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Review

Enhancing the Delivery of Chemotherapeutics: Role of Biodegradable Polymeric Nanoparticles

by
Jyoti Ahlawat
1,
Gabriela Henriquez
2 and
Mahesh Narayan
1,*
1
The Department of Chemistry & Biochemistry, The University of Texas at El Paso, El Paso, TX 79968, USA
2
Environment Science & Engineering Department, The University of Texas at El Paso, El Paso, TX 79968, USA
*
Author to whom correspondence should be addressed.
Molecules 2018, 23(9), 2157; https://doi.org/10.3390/molecules23092157
Submission received: 30 July 2018 / Revised: 12 August 2018 / Accepted: 15 August 2018 / Published: 27 August 2018
(This article belongs to the Special Issue Directed Drug Design and Molecular Therapy)
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Abstract

:
While pharmaceutical drugs have revolutionized human life, there are several features that limit their full potential. This review draws attention to some of the obstacles currently facing the use of chemotherapeutic drugs including low solubility, poor bioavailability and high drug dose. Overcoming these issues will further enhance the applicability and potential of current drugs. An emerging technology that is geared towards improving overall therapeutic efficiency resides in drug delivery systems including the use of polymeric nanoparticles which have found widespread use in cancer therapeutics. These polymeric nanoparticles can provide targeted drug delivery, increase the circulation time in the body, reduce the therapeutic indices with minimal side-effects, and accumulate in cells without activating the mononuclear phagocyte system (MPS). Given the inroads made in the field of nanodelivery systems for pharmaceutical applications, it is of interest to review and emphasize the importance of Polymeric nanocarrier system for drug delivery in chemotherapy.

Graphical Abstract

1. Introduction

Nanotechnology refers to the study of materials that have at least one dimension in the nanometer range. Therefore, it would not be wrong to call it as the technology of future since it involves designing nanostructures through methodologies that involve control over physical and chemical characteristics at molecular level i.e., nanoscale [1]. Since the famous 1959 lecture “There’s Plenty of Room at the Bottom”, by the Nobel laureate Richard P. Feynman, there have been many developments in the field of biology, chemistry, and physics that demonstrate his idea of managing and operating matter at the level of molecules and atoms [2]. Related to this, a more accurate definition of nanotechnology was given by Drexler in 1981 which involves production of material with dimensions and precision between 1 and 100 nm [3]. Nanomaterials are one of the fastest emerging research areas and is an interdisciplinary field that requires understanding and expertise in diverse areas such as biology, chemistry, electronics, engineering, physics and social sciences. As the research on nanomaterials is growing, it would not be wrong to call this period of development in nanomaterials as Nano era. Furthermore, Gutierrez in 2005 reported the possibility of conversion of all structures into nanostructures. For instance, it has been more than a decade now since nanomaterials are used to improve the quality and grit of products [4,5]. Therefore, success of nanotechnology lies in influencing the purity and composition (physical and chemical) of the parent material [6].
Nanotechnology encompasses two approaches: (1) A top-down approach; and (2) a bottom-up approach (Figure 1):
  • “Top-Down” approach: The nanoscale structures are deconstructed from larger structures while maintaining their original properties and chemical composition [2,6].
  • “Bottom-Up” approach: Involves engineering the materials at atomic or molecular level through a process of assembly or self-assembly [2].
The chemical synthesis methods involved have influence on the size and shape of the nanoparticle constructed using the bottom-up approach. Although the contemporary methods rely more on the top-down approach, the bottom-up approach produces more ordered or crystalline nanoparticles resulting in a greater change in their surface energies and morphologies. Apart from the various applications of bottom-up approach in materials and manufacturing, electronics, medicine and healthcare, energy and biotechnology, to name a few, the limitations include its high operational cost, limited suitability (for laboratory use only) and expertise requirement [2,7].
In this review, we will focus on the use of polymeric nanoparticles for cancer treatment. Currently, more than 90% of the available potential therapeutics have poor pharmacokinetic properties. Therefore, there is an urgent and unmet need to produce drug delivery systems that can distribute drug molecules to the targeted site without affecting surrounding healthy cells [7]. In this context, nanoparticles possess several advantages, such as: Lower doses, improved pharmacokinetics, increased delivery to target site, reduced drug toxicity, reduced liver clearance, improved solubility of hydrophobic drug in aqueous medium and bio-availability, and increased stability of therapeutic agents such as peptides and oligonucleotides. Furthermore, biocompatibility of nanoparticles helps in avoiding hypersensitivity reactions and peripheral neuropathy and can be injected without occluding needles [7].

2. Types of Nanoparticles for Drug Delivery

Nanoparticles used as drug conjugates can be classified into: Liposomes, Carbon Nanotubes, Dendrimers, Extracellular Vesicles, Tunneling Nanotubes and Polymeric nanoparticles (Figure 2).

2.1. Liposomes

Liposomes are bilayered vesicles composed of an outer lipid bilayer surrounding an inner aqueous core. The biocompatibility, amphiphilic nature, and ease of surface modification allow for increased circulation time. These properties enable the liposome to deliver the drug either by adhering to the cell membranes or by the process of endocytosis [8,9,10,11].
Due to their stability related issues, they have limited medical impact but are extensively used in cosmetic products. Moreover, functionalization using Polyethylene glycol (PEG) allows for enhanced circulation time. Liposomal formulations such as Doxil, Myocet and DaunoXome are approved for metastatic breast cancer treatment and Kaposi’s sarcoma [12,13,14].

2.2. Carbon Nanotubes (CNTs)

Nanotubes can be inorganic or organic (carbon nanotubes) in composition. Carbon nanotubes are self-assembling sheets of atoms arranged in tubes. For instance, they can have single or multi-walled structure with the latter one being more stable as the aggregation tendency decreases with reduced nanocurvature. Furthermore, the chemical modification of Carbon Nanotubes (CNTs) make them soluble and functionalized so that active substances like peptides or drugs can be attached on their surface [15]. They also have large internal volume. However, acute toxicity, carcinogenesis, immunogenicity arising due to the use of these nanoparticles cannot be overlooked. Therefore, they must be chemically or biologically modified before use for cellular delivery. Properties like low biocompatibility limit its use [16,17,18,19]. Although, they have been used as biosensors, drug delivery vehicle and as diagnostic tools, their insolubility in all solvents has caused health related issues.

2.3. Dendrimers

The term dendrimer was proposed due to its resemblance to a tree [20]. It is a synthetic polymer-based macromolecule in nanometer range having multiple branched monomers radiating out from the central core [21]. For instance, the void at the center, multivalence, ease of surface modification, well-defined globular-shape, predictable molecular weight, lack of immunogenicity, water solubility and size control make them a desirable candidate for drug delivery [21]; among these are PAMAM (polyamidoamine) and PPI (polypropylene). Although they can be conjugated with multiple substances, like imaging agent, drug, targeting ligand forming a multifunctional drug delivery system, biocompatibility and biodistribution problems limits their application [15,22].

2.4. Extracellular Vesicles (EVs) and Tunneling Nanotubes (TNTs)

These are basically lipid based bilayered structures composed mainly of cermaides, cholesterol and sphingolipids. Intracellular communication and cargo transfer via extracellular vesicles are well known and is gaining focus in research [23]. Furthermore, EVs is a generalized term and based on distinct biogenesis and release pathways these are further classified into various subtypes such as exosomes (50–100 nm), ectosomes (100–1000 nm) and oncosomes (1–10 um) [24]. For instance, these can be round, or cup shaped in morphology when observed under Scanning Electron Microscope (SEM). Moreover, these are well known for transfer of biological materials in paracrine fashion [23].
Rustom et al. in 2004, discovered an actin-based transient extension of cytoplasm between the cells, in the range of 50–200 nm, resembling nanotubes with open ends, called tunneling nanotubes [25]. The biological synthesis of this nanostructure is based on f-actin polymerization [26,27]. Furthermore, TNTs have role in intercellular communication, transfer of cargo, immunoregulation and inflammatory response [23].

2.5. Polymeric Nanoparticles

This review focuses on the application of polymeric nanoparticles for the delivery of anti-cancer drugs. These have a size between 10 to 1000 nm and are made up of polymers and copolymers protecting a drug, either encapsulated within particle or adsorbed on the surface or chemically linked to the surface, efficiently [28,29,30]. In 2002, Discher and Eisenberg described the structure of polymeric nanoparticles [31]. They state that it possesses a core-shell structure with the interior consisting of a polymeric matrix containing hydrophobic drug and the surface is made up of hydrophilic polymer e.g., PEG, PVP which provides stearic stability, reduces immunogenicity and phagocytosis of nanoparticles by reticuloendothelial system [32]. In another study, Alonso’s group showed that coating PLA nanoparticles with PEG enhanced their residence time in the GI fluids by protecting from enzymatic degradation [33]. Given these points, polymeric nanoparticles can exist as (1) nanocapsules; or (2) nanospheres (Figure 3).
  • Nanocapsules: They have an oily core and a polymeric outer surface. The drug can be adsorbed on the surface or encapsulated in the core.
  • Nanospheres: The core and outer surface are made up of polymeric material and the drug is either retained or adsorbed in this polymeric structure.
These polymeric nanoparticles are biodegradable, as the end products are non-harmful alcohols and other low molecular weight products [28]. Furthermore, these increase the solubility of active drug, provide good pharmacokinetic control, are stable, non-toxic, noninflammatory, non-immunogenic, do not activate neutrophils, and avoid reticuloendothelial clearance [34].
To summarize, the conventional medication has several side effects which can be overcome by using these polymeric nanoparticles. For instance, in ophthalmic administration, the nanoparticle releases drug following zero-kinetic order, increasing ocular bioavailability and reducing the side effects [34].
Overall, polymers used as drug delivery vehicle can be classified as synthetic and natural polymers (Table 1).
Synthetic polymers include N-(2-hydroxypropyl)-methacrylamide copolymer, polyethylene glycol, poly-l-glutamic acid, poly (lactic-co-glycolic acid), poly (sebacic acid), poly (acrylic acid), etc [29]. The United States Food and Drug Administration had approved Poly(lactic-co-glycolic acid) and Poly(lactic acid) for use by human. Poly(glycolic acid) was the first synthetic polymer used for conjugate building Doxorubicin loaded N-(2-Hydroxypropyl)methacrylamide conjugate (Protein-serine Kinase-1) was tested for its anti-cancerous activity [35].
Polymers such as heparin, albumin, chitosan, dextran, gelatin are present naturally and are preferred for the delivery of various active constituents such as DNA, drugs, oligonucleotide and proteins. Paclitaxel loaded albumin nanoparticles have been used for the treatment of metastatic cancer [35]. Natural polymeric nanoparticles are preferred because of their reduced side effects, sustained drug release and increased residence time [34].

3. Synthesis of Polymeric Nanoparticles

3.1. Solvent Evaporation Method

It involves addition of the polymer in an organic solvent like chloroform or ethyl acetate followed by dissolution of the drug into polymeric solution forming an oil (O) in water (W) emulsion in the presence of a surfactant like polysorbate-80 or poloxamer-188. Using various physical methods, like increasing the temperature, pressure or by continuous stirring, the organic solvent is evaporated (Figure 4). Given these points, this method is preferred for the synthesis of water-soluble drug-loaded NPs [37]. In short, the procedure is used for laboratory scale synthesis purpose only.

3.2. Spontaneous Emulsification/Solvent Diffusion Method

This is a modified version of the solvent evaporation method [38,39,40]. Here, the oil phase comprises of water-soluble solvent like methanol or acetone along with the organic solvent like dichloromethane. An interfacial turbulence between the two phases, due to spontaneous diffusion of methanol or acetone (water-soluble solvent), forms nanoparticles (Figure 5).

3.3. Salting Out Method

In brief, to avoid use of organic solvents, this method was developed. It involves dissolution of polymer and drug in a water-soluble solvent like acetone, which is then added to an aqueous solution containing stabilizer like hydroxyethylcellulose or PVP (polyvinylpyrrolidone) and a salting-out agent like magnesium chloride, calcium chloride, and sucrose (Figure 6). This O/W emulsion is then diluted to enhance the diffusion process of acetone into the aqueous phase, forming nanoparticles [41]. In conclusion, it works well for heat sensitive substances as it does not require increase in the temperature [42].

3.4. Nanoprecipitation/Solvent Displacement Method

This method is generally preferred for the encapsulation of lipophilic drugs and is not used for water-soluble drugs. It involves addition of polymer and drug into an organic solvent like dichloromethane in the presence or absence of the surfactant. This is then added to an aqueous solution containing stabilizer. An interfacial turbulence between the two phases due to diffusion causes polymer deposition on the interface (Figure 7). Overall, the method is adopted for various materials like PLGA, PLA, Polyvinylmethyl ether and maleic acid (PVM/MA). This method was used for the encapsulation of cyclosporin A, because of 98% entrapment efficiency [26,43,44,45].

3.5. Polymerization Methods

Nanoparticles can be synthesised by polymerization of monomers. In a study, Couvreur et al. in 1998 showed the polymerisation process of poly(alkyl cyanoacrylate) [46]. In the first place, the cyanoacrylic monomer is added to a polymerization medium in the presence of a surfactant like polysorbate-20 under vigorous stirring to polymerize ethyl or methyl cyanoacrylate at an ambient temperature. Later, drug is added before the introduction of the monomer or after the polymerization reaction. Usually, ultracentrifugation is used to purify the nanoparticles. Furthermore, to produce stable and high molecular mass NPs, pH (below 3.5), concentration of monomers, stirring speed, type and concentration of the surfactant/stabilizer must be monitored. For instance, a pH above 3 during the polymerization process results in aggregation of the nanoparticles [37].

3.6. Nanoparticles Developed from Hydrophilic Polymers

Nanoparticles from hydrophilic polymers like chitosan and gelatin have been synthesized using different methods (Figure 8). In a study, Calvo and coworkers in 1996 developed a method to synthesize chitosan nanoparticles involving ionic gelation using a mixture of two aqueous phases of which first one contained chitosan and EO (ethylene oxide) and the second one contained polyanion sodium-TPP (tripolyphosphate) [47].
In another study, Mao and co-workers in 2001 used complex coacervation method to develop DNA loaded chitosan nanoparticles for oral gene delivery. Additionally, alginate-based nanoparticles were synthesized for oligonucleotides delivery [37,48].

4. Chemotherapy and Its Limitations

Our body is composed of trillions of cells, the most common disease targeting these cells is Cancer. It is a group of diseases where a group of cells start to divide in an abnormal fashion, proliferate without stopping, invading other tissues [49]. Currently, over 100 different types of cancer have been characterized [49,50] they vary mainly in their behavior, location and treatment. For more than a century, cancer has been the focus of research for the scientist around the world. Even though the real reason is still unknown, it is believed to be caused by numerous different factors, such as chemicals, radiation, environmental factors (smoking, obesity, radiation, infections, etc.) acquired and inherited mutations and so on. Based on the Centres for Disease Control and Prevention in the United State, in 2016 1.6 million Americans were diagnosed with cancer (Figure 9). However, remarkable development has taken place in the field of early detection methods for various cancer types, but medical treatment needs attention for the development of efficient and safer medication. Finally, our hope remain in the biological application of nanoparticles, as is a rapidly developing area of nanotechnology that is rising with a new possibility in the diagnosis and treatment of human cancers. Table 2 gives an estimation of the number of new cases and deaths for each cancer type.
In a study, Feng and Chien, in 2003, described chemotherapeutic drugs as active substances that interfere with the activity of a cell by inducing apoptosis or by inhibiting DNA replication [57]. Due to their deleterious effects on rapidly proliferating cells, they have been employed in the treatment of cancer [57,58]. Furthermore, chemotherapeutic drugs, such as Daunorubicin, has been found to show cytotoxic effect on cancer cells and is currently used for the treatment of various tumors such as breast cancer, myeloblastic leukemia and lymphoma [59,60,61]. Related to this, drugs such as Paclitaxel and doxorubicin exert their effect by blocking the cell in the metaphase stage of mitosis [59,62]. Another chemotherapeutic agent, cisplatin, acts by making changes in the cellular DNA triggering apoptosis [59,63]. Doxorubicin also prevents DNA replication by targeting Topoisomerase-DNA complex [59,64].
As has been noted, the main challenge associated with the use of chemotherapeutic agents is their inability to discriminate between healthy and tumor cells [65]. These drugs attack any proliferating cells without differentiating between tumor cells or cells from body such as intestinal epithelial cells or hair cells [58]. Furthermore, side effects associated with doxorubicin such as nausea, fatigue, cardiotoxicity limits its use even after being the best anti-cancer drug available today [59,60]. Considering this, nanocarriers can be employed to overcome some, if not all, limitations associated with the use of these drugs and cytotoxicity against healthy cells is one of them [32,59]. Most notably, the nanocarriers will help in formulation problems such as hydrophobicity of the drug and, they will help in overcoming certain issues such as inappropriate dose and targeted delivery associated with chemotherapy.

5. Polymeric Nanoparticles in Cancer Treatment

An important aspect to be overcome by nanocarriers is the drug resistance in cancer cells which occurs over time during chemotherapy treatment. Various mechanisms by which this can be done include:
1
Cellular uptake of drug via endocytosis or receptor-mediated internalization [66,67,68]
2
Polymeric material such as Pluronic block copolymers can be used to inhibit the multidrug resistance proteins [67]
3
Increasing the concentration of drug around the tumor cell [66]
Both inhibitor and drug can be loaded inside the nanoparticle for synergistic effect [69]
Polymeric nanoparticles are promising candidates in the treatment of cancer due to their biodegradable nature, sustained release of drug, nanosize, biocompatibility, bioactivity, non-toxic nature, long circulation time, non-immunogenicity and ability to hold various active molecules such as drugs, oligonucleotide, peptides, etc. [70,71]. This part of review focuses on the ongoing research in the field of nanomedicine and the use of polymeric nanoparticles for the delivery of anti-cancer agents.

6. Poly-d,l-lactide-co-glycolide (PLGA)

PLGA is listed safe by US Food and Drug Administration for human use. It is the most successful candidate for use in nanomedicine due to the formation of biodegradable by products viz., lactic acid and glycolic acid, upon its hydrolysis. The various synthesis method includes solvent evaporation, interfacial deposition, emulsification-diffusion and nanoprecipitation (most commonly used). However, the acidic nature of PLGA makes it less suitable as carrier for drugs and bioactive molecules [71,72,73]. Therefore, this limitation is overcome by blending PLGA with other polymers such as poly(propylenefumarate) [71,74], polyvinylalcohol [71,73,75] chitosan etc. In this context, few of the PLGA based nanosystems as carriers for anti-cancer drugs are as follows.

6.1. Cisplatin

Cisplatin is a potent anti-cancer drug that interferes with the cell division. However, its use is limited due to its cytotoxicity against healthy cells [71,76]. Therefore, targeted delivery of this drug to tumor cells is increased by encapsulating it within PEG-PLGA nanosystem.

6.2. Curcumin

Curcumin is effective against prostate cancer, but the hydrophobicity of the drug limits its use. In a study by Mukherjee and Vishwanatha in 2012, they developed curcumin loaded PLGA nanospheres using emulsion solvent evaporation method with increased anti-cancer efficacy [77].

6.3. Docetaxel

Docetaxel is specific for cancer cells with folate receptors. Hence, its efficiency is increased by loading it inside PEG-PLGA nanoparticles synthesized using emulsion solvent diffusion [78]. Comparatively, it leads to enhanced cellular uptake by cancer cells.

6.4. 9-Nitrocamptothecin (9-NC)

9-NC is a promising anti-cancer agent that targets the topoisomerase-1 enzyme. But, due to its pH dependent fast and reversible hydrolysis its use is limited. Hence, the biological activity of this drug is enhanced by loading it inside PLGA nanoparticles by nanoprecipitation method [71,76].

6.5. Paclitaxel

Paclitaxel acts by interfering with the cell dynamics by promoting polymerization of tubulin and hence, initiating cell death. It is important to mention that it shows anti-cancer activity against breast, colon and ovarian cancer [71]. Given these points, the poor solubility issue is overcome by encapsulating the drug in a PLGA-Vit E-TPGS complex which is synthesized using solvent evaporation or extraction method.

6.6. Rose Bengal

Rose Bengal is specific for tumor cells and gets localized in the lysosomes. Therefore, it is used for the treatment of melanoma cancer [79]. However, the efficiency of the drug is enhanced by loading it inside PLGA nanoparticles by interfacial deposition method.

7. Poly-ε-caprolactone (PCL)

PCL has received great attention worldwide for use in nanomedicine because of the hydrolysis of its ester bond at physiological pH making it biodegradable. It is synthesized by nanoprecipitation, solvent displacement and solvent evaporation method [71]. Some of the anti-cancer drug loaded PCL based nanosystems are as follows.

7.1. Docetaxel

Docetaxel has anti-tumor effect. Hence, the surface modification of PCL nanoparticles with Me PEG, synthesized using nanoprecipitation method, allows effective killing of B 16 cells [80].

7.2. Vinblastine

Vinblastine is effective against breast cancer. Therefore, the Vinblastine loaded PCL nanoparticles synthesized using emulsion method allows efficient uptake of nanomedicine by the cancer cells with a slow drug release profile [81].

7.3. Tamoxifen

Tamoxifen works by binding to the estrogen receptors on the target cells and inhibiting estrogen effect. It is an anti-estrogen drug and competes with estrogen for the receptor binding on the breast and other tissues. Hence, it prevents proliferation of pre-cancerous cells by arresting the cell in G0 and G1 phase of the cell cycle [81]. Therefore, the tamoxifen encapsulated PCL nanoparticles are synthesized using solvent displacement method allowing enhanced circulation time and targeted delivery to the tumor site with increased drug accumulation level [82].

7.4. Taxol

Taxol has tumor growth inhibition activity. The extremely lipophilic characteristic of taxol could be overcome by encapsulating the drug in mPEG-PCl nanoparticles with enhanced anti-cancer activity due to higher drug loading [83].

8. Gelatin

Gelatin is a natural polymer with polyampholyte nature along with hydrophilic moiety. It is used for the sustained/controlled drug release due to its biodegradable, bioactive, biocompatibility, non-toxic, mechanical and thermal properties. It is synthesized using emulsion, coacervation/desolvation method [84,85].

Paclitaxel

Paclitaxel has anti-cancer activity against human-bladder transitional cancer cell. The paclitaxel encapsulated gelatin nanoparticles synthesized using desolvation method have increased anti-cancer efficacy compared to the free drug. The increased water solubility of the nanoparticle due to its amorphous nature allows rapid drug release at the target site [86].

9. Poly-alkyl-cyano-acrylates (PAC)

PAC have adverse effects on the central nervous system as the by-products are toxic and hence, PAC is not regarded as safe for human use, overshadowing its biodegradable and biocompatible nature. It is synthesized using emulsion, interfacial polymerization and nanoprecipitation method for use in nanomedicine [87,88]. An example of PAC loaded nanosystem is Ftorafur drug.

Ftorafur

Ftorafur is a mixture of tegafur and uracil. Tegafur when taken up by cancer cell breaks down into 5-FU subsequently killing it. Uracil on the other hand increases the level of 5-FU inside the cell, killing the cancer cell. Tegafur and uracil have synergistic effect. The ftorafur encapsulated PE-2-CA and PBC nanospheres have wide range of anti-tumor activity allowing rapid drug release at the target site [89].

10. Targeted Delivery of Nanoparticles

To begin with, two basic requirements must be met by the anti-cancer drugs for effective treatment of cancer [15]. These include:
1
Reaching the site of action after crossing all the biological barriers while retaining their activity with minimum loss of volume.
2
Attacking the tumor cells with minimal cytotoxic effect on the healthy neighboring cells or the tissues.
Nanoparticles fulfil both the requirements and hence act as a good drug carrier system. Types of targeting are as follows (Figure 10).

10.1. Passive Targeting

Increased permeability: The tumor cells and inflamed tissues have leaky microvasculature with numerous pores in the range of 380 and 780 nm [35], unlike healthy cells. This happens due to the increased demand of oxygen and nutrients by the hyper-proliferating cancer cells demanding neo-vascularization, called Enhanced Permeability and Retention effect (EPR) [90].
Tumor microenvironment: The tumor cells have an acidic environment as they use glycolysis pathway for meeting extra-energy demand due to increased metabolism [91].
For passive targeting, the nanoparticles must be able to accumulate in the tumor interstitium. Furthermore, the circulating life in blood should be long so that they have multiple chances to pass the target site. This can be achieved by coating the nanoparticles with surfactants such as PEG which is chemically inert, has low immunogenicity and antigenicity [92]. However, this may cause the passive distribution of drug to multiple sites. But, in some cases this situation may be beneficial too [15].

10.2. Active Targeting

Tumor and inflamed tissues not only have leaky vasculature but also have overexpression of certain epitopes and receptors that can be targeted. Once the nanocarriers have extravasated the tissue, the ligands on the surface of these nanocarriers can bind to the epitopes and receptors overexpressed on cancer cells allowing cellular uptake by receptor-mediated endocytosis. This is referred to as “active mode of targeting enhancing availability” of drug with poor permeability requiring intracellular site of action for bioactivity [93]. This can enhance the biodistribution of nanomedicine [94]. This method of targeting has been employed to delivery drug to drug resistant cancer cells. Key factor to be kept in mind while choosing ligands is its ability to activate Mononuclear Phagocytic system (MPS) (Table 3).
The active mode of targeting has several advantages over ligand-drug conjugates which includes:
1
High concentration of drug can be transported to the site of action.
2
The activity of the drug can be affected by conjugating ligand with the drug which is not the case in active targeting using ligand tagged nanocarriers.
3
Numerous ligands can be attached on the surface of nanocarriers increasing chance to pass the target site.

11. Polymeric Nanoparticles Related Toxicity Issues

Nowadays nanomaterials are of keen interest to the scientist in the biomedical field due to their wide range of applications in diagnosis, drug delivery, and development of human organs [103,104]. However, the biggest concern is the safety associated with the use of these NPs. The bare and small size of these particles have higher toxicity than modified and bulk materials, respectively. For instance, spherical nanoparticles have less toxicity than rod shaped nanoparticles due to their ability to trigger an immune response in the body. The toxicity of these materials can be reduced by chemical approaches such as surface treatment, functionalization, and composite formation [105]. There are many factors that could conceivably influence material’s toxicity, these includes surface chemistry, roughness, surface energy (hydrophobicity/hydrophilicity), level of degradation, products and release of by-products, particle size, oxidative stress functions, crystallinity, concentration, coating, and the longevity of particles [103]. The toxicity may vary in severity depending on the mode of administration and site of release, as a result, to preserve clinical purpose, information on toxicity is exhibited using a system-based approach focusing on lung, dermal, liver, and nervous system targets.
The interaction between NPs and living systems are not yet fully understood. The problem arises with the particles ability to bind and interact with biological material which can alter their surface characteristics, depending on the environment they are delivered to. Scientific knowledge about NPs cell-interaction mechanisms has been indicating that cells readily take up NPs via active or passive mechanisms.
At the end, even though these nanoparticles are a huge advancement in drug designing, it is better to have more understanding of the effects that they may have on human health before heading towards their clinical usage. They need to be evaluated on a particle-by-particle basis and must undergo better characterization strategy such as absorption, distribution, metabolism and excretion (ADME) tests and physicochemical, and toxicological characterization, involving both in vitro tests and in vivo animal studies.

12. Conclusions and Outlook

Nanoparticles used for drug delivery provide many advantages in medicine because of enhanced drug-therapeutic efficiency. They enter the body and bind to biological tissue and cells. After entry, they tend to dissolve and enter the biological environment, surrounded by proteins, high ionic strength, and low pH [106]. Nanoparticles interacts with the skin, the gastrointestinal tract, and the respiratory tract, and many others compartments that act as barriers to this nanosized material in the organism. A new development of a multifunctional Nanosystems have combined, different functions in a single nanoparticle, such as biocompatibility, biostability and biodistribution.
The polymeric nanoparticle is one of the most preferred nanoparticulate delivery systems in medicine and include synthetic polymers and natural polymers [107]. Polymeric nanoparticles, and its architecture, composition, stability, water solubility make them effective candidate for use in drug delivery. Based on several studies, it has been demonstrated that a polymeric carrier has controlled/sustained drug release, bioavailability and biodistribution in the body. Based on their polymeric characteristic, these nanoparticles have significance in medical field [108].
One of the best characteristics of polymeric nanoparticles is that they provide a buoyed-up release of encapsulated drugs, help to protect drugs from the body’s enzymatic, acidic, and degradation conditions, provide targeting capabilities from a tendency for passive accumulation in tumors, and display adjuvant characteristics. These and other properties make this type of nanoparticle a suitable mechanism to prevent cancer attacks. Priscilla B et al. 2017, used biocompatible Polymeric Nanoparticles derived from Castor Oil Derivatives for biomedical applications because of their biodegradability and biocompatibility [109].
Finally, multifunctional nanoparticles can facilitate visualization of malignant cells (using in vivo imaging), target them (through active targeting ligand) eventually killing the cancer cells without harming neighboring healthy cells via active targeting and controlled release of drug.

Funding

This research was funded by NIH grant number 1SC3 GM111200 01A1.

Acknowledgments

Authors are grateful to Lois Mendez for her suggestions while writing this article. MN acknowledges NIH 1SC3 GM111200 01A1.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

References

  1. Safar, J.; Zarnegar, Z. Advanced drug delivery systems: Nanotechnology of health design A review. J. Saudi Chem. Soc. 2012, 18, 85–99. [Google Scholar] [CrossRef]
  2. Sanchez, F.; Sobolev, K. Nanotechnology in concrete—A review. Constr. Build. Mater. 2010, 24, 2060–2071. [Google Scholar] [CrossRef]
  3. Pacheco-Torgal, F.; Jalali, S. Nanotechnology: Advantages and drawbacks in the field of construction and building materials. Constr. Build. Mater. 2010, 25, 582–590. [Google Scholar] [CrossRef] [Green Version]
  4. Amin, M.; Abu el-Hassan, K. Effect of using different types of nano materials on mechanical properties of high strength concrete. Constr. Build. Mater. 2014, 80, 116–124. [Google Scholar] [CrossRef]
  5. Gutiérrez, H.R.; Kim, J.U.; Kim, P.J.; Eklund, C.P. Thermal Conversion of Bundled Carbon Nanotubes into Graphitic Ribbons. Nano Lett. 2005, 5, 2195–2201. [Google Scholar] [CrossRef] [PubMed]
  6. Muhd Norhasri, M.S.; Hamidah, M.S.; Mohd Fadzil, A. Applications of using nano material in concrete: A review. Constr. Build. Mater. 2016, 133, 91–97. [Google Scholar] [CrossRef]
  7. Cevc, G.; Vierl, U. Nanotechnology and the transdermal route: A state of the art review and critical appraisal. J. Control. Release 2010, 141, 277–299. [Google Scholar] [CrossRef] [PubMed]
  8. Ryman, B. Potential applications of Liposomes to therapy. Ann. N. Y. Acad. Sci. 1978, 308, 281–307. [Google Scholar] [CrossRef] [PubMed]
  9. Lasic, D.D.; Frederik, P.M.; Stuart, M.C.; Barenholz, Y.; McIntosh, T.J. Gelation of liposome interior. A novel method for drug encapsulation. FEBS Lett. 1992, 312, 255–258. [Google Scholar] [CrossRef]
  10. Bangham, A.D. Surrogate cells or trojan horses. The discovery of liposomes. BioEssays 1995, 17, 1081–1088. [Google Scholar] [CrossRef] [PubMed]
  11. Papahadjopoulos, D. Liposomes and their uses in biology and medicine. Ann. N. Y. Acad. Sci. 1978, 308, 1–441. [Google Scholar] [CrossRef]
  12. Markman, M. Pegylated liposomal doxorubicin in the treatment of cancers of the breast and ovary. Expert Opin. Pharmacother. 2016, 7, 1469–1474. [Google Scholar] [CrossRef] [PubMed]
  13. Rivera, E. Current status of liposomal anthracycline therapy in metastatic breast cancer. Clin. Breast Cancer 2003, 4, 76–83. [Google Scholar] [CrossRef]
  14. Rosenthal, E.; Poizot-Martin, I.; Saint-Marc, T.; Spano, J.P.; Cacoub, P. Phase IV study of liposomal daunorubicin (DaunoXome) in AIDS-related Kaposi sarcoma. Am. J. Clin. Nutr. 2002, 25, 57–59. [Google Scholar] [CrossRef]
  15. Cho, K.; Wang, X.; Nie, S.; Chen, Z.; Shin, D.M. Therapeutic nanoparticles for drug delivery in cancer. Clin. Cancer Res. 2008, 14, 1310–1316. [Google Scholar] [CrossRef] [PubMed]
  16. Kango, S.; Kalia, S.; Celli, A.; Njuguna, J.; Habibi, Y.; Kumar, R. Surface modification of inorganic nanoparticles for development of organic–inorganic nanocomposites—A review. Prog. Polym. Sci. 2013, 38, 1232–1261. [Google Scholar] [CrossRef]
  17. Kagan, V.E.; Tyurina, Y.Y.; Tyurin, V.A.; Konduru, N.V.; Potapovich, A.I.; Osipov, A.N.; Kisin, E.R.; Schwegler-Berry, D.; Mercer, R.; Castranova, V.; et al. Direct and indirect effects of single walled carbon nanotubes on RAW 264.7 macrophages: Role of iron. Toxicol. Lett. 2006, 165, 88–100. [Google Scholar] [CrossRef] [PubMed]
  18. Porter, A.E. Direct imaging of single-walled carbon nanotubes in cells. Nat. Nanotechnol. 2007, 2, 713–717. [Google Scholar] [CrossRef] [PubMed]
  19. Manna, S.K. Single-walled carbon nanotube induces oxidative stress and activates nuclear transcription factor-kappaB in human keratinocytes. Nanotechnol. Lett. 2005, 5, 1676–1684. [Google Scholar]
  20. Tomalia, D.A.; Naylor, M.A.; Goddord, A.W., III. Starburst Dendrimers: Molecular-Level Control of Size, Shape, Surface Chemistry, Topology, and Flexibility from Atoms to Macroscopic Matter. Angew. Chem. Int. 1990, 29, 138–175. [Google Scholar] [CrossRef]
  21. Faraji, A.H.; Wipf, P. Nanoparticles in cellular drug delivery. Bioorg. Med. Chem. 2009, 17, 2950–2962. [Google Scholar] [CrossRef] [PubMed]
  22. Svenson, S.; Tomalia, D.A. Dendrimers in biomedical applications-reflections on the field. Adv. Drug Deliv. Rev. 2005, 57, 2106–2129. [Google Scholar] [CrossRef] [PubMed]
  23. Nawaz, M.; Fatima, F. Extracellular Vesicles, Tunneling Nanotubes, and Cellular Interplay: Synergies and Missing Links. Front. Mol. Biosci. 2017, 4, 50. [Google Scholar] [CrossRef] [PubMed]
  24. Nawaz, M.; Camussi, G.; Valadi, H.; Nazarenko, I.; Ekstrom, K.; Wang, X.; Principe, S.; Shah, N.; Ashraf, N.M.; Fatima, F.; et al. The emerging role of extracellular vesicles as biomarkers for urogenital cancers. Nat. Rev. Urol. 2014, 11, 688–701. [Google Scholar] [CrossRef] [PubMed]
  25. Rustom, A.; Saffrich, R.; Markovic, I.; Walther, P.; Gerder, H.H. Nanotubular highways for intercellular organelle transport. Science 2004, 303, 1007–1010. [Google Scholar] [CrossRef] [PubMed]
  26. Austefjord, M.W.; Gerdes, H.H.; Wang, X. Tunneling nanotubes: Diversity in morphology and structure. Commun. Integr. Biol. 2014, 7, e27934. [Google Scholar] [CrossRef] [PubMed]
  27. Benard, M.; Schapman, D.; Lebon, A.; Monterroso, B.; Bellenger, M.; Le Foll, F.; Pasquier, J.; Vaudry, H.; VAudry, D.; Galas, L. Structural and functional analysis of tunneling nanotubes (TnTs) using gCW STED and gconfocal approaches. Biol. Cell 2015, 107, 419–425. [Google Scholar] [CrossRef] [PubMed]
  28. Bonifácio, B.V.; da Silva, P.B.; dos Santos Ramos, M.A.; Silveira Negri, K.M.; Bauab, T.M.; Chorilli, M. Nanotechnology-based drug delivery systems and herbal medicines: A review. Int. J. Nanomed. 2014, 9, 1–15. [Google Scholar]
  29. Hu, L.; Han, S.; Parveen, S.; Yuan, Y.; Zhang, L.; Xu, G. Highly sensitive fluorescent detection of trypsin based on BSA-stabilized gold nanoclusters. Biosens. Bioelectron. 2012, 32, 297–299. [Google Scholar] [CrossRef] [PubMed]
  30. Zensi, A.; Begley, D.; Pontikis, C.; Legros, C.; Mihoreanu, L.; Wagner, S.; Büchel, C.; Kreuter, J. Albumin nanoparticles targeted with Apo E enter the CNS by transcytosis and are delivered to neurons. Off. J. Control. Release Soc. 2009, 137, 78–86. [Google Scholar] [CrossRef] [PubMed]
  31. Discher, E.D.; Eisenberg, A. Polymer vesicles. Science 2002, 297, 967–973. [Google Scholar] [CrossRef] [PubMed]
  32. Letchford, K.; Burt, H. A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: Micelles, nanospheres, nanocapsules and polymers. Eur. J. Pharm. Biopharm. 2007, 65, 259–269. [Google Scholar] [CrossRef] [PubMed]
  33. Vila, A.; Gill, H.; McCallion, O.; Alonso, M.J. Transport of PLA-PEG particles across the nasal mucosa: Effect of particle size and PEG coating density. J. Control. Release 2004, 98, 231–244. [Google Scholar] [CrossRef] [PubMed]
  34. Xu, Z.P.; Zeng, Q.H.; Lu, G.Q.; Yu, A.B. Inorganic nanoparticles as carriers for efficient cellular delivery. Chem. Eng. Sci. 2006, 61, 1027–1040. [Google Scholar] [CrossRef]
  35. Ensign, M.L.; Cone, R.; Hanes, J. Oral drug delivery with polymeric nanoparticles: The gastrointestinal mucus barriers. Adv. Drug Deliv. Rev. 2012, 64, 557–570. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Coulembier, O.; Degee, P.; Hedrick, L.J.; Dubois, P. From controlled ring-opening polymerization to biodegradable aliphatic polyester: Especially poly(beta-malic acid) derivatives. Prog. Polym. Sci. 2006, 31, 723–747. [Google Scholar] [CrossRef]
  37. Soppimath, S.K.; Aminabhavi, M.T.; Kulkarni, R.A.; Rudzinski, E.W. Biodegradable polymeric nanoparticles as drug delivery devices. J. Control. Release 2001, 70, 1–20. [Google Scholar] [CrossRef]
  38. Niwa, T.; Takeuchi, H.; Hino, T.; Kunou, N.; Kawashima, Y. Preparations of biodegradable nanospheres of water-soluble and insoluble drugs with d,l-lactide/glycolide copolymer by a novel spontaneous emulsification solvent diffusion method and the drug release behavior. J. Control. Release 1993, 25, 89–98. [Google Scholar] [CrossRef]
  39. Wehrle, P.; Magenheim, B.; Benita, S. The Influence of process parameters on the PLA nanoparticle size distribution evaluated by means of factorial design. Eur. J. Pharm. Biopharm. 1995, 41, 19–26. [Google Scholar]
  40. Murakami, H.; Yoshino, H.; Mizobe, M.; Kobayashi, M.; Takeuchi, H.; Kawashima, Y. Preparation of poly(d,l-lactide-co-glycolide) latex for surface modifying material by a double coacervation method. Proc. Int. Symp. Control. Release Bioact. Mater. 1996, 23, 361–362. [Google Scholar]
  41. Bodmeier, R.; McGinity, W. Solvent selection in the preparation of poly(d,l-lactide) microspheres prepared by the solvent evaporation method. Int. J. Pharm. 1998, 43, 179–186. [Google Scholar] [CrossRef]
  42. Guo, C.; Yang, C.; Li, Q.; Li, Q.-L.; Xi, Y.-W.; Liu, W.-N.; Zhai, G.-X. Development of a quercetin-loaded nanostructured lipid carrier formulation for topical delivery. Int. J. Pharm. 2012, 430, 292–298. [Google Scholar]
  43. Wu, T.; Yen, F.-L.; Lin, L.-T.; Tsai, T.-R.; Lin, C.-C.; Cham, T.-M. Preparation, physicochemical characterization, and antioxidant effects of quercetin nanoparticles. Int. J. Pharm. 2008, 346, 160–168. [Google Scholar] [CrossRef] [PubMed]
  44. Min, K.H.; Park, K.; Kim, Y.-S.; Bae, S.M.; Lee, S.; Jo, H.G.; Park, R.-W.; Kim, I.-S.; Jeong, S.Y.; Kim, K.; et al. Hydrophobically modified glycol chitosan nanoparticles-encapsulated camptothecin enhance the drug stability and tumor targeting in cancer therapy. J. Control. Release 2008, 127, 208–218. [Google Scholar] [CrossRef] [PubMed]
  45. Yen, F.Y.; Wu, T.H.; Lin, L.T.; Cham, T.M.; Lin, C.C. Naringenin-loaded nanoparticles improve the physicochemical properties and the hepatoprotective effects of naringenin in orally-administered rats with CCl4-induced acute liver failure. Pharm. Res. 2009, 26, 893–902. [Google Scholar] [CrossRef] [PubMed]
  46. Vauthier, C.; Dubernet, C.; Fattal, E.; Pinto-Alphandary, H.; Couvreur, P. Poly(alkylcyanoacrylates) as biodegradable materials for biomedical applications. Adv. Drug Deliv. Rev. 2003, 55, 519–548. [Google Scholar] [CrossRef]
  47. Calvo, P.; Sanchez, A.; Martinez, J.; Lopez, I.M.; Calonge, M.; Pastor, C.J.; Alonso, J.M. Polyester Nanocapsules as New Topical Ocular Delivery Systems for Cyclosporin A. Pharm. Res. 1996, 13, 311–315. [Google Scholar] [CrossRef] [PubMed]
  48. Mao, H.Q.; Roy, K.; Troung-Le, V.L.; Janes, K.A.; Lin, K.Y.; Wang, Y.; August, J.T.; leong, K.W. Chitosan-DNA nanoparticles as gene carriers: Synthesis, characterization and transfection efficiency. J. Control. Release 2001, 70, 399–421. [Google Scholar] [CrossRef]
  49. Cooper, G.M. The Cell: A Molecular Approach, 2nd ed.; Sunderland (MA), Sinauer Associates: New York, NY, USA, 2000. [Google Scholar]
  50. Albert, B.; Johnson, A.; Lewis, J.; Raff, M.; Roberts, K.; Walter, P. Molecular Biology of the Cell, 4th ed.; Garland Science: New York, NY, USA, 2002. [Google Scholar]
  51. Cancer Facts & Figures; American Cancer Society. 2018. Available online: https://www.cancer.org/research/cancer-facts-statistics/all-cancer-facts-figures/cancer-facts-figures-2017.html (accessed on 15 April 2018).
  52. Antoni, S.; Ferlay, J.; Soerjomataram, I.; Znaor, A.; Jemal, A.; Bray, F. Bladder cancer incidence and mortality: A global overview and recent trends. Eur. Urol. 2017, 71, 96–108. [Google Scholar] [CrossRef] [PubMed]
  53. Smith, R.A.; von Eschenbach, A.C.; Wender, R.; Levin, B.; Byers, T.; Rothenberger, D.; Saslow, D. American Cancer Society guidelines for the early detection of cancer: Update of early detection guidelines for prostate, colorectal, and endometrial cancers: Also: Update 2001-Testing for early lung cancer detection. CA Cancer J. Clin. 2001, 51, 38–75. [Google Scholar] [CrossRef] [PubMed]
  54. Lane, B.R.; Canter, D.J.; Rini, B.I.; Uzzo, R.S.; Rosenber, S.A. Cancer: Principles and Practice of Oncology, 10th ed.; Pili, R., Kauffman, E., Rodriguez, R., Eds.; Ch 82-Cancer of the Kidney; Lippincott Williams & Wilkins: Philadelphia, PA, USA, 2015. [Google Scholar]
  55. National Cancer Institute (NCI). 2018. Available online: https://www.cancer.gov/types/skin (accessed on 15 April 2018).
  56. Centers for Disease Control and Prevention 2018. Available online: https://www.cdc.gov/cancer/prostate/index.htm (accessed on 15 April 2018).
  57. Feng, S.S.; Chein, S. Chemotherapeutic engineering: Application and further development of chemical engineering principles for chemotherapy of cancer and other diseases. Chem. Eng. Sci. 2003, 58, 4087–4114. [Google Scholar] [CrossRef]
  58. Feng, S.S. Interpretation of mechanochemical properties of lipid monolayers at the air-water or oil-water interface and bilayer vesicles from equation of state or pressure-area measurement. Langmuir 1999, 15, 998–1010. [Google Scholar] [CrossRef]
  59. Steichen, D.S.; Moore, C.M.; Peppas, A.N. A review of current nanoparticle and targeting moieties for the delivery of cancer therapeutics. Eur. J. Pharm. Sci. 2013, 14, 416–427. [Google Scholar] [CrossRef] [PubMed]
  60. Minotti, G.; Menna, P.; Salvatorelli, E.; Cairo, G.; Gianni, L. Anthracyclines: Molecular Advances and Pharmacologic Developments in Antitumor Activity and Cardiotoxicity. Pharmacol. Rev. 2004, 56, 185–229. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  61. Weiss, L.M.; Jaffe, E.S.; Liu, X.F.; Chen, Y.Y.; Shibata, D.; Medeiros, L.J. Detection and localization of Epstein-Barr viral genomes in angioimmunoblastic lymphadenopathy and angioimmunoblastic lymphadenopathy-like lymphoma. Blood 1992, 79, 1789–1795. [Google Scholar] [PubMed]
  62. Rowinsky, E. The development and clinical utility of taxane class of antimicrotubule chemotherapy agents. Ann. Rev. 1997, 48, 353–374. [Google Scholar] [CrossRef] [PubMed]
  63. Boulikas, T.; Vougiouka, M. Cisplatin and platinum drugs at the molecular level. Oncol. Rev. 2003, 10, 1663–1682. [Google Scholar] [CrossRef]
  64. Hurley, H.L. DNA and its associated processes as targets for cancer therapy. Nat. Rev. Cancer 2002, 2, 188–200. [Google Scholar] [CrossRef] [PubMed]
  65. Maeda, H. SMANCS and polymer-conjugated macromolecular drugs: Advantages in cancer chemotherapy. Adv. Drug Deliv. Rev. 2001, 46, 169–185. [Google Scholar] [CrossRef]
  66. Vauthier, C.; Dubernet, C.; Chauvierre, C.; Brigger, I.; Couvreur, P. Drug delivery to resistant tumors: The potential of poly(alkyl cyanoacrylate) nanoparticles. J. Control. Release 2009, 3, 151–160. [Google Scholar] [CrossRef]
  67. Miller, D.W.; Batrakova, E.V.; Kabanov, A.V. Inhibition of multidrug resistance-associated protein (MRP) functional activity with pluronic block copolymers. Pharm. Res. 1999, 16, 396–401. [Google Scholar] [CrossRef] [PubMed]
  68. Mamot, C.; Drummond, D.C.; Hong, K.; Kirpotin, D.B.; Park, J.W. Liposome-based approaches to overcome anticancer drug resistance. Drug Resist. Updates 2003, 6, 271–279. [Google Scholar] [CrossRef]
  69. Soma, C.E.; Dubernet, C.; Bentolila, D.; Benita, S.; Couvreur, P. Reversion of multidrug resistance by co-encapsulation of doxorubicin and cyclosporin A in polyalkylcyanoacrylate nanoparticles. Biomaterials 2000, 21, 1–7. [Google Scholar] [CrossRef]
  70. Bonduelle, S.; Foucher, C.; Leroux, J.-C.; Chouinard, F.; Caieux, C.; Lenaerts, V. Association of cyclosporin to isohexylcyanoacrylate nanospheres and subsequent release in human plasma in vitro. J. Microencapsul. 1992, 9, 173–182. [Google Scholar] [CrossRef] [PubMed]
  71. Kumari, A.; Yadav, K.S.; Yadav, C.S. Biodegradable polymeric nanoparticles based drug delivery systems. Colloids Surf. B Biointerfaces 2010, 75, 1–18. [Google Scholar] [CrossRef] [PubMed]
  72. Carrasquillo, K.G.; Stanley, A.M.; Aponte-Carro, J.C.; De Jésus, P.; Costantino, H.R.; Bosques, C.J.; Griebenow, K. Non-aqueous encapsulation of excipient-stabilized spray-freeze dried BSA into poly(lactide-co-glycolide) microspheres results in release of native protein. J. Control. Release 2001, 76, 199–208. [Google Scholar] [CrossRef]
  73. RaviKumar, M.N.; Mohapatra, S.S.; Kong, X.; Jena, P.K.; Bakowsky, U.; Lehrd, C.M. Cationic poly(lactide-co-glycolide) nanoparticles as efficient in vivo gene transfection agents. J. Nanosci. Nanotechnol. 2004, 4, 990–994. [Google Scholar] [CrossRef]
  74. Hedberg, E.L.; Kroese-Deutman, H.C.; Shih, C.K.; Crowther, R.S.; Carney, D.H.; Mikos, A.G.; Jansen, J.A. In vivo degradation of porous poly(propylenefumarate)/poly(dl-lactic-co-glycolic acid) composite scaffolds. Biomaterials 2005, 26, 4616–4623. [Google Scholar] [CrossRef] [PubMed]
  75. Patil, D.S.; Papadimitrakopoulos, F.; Burgess, J.D. Dexamethasone-loaded poly(lactic-co-glycolic) acid microspheres/poly(vinyl alcohol) hydrogel composite coatings for inflammation control. Diabetes Technol. Ther. 2004, 6, 887–897. [Google Scholar] [CrossRef] [PubMed]
  76. Avgoustakis, K.; Beletsi, A.; Panagi, Z.; Lepetsanis, K.P.; Karydas, G.A.; Lthakissios, S.D. PLGA-mPEG nanoparticles of cisplatin: In vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties. J. Control. Release 2002, 79, 123–135. [Google Scholar] [CrossRef]
  77. Ranjan, P.A.; Mukherjee, A.; Helson, L.; Vishwanantha, K.J. Scale up, optimization and stability analysis of Curcumin C3 complex-loaded nanoparticles for cancer therapy. J. Nanobiotechnol. 2012, 10, 38. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Esmaeili, F.; Ghahremani, M.H.; Ostad, S.N.; Atyabi, F.; Seyedabadi, M.; Malekshahi, M.R.; Amini, M.; Dinarvand, R. Folate-receptor-targeted delivery of docetaxel nanoparticles prepared by PLGA–PEG–folate conjugate. J. Drug Target 2008, 16, 415–423. [Google Scholar] [CrossRef] [PubMed]
  79. Redhead, M.H.; Davis, S.S.; Illum, L. Drug delivery in poly(lactide-co-glycolide) nanoparticles surface modified with poloxamer 407 and poloxamine 908: In vitro characterisation and in vivo evaluation. J. Control. Release 2001, 70, 353–363. [Google Scholar] [CrossRef]
  80. Zheng, D.; Li, X.; Xu, H.; Lu, X.; Hu, Y.; Fan, W. Study on docetaxel-loaded nanoparticles with high antitumor efficacy against malignant melanoma. Acta Biochim. Biophys. Sin. 2009, 41, 578–587. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  81. Prabu, P.; Chaudhari, A.A.; Dharmaraj, N.; Khil, M.S.; Park, S.Y.; Kim, H.Y. Preparation, characterization, in-vitro drug release and cellular uptake of poly(caprolactone) grafted dextran copolymeric nanoparticles loaded with anticancer drug. J. Biomed. Mater. Res. 2008, 90, 1128–1136. [Google Scholar]
  82. Shenoy, B.D.; Amiji, M.M. Poly(ethylene oxide)-modified poly(epsiloncaprolactone) nanoparticles for targeted delivery of tamoxifen in breast cancer. Int. J. Pharm. 2005, 293, 261–270. [Google Scholar] [CrossRef] [PubMed]
  83. Gao, H.; Wang, Y.N.; Fan, Y.G.; Ma, J.B. Synthesis of a biodegradable tadpole-shaped polymer via the coupling reaction of polylactide onto mono(6-(2-aminoethyl)amino-6-deoxy)-beta-cyclodextrin and its properties as the new carrier of protein delivery system. J. Control. Release 2005, 107, 158–173. [Google Scholar] [CrossRef] [PubMed]
  84. Zambaux, M.F.; Bonneaux, F.; Gref, R.; Dellacherie, E.; Vigneron, C. Preparation and characterization of protein C-loaded PLA nanoparticles. J. Control. Release 1999, 60, 179–188. [Google Scholar] [CrossRef]
  85. Oppenhiem, C.R. Paclitaxel loaded gelatin nanoparticles for intravesical bladder cancer therapy. Int. J. Pharm. 1981, 8, 217. [Google Scholar]
  86. Lu, Z.; Yeh, T.K.; Tsai, M.; Au, J.L.; Wientjes, M.G. Paclitaxel-loaded gelatin nanoparticles for intravesical bladder cancer therapy. Clin. Cancer Res. 2004, 10, 7677–7684. [Google Scholar] [CrossRef] [PubMed]
  87. Reis, P.C.; Neufeld, R.J.; Ribeiro, A.J.; Veiga, F. Nanoencapsulation I. Methods for preparation of drug loaded polymeric nanoparticles. Nanomedicine 2006, 2, 8–21. [Google Scholar] [CrossRef] [PubMed]
  88. Davis, S. Drug delivery systems. Interdiscip. Sci. Rev. 2000, 25, 175–183. [Google Scholar] [CrossRef]
  89. Arias, J.L.; Gallardo, V.; Ruiz, M.A.; Delgado, A.V. Ftorafur loading and controlled release from poly(ethyl-2-cyanoacrylate) and poly(butylcyanoacrylate) nanospheres. Int. J. Pharm. 2007, 337, 282–290. [Google Scholar] [CrossRef] [PubMed]
  90. Carmeliet, P.; Jain, R.K. Angiogenesis in cancer and other diseases. Nature 2000, 40, 7249–7257. [Google Scholar] [CrossRef] [PubMed]
  91. Yatvin, M.B.; Kreutz, W.; Horwitz, B.A.; Shinitzky, M. pH-sensitive liposomes: Possible clinical implications. Science 1980, 210, 1253–1255. [Google Scholar] [CrossRef] [PubMed]
  92. Bianco, A.; Kostarelos, K.; Partidos, C.D.; Prato, M. Biomedical applications of functionalised carbon nanotubes. Chem. Commun. 2005, 5, 571–577. [Google Scholar] [CrossRef] [PubMed]
  93. Farokhzad, C.O.; Langer, R. Impact of Nanotechnology on Drug Delivery. ACS Nano 2009, 3, 16–20. [Google Scholar] [CrossRef] [PubMed]
  94. Farokhzad, O.C.; Karp, J.M.; Langer, R. Nanoparticle-Aptamer Bioconjugates for Cancer Targeting. Expert Opin. Drug Deliv. 2006, 3, 311–324. [Google Scholar] [CrossRef] [PubMed]
  95. Koo, O.M.; Rubinstein, I.; Onyksel, H. Role of nanotechnology in targeted drug delivery and imaging: A concise review. Nanomed. Nanotechnol. Biol. Med. 2005, 1, 193–212. [Google Scholar] [CrossRef] [PubMed]
  96. Missailidis, S.; Thomaidou, D.; Borbas, K.E.; Price, M.R. Selection of aptamers with high affinity and high specificity against C595, an anti-MUC1 IgG3 monoclonal antibody, for antibody targeting. J. Immunol. Methods 2005, 296, 45–62. [Google Scholar] [CrossRef] [PubMed]
  97. Farokhzad, O.C.; Jon, S.; Khademhosseini, A.; Tran, T.N.; Lavan, D.A.; Langer, R. Nanoparticle-Aptamer Bioconjugates. Cancer Res. 2004, 64, 7668–7672. [Google Scholar] [CrossRef] [PubMed]
  98. Gabizon, A.; Horowitz, T.A.; Goren, D.; Tzemach, D.; Shmeeda, H.; Zalipsky, S. In Vivo Fate of Folate-Targeted Polyethylene-Glycol Liposomes in Tumor-Bearing Mice. Clin. Cancer Res. 2003, 9, 6551–6559. [Google Scholar] [PubMed]
  99. Medina, O.P.; Kairemo, K.; Valtanen, H.; Kangasniemi, A.; Kaukinen, S.; Ahonen, I.; Permi, P.; Annila, A.; Sneck, M.; Holopainen, M.J.; et al. Radionuclide Imaging of Tumor Xenografts in Mice Using a Gelatinase-targeting Peptide. Anticancer Res. 2005, 25, 33–42. [Google Scholar] [PubMed]
  100. Dharap, S.S. Tumor-specific targeting of an anticancer drug delivery system by LHRH peptide. Proc. Natl. Acad. Sci. USA 2003, 102, 12962–12967. [Google Scholar] [CrossRef] [PubMed]
  101. Mitra, A.; Mulholland, J.; Nan, A.; McNeil, E.; Ghandehari, H.; Line, R.B. Targeting tumor angiogenic vasculature using polymer–RGD conjugates. J. Control. Release 2005, 102, 191–201. [Google Scholar] [CrossRef] [PubMed]
  102. Temming, K.; Schiffelers, M.R.; Molema, G.; Kok, J.R. RGD-based strategies for selective delivery of therapeutics and imaging agents to the tumour vasculature. Drug Resist. Updates 2005, 8, 381–402. [Google Scholar] [CrossRef] [PubMed]
  103. Adabi, M. Biocompatibility and nanostructured materials: Applications in nanomedicine. Artif. Cells Nanomed. Biotechnol. 2016, 45, 833–842. [Google Scholar] [CrossRef] [PubMed]
  104. Naahidi, S.; Mousa, J.; Faramarz, E.; Kevin, R.; Khademhosseini, A.; Chen, P. Biocompatibility of engineered nanoparticles for drug delivery. J. Control. Release 2013, 166, 182–194. [Google Scholar] [CrossRef] [PubMed]
  105. Singh, S.; Singh, H.N. Nanotechnology and Health Safety-Toxicity and Risk Assessments of Nanostructured Materials on Human Health. J. Nanosci. Nanotechnol. 2007, 23, 3048–3070. [Google Scholar] [CrossRef]
  106. Li, X.; Wang, L.; Fan, Y.; Feng, Q.; Cui, F.Z. Biocompatibility and toxicity of nanoparticles and nanotubes. J. Nanomater. 2012, 2012, 6. [Google Scholar] [CrossRef]
  107. Brocchini, S.; Duncan, R. Pendent drugs, release from polymers. Encycl. Control. Drug Deliv. 1999, 2, 786–816. [Google Scholar]
  108. Shiah, J.G.; Sun, Y.; Kopečková, P.; Peterson, C.M.; Straight, R.C.; Kopeček, J. Combination chemotherapy and photodynamic therapy of targetable N-(2-hydroxypropyl) methacrylamide copolymer–doxorubicin/mesochlorin e6-OV-TL 16 antibody immunoconjugates. J. Control. Release 2001, 74, 249–253. [Google Scholar] [CrossRef]
  109. Cardoso, P.B.; Machado, T.O.; Feuser, P.E.; Sayer, C.; Meier, M.A.; Araujo, P.H. Biocompatible Polymeric Nanoparticles from Castor Oil Derivatives via Thiol-Ene Miniemulsion Polymerization. Eur. J. Lipid Sci. Technol. 2018, 120, 1700212. [Google Scholar] [CrossRef]
Sample Availability: Since this is a review, no samples are available.
Molecules 23 02157 g001 550
Figure 1. Schematic representation of (a) bottom-up; and (b) top-down approach.
Figure 1. Schematic representation of (a) bottom-up; and (b) top-down approach.
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Molecules 23 02157 g002 550
Figure 2. Schematic illustration of nanocarriers for the delivery of drug.
Figure 2. Schematic illustration of nanocarriers for the delivery of drug.
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Molecules 23 02157 g003 550
Figure 3. Schematic illustration of (a) nanocapsule; and (b) nanosphere.
Figure 3. Schematic illustration of (a) nanocapsule; and (b) nanosphere.
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Molecules 23 02157 g004 550
Figure 4. Solvent evaporation method.
Figure 4. Solvent evaporation method.
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Figure 5. Solvent diffusion method.
Figure 5. Solvent diffusion method.
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Molecules 23 02157 g006 550
Figure 6. Salting out method.
Figure 6. Salting out method.
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Figure 7. Nanoprecipitation method.
Figure 7. Nanoprecipitation method.
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Figure 8. Ion gelation method.
Figure 8. Ion gelation method.
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Molecules 23 02157 g009 550
Figure 9. Most common type of cancer in 2018 reported by the American Cancer Society.
Figure 9. Most common type of cancer in 2018 reported by the American Cancer Society.
Molecules 23 02157 g009
Molecules 23 02157 g010 550
Figure 10. Schematic illustration of (a) Passive targeting; (b) Active targeting.
Figure 10. Schematic illustration of (a) Passive targeting; (b) Active targeting.
Molecules 23 02157 g010
Table
Table 1. Synthetic and natural biodegradable polymers used as drug delivery vehicles adapted from [36].
Table 1. Synthetic and natural biodegradable polymers used as drug delivery vehicles adapted from [36].
Synthetic Biodegradable PolymersNatural Biodegradable Polymers
PolyestersPolyoxalatesStarchChitosan
PolyorthoestersPolyiminocarbonatesHyaluronic acidDextran
PolyanhydridesPolyurethanesHeparin
PolydioxanonesPolyphosphazenesGelatin
Poly(a-cyanoacrylates) Albumin
Table
Table 2. List of cancers, their cause, common types, and estimated deaths.
Table 2. List of cancers, their cause, common types, and estimated deaths.
Most Prevalent CancersCauseMost Common TypeEstimated DeathReferences
BladderSmoking, Exposition to certain chemicals, chronic bladder infections, Abnormal cell growth in the muscular sac that stores urine, urothelium, infection with Schistosoma haematobiumUrothelial carcinoma, squamous cell carcinoma, adenocarcinoma, Superficial bladder cancer, Invasive bladder cancer17,240[51,52]
Breast (Men and Female)Malignant tumor in the breast, gene mutation, family historyDuctal carcinoma in situ (DCIS), Invasive Ductal Carcinoma (IDC), Mammogram, Lumpectomy, Mastectomy268,670[51]
Colon and RectalGenetic mutation, an inherited or acquire mutation to the APC gene.More than 95% of colon cancer can be classified as adenocarcinomas.50,630[51]
EndometrialIncreasing age, unopposed estrogen therapy, late menopause, tamoxifen therapy, nulliparity, infertility or failure to ovulate, obesity, hypertension, diabetes, and HNPCC.Adenocarcinoma, Carcinosarcoma, Squamous cell carcinoma, Undifferentiated carcinoma, Small cell carcinoma, Transitional carcinoma11,350[53]
Kidney (Renal Cell and Renal Pelvis)Smoking, obesity, Workplace exposures, Family history of kidney cancer, High blood pressure, Certain medicinesRenal cell carcinoma (RCC), Clear cell renal cell carcinoma, Papillary renal cell carcinoma, Chromophobe renal cell carcinoma, transitional cell carcinomas, Wilms tumors, and renal sarcomas.14,970[51,54]
Leukemia (All Types)DNA of immature blood cells, mainly white cells, becomes damaged.Acute lymphoblastic leukemia, Acute myeloid leukemia, Chronic lymphocytic leukemia (CLL), Chronic myeloid leukemia (CML), Chronic myelomonocytic leukemia (CMML), Leukemia in children24,370[51]
Liver and Intrahepatic Bile DuctAlcohol, age, smoking, genetic, hepatitis, obesity, cirrhosis, genderHepatocellular carcinoma, Hepatoblastoma, Hepatocellular carcinoma30,200[51]
Lung (Including Bronchus)Smoking tobacco, second hand smoke, genetic undergoing radiation therapy and environmental exposureSmall Cell Lung Cancer (SCLC) Non-Small Cell Lung Cancer (NSCLC)154,050[51,55]
SkinExposure to Ultraviolet (UV) light, tanning beds or sunlamps.Melanoma, Basal, Squamous and Merkel Cell Carcinoma, Epidermoid cysts9320[51,55]
Non-Hodgkin LymphomaInfection-fighting cells of the immune system, called lymphocytes, immune deficiency.Hodgkin lymphoma and non-Hodgkin lymphoma (NHL), Skin lymphoma, pediatric lymphoma, AIDS-related lymphoma, Waldenstrom macroglobulinemia (WM)19,910[51]
PancreaticDNA mutations, Diabetes, smoking, pancreatitis, smoking, ObesityExocrine cancers, Pancreatic adenocarcinoma, endocrine44,330[51]
ProstateOncogenes change or mutation in the DNA, Age, growth of abnormal cells, which may invader healthy cells in the body.Acinar, ductal adenocarcinoma, ductal, urothelial, squamous cell cancer, Small all prostate cancer29,430[56]
ThyroidRadiation, low iodine consumptions, family history, gender, age, hereditary conditions, DNA mutationspapillary, follicular, medullary, and anaplastic thyroid cancer.2060[51]
Table
Table 3. Example of some ligands used in active drug targeting adapted from [95].
Table 3. Example of some ligands used in active drug targeting adapted from [95].
Targeting LigandsTargetsReferences
AptamersAntibodies, cell surface receptors, enzymes, small organic molecules, peptides, proteins[96,97]
FolateFolate receptor[98]
Gelatinase inhibitor peptide CTTHWGFTLCMatrix Metalloprotease-2 and Matrix Metalloprotease-9 gelatinase[99]
Luteinizing hormone-releasing hormoneLuteinizing hormone-releasing hormone receptor[100,101]
RGD peptideIntegrin[102]

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Ahlawat, J.; Henriquez, G.; Narayan, M. Enhancing the Delivery of Chemotherapeutics: Role of Biodegradable Polymeric Nanoparticles. Molecules 2018, 23, 2157. https://doi.org/10.3390/molecules23092157

AMA Style

Ahlawat J, Henriquez G, Narayan M. Enhancing the Delivery of Chemotherapeutics: Role of Biodegradable Polymeric Nanoparticles. Molecules. 2018; 23(9):2157. https://doi.org/10.3390/molecules23092157

Chicago/Turabian Style

Ahlawat, Jyoti, Gabriela Henriquez, and Mahesh Narayan. 2018. "Enhancing the Delivery of Chemotherapeutics: Role of Biodegradable Polymeric Nanoparticles" Molecules 23, no. 9: 2157. https://doi.org/10.3390/molecules23092157

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