Accepted Manuscript

Title: Synthetic biopolymer nanocomposites for tissue

engineering scaffolds

Author: Masami Okamoto Baiju John

PII: S0079-6700(13)00064-6
DOI: http://dx.doi.org/doi:10.1016/j.progpolymsci.2013.06.001
Reference: JPPS 801

To appear in: Progress in Polymer Science

Received date: 1-5-2012

Revised date: 6-5-2013
Accepted date: 13-5-2013

Please cite this article as: Okamoto M, John B, Synthetic biopolymer

nanocomposites for tissue engineering scaffolds, Progress in Polymer Science (2013),
http://dx.doi.org/10.1016/j.progpolymsci.2013.06.001

This is a PDF file of an unedited manuscript that has been accepted for publication.
As a service to our customers we are providing this early version of the manuscript.
The manuscript will undergo copyediting, typesetting, and review of the resulting proof
before it is published in its final form. Please note that during the production process
errors may be discovered which could affect the content, and all legal disclaimers that
apply to the journal pertain.
Synthetic biopolymer nanocomposites for tissue engineering scaffolds

Masami Okamoto*, Baiju John

Advanced Polymeric Nanostructured Materials Engineering, Graduate School of Engineering,

t
Toyota Technological Institute, 2-12-1 Hisakata, Tempaku, Nagoya 468-8511, Japan

ip
___________________________________________________

cr
* To whom correspondence should be addressed

E-mail: [email protected] (M. Okamoto), Fax: +81 052 809 1864

us
Abstract
an
With tissue engineering we can create biological substitutes to repair or replace failing organs
or tissues. Synthetic biopolymer-based nanocomposites are of interest for use in tissue
engineering scaffolds due to their biocompatibility and adjustable biodegradation kinetics.
M
The most often utilized synthetic biopolymers for three dimensional scaffolds in tissue
engineering are saturated poly(-hydroxy esters), including poly(lactic acid) (PLA),
ed

poly(glycolic acid) (PGA), poly(lactic acid-co-glycolic acid) (PLGA), and poly(-

caprolactone) (PCL). To enhance the mechanical properties and cellular adhesion and
pt

proliferation, the incorporation of nanoparticles (e.g., apatite component, carbon

nanostructures and metal nanoparticles) has been extensively investigated. At the same time,
ce

current research is focused on the interaction between stromal cells and biopolymer
interfaces. In this review, current research trends in nanocomposite materials for tissue
engineering, including strategies for fabrication of nanocomposite scaffolds with highly
Ac

porous and interconnected pores are presented. The results of the in-vitro cell culture analysis
of the cell-scaffold interaction using the colonization of mesenchymal stem cells (MSCs) and
degradation of the scaffolds in-vitro are also discussed.

Keywords: Biopolymer; Nanocomposites; Tissue engineering; Scaffolds; Mesenchymal stem

cell; Nanoparticles

1
Page 1 of 54
Abbreviations:
Ag silver
BMNC bone marrow mononuclear cell
BMSC bone marrow stromal cell
CNF carbon nanofiber
CNT carbon nanotube
CO2 carbon dioxide
ECM extracellular matrix

t
ip
EGFP enhanced green fluorescent protein
ES embryonic stem

cr
FDA US Food and Drug Administration
GF/PL carbon dioxide foaming and solid porogen leaching

us
g-HA surface-grafted-hydroxyapatite
HA hydroxyapatite
HEK human epidermal keratinocyte
hMSC
HRP
human mesenchymal stem cell
horseradish peroxidase
an
LA bare poly(L-lactic acid) microsphere
M
mHA micro-hydroxyapatite
MSC mesenchymal stem cell
MWNT multi-walled nanotube
ed

ND nanodiamond
ND-ODA octadecylamine-functioalized nanodiamond
nHA nano-sized hydroxyapatite
pt

NS nano-scaffold
nTiO2 TiO2 nanoparticles
ce

PBS poly(butylene succinate)

PBSPTDGS poly(butylene/thiodiethylene succinate) block copolymer
Ac

PCL poly(-caprolactone)
PDLLA racemic mixture of D,L- poly(lactic acid)
PGA poly(glycolic acid)
PHB poly(hydroxy butyrate)
PLA poly(lactic acid)
PLGA poly(lactic acid-co-glycolic acid)
PLLA poly(L-lactic acid)
PPF poly(prpylene fumarate)
PVA polyvinyl alcohol
RGD Arg-Gly-Asp

2
Page 2 of 54
SBF simulated body fluid
SEM scanning electron microscope
SWNT single-walled carbon nanotube
3D three dimensional
TIPS thermally-induced phase separation
WHO World Health Organization

t
ip
cr
us
an
M
ed
pt
ce
Ac

3
Page 3 of 54
Table of Contents

1 Introduction
2 Tissue engineering applications
3 Synthetic biopolymer and its nanocomposites for tissue engineering
3.1. Hydroxyapatite (HA)-base nanocomposites
3.2. Metal nanoparticles-base nanocomposites

t
3.3. Carbon-base nanocomposites

ip
4. Three dimensional porous scaffolds
4.1. Solvent casting and particulate leaching

cr
4.2. Thermally-induced phase separation
4.3. Electrospinning

us
5. In-vitro degradation
6. Stem cell-scaffolds interactions
7. Health implication of nanoparticles
8. Conclusions
an
Acknowledgment
M
References
ed
pt
ce
Ac

4
Page 4 of 54
1. Introduction

Since the industrial revolution and particularly after World War II, the breakthrough

in materials research has become increasingly more rapid, and has resulted in the wide use of

materials such as polymers, metals, semi-conductors, and agricultural chemicals (e.g.,

pesticides and fertilizers). The production of these materials in increasing quantities to meet

t
the demands of a growing population has led to the increased consumption of fossil fuel and

ip
the release of wastes, resulting in regional and global environmental problems ranging from

cr
air, water and soil pollution, to climate changes.

us
These problems in turn limit the amount and extent to which such materials can be

used, and call for a re-thinking of the design, synthesis, and production of materials in mass
an
use. In this regard, natural materials provide not only a baseline for a comparison of the

performance of man-made materials, but also a clue to the development of new materials that
M
are more environmentally sustainable, in addition to having a desirable functionality.

Hence, with this background, biopolymers are well-known examples for renewable
ed

source based, environmental benign polymeric materials [1]. These include polysaccharides,

such as cellulose, starch, alginate and chitin/chitosan, carbohydrate polymers produced by

pt

bacteria and fungi [2], and animal protein-based biopolymers such as wool, silk, gelatin and
ce

collagen. Naturally derived polymers offer interesting properties of biocompatibility and

biodegradability. One of the advantages of naturally derived polymers is the biological

Ac

recognition that may positively support cell adhesion and function, However, many have

poor mechanical properties, and are also limited in supply and can therefore be costly [3].

On the other hand, polyvinyl alcohol (PVA), poly(-caprolactone) (PCL), poly(lactic

acid) (PLA), poly(glycolic acid) (PGA), poly(hydroxy butyrate) (PHB) and poly(butylene

succinate) (PBS) are examples of synthetic biodegradable polymers; it [4]. In todays

commercial environment, synthetic biopolymers have proven to be relatively expensive and

available only in small quantities, with applications in the textile and medical industries, as

5
Page 5 of 54
well as the packaging industry. Although this has led to limited applications, they can be

produced in large-scale under controlled conditions and with predictable and reproducible

mechanical properties, degradation rate and microstructure [4, 5].

In this context, one of the most promising synthetic biopolymers is PLA because it is

made from agriculture products. Although PLA is not a new polymer, developments in the

t
capability to manufacture the monomer economically from agriculture products have placed

ip
this material at the forefront of the emerging biodegradable plastics industries.

cr
PLA, PGA and their copolymers, poly(lactic acid-co-glycolic acid) (PLGA) are

us
extensively used in tissue engineering for treating patients suffering from damaged or lost

organs or tissues [6, 7]. They have been demonstrated to be biocompatible, degrading into
an
non-toxic components, and have a long history as degradable surgical sutures with FDA (US

Food and Drug Administration) approval for clinical use. PCL and PHB are also used in
M
tissue engineering research.

The task of tissue engineering demands a combination of molecular biology and

ed

materials engineering, since in many applications a scaffold is needed to provide a temporary

artificial matrix for cell seeding. In general, scaffolds must exhibit high porosity, proper pore
pt

size, biocompatibility, biodegradability and proper degradation rate [8]. The scaffold must
ce

provide sufficient mechanical support to maintain stresses and loadings generated during in-

vitro or in-vivo regeneration.

Ac

For some of aforementioned applications, enhancement of the mechanical properties

is often needed [9]. This can be achieved by the incorporation of nanoparticles, such as

hydroxyapatite (HA) carbon nanotubes and layered silicates. Polymer/layered silicate

nanocomposites have become the focus of academic and industrial attention [10]. Introduction

of small quantities of high aspect ratio nano-sized silicate particles can significantly improve

mechanical and physical properties of the polymer matrix [11]. However, the pore structure,

the porosity, the crystallinity and the degradation rate may alter the mechanical properties

6
Page 6 of 54
and, thus, the efficiency of a scaffold. As a consequence, the scaffold fabrication method

should allow for the control of its pore size and shape and should enhance the maintenance of

its mechanical properties and biocompatibility [6, 8].

During the past year, many techniques have been applied for making porous

scaffolds. Among the most popular are particulate leaching [12], temperature-induced phase

t
separation [13], phase inversion in the presence of a liquid non-solvent [14], emulsion freeze-

ip
drying [15], electrospining [16], and rapid prototyping [6]. On the other hand, foaming of

cr
polymers using supercritical fluids is a versatile method in obtaining porous structure [8, 17].

us
This review highlights the synthetic biopolymer-based nanocomposites with the aim

of producing porous scaffolds in tissue engineering applications during the last decade. In
an
addition, current research trends on nanocomposite materials for tissue engineering are also

reviewed, including strategies for fabrication of nanocomposite scaffolds with highly porous
M
and interconnected pores. The results of the in-vitro cell culture analysis of the cell-scaffold

interaction using the colonization of mesenchymal stem cells (MSCs), and in-vitro
ed

degradation of the scaffolds are also discussed.

pt

2. Tissue engineering applications

ce

Tissue engineering applies methods from materials engineering and life science to

create artificial constructs for regeneration of new tissue [6, 7]. Tissue engineering facilitates
Ac

the creation of biological substitutes to repair or replace the failing organs or tissues. One of

the most promising approaches towards this direction is to grow cells on scaffolds that act as

temporary support for cells during the regeneration of the target tissues, without losing the

three dimensional (3D) stable structure.

Polymeric scaffolds play a pivotal role in tissue engineering through cell seeding,

proliferation, and new tissue formation in three dimensions, showing great promise in the

research of engineering a variety of tissues. Pore size, porosity, and surface area are widely

7
Page 7 of 54
recognized as important parameters for a tissue engineering scaffold. Other architectural

features such as pore shape, pore wall morphology, and interconnectivity between pores of

the scaffolding materials are also suggested to be important for cell seeding, migration,

growth, mass transport and tissue formation [6].

Scaffolds made from collagen are being rapidly replaced with ultraporous scaffolds

t
from biodegradable polymers. Biodegradable polymers are attractive candidates for

ip
scaffolding materials because they degrade as the new tissues are formed, eventually leaving

cr
nothing foreign to the body. The major challenges in scaffold manufacture lies in the design

us
and fabrication of customizable biodegradable constructs with properties that promote cell

adhesion and cell porosity, along with sufficient mechanical properties that match the host
an
tissue, with predictable degradation rate and biocompatibility [6, 7, 18].

The biocompatibility of the materials is imperative. That is, the substrate materials
M
must not elicit an inflammatory response nor demonstrate immunogenicity of cytotoxicity.

The scaffolds must be easily sterilizable in both the surface and the bulk to prevent infection
ed

[19]. For scaffolds particularly in bone tissue engineering, a typical porosity of 90% with a

pore diameter of about 100 m is required for cell penetration and a proper vascularization of
pt

the ingrown tissue [20].

ce

Bioactive ceramics such as HA and calcium phosphates are another major class of

biomaterials for bone repair is [21, 22]. They showed appropriate osteoconductivity and
Ac

biocompatibility because of chemical and structural similarity with the mineral phase to

native bone. However, their inherent brittleness and the difficulty to shape them are

disadvantages. For this reason, polymer/bioactive ceramic composite scaffolds have been

developed in applications for the bone tissue engineering. They exhibit good bioactivity,

manipulation and control microstructure in shaping to fit bone defects [23].

3. Synthetic biopolymer and its nanocomposites for tissue engineering

8
Page 8 of 54
 The extensive literature on nanocomposite research (e.g., polymer/layered silicate)

is covered in reviews [10, 24-26]. The study on nanocomposites has gained greater

momentum. This new class of materials is now being introduced in structural applications,

such as gas barrier film, flame retardant product, and other load-bearing applications [27].

Among these nanocomposites, biopolymer-based nancomposites are considered to be a

t
stepping stone towards a greener and sustainable environment. Biopolymer-based

ip
nanocomposites are described in detailed studies and reviews elsewhere [28-30].

cr
The most often utilized synthetic biopolymers for 3D scaffolds in tissue

us
engineering are saturated poly(-hydroxy esters) including PLA, racemic mixture of D,L-

PLA (PDLLA) and PGA, as well as PLGA [31-33]. These polymers degrade through
an
hydrolysis of the ester bonds. Once degraded, the monomeric components are removed by

natural pathways. The body contains highly regulated mechanisms for completely removing
M
monomeric components of lactic and glycolic acids. PGA is converted to metabolites or

eliminated by other mechanisms. On the other hand, PLA is cleared via the tricarboxylic
ed

acid cycle. Due to these properties PLA and PGA have been used in products and devices,

including degradable sutures, approved by the US FDA. The cost of PLA for medical use is
pt

about 3 $/g, which is three order of magnitude higher than conventional injection moldable
ce

PLA (3 $/kg) [34]. PLA and PGA may be processed easily, and their degradation rates,

physical and mechanical properties are adjustable over a wide range by using various
Ac

molecular weights and copolymer composition. These polymers undergo a bulk erosion

process such that can cause scaffolds to fail prematurely. The abrupt release of their acidic

degradation products can cause a strong inflammatory response [35]. Table 1 shows an

overview of the discussed biopolymers and their physical properties. Their degradation

rates decreases in the following order:

PGA > PDLLA > PLLA > PCL ~ PPF

9
Page 9 of 54
 Table 1

PGA degrades rapidly in aqueos solution or in-vivo, and loses mechanical integrity

between two and four weeks. The extra methy group in the PLA repeating unit makes it

more hydrophobic, reduces the molecular affinity to water, and leads to a slower

t
degradation. Therefore, the scaffolds made from PLA degrade slowly both in-vitro and in-

ip
vivo, maintaining mechanical properties over several months [45].

cr
PCL degrades at a significantly slower rate than PLA, PGA, and PLGA. The slow

us
degradation makes PCL less attractive for biomedical applications, but more attractive for

long-term implants and controlled release application [6, 36]. PCL has been used as a
an
candidate polymer for bone tissue engineering, where scaffolds should maintain physical

and mechanical properties for at least 6 months [37].

M
Poly(propylene fumarate) (PPF), an unsaturated linear polyester, has been developed

for orthopedic and dental applications [38]. Its degradation products are biocompatible and
ed

readily removed from the body. The double bond of PPF main chains leads to in situ cross-

linking, which causes results in a moldable composite. The preservation of the double bond
pt

and molecular weight are key characteristics to control the final mechanical properties and
ce

degradation time.

However, PPF and other biodegradable polymers lack the mechanical strength
Ac

required for tissue engineering of load-bearing bones [39]. The development of composite and

nanocomposite materials utilizing inorganic particles, e.g., apatite components (i.e., the main

constituent of the inorganic phase of bone [6]), bioactive glasses, carbon nanostructures (e.g.,

nanotubes, nanofibers, and graphene), and metal nanoparticles has been investigated.

3.1. Hydroxyapatite (HA)-base nanocomposites

HA promotes bone ingrowth and biocompatible because around 65 wt% of bone is

10
Page 10 of 54
made of HA, Ca10(PO4)6(OH)2. Natural or synthetic HA has been intensively investigated as

the major component of scaffold materials for bone tissue engineering [40]. The Ca/P ratio of

1.50-1.67 is the key issue to promote bone regeneration. Much better osteoconductive

properties have been reported in HA by changing composition, size and morphology [41].

The nano-sized HA (nHA) may have other special properties due to its small size and huge

t
specific surface area. A significant increase in protein adsorption and osteoblast adhesion on

ip
the nano-sized ceramic materials was reported by Webster et al. [42].

cr
Figure 1 shows the rod shaped morphology of the nHA with particle width ranging

us
from 37-65 nm and length from 100 to 400 nm [43]. The compressive strength of bioceramics

increases when their grain size reduced to nanolevels [44].

an
Figure 1
M
Nanocomposites based on HA particles and biopolymers have attracted attention for
ed

their good osteoconductivity, osteoinductivity, biodegradability and high mechanical

strengths. The Ma group mimicked the size scale of HA in natural bone and showed the
pt

incorporation of nHA improved the mechanical properties and protein adsorption of the
ce

composite scaffolds, while maintaining high porosity and suitable microarchitecture [44].

Nejati et al. [43] reported that the effect of the synthesis nHA on the scaffolds
Ac

morphology and mechanical properties in poly(L-lactic acid) (PLLA)-based nanocomposites.

The morphology and microstructure of the scaffolds were examined using scanning electron

microscope (SEM) (Figure 2). The nanocomposite scaffold (Fig. 2c and d) maintain a regular

internal ladder-like pore structure, similar to neat PLLA scaffold (Fig. 2a and b) with a typical

morphology processed by thermally-induced phase separation [13]. Rod-like nHA particles

are distributed within the pore walls, n with no aggregation in the pores (Fig. 2e and f).

However, the nanocomposite exhibits little effect of nHA on the development of the pore

11
Page 11 of 54
morphology as compared with that of neat PLLA. Pore size of neat PLLA and nanocomposite

scaffolds are in the range of 175-97 m, respectively. In the case of microcomposite scaffold

(Fig. 2g and h), micro-HA (mHA) particles are randomly distributed in PLLA matrix. Some

are embedded in the pore wall and some are piled together between or within the pores.

Among composite and neat PLLA scaffolds, nanocomposites scaffolds showed the highest

t
compressive strength (8.67 MPa) with 85.1 % porosity, comparable to the high end of

ip
compressive strength of cancellous bone (2-10 MPa) [46].

cr
us
Figure 2

an
PCL/nHA nanocomposites were prepared and they combine the osteoconductivity

and biocompatibility shown by HA ceramic with PCL properties [45, 47-49]. The structural
M
characterization of a novel electrospun nanocomposite and the analysis of cell response by a

highly sensitive cell, embryonic stem cell for PCL/Ca-deficient nHA system have been
ed

investigated [47]. For higher Ca-deficient nHA contents (~ 55 wt%), the mechanical

properties significantly decreased, and the onset decomposition temperature and crystallinity
pt

considerably decreased.
ce

Due to the brittleness of HA and lack of interaction with polymer matrix, the ceramic

nanoparticles may present deleterious effects on the mechanical properties, when loaded at
Ac

high levels. Coupling agents are generally used to overcome both the lack of interaction with

polymer and nHA aggregation [49-51]. In order to increase the interfacial strength between

PLLA and HA, and hence increase the mechanical properties, the nHA particles were surface-

grafted (g-HA) with the polymer and further blended with PLLA [50]. The PLLA/g-HA

nanocomposites also demonstrated improved cell compatibility due to the favorable

biocompatibility of the nHA particles and more uniform distribution of the g-HA

nanoparticles on the film surface [50, 51]. These nanocomposites are of interest to the

12
Page 12 of 54
biomedical community because the materials have a structure that induces and promotes new

bone formation at the required site.

Calcium phosphate biomaterials certainly posses osteoconductive properties and may

bind directly to bone under certain conditions [43]. Calcium phosphate materials are suitable

for the calcified tissue generation.

t
ip
3.2. Metal nanoparticles-base nanocomposites

cr
Currently, metal nanoparticle-based nanocomposites are used in various biomedical

us
applications, such as probes for electron microscopy to visualize cellular structure, drug

delivery, diagnosis and therapy. The unique physical characteristics of gold nanoparticle-
an
based nanocomposites are used in the optical and photonic fields [52], not medical

applications.
M
Silver (Ag) is known to have a disinfecting effect, and has found applications in

traditional medicines. Ag nanoparticles have aptly been investigated for their antibacterial
ed

property [53]. Biopolymer-embedded Ag nanoparticles have been investigated [54]. The

nano-sized Ag permits a controlled antibacterial effect due to the high surface area. For
pt

PLLA-based nanocomposite fibers including Ag nanoparticles, a antibacterial effect longer

ce

than 20 days was shown [55]. PLGA-based nanocomposites have also been [56, 57]. The

metal nanoparticles induce a thermal conductivity in the nanocomposites that enhances the
Ac

degradation rate [55]. Furthermore, the Ag nanoparticles change the surface wettability and

roughness of the nanocomposites. For these reasons it is very difficult to control the bacterial

adhesion process.

Of particular interest, it is important to note that Ag nanoparticles are recognized and

listed under carcinogenic materials by the World Health Organization (WHO). These

hazardous signs require immediate and thorough action not only from the environment and

human health view-points, but also from the perspective of socio-economic benefits [58].

13
Page 13 of 54
3.3. Carbon-base nanocomposites

Carbon nanostructures in polymer matrix have been extensively investigated for

biomedical applications [59]. Carbon nanotubes (CNTs) have potential for use in biomedical

scaffolds. Honeycomb-like matrices of multi-walled nanotube (MWNT) have been fabricated

t
as potential scaffolds for tissue engineering [60]. Mouse fibroblast cells were cultured on the

ip
nanotube networks, prepared by treatment with an acid solution that generates carboxylic acid

cr
groups at the defect of the nanotubes. The carbon networks can be used as a biocompotible

us
mesh for restoring or reinforcing damaged tissues because of no cytotoxicity of the networks.

The electrical conductivity of the nanocomposites including carbon nanostructures is a useful

an
tool to direct cell growth because they can conduct an electrical stimulus in the tissue healing

process. An osteoblast proliferation on PLLA/MWNT nanocomposites under an alternating

M
current stimulation was investigated [61]. The results showed an increase in osteoblast

proliferation and extra-cellular calcium deposition on the nanocomposites as compared with

ed

the control samples. Unfortunately, no comparison was made with a currently used orthopedic

reference material under electrical stimulation.

pt

Mikos et al. [62] investigated in vitro cytotoxicity of single-walled CNT

ce

(SWNT)/PPF nanocomposites. The results did not reveal any in vitro cytotoxicity for

PPF/SWNT fucctionalized with 4-tert-butylphenylene nanocomposites. Moreover, nearly

Ac

100% cell viability was observed on the nanocomposites and cell attachment on their surfaces

was comparable with that on tissue culture polystyrene. The nature of the functional group at

the CNT surface seems to play an important role to improve the dispersion of CNTs in

polymer matrix and in the mechanism of interaction with cells. The sidewall carboxylic

functionalized SWNTs exhibited an nucleation surface to induce the formation of a

biomimetic apatite coating [63].

Nanodiamonds (NDs) synthesized by detonation are one of the most promising

14
Page 14 of 54
materials for use in multifunctional nanocomposites for various applications, including

biomedical [64-66]. To Fully benefit from the advantages of NDs as nanofillers for

biopolymeric bone scaffolds, they need to be dispersed into single particles. The quality of the

filler dispersion in the matrix is important, because it determines the surface area of the

nanoparticles available for interaction with the matrix. When adequately dispersed, NDs

t
increase the strength, toughness, and thermal stability of the nanocomposites [67]. The

ip
purified NDs are composed of particles with 5 nm average diameter. They contain an inert

cr
diamond core and are decorated by functional groups such as COOH, OH, NH2, etc. [64].

us
Zhou et al. [68] prepared multifunctional bone scaffold materials composed of PLLA

and octadecylamine-functioalized ND (ND-ODA) via solution casting, followed by

an
compression molding. Addition of 10 wt% of ND-ODA resulted in a 280 % increase in the

strain to failure and a 310 % increase in fracture energy as compared to neat PLLA. Both of
M
these parameters are crucial for bone tissue engineering and for manufacturing of orthopedic

surgical fixation devices. The biomineralization of the nanocomposite scaffolds was tested in
ed

simulated body fluid (SBF) [69]. The apatite nucleation and growth occurred faster on the

nanocomposites than on neat PLLA (Figure 3) [68]. The increased mechanical properties and
pt

enhanced biomineralization make PLLA/ND-ODA nanocomposites a promising materials for

ce

bone surgical fixation devices and regenerative medicine.

Ac

Figure 3

Despite the evidence of research into potential biomedical applications of carbon-

based nanocomposites, there have been many published studies on the cytotoxicity of the

carbon nanostructures [70]. Some research groups detected high toxicity in both cells [71-78]

and animals [79-81], and explained mechanisms to cell damage at molecular and gene

expression levels [82].

15
Page 15 of 54
 Exposure to SWNT resulted in accelerated oxidative stress (increased free

radical and peroxide generation and depletion of total antioxidant reserves), loss in cell

viability and morphological alterations to cellular structure. It was concluded that these

effects were the results of high levels of iron catalyst present in the unrefined SWNT. As a

result, possible dermal toxicity in handling unrefined CNT was warned. Similar dermal

t
toxicity warnings were echoed in 2005, in a study which found that MWNT initiated an

ip
irritation response in human epidermal keratinocyte (HEK) cells [74]. Purified MWNT

cr
incubated (at doses of 0.1-0.4 mg/mL) with HEK cells for up to 48 h were observed to

us
localize within cells (Figure 4), eliciting the production of the pro-inflammatory cytokine

release and decreasing cell viability in a time- and dose-dependent manner.

an
Figure 4
M
These controversial results reported by different researchers reflect the complex
ed

material properties of CNTs such as SWNTs or MWNTs. In addition, different synthesis

methods may produce CNTs with different diameters, lengths and impurities. The results urge
pt

caution when handling CNTs and the introduction of safety measures in laboratories should
ce

be seriously considered. Most importantly, the success of CNT technology is dependent upon

the continuation of research into the toxicology of CNT and CNT-based nanocomposites. At
Ac

the same time, the pharmacological development must continue in parallel before providing

the guidelines for the safe use in biomedical applications.

4. Three dimensional (3D) porous scaffolds

Development of composite scaffolds is attractive as advantageous properties of two

or more types of materials can be combined to better suit the mechanical and physiological

demands of the host tissue. The tissues in the body are organized into 3D structure as a

16
Page 16 of 54
function of organs. The scaffolds with designed microstructures provide structural support

and adequate mass transport to guide the tissue regeneration . To achieve the goal of tissue

regeneration, scaffolds must meet some specific needs. A high porosity and an adequate pore

size are necessary to facilitate cell seeding and diffusion throughout the whole structure of

both cells and nutrients [48].

t
Nanocomposites 3D scaffolds based on biopolymers have been developed by using

ip
different processing methods. Most popular techniques include solvent casting and porogen

cr
(particulate) leaching, gas foaming, emulsion freeze-drying, electrospinning, rapid

us
prototyping, and thermally-induced phase separation [6, 12-17, 43, 48, 83].

4.1. Solvent casting and particulate leaching

an
Organic solvent casting particulate leaching is a very easy process that has been
M
widely used to fabricate biocomposite scaffolds [84]. This process involves the dissolution of

the polymer in an organic solvent, mixing with nanofillers and porogen particles, and casting
ed

the mixture into a predefined 3D mold. The solvent is subsequently allowed to evaporate, and

the porogen particles are removed by leaching [85]. However, residual solvents in the
pt

scaffolds may be harmful to transplanted cells or host tissues. To avoid toxicity effects of the
ce

organic solvent, gas foaming can be used to prepare a highly porous biopolymer foam [28].

Kim et al. [86] fabricated PLGA/nHA scaffolds by carbon dioxide (CO2) foaming and solid
Ac

porogen (i.e., sodium chloride crystals) leaching (GF/PL) without the use of organic solvents.

Selective staining of nHA particles indicated that nHA exposed to the scaffold surface were

observed more abundantly in the GF/PL scaffold than in the conventional solvent casting and

particulate leaching scaffold. The GF/PL scaffolds exhibited significant enhanced bone

regeneration when compared with conventional scaffolds.

In our previous paper [87], highly porous crosslinked PLA scaffolds were

successfully prepared through particulate leaching and foaming followed by leaching

17
Page 17 of 54
methods. The scaffolds were porous with good inter-connectivity and thermal stability. The

SEM images confirmed the pore connectivity and structural stability of the crosslinked PLA

scaffold (Figure 5).

Figure 5

t
ip
The Lait-X/b and Lait-X/c scaffolds have the same percentage of salt particulate with

cr
similar particle size; the former was turned into a scaffold through simple leaching, while the

us
latter was through batch foaming followed by leaching. The qualitative evaluation of the SEM

images of Lait-X/b and Lait-X/c showed a well-developed porosity and interconnectivity with
an
pore sizes spanning over a very wide range, from a few microns to hundreds of microns.

Figure 6 shows the relation between the pore size diameter and the cumulative and
M
differential intrusions of mercury in Lait-X/b and Lait-X/c scaffolds. The maximum intrusion

and interconnectivities of Lait-X/b was from 0.1 to 1 m pore diameter regions and Lait-X/c
ed

it was from 0.1 to 10 m. The porosity, total intrusion volume, total pore area and median

pore diameter (volume) of Lait-X/b calculated by mercury porosimetry were 43%, 0.511
pt

mL/g, 13.4 m2/g and 0.520 m whereas for Lait-X/c it was 49%, 0.688 mL/g, 27.6 m2/g and
ce

1.26 m respectively. The shift in the values of Lait-X/b and Lait-X/c was due to the effect of

batch foaming which lead to the movement of salt particulate during foaming, resulting in
Ac

increased porosity and total intrusion volume. The in-vitro cell culture demonstrated the

ability of the scaffold to support human mesenchymal stem cells (hMSCs) adhesion

confirming the biocompatibility through the cellscaffold interaction. The in-vitro

degradation of the PLA thermoset scaffolds in phosphate buffered solution was faster with

those prepared by foaming and subsequent leaching [87]. The agglomeration of the

smallercrystal (solid porogen) within 3D polymer matrix enables creation of an

interconnected pore network with well-defined pore sizes and shapes.

18
Page 18 of 54
 Figure 6

4.2. Thermally-induced phase separation (TIPS)

t
3D resorbable polymer scaffolds with very high porosities (~ 97 %) can be produced

ip
using the TIPS technique to give controlled microstructures as scaffolds for tissues, such as

cr
nerve, muscle, tendon, intestine, bone, and teeth [88]. The scaffolds are highly porous with

us
anisotropic tubular morphology and extensive pore interconnectivity. Microporosity of TIPS

produced foams, their pore morphology, mechanical properties, bioactivity and degradation
an
rates can be controlled by varing the polymer concentration in solution, volume fraction of

secondary phase, quenching temperature and the polymer and solvent used [88].
M
When dioxane was used alone, the porous structure resulted from a solid-liquid phase

separation of the polymer solution. During quenching, the solvent crystallized and the
ed

polymer was expelled from the solvent crystallization front. Solvent crystals became pores

after subsequent sublimation. To better mimic the mineral component and the microstructure
pt

of natural bone, novel nHA nanocomposite scaffolds with high porosity and well-controlled
ce

pore architectures were prepared using the TIPS techniques (Fig. 2 [43]). The incorporation of

nHA particles into PLLA solution perturbed the solvent crystallization to some extent and
Ac

thereby made the pore structure more irregular and isotropic. The perturbation by nHA

particles, however, was small even in high proportion up to 50% due to their nanometer size

scale and uniform distribution. The SEM images showed that the nHA particles were

dispersed in the pore walls of the scaffolds and bound to the polymer very well. PLLA/nHA

scaffolds prepared using pure solvent system had a regular anisotropic, but open 3D pore

structure similar to neat polymer scaffolds, whereas PLLA/mHA scaffolds had an isotropic

and a random irregular pore structure.

19
Page 19 of 54
 TiO2 nanoparticles (nTiO2) have been proposed as attractive fillers for

biodegradable PDLLA matrix [89]. 3D PDLLA foams containing both nTiO2 and Bioglass

additions have been synthesized by TIPS. The foams demonstrated the enhancement of the

bioactivity and the surface nanotopography.

t
ip
4.3. Electrospinning

Electrospinning technique has attracted great interest since it facilitates the

cr
production of fibrous non-woven micro/nano fabrics for tissue engineering, mainly due to the

us
structural similarity to the tissue extracellular matrix (ECM) [47, 90]. The composition and

topology of the ECM has been found to affect cell morphology, function, and physiological
an
response [91]. The electrospun nanofibrous scaffolds aimed to mimic the architecture and

biological functions of ECM, are considered as very promising substrates for tissue
M
engineering. PCL scaffolds, a bioresorbable aliphatic polyester, have been used to provide a

3D environment for in vitro embryonic stem cell culture and differentiation. Electrospun
ed

nanocomposite scaffolds based on bioresorbable polymers and conventional HA allow

osteoblast proliferation and differentiation, and are thus considered very promising as bone
pt

scaffolding materials [47].

ce

Fibrous PCL/Ca-deficient nHA nanocomposites have been obtained by

electrospinning. The electrospun mats showed a non-woven architecture, average fiber size
Ac

was 1.5 m, porosity 8090%, and specific surface area 16 m2/g (Figure 7). Murine

embryonic stem (ES) cell response to neat PCL and to PCL/Ca-deficient nHA (6.4 wt.%)

mats was evaluated by analyzing morphological, metabolic and functional markers. Cells

growing on either scaffold proliferated and maintained pluripotency markers at essentially the

same rate as cells growing on standard tissue culture plates, with no detectable signs of

cytotoxicity, despite a lower cell adhesion at the beginning of culture. These results indicate

that electrospun PCL scaffolds may provide adequate supports for murine ES cell

20
Page 20 of 54
proliferation in a pluripotent state, and that the presence of Ca-deficient nHA within the mat

does not interfere with their growth.

Figure 7

t
Aligned nanocomposite fibers of PLGA/nHA were fabricated by using a rotating

ip
collector by electrospinning. At low concentrations the fibers had no agglomerates and good

cr
dispersion was achieved [92]. The presence of well-dispersed nHA particles reduced the chain

us
mobility and hence helped to prevent shrinkage to some degree. The glass transition was

affected by the incorporation of nHA into the polymer matrix which hinders chain mobility.
an
Interestingly, the electrospinning technique provides the opportunity to align

conductive nanoparticles with high aspect ratio within the polymeric fibers. Carbo nanofibers
M
(CNFs) can orientate along the axis of electrospun fibers due to the sink flow and the high

extension of the electrospun jet [93]. The CNF alignment depends upon the CNF dispersion in
ed

the polymer solution. The idea of dispersing and aligning carbon nanostructures in polymer

matrix to form highly ordered structures. The mechanical properties of PCL/CNF mats
pt

however, were only slightly affected by CNF introduction [94].

ce

Ternary nanocomposite scaffolds involving three different materials have been

developed [95, 96]. The addition of MWNTs to the biopolymer creates new highly conductive
Ac

material due to the 3D electrical conducting network. The results exhibited that combining

two different nanostructures (e.g., MWNT/nHA or MWNT/ Bioglass) led to multifunctional

biomaterials with tailored bioactivity, structural and mechanical integrity as well as electrical

conductivity of the porous scaffolds.

5. In-vitro degradation

21
Page 21 of 54
 Since tissue engineering aims at the regeneration of new tissues, biomaterials are

expected to be degradable and absorbable with a proper rate to match the speed of new tissue

formation. The degradation behavior has a crucial impact on the long-term performance of a

tissue-engineered cell/polymer construct. The degradation kinetics may affect a range of

processes, such as cell growth, tissue regeneration, and host response. The mechanism of

t
aliphatic polyester biodegradation is the bio-erosion of the material mainly determined by the

ip
surface hydrolysis of the polymer. The scaffolds can lead to heterogeneous degradation, with

cr
the neutralization of carboxylic end groups located at the surface by the external buffer

us
solution (in-vitro or in-vivo). These phenomena contribute to reduce the acidity at the surface

whereas, in the bulk, degradation rate is enhanced by autocatalysis due to carboxylic end
an
groups of aliphatic polyesters. In general, the amount of absorbed water depends on diffusion

coefficients of chain fragment within the polymer matrix, temperature, buffering capacity,
M
pH, ionic strength, additions in the matrix, in the medium and processing history. Different

polyesters can exhibit quite distinct degradation kinetics in aqueous solutions. For example,
ed

PGA is a stronger acid and is more hydrophilic than PLA, which is hydrophobic due to its

methyl groups.
pt

Of particular significance for application in tissue engineering are debris and

ce

crystalline by-products, as well as particularly acidic degradation products of PLA, PGA,

PCL and their copolymers [97]. Several groups have incorporated basic compounds to
Ac

stabilize the pH of the environment surrounding the polymer and to control its degradation.

Bioglass and calcium phosphates have been introduced [98]. Naocomposites showed a

strongly enhanced polymer degradation rate when compared to the neat polymer [99]. As

mentioned. in PLLA/ND nanocomposites (Fig. 3), improvement of osteoconductivity of

PLLA nanocomposites, i.e., the deposition of the HA crystal on the surfac was observed. Fast

degradation and the superior bioactivity make these nanocomposites a promising material for

orthopaedic medicine application [99].

22
Page 22 of 54
 In contrast, the degradation rates of the biopolyester elastomer/MWNT

nanocomposites tended to decrease with the increase of MWNT loadings (above 1 wt%) in

SBF solution [100]. Continued investigation of the degradation behavior of biopolymer-based

nanocomposites is required for the nanostructures incorporated into matrices.

Allen et al. [101] reported the biodegradation of SWNTs through natural, enzymatic

t
catalysis. By incubating SWNTs with a natural horseradish peroxidase (HRP) and low

ip
concentration of H2O2 (~ 40 M), the degradation of SWNTs proceeded at 4 C over 12

cr
weeks under static conditions. It is tempting to speculate that other peroxidases in plants and

us
animals may be effective in oxidative degradation of CNTs. More studies are necessary to

ascertain the byproducts of the biodegradation, as well as cellular studies for practical

applications.
an
M
6. Stem cell-scaffolds interactions

Synthetic biopolymers are widely used for the preparation of porous scaffolds by
ed

different techniques set up for the purpose. The main limitation to the use of PLA-based

systems is their low hydrophilicity that causes a low affinity for the cells as compared with
pt

the biological polymers. Therefore the addition of biological components to a synthetic

ce

biopolymer represents an interesting way to produce a bioactive scaffold that can be

considered as a system showing at the same time adequate mechanical stability and high cell
Ac

affinity [102-104]. A variety of ECM protein components such as gelatin, collagen, laminin,

and fibronectin could be immobilized onto the plasma treated surface of the synthetic

biopolymer to enhance cellular adhesion and proliferation. Arg-Gly-Asp (RGD) is the most

effective and often employed peptide sequence for stimulating cell adhesion on synthetic

polymer surfaces. This peptide sequence is present in many ECM proteins and can interact

with the integrin receptors at the focal adhesion points. Once the RGD sequence is recognized

by and binds to integrins, it will initiate an integrin-mediated cell adhesion process and active

23
Page 23 of 54
signal transduction between the cell and ECM [105, 106]. Hollister et al. [106] reported a

simple method to immobilize RGD peptide on PCL 3D scaffold surfaces. They demonstrated

that rat bone marrow stromal cell (BMSC) adhesion was significantly improved on the RGD-

modified PCL scaffolds in a serum-free culture condition.

Surface treatment techniques, such as plasma treatment, ion sputtering, oxidation and

t
corona discharge, affect the chemical and physical properties of the surface layer without

ip
changing the bulk material properties. The effect of the oxygen plasma treatments on the

cr
surface of the materials have been shown to charge wettability, roughness and to enable the

us
selective interaction between PLLA surface and the protein, further improved stem cell

attachment [107].
an
Bone marrow derived hMSCs are an important cell source for cell therapy and tissue

engineering applications. The interactions between stem cell and their environment are very
M
complex and not fully clarified. Previous work showed that cells respond to the mechanical

properties of the scaffolds on which they are growing [108]. Rohman et al. [109] reported that
ed

PLGA and PCL are biocompatible for the growth of normal human urothelial and human

bladder smooth muscle cells. Their analysis of the potential mechanism has indicated that
pt

differences in degradation behaviors between polymers are not significant, but that the elastic
ce

modulus is a critical parameter, relevant to biology at the microscopic (cellular) level and may

also have impact at macroscopic (tissue/organ) scales. They concluded that the elastic
Ac

modulus is a property that should be considered in the development and optimization of

synthetic biopolymers for tissue engineering.

MSCs provided striking evidence that ECM elasticity influences differentiation.

Indeed, multipotent cells are able to start a transdifferentiation process towards very soft

tissues, such as nerve tissues, when the elastic modulus (E) of the substrate is about 0.5 kPa.

Intermediate stiffness (~ 10 kPa) addresses cells toward a muscle phenotype and higher E (

30 kPa) to cartilage/bone [110]. This should br relevant to the intelligent design of new

24
Page 24 of 54
biopolymer intended for specific applications [111]. Biopolymers presently used in tissue

engineering are extremely stiff. PLA has a bulk elasticity of E ~ 1 GPa, that is ten-thousand

times stiffer than most soft tissues. Thus engineering of soft tissue replacements needs to

explore biopolymers softer than those presently available.

Poly(butylene/thiodiethylene succinate) block copolymers (PBSPTDGS) were

t
prepared by reactive blending of the parent homopolymers (PBS and PTDGS) in the presence

ip
of Ti(OBu)4 [112]. The random copolymer, characterized by the lowest crystallinity degree,

cr
exhibits the lowest elastic modulus and the highest deformation at break. When evaluated for

us
indirect citotoxicity, films of block PBSPTDGS30 and random PBSPTDGS240 copolymers

appeared entirely biocompatible. In addition, cellular adhesion and proliferation of H9c2 cells
an
[113] (derived from embryonic rat heat) seeded and grown up to 14 days in culture over the

same films demonstrate that these new materials might be of interest for tissue engineering
M
applications.

The biocompatibility of neat PLLA, PLLA/nHA and PLLA/mHA composite

ed

scaffolds were evaluated in vitro by observing the behavior of the stained MSCs cultured in

close contact with the scaffolds [43]. Cell growth in material-free organ culture can be
pt

distinguished into four stages: Cells adhered on the surface of the composite in a round shape
ce

during the initial two days. Then the round cell attached, spread, and proliferated into the

inner pores of the scaffold, exhibiting morphologies ranging from spindle shaped to
Ac

polygonal. After one week, the cells reached confluence on the material while the material-

free group did not reach this status (Figure 8). The representative cell culture micrographs of

cell attachment into the scaffolds after seven days are observed. It is seen that round shaped

cells attached and proliferated to the scaffolds surface, became spindle like and migrated

through the pores (Fig. 8a-c). The number of round shaped cells is noticeable on the surface

of pure PLLA scaffold (Fig. 8a) while proliferated cells on the micro and nanocomposite

25
Page 25 of 54
scaffolds exhibit spindle shaped morphology (Fig. 8b, c). The PLLA/HA scaffolds appeared

to be in vitro biocompatible and noncytotoxic to cells.

Figure 8

t
Clinical trials demonstrate the effectiveness of cell-based therapeutic angiogenesis in

ip
patients with severe ischemic diseases, however, their success remains limited. Maintaining

cr
transplanted cells in place are expected to augment the cell-based therapeutic angiogenesis.

us
In 2012, nHA-coated PLLA microspheres, named nano-scaffold (NS), were, for the first time,

generated as a non-biological, biodegradable and injectable cell scaffold [114]. Fukumoto et

an
al. investigated the effectiveness of NS on cell-based therapeutic angiogenesis. NS are

microspheres approximately 100 nm in diameter (Figure 9A-a), the surfaces of which are
M
coated with a monolayer of nHA particles with 50 nm in diameter (Fig. 9A-b, -c, -d). To

assess the cell adhesiveness of NS, SEM was performed after incubation of NS and bare
ed

PLLA microspheres (LA) as controls with murine bone marrow mononuclear cells (BMNCs)

at 37 C for 8 h in-vitro. The number of cells adhering to NS was much greater than that to
pt

LA (Fig. 9B-a and b). High-magnification SEM images showed active cell adhesion to NS
ce

(Fig. 9B-c).
Ac

Figure 9

BMNCs from enhanced green fluorescent protein (EGFP)-transgenic mice and

rhodamine B-containing PLLA microspheres (orange) as a scaffold core or control

microspheres were implanted into the ischemic hind limbs of eight-week-old male

(C57BL/6NCrSlc) mice to determine the co=localization of implanted cells with injected

microspheres (Figure 10A). Few implanted BMNCs were observed around LA (Fig. 10A-a),

26
Page 26 of 54
while markedly larger numbers of cells were seen with NS (Fig. 10A-b) in ischemic thigh

tissue 7 days after transplantation. Intramuscular levels of GFP derived from transplanted

BMNCs were consistently and significantly higher in the group injected with NS than that

injected with LA or BMNCs alone at 3, 7 and 14 days after implantation, while GFP levels

were not significantly different between BMNCs alone and LA+BMNCs groups (Fig. 10B).

t
ip
Figure 10

cr
us
Kaplan-Meier analysis demonstrated that NS+BMNC markedly prevented hindlimb

necrosis. NS+BMNC revealed much higher induction of angiogenesis in ischemic tissues and
an
collateral blood flow confirmed by 3D computed tomography angiography than those of

BMNC or LA+BMNC groups [114]. NS-enhanced therapeutic angiogenesis and

M
arteriogenesis showed good correlations with increased intramuscular levels of vascular

endothelial growth factor and fibroblast growth factor-2. NS co-implantation also prevented
ed

apoptotic cell death of transplanted cells, resulting in prolonged cell retention.

This nano-scaffold provides promising local environment for implanted cells for the
pt

effects on angiogenesis and arteriogenesis through cell clustering, augmented expression of

ce

proangiogenic factors, and supporting cell survival without gene manipulation or artificial

ECM.
Ac

7. Health implication of nanoparticles

The degree of exposure to nanoparticles (TiO2, ZnO, NiO, CNTs, Al, Cu, and Ag )

and the percentage of exposed people will grow in the next few years [115]. Some properties

of nanoparticles in industrial applications might be detrimental both for biological systems

and environment. This led to the development of nanotoxicology, i.e., the systematic

evaluation of possible toxic effects elicited by nanotechnology products on cells or biological

27
Page 27 of 54
fluids and animals. Data regarding humans are still lacking, except for isolated case-reports

on accidental high dose exposure in the workplace [116]. The issue of nanoparticles toxicity

for humans remains controversial, as described in section 3.3. The main factors limiting

extrapolation to humans of available finding are:

1. To date, there is no conclusive evidence of a known human toxic response that is

t
specifically caused by nanoparticles. Effects seen in animals cannot be automatically

ip
translated to humans.

cr
2. Data are not univocal. Some well-performed studies show no toxicity from the same

us
nanoparticles showing adverse effects in other experiments [117]. This is due to the lack

of standardization both in characterizing the nanoparticle and in the methods used to

an
challenge the nanoparticles with biologic systems.

On the other hand, in several studies in which a direct comparison between CNTs
M
and asbestos has been made, similar toxicity has been reported [118].

We must be clear that the nanoparticle-linked diseases related to the realm of

ed

possible risk.
pt

8. Conclusions
ce

The synthetic biopolymer-based nanocomposites reviewed in this article are

particularly attractive as tissue engineering scaffolds due to their biocompatibility and

Ac

adjustable biodegradation kinetics. Conventional materials processing methods have been

adapted and incorporation of inorganic nanoparticles into porous and interconnected 3D

porous scaffolds. The incorporation of nanoparticles and immobilization of biological

components on the surface to enhance cellular adhesion and proliferation are promising and

currently under extensive research. Current research is focused on the interaction between

stromal cells and biopolymer interfaces. The synthetic biopolymer-based nanocomposite

scaffolds with bioactive inorganic phases will be in the center of attention in combination

28
Page 28 of 54
with stem cell seeding.

The fundamentals for biomaterials seem to originate from introducing stem cells. In

this direction, the new approach of biopolymer-based nanocomposite enables the scaffold

surface to mimic complex local biological functions and may lead in the near future to in-

vitro and in-vivo growth of tissues and organs.

t
In the present scenario, bioceramics entities have been used for bone tissue

ip
engineering scaffolds and drug delivery [119-121]. Osteomyelitis is a most common medical

cr
problem related to bones caused by an inflammatory process leading to bone destruction

us
caused by infective microorganisms found worldwide in children, where the bone tissue

regeneration is required [122]. Although, bioceramics scaffolds serve the purpose of tissue
an
regeneration and drug release, but they present formidable limitations such as the lack of

information relating to the long-term effects in the body. The bioceramics, especially HA,
M
when resorbed into the biological system for a long term shall give secondary fixation (70%

remains in dogs after 4 months and for humans 90% remains even after 4 years) [123]. HA
ed

crystals released from the bone scaffolds will accumulate in the joints and can stimulate an

inflammatory response in the prosthesis area [124]. In order to target clinical and medical
pt

applications, in-vitro and in-vivo studies are inevitable and the need for additional
ce

investigations in biological system is imperative.

Ac

Acknowledgment

This work was supported by KAKENHI (22656148) and the Strategic Research

Infrastructure Project of the Ministry of Education, Sports, Science and Technology, Japan

(2010-2014).

29
Page 29 of 54
References

[1] Smith R, editor. Biodegradable polymer for industrial applications. New York: CRC

Press, 2005. 552 pp.

[2] Chandra R, Rustgi R. Biodegradable polymers. Prog Polym Sci 1998;23:1273-1335.

t
[3] Johnson RM, Mwaikambo LY, Tucker N. Biopolymer. Rapra Review Report No 159.

ip
London: Rapra Technology Ltd, 2003. 148 pp.

cr
[4] Platt DK. Biodegradable polymers, market report. London: Rapra Technology Ltd,

us
2006. 158 pp.

[5] Sinha Ray S, Okamoto M. Biodegradable polylactide and its nanocomposites: Opening
an
a new dimension for plastics and composites. Macromol Rapid Commun 2003;24:815-

840.
M
[6] Ma PX. Scaffolds for tissue fabrication. Mater Today 2004;7:30-40.

[7] Langer R, Vacanti JP. Tissue engineering. Science 1993;260:920-926.

ed

[8] Quirk RA, France RM, Shakesheff KM, Howdle SM. Supercritical fluid technologies

and tissue engineering scaffolds. Curr Opin Solid State Mater Sci 2004;8:313-821.
pt

[9] Tsivintzelis I, Marras SI, Zuburtikudis I, Panayiotou C. Porous poly(L-lactic acid)

ce

nanocomposite scaffolds prepared by phase inversion using supercritical CO2 as

antisolvent. Polymer 2007;48:6311-6318.

Ac

[10] Sinha Ray S, Okamoto M. Polymer/layered silicate nanocomposites: a review from

preparation to processing. Prog Polym Sci 2003;28:1539-1641.

[11] Lee JH, Park TG, Park HS, Lee DS, Lee YK, Yoon SC, Nam JD. Thermal and

mechanical characteristics of poly(l-lactic acid) nanocomposite scaffold. Biomaterials

2003;24:2773-2778.

[12] Mikos AG, Sarakinos G, Leite SM, Vacanti JP, Langer R. Laminated three-

dimensional biodegradable foams for use in tissue engineering. Biomaterials

30
Page 30 of 54
 1993;14:323-330.

[13] Nam YS, Park TG. Biodegradable polymeric microcellular foams by modified

thermally induced phase separation method. Biomaterials 1999;20:1783-1790.

[14] Van de Witte P, Esselbrugge H, Dijkstra PJ, Van den Berg JWA, Feijen J. Phase

transitions during membrane formation of polylactides. I. A morphological study of

t
membranes obtained from the system polylactide-chloroform-methanol. J Membr Sci

ip
1996;113:223-236.

cr
[15] Whang K, Thomas CH, Healy KE, Nuber GA. A novel method to fabricate

us
bioabsorbable scaffolds. Polymer 1995;36:837-842.

[16] Bognitzki M, Czad W, Frese T, Schaper A, Hellwig M, Steinhart M, Greiner A,

an
Wendorff JH. Nano-structured fibers via electrospinning. Adv Mater 2001;13:70-72.

[17] Goel SK, Beckman EJ. Generation of microcellular polymeric foams using
M
supercritical carbon dioxide. I: Effect of pressure and temperature on nucleation. Polym

Eng Sci 1994;34:1137-1147.

ed

[18] Mohanty AK, Misra M, Hinrichsen G. Biofibers. Biodegradable polymers and

biocomposites: an overview. Macromol Mater Eng 2000;276:1-24.

pt

[19] Gilding D, Reed AM. Biodegradable polymers for use in surgery

ce

polyglycolic/poly(lactic acid) homo- and copolymers. Polymer 1979;20:1459-1464.

[20] Karageorgiou V, Kaplan D. Porosity of 3D biomaterial scaffolds and osteogenesis.

Ac

Biomaterials 2005;26:5474-5491.

[21] Hench LL. Bioceramics. J Am Ceram Soc 1998;81:1705-1728.

[22] Kim HW, Knowles JC, Kim HE. Hydroxyapatite/poly(epsilon)-caprolactone)

composite coating on hydroxyapatite porous bone scaffold for drug delivery.

Biomaterials 2004;25:1279-1287.

[23] Zhang R, Ma PX. Porous poly(l-lactic acid)/apatite composites created by biomimetic

process. J Biomed Mater Res 1999;45:285-293.

31
Page 31 of 54
[24] Alexandre M, Dubois P. Polymer-layered silicate nanocomposites: preparation,

properties and uses of a new class of materials. Mater Sci Eng R 2000;28:1-63.

[25] Gao F. Clay/polymer composites: the story. Mater Today 2004;7:50-55.

[26] Okada A, Usuki A. Twenty Years of Polymer-Clay Nanocomposites. Macromol Mater

Eng 2006;291:1449-1476.

t
[27] Okamoto M. Recent Advances in Polymer/Layered Silicate Nanocomposites: An

ip
overview from science to technology. Mater Sci Technol. 2006;22:756-779.

cr
[28] Okamoto M. Biodegradable polymer/layered silicate nanocomposites: A review. In:

us
Mallapragada S, Narasimhan B, editors. Handbook of Biodegradable polymeric

materials and their applications. Los Angeles: American Scientific Publishers, 2006. p.

153-197.
an
[29] Sinha Ray S, Bousmina M. Biodegradable polymer and their layered silicate
M
nanocomposits: In greeing the 21st century materials world. Prog Mater Sci

2005;50:962-1079.
ed

[30] Bordes P, Pollet E, Averous L. Nano-biocomposites: Biodegradable polyester/nanoclay

systems. Prog Polym Sci 2009;34:125-155.

pt

[31] Seal BL, Otero TC, Panitch A. Polymeric biomaterials for tissue and organ
ce

regeneration. Mater Sci Eng R 2001;34:147-230.

[32] Kohn J, Langer R. Bioresorbable and bioerodible materials. In: Ratner BD, Hoffman
Ac

AS, Schoen FJ, Lemmons JE, editors. Biomaterials science: an introduction to

materials in medicine. New York: Academic Press, 1996. p. 64-72.

[33] Jagur-Grodzinski J. Biomedical application of functional polymers. React Funct Polym

1999;39:99-138.

[34] Anonymous. PLA degradable. Kyoto: BMG Inc. http://www.bmg-

inc.com/en/prod_and_res/index.html Accessed March 2013 2012. 1 pp.

[35] Martin C, Winet H, Bao JY. Acidity near eroding polylactidepolyglycolide in vitro and

32
Page 32 of 54
 in vivo in rabbit tibial bone chambers. Biomaterials 1996;17:2373-2380.

[36] Pitt CG, Gratzel MM, Kimmel GL. Aliphatic polyesters. 2. The degradation of

poly(DL-lactide), poly(e-caprolactone) and their copolymers in vivo. Biomaterials

1981;2:215-220.

[37] Pektok E, Nottelet B, Tille JC, Gurny R, Kalangos A, Moeller M, Walpoth BH.

t
Degradation and healing characteristics of small-diameter poly(-caprolactone)

ip
vascular grafts in the rat systemic arterial. Circulation 2008;118:2563-2570.

cr
[38] Shi X, Mikos AG. Poly(propylene fumarate). In: Guelcher SA, Hollinger JO, editors.

us
An Introduction to Biomaterials. Boca Raton FL: CRC Press, 2006. p. 205-218.

[39] Mistry AS, Mikos AG. Tissue engineering strategies for bone regeneration. Adv

Biochem Eng Biotechnol 2005;94:1-22.

an
[40] Knowles JC. A review article: phosphate glasses for biomedical applications. J Mater
M
Chem 2003;13:2395-2401.

[41] Gay S, Arostegui S, Lemaitre J. Preparation and characterization of dense

ed

nanohydroxyapatite/PLLA composites. Mater Sci Eng C 2009;29:172-177.

[42] Webster TJ, Ergun C, Doremus RH, Siegel RW, Bizios R. Enhanced functions of
pt

osteoblasts on nanophase ceramics. Biomaterials 2000;21:1803-1810.

ce

[43] Nejati E, Mirzadeh H, Zandi M. Synthesis and characterization of nanohydroxyapatite

rods/poly(L-lactide acid) composite scaffolds for bone tissue engineering. Composites

Ac

Part A 2008;39:1589-1596.

[44] El-Ghannam A, Ning CQ, Mehta J. Cyclosilicate nanocomposite: a novel resorbable

bioactive tissue engineering scaffold for BMP and bone-marrow cell delivery. J

Biomed Mater Res Part A 2004;71:377-390.

[45] Wei G, Ma PX. Structure and properties of nano-hydroxyapatite/polymer composite

scaffolds for bone tissue engineering. Biomaterials 2004;25:4749-4757.

[46] Ramay Hassna RR, Zhang M. Biphasic calcium phosphate nanocomposite porous

33
Page 33 of 54
 scaffolds for load-bearing bone tissue engineering. Biomaterials 2004;25:5171-5180.

[47] Bianco A, Di Federico E, Moscatelli I, Camaioni A, Armentano I, Campagnolo L,

Dottori M, Kenny JM, Siracusa G, Gusmano G. Electrospun poly(
-caprolactone)/Ca-

deficient hydroxyapatite nanohybrids: microstructure, mechanical properties and cell

response by murine embryonic stem cells. Mater Sci Eng C 2009;29:2063-2071.

t
[48] Rezwan K, Chen QZ, Blaker JJ, Boccaccini AR. Biodegradable and bioactive porous

ip
polymer/inorganic composite scaffolds for bone tissue engineering. Biomaterials

cr
2006;27:3413-3431.

us
[49] Hong Z, Zhang P, He C, Qiu X, Liu A, Chen L, Chen X, Jing X. Nano-composite of

poly(L-lactide) and surface grafted hydroxyapatite: mechanical properties and

an
biocompatibility. Biomaterials 2005;26:6296-304.

[50] Li J, Lu XL, Zheng YF. Effect of surface modified hydroxyapatite on the tensile
M
property improvement of HA/PLA composite. Appl Surf Sci 2008;255:494-497.

[51] Hong ZK, Qiu XY, Sun JR, Deng MX, Chen XS, Jing XB. Grafting polymerization of
ed

L-Lactide on the surface of hydroxyapatite nano-crystals. Polymer 2004;45:6705-6713.

[52] Gansel JK, Thiel M, Rill MS, Decker M, Bade K, Saile V, von Freymann G, Linden S,
pt

Wegener M. Gold helix photonic metamaterial as broadband circular polarizer. Science

ce

2009;325:1513-1515.

[53] Rai M, Yadav A, Gade A. Silver nanoparticles as a new generation of antimicrobials.

Ac

Biotechnol Adv 2009;27:76-83.

[54] Lee JY, Nagahata JLR, Horiuchi S. Effect of metal nanoparticles on thermal

stabilization of polymer/metal nanocomposites prepared by a one-step dry process.

Polymer 2006;47:7970-7979.

[55] Xu X, Yang Q, Wang Y, Yu H, Chen X, Jing X. Biodegradable electrospun poly (l-

lactide) fibers containing antibacterial silver nanoparticles. Eur Polym J 2006;42:2081-

2087.

34
Page 34 of 54
[56] Schneider OD, Loher S, Brunner TJ, Schmidlin P, Stark WJ. Flexible, silver containing

nanocomposites for the repair of bone defects: antimicrobial effect against E. coli

infection and comparison to tetracycline containing scaffolds. J Mater Chem

2008;18:2679-2684.

[57] Xu X, Yang Q, Bai J, Lu T, Li Y, Jing X. Fabrication of biodegradable electrospun

t
poly(L-lactide-co-glycolide) fibers with antimicrobial nanosilver particles. J Nanosci

ip
Nanotechnol 2008;8:5066-5070.

cr
[58] Anonymous. The international decade for action: water for life-2005-2015. Geneva

us
Switzerland: World Health Organization. http://www.who.

int/water_sanitation_health/wwd7_water_scarcity_final_rev_1.pdf Accessed March

2013, 2007. 2 pp.

an
[59] Harrison BS, Atala A. Review, carbon nanotube applications for tissue engineering.
M
Biomaterials 2007;28:344-353.

[60] Mwenifumbo S, Shaffer MS, Stevens MM. Exploring cellular behavior with multi-
ed

walled carbon nanotube constructs. J Mater Chem 2007;17:1894-1902.

[61] Supronowicz PR, Ajayan PM, Ullmann KR, Arulanandam BP, Metzger DW, Bizios R.
pt

Novel current-conducting composite substrates for exposing osteoblaststo alternating

ce

current stimulation. J Biomed Mater Res 2002;59:49-506.

[62] Shi X, Sitharaman B, Pham QP, Spicer PP, Hudson JL, Wilson LJ, Tour JM, Raphael
Ac

RM, Mikos AG. In vitro cytotoxicity of single-walled carbon nanotube/biodegradable

polymer nanocomposites. J Biomed Mater Res Part A 2008;86A:813-823.

[63] Armentano I, Alvarez-Prez MA, Carmona-Rodrguez B, Gutirrez-Ospina I, Kenny

JM, Arzate H. Analysis of the biomineralization process on SWNT-COOH and F-

SWNT films. Mater Sci Eng C 2008;28:1522-1529.

[64] Mochalin VN, Shenderova O, Ho D, Gogotsi Y. The properties and applications of

nanodiamonds. Nat Nanotechnol 2012;7:11-23.

35
Page 35 of 54
[65] Huang HJ, Pierstorff E, Osawa E, Ho D. Protein-mediated assembly of nanodiamond

hydrogels into a biocompatible and biofunctional multilayer nanofilm. ACS Nano

2008;2:203-212.

[66] Zhang QW, Mochalin VN, Neitzel I, Knoke IY, Han JJ, Klug CA, Zhou JG, Lelkes PI,

Gogotsi Y. Fluorescent PLLA-nanodiamond composites for bone tissue engineering.

t
Biomaterials 2011;32:87-94.

ip
[67] Karbushev VV, Konstantinov II, Parsamyan IL, Kulichikhin VG, Popov VA, George

cr
TF. Preparation of polymer-nanodiamond composites with improved properties. Adv

us
Mater Res 2009;59:275-278.

[68] Zhang Q, Mochalin VN, Neitzel I, Hazeli K, Niu J, Kontsos A, Zhou JG, Lelkes PI,
an
Gogotsi Y. Mechanical properties and biomineralization of multifunctional

nanodiamond-PLLA composites for bone tissue engineering. Biomaterials

M
2012;33:5067-5075.

[69] Kokubo T, Takadama H. How useful is SBF in predicting in vivo bone bioactivity?
ed

Biomaterials 2006;27:2907-2915.

[70] Smart SK, Cassady AI, Lu GQ, Martin DJ. The biocompatibility of carbon nanotubes.
pt

Carbon 2006;44:1034-1047.
ce

[71] Shvedova AA, Castranova V, Kisin ER, Schwegler-Berry D, Murray AR, Gandelsman

VZ, Maynard A, Baronn P. Exposure to carbon nanotube material: Assessment of

Ac

nanotube cytotoxicity using human keratinocyte cells. J Toxicol Environ Health Part A

2003;66:1909-1926.

[72] Cui DX, Tian FR, Ozkan CS, Wang M, Gao HJ. Effect of single wall carbon nanotubes

on human HEK293 cells. Toxicol Lett 2005;155:73-85.

[73] Jia G, Wang HF, Yan L, Wang X, Pei RJ, Yan T, Zhao YL, Guo XB. Cytotoxicity of

carbon nanomaterials: Single-wall nanotube, multi-wall nanotube, and fullerene.

Environ Sci Technol 2005;39:1378-1383.

36
Page 36 of 54
[74] Monterio-Riviere NA, Nemanich RJ, Inman AO, Wang YYY, Riviere JE. Multi-walled

carbon nanotube interactions with human epidermal kerationcytes. Toxicol Lett

2005;155:377-384.

[75] Chen X, Tam UC, Czlapinski JL, Lee GS, Rabuka D, Zettle A, Bertozzi CR.

Interfacing carbon nanotubes with living cells. J Am Chem Soc 2006;128:6292-6293.

t
[76] Margrez A, Kasas S, Salicio V, Pasquier N, Seo JW, Celio M, Catsicas S, Schwaller B,

ip
Forro L. Cellular toxicity of carbon-based nanomaterials. Nano Lett 2006;6:1121-1125.

cr
[77] Nimmagadda A, Thurston K, Nollert MU, McFetridge PSF. Chemical modification of

us
SWNT alters in vitro cell-SWNT interactions. J Biomed Mater Res Part A

2006;76:614-625.
an
[78] Sayes CM, Liang F, Hudson JL, Mendez J, Guo WH, Beach JM, Moore VC, Doyle

CD, West JL, Billups WE, Ausman KD, Colvin VL. Functionalization density
M
dependence of single-walled carbon nanotubes cytotoxicity in vitro. Toxicol Lett

2006;161:135-142.
ed

[79] Warheit DB, Laurence BR, Reed KL, Roach DH, Reynolds GAM, Webb TR.

Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats.

pt

Toxicol Sci 2004;77:117-125.

ce

[80] Huczko A, Lange H, Bystrzejewski M, Baranowski P, Grubek-Jaworska H, Nejman P,

Przybylowski T, Czuminska K, Glapinski J, Walton DRM, Kroto HW. Pulmonary

Ac

toxicity of 1-D nanocarbon materials. Fullerenes Nanotubes Carbon Nanostruct

2005;13:141-145.

[81] Muller J, Huaux F, Moreau N, Misson P, Heilier JF, Delos M, Arras M, Fonseca A,

Nagy JB, Lison D. Respiratory toxicity of multi-wall carbon nanotubes. Toxicol Appl

Pharmacol 2005;207:221-231.

[82] Ding LH, Stilwell J, Zhang TT, Elboudwarej O, Jiang HJ, Selegue JP, Cooke PA, Gray

JW, Chen FQF. Molecular characterization of the cytotoxic mechanism of multiwall

37
Page 37 of 54
 carbon nanotubes and nano-onions on human skin fibroblast. Nano Lett 2005;5:2448-

2464.

[83] Kretlow JD, Mikos AG. Review: mineralization of synthetic polymer scaffolds for

bone tissue engineering. Tissue Eng 2007;13:927-938.

[84] Mikos AG, Thorsen AJ, Czerwonka LA, Bao Y, Winslow DN, Vacanti JP. Preparation

t
and characterization of poly(l-lactic acid) foams. Polymer 1994;35:1068-1077.

ip
[85] Lu L, Peter SJ, Lyman MD, Lai HL, Leite SM, Tamada JA, Vacanti JP, Langer R,

cr
Mikos AG. In vitro degradation of porous poly(l-lactic acid) foams. Biomaterials

us
2000;21:1595-1605.

[86] Kim SS, Ahn KM, Park MS, Lee JH, Choi CY, Kim BS. A poly(lactide-co-
an
glycolide)/hydroxyapatite composite scaffold with enhanced osteoconductivity. J

Biomed Mater Res Part A 2007;80A:206-215.

M
[87] Sakai R, John B, Okamoto M, Seppl JV, Vaithilingam J, Hussein H, Goodridge R.

Fabrication of Polylactide based Biodegradable Thermoset Scaffolds for Tissue

ed

Engineering Applications Macromol Mater Eng 2013;298:45-52.

[88] Boccaccini AR, Maquet V. Bioresorbable and bioactive polymer/Bioglass(R)

pt

composites with tailored pore structure for tissue engineering applications. Compos Sci
ce

Technol 2003;63:2417-2429.

[89] Boccaccini AR, Blaker JJ, Maquet M, Chung W, Jerome R, Nazhat SN. Poly(DL-
Ac

lactide) (PDLLA) foams with TiO2 nanoparticles and PDLLA/TiO2-Bioglass foam

composites for tissue engineering scaffolds. J Mater Sci 2006;41:3999-4008.

[90] Greiner A, Wendorff JH. Electrospinning: a fascinating method for the preparation of

ultrathin fibers. Angew Chem Int Ed 2007;46:5670-5703.

[91] Causa F, Netti PA, Ambrosio L. A multi-functional scaffold for tissue regeneration:

The need to engineer a tissue analogue. Biomaterials 2007;28:5093-5099.

[92] Jose MV, Thomas V, Johnson KT, Dean DR, Nyairo E. Aligned PLGA/HA

38
Page 38 of 54
 nanofibrous nanocomposite scaffolds for bone tissue engineering. Acta Biomater

2009;5:305-315.

[93] Ago H, Tobita M. Polymer composites of carbon nanotubes aligned by a magnetic

field. Adv Mater 2002;14:1380-1383.

[94] Armentano I, Del Gaudio C, Bianco A, Dottori M, Nanni F, Fortunati E, Kenny JM.

t
Processing and properties of poly(e-caprolactone)/carbon nanofiber composite mats

ip
and films obtained by electrospinning and solvent casting. J Mater Sci 2009;44:4789-

cr
4795.

us
[95] Misra SK, Watts PCP, Valappil SP, Silva SRP, Roy I, Boccaccini AR. Poly(3-

hydroxybutyrate)/bioglass composite films containing carbon nanotubes.

Nanotechnology 2007;18:075701/1-8.
an
[96] Mei F, Zhong J, Yang X, Ouyang X, Zhang S, Hu X, Ma Q, Lu J, Ryu S, Deng X.
M
Improved biological characteristics of poly(L-Lactic Acid) electrospun membrane by

incorporation of multiwalled carbon nanotubes/hydroxyapatite nanoparticles.

ed

Biomacromolecules 2007;8:3729-3735.

[97] Niiranen H, Pyhlt T, Rokkanen P, Kellomki M, Trml P. In vitro and in vivo

pt

behavior of self-reinforced bioabsorbable polymer and self-reinforced bioabsorbable

ce

polymer/bioactive glass composites. J Biomed Mater Res Part A 2004;69:699-708.

[98] Rich J, Jaakkola T, Tirri T, Narhi T, Yli-Urpo A, Seppala J. In vitro evaluation of

Ac

poly([var epsilon]-caprolactone-co-DL-lactide)/bioactive glass composites.

Biomaterials 2002;23:2143-2150.

[99] Dunn AS, Campbell PG, Marra KG. The influence of polymer blend composition on

the degradation of polymer/hydroxyapatite biomaterials. J Mater Sci Mater Med

2001;12:673-677.

[100] Liu Q, Wu J, Tan T, Zhang L, Chen D, Tian W. Preparation, properties and

cytotoxicity evaluation of a biodegradable polyester elastomer composite. Polym

39
Page 39 of 54
 Degrad Stab 2009;94:1427-1435.

[101] Allen BL, Kichambare PD, Gou P, Vlasova II , Kapralov AA, Konduru N, Kagan VE,

Star A. Biodegradation of single-walled carbon nanotubes through enzymatic catalysis.

Nano Lett 2008;8:3899-3903.

[102] Lazzeri L, Cascone MG, Danti S, Serino LP, Moscato S, Bernardini N. Geratine/PLLA

t
sponge-like scaffolds: morphological and biological characterization. J Mater Sci Mater

ip
Med 2007;18:1399-1405.

cr
[103] Baek HS, Park YH, Ki CS, Park JC, Rah DK. Enhanced chondrogenic responses of

us
articular chondrocytes onto porous silk fibroin scaffolds treated with microwave-

induced argon plasma. Surf Coat Technol 2008;202:5794-5797.

an
[104] He W, Yong T, Ma ZW, Inai R, Teo WE, Ramakrishna S. Biodegradable polymer

nanofiber mesh to maintain functions of endothelial cells. Tissue Eng 2006;12:2457-

M
2466.

[105] Hersel U, Dahmen C, Kessler H. RGD modified polymers: biomaterials for stimulated
ed

cell adhesion and beyond. Biomaterials 2003;24:4385-4415.

[106] Zhang H, Lin CY, Hollister SJ. The interaction between bone marrow stromal cells and
pt

RGD-modified three-dimensional porous polycaprolactone scaffolds. Biomaterials

ce

2009;30:4063-4069.

[107] Armentano I, Ciapetti G, Pennacchi M, Dottori M, Devescovi V, Granchi D, Baldini N,

Ac

Olalde B, Jurado MJ, Alava JIM, Kenny JM. Role of PLLA plasma surface

modification in the interaction with human marrow stromal cells. J Appl Polym Sci

2009;114:3602-3611.

[108] Discher DE, Janmey P, Wang YL. Tissue cells feel and respond to the stiffness of their

substrate. Science 2005;310:1139-1143.

[109] Rohman G, Pettit JJ, Isaure F, Cameron NR, Southgate J. Influence of the physical

properties of two-dimensional polyester substrates on the growth of normal human

40
Page 40 of 54
 urothelial and urinary smooth muscle cells in vitro. Biomaterials 2007;28:2264-2274.

[110] Engler AJ, Sen S, Sweeney HL, Disher DE. Matrix Elasticity Directs Stem Cell

Lineage Specification. Cell 2006;126:677-689.

[111] Mitragotri S, Lahann J. Cell and biomolecular mechanics in silico. Nat Mater

2009;8:15-23.

t
[112] Soccioa M, Lottia N, Finellia L, Gazzanob M, Munari A. Influence of

ip
transesterification reactions on the miscibility and thermal properties of

cr
poly(butylene/diethylene succinate) copolymers. Eur Polym J 2008;44:1722-1732.

us
[113] Tantini B, Fiumana E, Cetrullo S, Pignatti C, Bonavita F, Shantz LM, Giordano E,

Muscari C, Flamigni F, Guarnieri C, Stefanelli C, Caldarera CM. Involvement of

an
polyamines in apoptosis of cardiac myoblasts in a model of simulated ischemia. J Mol

Cell Cardiol 2006;40:775-782.

M
[114] Mima Y, Fukumoto S, Koyama1 H, Okada M, Tanaka S, Shoji T, Emoto M, Furuzono

T, Nishizawa Y, Inaba M. Enhancement of cell-based therapeutic angiogenesis using a

ed

novel type of injectable scaffolds of hydroxyapatite-polymer nanocomposite

microspheres. Plos One 2012;7:e35199/1-12

pt

[115] Pietroiusti A. Health implications of engineered nanomaterials Nanoscale 2012;4:1231-

ce

1247.

[116] Phillips JI, Green FY, Davies JC, Murray J. Pulmonary and systemic toxicity following
Ac

exposure to nickel nanoparticles. Am J Ind Med 2010,;53:763-767.

[117] Hauck TS, Anderson RE, Fischer HC, Newbigging S, Chan WCW. In vivo quantum-

dot toxicity assessment. Small 2010;6:138-144.

[118] Poland CA, Duffin R, Kinlock I, Maynard A, Wallace WAH, Seaton A, Stone V,

Brown S, MacNee W, Donaldson K. Carbon nanotubes introduced into the abdominal

cavity of mice show asbestos-like pathogenicity in a pilot study. Nat Nanotechnol

2008;3:423-438.

41
Page 41 of 54
 [119] Dvir T, Timko BP, Brigham MD, Naik SR, Karajanagi SS, Levy O, Jin H, Parker KK,

Langer R, Kohane DS. Nanowired three-dimensional cardiac patches. Nat Nanotechnol

2011;6:720-725.

[120] Wu S, Liu X, Hu T, Chu PK, Ho JPY, Chan YL, Yeung KWK, Chu CL, Hung TF, Huo

KF, Chung CY, Lu WW, Cheung KMC, Luk KDK. A Biomimetic Hierarchical

t
Scaffold: Natural Growth of Nanotitanates on Three-Dimensional Microporous Ti-

ip
Based Metals. Nano Lett 2008;8:3803-3808.

cr
[121] Rahaman MN, Day DE, Bal BS, Fu Q, Jung SB, Bonewald LF, Tomsia AP. Bioactive

us
glass in tissue engineering. Acta Biomater 2011;7:2355-2373.

[122] Gristina AG, Oga M, Webb LX, Hobgood CD. Adherent bacterial colonization in the
an
pathogenesis of osteomyelitis. Science 1985;228:990-993.

[123] Heisel J. Animal experiment studies of callus formation by hydoxyapatite injection.

M
Unfallchirurgie 1987;13:179-186.

[124] White RA, Weber JN, White EW. Replamineform: A New Process for Preparing
ed

Porous Ceramic, Metal, and Polymer Prosthetic Materials. Science 1972;176:922-924.

pt

Table 1 Physical properties of synthetic biopolymers used as scaffold materials

ce

Thermal Properties Tensile Biodegradation time

Biopolymers Tm (C)a) Tg (C) b) Modulus (GPa) (months)
PLLA 173-178 60-65 1.2 - 3.0 > 24
Ac

PDLLA - 55-60 1.9 - 2.4 12 - 16

PGA 225-230 35-40 5-7 3-4
PLGA (50/50) - 50-55 1.4 - 2.8 Adjustable: 3 - 6
PCL 58-63 -60 0.4 - 0.6 > 24
PPF 30-50 -60 2-3 > 24
a)
Melting temperature.
b)
Glass transition temperature.
Reproduced from [48].
Figure 1. SEM micrographs of the synthetic nHA rods [43], Copyright 2008. Reproduced

42
Page 42 of 54
with permission from Elsevier Ltd.

Figure 2. SEM micrographs of pure PLLA, PLLA/nHA and PLLA/mHAP scaffolds. (a, b)
Neat PLLA and cross-section; (c, d) PLLA/nHA: 50/50 and cross-section; (e, f) PLLA/nHAP:
50/50; (g, h) PLLA/mHAP: 50/50 scaffold [43], Copyright 2008. Reproduced with permission
from Elsevier Ltd.

t
ip
Figure 3. A schematic representation of a biomineralization process on PLLA/ND-ODA
scaffolds in SBF. (1) The initial stage. (2) While in contact with SBF, PLLA is hydrolyzed,

cr
resulting in the formation of -COOH groups on the surface of the scaffold. Due to the
degradation of PLLA, ND-ODA is exposed to SBF. The exposed -COOH groups of ND-ODA

us
dissociate and form negatively charged -COO- on the surface. In addition, the ND-ODA may
speed up the degradation of PLLA to produce more -COOH groups on the PLLA surface. The
an
negatively charged surface attracts Ca2+. (3) The deposited calcium ions, in turn, interact with
phosphate ions in the SBF and form bonelike apatite. (4) The bonelike apatite then grows
spontaneously, consuming the calcium and phosphate ions to form apatite clusters [68] ,
M
Copyright 2012. Reproduced with permission from Elsevier Ltd.
ed

Figure 4. Transmission electron micrograph of human epidermal keratinocytes (HEKs): (a)

intracellular localization of the MWNT-arrows depict the MWNT present within the
cytoplasmic vacuoles of a HEK; (b) keratinocyte monolayer grown on a Permanox surface-
pt

arrow depicts the intracytoplasmic localization of the MWNT [70], Copyright 2006.
Reproduced with permission from Elsevier Ltd.
ce

Figure 5. SEM images of crosslinked PLA porous scaffolds: Lait-X/b and Lait-X/c, for 350X
Ac

and 750X magnifications [87], Copyright 2012. Reproduced with permission from John

Wiley & Sons.

Figure 6. Pore size distribution in crosslinked PLA porous scaffolds: Lait-X/b and Lait-X/c.
Reproduced with permission from [87], Copyright 2012. Reproduced with permission from
John Wiley & Sons. & Sons.

Figure 7. SEM micrographs of neat PCL mat (A), SEM micrograph of PCL/ Ca-deficient

43
Page 43 of 54
nHA 2.0 wt.% (B), SEM micrograph and EDS mappings of PCL/ Ca-deficient nHA 6.4 wt.%
(C), and SEM microraph of PCL/ Ca-deficient nHA 24.9 wt.% (D) [47], Copyright 2009.
Reproduced with permission from Elsevier Ltd.
Figure 8. Optical microscopy photographs of the colored MSCs (H&E staining) attached to
the (a) neat PLLA, (b) PLLA/mHAP and (c) PLLA/nHAP [43], Copyright 2008. Reproduced
with permission from Elsevier Ltd.
Figure 9. SEM image of NS (A) and marked cell adhesiveness to NS in-vitro (B).

t
ip
(A) NS are microspheres approximately 100 m in diameter (a). The NS surface uniformly
coated with nano-scale hydroxyapatite (nHA) crystals was observed at different

cr
magnifications (low and high magnification in b and c, respectively). SEM image of an NS
cross-section indicating a single layer of nHA particles on the NS surface (d).

us
(B) Murine BMNCs were incubated with LA (a) or NS (b, c) at 37C for 8 h. Large numbers
of BMNCs adhered to NS (b, c) but not to LA (a). Scale bars: 100 m (A-a, B-a, B-b), 5 m
an
(B-c), 1 m (A-b), 100 nm (A-c, A-d) [114], Copyright 2012. Reproduced with permission
from Plos ONE.
Figure 10. Prolonged localization of implanted BMNCs in ischemic tissues by NS.
M
(A) Colocalization of BMNCs with NS and LA in-vivo. Murine BMNCs derived from EGFP-
transgenic mice were transplanted together with LA or NS into the thighs in the hind limb
ed

ischemic model. Cores of NS and LA containing rhodamine B (orange) were used to indicate
localisation of the injected microspheres in ischemic tissues. Tissue sections 7 days after
transplantation of LA+BMNCs (a) or NS+BMNCs (b) were counterstained with DAPI (blue),
pt

and merged images of DAPI, GFP and rhodamine B are shown. BMNCs (green) were
observed as densely clustered around NS (b) but not LA (a). Scale bars: 100 mm.
ce

(B) Quantitative evaluation of implanted cells existing in ischemic tissues. Quantitative

analysis of intramuscular GFP was performed 3, 7 and 14 days after transplantation. BMNCs
Ac

were derived from EGFP-transgenic mice. BMNCs were transplanted alone or together with
LA or NS into ischemic thigh muscles. Intramuscular GFP values of whole thigh muscles
were corrected for total protein and expressed in arbitrary units (n = 6 in each group). *P<0.05
for the NS+BMNCs group compared to the BMNCs alone and LA+BMNCs groups. GFP
concentration in normal murine muscle was measured as background (BG) [114], Copyright
2012. Reproduced with permission from Plos ONE.

44
Page 44 of 54
 t
ip
cr
us
an
M

Figure 1.
ed
pt
ce
Ac

45
Page 45 of 54
 t
ip
cr
us
an
M
ed
pt
ce
Ac

Figure 2.

46
Page 46 of 54
 t
ip
Figure 3.

cr
us
an
M
ed
pt
ce
Ac

47
Page 47 of 54
 t
ip
cr
us
an
M
Figure 4.
ed
pt
ce
Ac

48
Page 48 of 54
 t
ip
cr
us
Figure 5. an
M
ed
pt
ce
Ac

49
Page 49 of 54
 0.7
0.5 Lait-X/b Fig
0.6 ure
6
0.4 0.5

0.3 0.4

t
Log

ip
g/ 0.3
L 0.2 D

cr
m 0.2 fefi
/
noi 0.1 re

us
s 0.1 n
ur
t ati
nI 0 0 l
an In
Lait-X/c 0.4
vei 0.6 ur
t
atl s
oi
M
u 0.5 n
0.3
m m /
u 0.4
C
ed

L
0.3 0.2 g/
pt

0.2
0.1
ce

0.1

0 0
Ac

0.001 0.01 0.1 1 10 100 1000

Pore size Diameter / m

50
Page 50 of 54
 t
ip
cr
us
Figure 7.
an
M
ed
pt
ce
Ac

51
Page 51 of 54
 t
ip
cr
us
an
M
ed
pt
ce
Ac

Figure 8.

52
Page 52 of 54
 t
ip
cr
us
Figure 9.

an
M
ed
pt
ce
Ac

53
Page 53 of 54
 t
ip
cr
us
an
M
ed

Figure 10.
pt
ce
Ac

54
Page 54 of 54