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polymers

Article
Polyoxyethylene Diamine Modification of
Poly(amide-imide)-polyethylene Glycol Exhibits Excellent
Hydrophilicity, Degradability, and Biocompatibility
Ran Yu 1,2 , Chao Xu 2 , Xiaopei Wu 1,2 and Honglian Dai 1,2, *

1 Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory,
Xianhu Hydrogen Valley, Foshan 528200, China
2 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing,
Wuhan University of Technology, Wuhan 430070, China
* Correspondence: daihonglian@whut.edu.cn; Tel.:+86-13697333860

Abstract: We designed and synthesized the polyoxyethylene diamine (H2 N-PEG-NH2 ) and
poly(amide-imide)-polyethylene glycol (PAI-PEG) copolymers. The physical and chemical properties,
mechanical properties, and in vitro biocompatibility of the materials were characterized. The results
showed that the best elongation at break and recovery were obtained when the amount of PEG
was 5 wt%. With the increase in PEG content, the degradation rate, hydrophilic property, tensile
strength and tensile modulus of the copolymer decreased to a certain extent. The material had the
best thermal stability and mechanical properties when 5 wt% PEG was added. Cytocompatibility
evaluation showed that the addition of PEG could enhance the cell compatibility of the material and
make it potentially suitable for application in bone repair.

Keywords: polyoxyethylene diamine (H2 N-PEG-NH2 ); poly(amide-imide) (PAI); biocompatibility


Citation: Yu, R.; Xu, C.; Wu, X.; Dai,
H. Polyoxyethylene Diamine
Modification of
Poly(amide-imide)-polyethylene 1. Introduction
Glycol Exhibits Excellent
In the United States and the European Union, there are approximately 1 million cases
Hydrophilicity, Degradability, and
of bone defects each year, and bone graft surgery is required to achieve fusion [1]. Bone is
Biocompatibility. Polymers 2022, 14,
a dynamic, highly vascularized tissue with a unique ability to heal and reshape without
4694. https://doi.org/10.3390/
leaving scars [2,3]. Therefore, materials are booming in the medical field of artificial bones,
polym14214694
and among them, synthetic polymers have attracted more and more attention due to their
Academic Editor: Ilaria Armentano designable properties [4–6]. Although polymer materials have been widely used in the field
Received: 21 June 2022
of bone repair, artificial polymer materials still have disadvantages that cannot be ignored,
Accepted: 24 October 2022
such as non-degradability, stress shielding and lack of biological activity. Therefore, the
Published: 3 November 2022
ideal bone repair material should have good biocompatibility, biodegradability and suitable
mechanical properties.
Publisher’s Note: MDPI stays neutral
Poly(amide-imide) (PAI) was chosen in our work because it has been widely used in
with regard to jurisdictional claims in
the industrial field as an engineering plastic due to its excellent mechanical properties and
published maps and institutional affil-
extremely high thermal stability. However, its lack of biodegradability limits its application
iations.
in the field of biomaterials. Previous studies have introduced L-amino acids into non-
degradable polymers [7–9] to make the non-degradable materials biodegradable. The
reason is that amino acids can endow the polymer materials with bioactive sites similar
Copyright: © 2022 by the authors.
to peptide materials, and also provide enzymatic hydrolysis sites for the biodegradation
Licensee MDPI, Basel, Switzerland. of polymers [10–12]. In our previous research [13], the synthesized PAI derived from
This article is an open access article L-phenylalanine showed good biocompatibility, biodegradability, and potential application
distributed under the terms and value in the field of biological materials. However, the hydrophilicity of PAI is poor.
conditions of the Creative Commons Therefore, we hope to improve the hydrophilicity of PAI by introducing the hydrophilic
Attribution (CC BY) license (https:// polyether segment to form copolymers with PAI.
creativecommons.org/licenses/by/ Polyethylene glycol (PEG) is a polymer widely used in the field of biomaterials with
4.0/). good hydrophilicity. In an aqueous medium, the molecular conformation of PEG will

Polymers 2022, 14, 4694. https://doi.org/10.3390/polym14214694 https://www.mdpi.com/journal/polymers


Polymers 2022, 14, 4694 2 of 14

change, and the ether bond (R-O-R) in PEG will be distributed on the chain surface,
making it easy to combine with water around the polymer [14]. Its main applications in
biomaterials include increasing membrane permeability and modifying some materials
with poor biocompatibility. PEG with higher molecular weight can be cleared by the kidney,
so it has safe toxicity characteristics and bio-tolerance. Due to the wide range of PEG
molecular weight selection, the range of mechanical and physical properties can be realized
by simply changing the molecular weight and concentration of PEG, and biological activity
can be controlled by introducing specific biological active agents [15]. The activity of the
terminal hydroxyl in polyethylene glycol is relatively low, and a large number of studies
have modified the terminal hydroxyl into more reactive functional groups such as amino
(-NH2 ), carboxyl (-COOH), and ester groups [16,17]. The modified PEG can be used to
further synthesize new polymer materials. With the development of material technology,
in the field of medical materials the single function of a material cannot meet its application
requirements, so more and more studies have been devoted to the preparation of composite
polymers and copolymers.
PAI can provide good mechanical properties and thermal stability for the copolymer,
while PEG can provide excellent hydrophilicity and biocompatibility. To make up for
the lack of hydrophilicity of PAI, PEG was copolymerized with PAI. It was hoped that
PAI-PEG copolymer could have good hydrophilicity, biocompatibility, and suitable me-
chanical properties. In our work, PAI-PEG copolymers were prepared by chemical bonding.
Finally, we tested the cell compatibility of the copolymer to evaluate its potential as a bone
repair material.

2. Materials and Methods


2.1. Materials
The following materials were used: polyethylene glycol (Mn = 2000), dichloromethane
(AR, ≥99.5%), triethylamine (AR, 99%), p-toluene sulfonyl chloride (TsCl; ≥99%), ethyl
ether (AR, ≥99%), L-phenylalanine (99%), glacial acetic acid (AR, ≥99.5%), anhydrous
ethanol (AR, ≥99.7%), hydrochloric acid (AR, 36~38%), sodium bicarbonate (NaHCO3 ;
AR, ≥99.5%), sodium hydroxide (NaOH; AR, ≥96%), calcium nitrate tetrahydrate (AR,
99%), diammonium phosphate (AR, ≥99%), ethyl orthosilicate (TEOS; AR), N, N-dimethyl
acetamide (10-channel DMAc; AR, ≥99%), and ammonia water (AR, 25~28%) were pur-
chased from Sinopharm Chemical ReagentCo., Ltd. (Shanghai, China). 3,30 ,4,40 -biphenyl
tetracarboxylic acid dianhydride (BPDA; 99%), 4,40 -two carboxyl diphenyl ether (ODA;
98%), tetrabutylammonium bromide (TBAB; AR, 99%), triphenyl phosphite (TPP; 98%) and
tetrabutyl ammonium bromide (TBAB; AR, 99%) were purchased from Shanghai Aladdin
Biochemical Technology Co., Ltd. (Shanghai, China). Mouse bone marrow mesenchymal
stem cells (BMSCs) were extracted from the bone marrow of male Sprague-Dawley (SD)
rats (Hubei Provincial Center for Disease Control and Prevention, Wuhan, China). alpha
MEM medium, 10% Fetal Bovine Serum (FBS), penicillin-streptomycin, phosphate buffer
saline (PBS), and trypsin-edta were purchased from Hyclone (Logan, UT, USA). Addi-
tionally, we used Cell Counting Kit-8 (CCK-8; Beyotime Biotechnology., Wuhan, China),
fitc-phalloidin (Solarbio, Beijing, China), 40 ,6-diamidine-2-phenylindoles (DAPI; Beijing
solarbio science & technology Co., Ltd., Beijing, China), and 4% paraformaldehyde (Wuhan
Boster Biological Technology., LTD, Wuhan, China).

2.2. Synthesis of Polyoxyethylene Diamine (H2 N-PEG-NH2 )


Polyethylene glycol (PEG, molecular weight 2000, PEG 2000) and p-toluene sulfonyl
chloride (TsCl) were dissolved in dichloromethane (CH2 Cl2 ) and triethylamine to form
a solution. The reaction was terminated after stirring the solution for 12 h at room tem-
perature, then the organic phase solution was washed with HCl (3M). The solid sodium
bicarbonate was then slowly added to the organic phase to react with the HCl away. The
solution was stirred vigorously until there were no bubbles, then filtered under reduced
pressure to produce a concentrated solution. Excess diethyl ether was slowly added to
Polymers 2022, 14, x FOR PEER REVIEW 3 of 16

ature, then the organic phase solution was washed with HCl (3M). The solid sodium bi-
carbonate was then slowly added to the organic phase to react with the HCl away. The
Polymers 2022, 14, 4694 3 of 14
solution was stirred vigorously until there were no bubbles, then filtered under reduced
pressure to produce a concentrated solution. Excess diethyl ether was slowly added to the
concentrated solution to precipitate a large amount of sediment. After filtration and vac-
the concentrated
uum solution
drying, the white waxy tosolid
precipitate
product a large amount glycol
polyethylene of sediment. After
p-toluene filtration
sulfonate and
(TsO-
vacuum drying, the
PEG-OTs) was obtained. white waxy solid product polyethylene glycol p-toluene sulfonate
(TsO-PEG-OTs)
TsO-PEG-OTs wasandobtained.
ammonia water were added to a 150 mL autoclave and sealed at
TsO-PEG-OTs and
140 °C for 6 h, then cooled ammonia
to room water were added
temperature, andtothe
a 150 mL autoclave
aqueous phase wasandextracted
sealed at
140 ◦ C for 6 h, then cooled to room temperature, and the aqueous phase was extracted
with dichloromethane; sodium hydroxide aqueous solution (1M) was added, and the mix-
withwas
ture dichloromethane;
left standing aftersodium hydroxide
stirring aqueous
for 4 h. The solution
organic phases(1M)
werewas added, washed
combined, and the
mixture
with was left
deionized standing
water to pHafter
= 7,stirring for 4 h. The
and freeze-dried to organic
obtain aphases
white were combined,
powder productwashed
(H2N-
with deionized water to pH = 7, and freeze-dried
PEG-NH2). The reaction process is shown in Figure 1. to obtain a white powder product
(H2 N-PEG-NH2 ). The reaction process is shown in Figure 1.

Thesynthesis
Figure1.1.The
Figure synthesisofofpolyoxyethylene
polyoxyethylenediamine.
diamine.

2.3. Synthesis of Poly(amide-imide)—Polyethylene Glycol Copolymer (PAI-PEG)


2.3. Synthesis of Poly(amide-imide)—Polyethylene Glycol Copolymer (PAI-PEG)
BPDA and L-phenylalanine were uniformly dispersed in glacial acetic acid to form
BPDA and L-phenylalanine were uniformly dispersed in glacial acetic acid to form a
a homogeneous solution. The reaction system was stirred at room temperature (25 ◦ C)
homogeneous solution. The reaction system was stirred at room ◦temperature (25 °C) for
for 12 h. Then, in an oil bath the temperature was raised to 110 C, and the reaction was
12 h. Then, in an oil bath the temperature was raised to 110 °C, and the reaction was re-
refluxed for 5 h. After the reaction was completed, vacuum distillation was performed to
fluxed for 5 h. After the reaction was completed, vacuum distillation was performed to
distill off the reaction solvent. The distillation temperature was 63 ◦ C and the flow rate was
distill off the reaction solvent. The distillation temperature was 63 °C and the flow rate
1 to 2 drops per second. Finally, the reaction product was washed 3 times with 1 mol/L
was 1 to 2 drops per second. Finally, the reaction product was washed 3 times with 1
hydrochloric acid aqueous solution. Suction filtration and vacuum drying at 30 ◦ C for 12 h
mol/L hydrochloric acid aqueous solution. Suction filtration and vacuum drying at 30 °C
were performed to obtain L-phenylalanine-based imide diacid monomer [13].
for 12ODA,
h werepolyoxyethylene
performed to obtain L-phenylalanine-based
diamine, and L-phenylalanine imide diacidacid
diamino monomer
monomer [13].were
added to molten tetrabutylammonium bromide to form a homogeneous solution,were
ODA, polyoxyethylene diamine, and L-phenylalanine diamino acid monomer and
added
TPP was to molten
addedtetrabutylammonium
dropwise. The reaction bromide
system to was
formplaced
a homogeneous solution,
in an oil bath at 110and
◦ CTPP
and
was added dropwise. The reaction system was placed in an oil bath at 110 °C and
stirred for 2.5 h under the protection of N2 . After the reaction was completed, anhydrous stirred
for 2.5 h under
ethanol the protection
was added dropwiseoftoNthe
2. After the reaction was completed, anhydrous ethanol
reaction solution, and the precipitated product was
was added dropwise to the reaction
stirred, washed three times with anhydroussolution, and the
ethanol, precipitated
filtered product
with suction, andwas stirred,
dried under

vacuum at 60 C for 12 h to obtain the copolymer containing L-phenylalanine poly(amide-
imide)—PEG block in the main chain (PAI-PEG). The reaction process is shown in Figure 2.
Different samples’ names and compositions are shown in Table 1 and the ingredients are
shown in Table 2.
washed three times with anhydrous ethanol, filtered with suction, and dried under vac-
uum at 60 °C for 12 h to obtain the copolymer containing L-phenylalanine poly(amide-
imide)—PEG block in the main chain (PAI-PEG). The reaction process is shown in Figure
2. Different samples’ names and compositions are shown in Table 1 and the ingredients
Polymers 2022, 14, 4694 are shown in Table 2. 4 of 14

Figure 2. The synthesis of Poly(amide-imide)-polyethylene glycol copolymer(PAI-PEG).


Figure 2. The synthesis of Poly(amide-imide)-polyethylene glycol copolymer(PAI-PEG).
Table 1. Different samples’ names and compositions.

Table 1. Different samples’Names


Specimens’ names and compositions. Compositions
S1 Names
Specimens’ PAI-PEG-0
Compositions
S2 PAI-PEG-5
S1
S3 PAI-PEG-0
PAI-PEG-10
S2
S4 PAI-PEG-5
PAI-PEG-15
S3 PAI-PEG-10
S4 PAI-PEG-15
Polymers 2022, 14, 4694 5 of 14

Table 2. The synthesis of PAI-PEG composites with different amounts of PEG.

Imide Diacid
Sample wt% a PEG2000 (g) ODA (g)
Monomer (g)
S1 0 0 5.97 1.9624
S2 5 1 5.97 1.9
S3 10 2 5.97 1.8
S4 15 3 5.97 1.7
a represents the mass percentage of PEG added.

2.4. Characterization of S1–S4


2.4.1. Fourier Transform Infrared Spectrum Analysis (FTIR)
An infrared spectrometer (Nicolet 6700, Thermo Electron Scientific Instruments, Madi-
son, WI, USA) was used to analyze the structure of PEG, TsO-PEG-OTs, H2 N-PEG-NH2 , and
samples S1 to S4. The KBr tablet was used and the measurement range was 4000–400 cm−1 .

2.4.2. 1 H NMR Analysis


A nuclear magnetic resonance spectrometer (Bruker Avance500, Bruker, Karlsruhe,
Germany) was used to detect the hydrogen atom environment of synthetic polymers.
Tetramethylsilane (Si(OH3 )4 ) was used as the internal standard, and DMSO-d6 was used as
the solvent.

2.4.3. Hydrophilic Performance Analysis


The hydrophilic property of the polymer surface was detected by a water contact
angle measuring instrument (JC2000C 50Hz, KRUSS, Hamburg, Germany). A point was
measured every 5 mm. Each polymer was measured at least three times: points, multiple
measurements, and average.

2.4.4. Thermal Analysis


The thermal analysis (STA449F3/STA449F3, NETZSCH, Hamburg, Germany) was
used to analyze the thermal properties of synthetic polymers. Nitrogen was used as the
protective gas, the heating rate was 10 ◦ C/min, and the test temperature range was 25 ◦ C
to 1000 ◦ C.

2.4.5. Mechanical Testing


The mechanical properties of the sample splines were tested according to GB/T1040-
2006 “Plastic tensile test method”. Dumbbell-shaped test specimens with molded product
specifications of 4 × 35 mm were tested for tensile properties and elongation at break using a
universal material testing machine (M350/500, LLOYD, British). The speed was 1 mm/min. At
least 5 samples were tested in each group.
To measure the recovery rate, a sample with a width of 4 mm and a length of
L0 = 25 mm was used with a tensile speed of 50 mm/min. The tensile length was based on
the stress-strain curve before the yield point. In this experiment, it was taken as 10 mm.
Then, we waited for the sample to recover and measured the length as L. We used the follow-
ing formula to determine the elastic recovery rate of the sample: X = (2L0 − L)/L0 × 100%.

2.4.6. In Vitro Degradation Experiment


The degradation of S1–S4 of PAI-PEG was performed in vitro, mainly by immersing
the material in PBS for 28 days. Samples at different time points were weighed, and the pH
of the degradation solution and residual mass were measured. The surface morphology of
the soaking material was observed with an electron microscope (SEM) (JSM IT200, JEOL,
Akishima, Japan). A test sample with a regular shape was prepared, and the mass–volume
ratio of the sample to the PBS was 1:20. The degradation device was placed in a 37 ◦ C
constant-temperature shaking box. Three samples were taken from each group on days 1,
3, 5, 7, 14, 21, and 28, and dried in a blast drying oven at 37 ◦ C to constant weight.
Polymers 2022, 14, 4694 6 of 14

2.4.7. In Vitro Biocompatibility Assay


The in vitro biocompatibility of S1, S2, S3, and S4 was characterized through the
observation of cell adhesion, proliferation, and differentiation. BMSCs were seeded onto
the specimens with densities of 5 × 104 cell/mL, 2 × 104 cell/mL and 2.5 × 104 cell/mL,
for cell adhesion, proliferation, and differentiation, respectively [18,19]. After the BMSCs
were cultured normally for 24 h, the cells adhered to the wall and were replaced with S1–S4
extract and the culture continued for 5 days. Then, 100 µL live/dead staining working
solution was added to each well. After 10 min, images were observed and taken under a
fluorescence microscope. S1–S4 samples were co-cultured with BMSCs for 3 days, and the
cell morphology was observed by a confocal laser scanning microscope (CLSM) (FV1000,
Olympus, Tokyo, Japan). The cell proliferation rate was assessed using the CCK-8 method.
At 1, 3, and 5 days the formazan product was quantified by a microplate reader (Multiskan
GO, Thermo SCIENTIFIC, Waltham, MA, USA).

3. Results and Discussion


3.1. Structure Characterization of PAI-PEG
Figure 3A shows the FTIR spectrum of PEG, polyethylene glycol p-toluene sulfonates
(TsO-PEG-OTs), and double-terminal amino polyethylene glycols (H2 N-PEG-NH2 ). Sym-
metrical stretching vibration, deformation vibration, and in-plane swing vibration of C-H
were observed at 2877 cm− 1 , 1487 cm− 1 , and 802 cm− 1 in the spectra of TsO-PEG-OTs
and H2 N-PEG-NH2 . The characteristic C-O-C peak appears at 1100 cm− 1 . This peak was
the main characteristic peak of PEG-Ots. The bond stretching peak, 1645 cm− 1 , was the
characteristic peak of N-H of -NH2 . FTIR analysis results showed that the synthesized
structures TsO-PEG-OTs and H2 N-PEG-NH2 were consistent with the expected structure.
Figure 3B shows the FTIR spectrum of the copolymers (S1, S2, S3, and S4) of block
poly(amido-imide)-polyethylene glycols with different contents of polyethylene glycol. It
could be seen from the figure that 2933 cm− 1 was an asymmetric stretching vibration of
-CH2 -. As the amount of polyethylene glycol increased, the absorption peak strength also
increased; 1774 and 1716 cm− 1 were symmetrical stretching vibrations of C=O on the imide
ring; 1374 cm− 1 was the stretching vibration of C-N on the imide ring; 1533 and 3380 cm− 1
were the bending vibration and stretching vibration of N-H on amide group; 1223 cm− 1
was the stretching vibration of C-N in amide group. The stretching vibration of C-N on
the imide ring was 1394 cm− 1 ; 842 cm− 1 and 742 cm− 1 were the characteristic peaks of
benzene rings, and 1102 cm− 1 was the characteristic peak of benzene ring ether. The
characteristic peak of the bond was also the characteristic peak of the polyethylene glycol
ether bond. The characteristic peak intensity increased with the increase in polyethylene
glycol. FTIR spectrum results confirmed the successful preparation of block poly(amido-
imide)-polyethylene glycol copolymers with different levels of polyethylene glycol.
As shown in Figure 3C, δ H (ppm): 3.52 was the absorption peak of the repeating
segment (-CH2 CH2 O-); δ H (ppm): 2.51 and 3.50 peaks 1 and 2 were the amino-linked
fluorene and β carbon Proton absorption peak. Combined with infrared spectroscopy
analysis, we could see that the terminal hydroxyl group of PEG had been converted to the
amino group of H2 N-PEG-NH2 .
In Figure 3D, the proton peak at 9.996 ppm was the N-H proton on the amide group,
which proved that the polymer skeleton contained the amide group. The peak at 5.198 ppm
corresponded to the proton on the chiral carbon atom where L-phenyl propionic acid
was connected to BPDA. The peak -CH-, and the H proton on the aromatic ring were in
5 different chemical environments. At position 5, due to the π–π conjugate effect between
two adjacent benzene rings and the π–π conjugate effect of the carbon–oxygen double
bond on the benzene ring and the imide ring, the chemical shift value moved to a low
field, and the chemical shift value was high. However, because the π–π conjugate effect
between the benzene rings was greater than the π–π conjugate effect of the carbon–oxygen
double bond on the benzene ring and the imide ring, the density of the electron cloud
around position 7 was slightly lower than position 6. Therefore, the chemical shift value
Polymers 2022, 14, 4694 7 of 14

of 7H on the benzene ring was higher than 6H. Similarly, the electron conjugation effect
of p–π formed by the N atom and the benzene ring was lower than that of the O atom,
so the density of the electron cloud at position 8 on the benzene ring was lower than that
around position 9, and the chemistry displacement value of 8H on benzene ring was higher
than 9H. The proton characteristic peak of polyethylene glycol-CH2 CH2 O- was at 3.51.
Combined with the analysis of the infrared spectrum, it could be concluded that the block
poly(amide imide)-polyethylene glycol copolymer was successfully prepared.

Figure 3. Structural characterization. (A): FTIR spectrum of PEG, TsO-PEG-OTs and H2 N-PEG-NH2 ;
(B): FTIR of S1–S4; (C): 1 H NMR spectrum of PEG, TsO-PEG-OTs, and H2 N-PEG-NH2 ; (D): 1 H NMR
spectrum of S1–S4; (E): S1–S4 surface SEM image. Scale bar = 500 µm.

3.2. Thermal Analysis


Figure 4A shows the DSC curve of copolymer S1–S4. The crystallization temperatures
(Tc) of S1–S4 were 138.3 ◦ C, 136.8 ◦ C, 130 ◦ C, and 118 ◦ C. With the increase in PEG content,
the Tc of the copolymer moved to a lower temperature direction. This showed that as the
soft segment increased, the ability of the copolymer to aggregate and crystallize decreased.
We speculated that this phenomenon might be related to the following factors. First, it could
be seen from Figure 3E that there was a certain degree of phase separation between PEG and
PAI. The introduction of the random phase separation destroyed the chain structure of PAI
and PEG, respectively, making the originally regular structure disordered, which affected
the crystal growth of the respective segments, resulting in smaller grains or imperfect
crystals. Second, with the increase in the content of the soft segment, the hard segment
Polymers 2022, 14, 4694 8 of 14

Polymers 2022, 14, x FOR PEER REVIEW 9 of 16

molecular chain would be restricted by the soft segment molecular chain, which made it
difficult
weight to crystallize
at the after forming
same temperature. Tablehydrogen
3 showed bonds between amide
the weightlessness groups.
of the When
samples the
at dif-
PEG content increased
ferent temperatures. from 10% to 15%, these effects changed dramatically, as shown in
Figure 4A; DSC curves of S3 and S4 showed great differences.

Figure
Figure4.4.S1–S4
S1–S4comprehensive
comprehensivethermal
thermalanalysis
analysis spectrum. (A): S1–S4
spectrum. (A): S1–S4 DSC
DSCcurve;
curve;(B):
(B):S1–S4
S1–S4Tg
Tgcurve.
curve.
It can be seen from Figure 4B that at 200 ◦ C, the Tg curves of all the groups began to
Table
drop.3. The
The weightlessness of the
weight loss rate samples
of the at different
S4 group temperatures.
had always been the highest, while the weight
loss rate of the S1 group (T
Mass/% was the lowest, with S2 and S3Mass/%
= 200/℃) in between. A second thermal
(T = 500/℃)
decomposition occurred at 450 ◦ C. At this time, the weight loss rate of S4 was 48.7%, and
S1 7.5 28.8
the weight loss rate of S1 was 28.8%. This may indicate that as the content of the hard
S2 1.8 37.4
segment increased, the thermal decomposition of the soft segment was delayed, and the
S3 the content of the 5.63
higher 40.4
hard segment, the more PAI tended to agglomerate and lose less
S4 8.38
weight at the same temperature. Table 3 showed the weightlessness 48.7 of the samples at
different temperatures.
3.3. In Vitro Degradation Analysis
Table 3. The weightlessness of the samples at different temperatures.
Figure 5A shows the surface morphology changes of S1–S4 after degradation for 1, 7,
14, and 28 days. After degradation
Mass/% (T for 7 days, cracks occurred on
= 200/°C) the surface
Mass/% of S1–S4. The
(T = 500/°C)
cracks became larger with the higher PEG content. Large cracks appeared on the surface
S1 7.5 28.8
of S4 after
S2 28 days of degradation, 1.8and the trend of increasing cracks with 37.4 the increase of
PEG content
S3 was consistent at 7, 14,
5.63 and 28 days, which indicated that
40.4the surface mor-
phology S4of degraded material was 8.38strongly related to the PEG content. 48.7The degradation
data shows (Figure 5B) that the weight loss rate of the material in the initial stage of deg-
radation displayed
3.3. In Vitro a decreasing
Degradation Analysistrend, which means that the mass of the material did not
decrease at the initial stage of degradation, but increased, and tended to degrade normally
Figure 5A shows the surface morphology changes of S1–S4 after degradation for 1, 7,
in the later stage of degradation, which may be related to the material’s adsorption of
14, and 28 days. After degradation for 7 days, cracks occurred on the surface of S1–S4. The
crystal
crackswater
became in PBS.
largerAs shown
with in Figure
the higher PEG 5D,E, in the
content. infrared
Large crackscharacterization
appeared on the ofsurface
the ma-of
terial after287 days
S4 after days of
of degradation,
degradation, and compared with
the trend ofthe undegraded
increasing cracksmaterial,
with theaincrease
characteristic
of PEG
peak
content was consistent at 7, 14, and 28 days, which indicated that the surfacethe
of crystal water appeared. This may explain why the weight loss rate of material
morphology
decreased
of degraded during the initial
material stage ofrelated
was strongly degradation,
to the PEGand content.
the quality
Theofdegradation
degradationdata wasshows
less
than the mass of crystal water adsorbed by the material. However, the
(Figure 5B) that the weight loss rate of the material in the initial stage of degradationcontent of PEG is
not the only factor affecting the degradation rate of the copolymer. We
displayed a decreasing trend, which means that the mass of the material did not decrease atspeculated that
when the amount
the initial stage ofof PEG was small,
degradation, the hard and
but increased, segment
tendedPAI could tightly
to degrade wrapinthe
normally thesoft
later
segment, slowing down the degradation rate of the copolymer. With the
stage of degradation, which may be related to the material’s adsorption of crystal water inincrease in PEG
content,
PBS. Asashown
large number
in Figureof5D,E,
PEGinchain segments
the infrared were exposedoftothe
characterization the degradation
material after 7 liquid
days of
environment, which increased the overall degradation rate of the copolymer.
degradation, compared with the undegraded material, a characteristic peak of crystal water
appeared. This may explain why the weight loss rate of the material decreased during
the initial stage of degradation, and the quality of degradation was less than the mass of
crystal water adsorbed by the material. However, the content of PEG is not the only factor
Polymers 2022, 14, 4694 9 of 14

affecting the degradation rate of the copolymer. We speculated that when the amount of
PEG was small, the hard segment PAI could tightly wrap the soft segment, slowing down
the degradation rate of the copolymer. With the increase in PEG content, a large number of
PEG chain segments were exposed to the degradation liquid environment, which increased
the overall degradation rate of the copolymer.

Figure 5. In vitro degradation experiment. (A): SEM surface morphology of S1–S4 degraded in PBS
at 37 ◦ C for 1, 7, 14, and 28 days. (B): residual mass during S1–S4 degradation; (C): during S1–S4
degradation pH value of degradation solution; (D): Infrared characterization chart of S1 without
degradation and degradation for 7 days; (E): Infrared characterization chart of S4 without degradation
and degradation for 7 days.
Polymers 2022, 14, 4694 10 of 14

The experimental data shows that the pH value of the degradation solution of different
samples decreased with the increase in degradation time (Figure 5C), and the change
Polymers 2022, 14, x FOR PEER REVIEW 11 of 16
rate of pH was different with the increase in PEG content, which was related to PEG
degradation products. In the presence of enzyme-catalyzed alcohol dehydrogenase, PEG
is metabolized to carboxylic acid, diacid and hydroxy acid metabolites by oxidation of
The experimental data shows that the pH value of the degradation solution of differ-
its alcohol group [20]. However,
ent samples decreased the
with thepH of the
increase degradation
in degradation timesolution could
(Figure 5C), be change
and the maintained
between 7.0 rateandof7.2
pHwhich was conducive
was different to cell
with the increase growth
in PEG when
content, whichthe amount
was ofPEG
related to 5 wt%
deg- of the
material wasradation
addedproducts.
[21,22]. In the presence of enzyme-catalyzed alcohol dehydrogenase, PEG is
metabolized to carboxylic acid, diacid and hydroxy acid metabolites by oxidation of its
alcohol
3.4. Mechanical group [20].Analysis
Performance However, the pH of the degradation solution could be maintained
between 7.0 and 7.2 which was conducive to cell growth when the amount of 5 wt% of the
Figure material
6A,B reflects
was addedthe[21,22].
tensile strength and tensile modulus of the material. With
the increase of the PEG content, the tensile strength and tensile modulus of the copolymer
both showed3.4. Mechanical Performance Analysis
a downward trend. This might be because the addition of PEG destroyed the
Figure 6A,B reflects the tensile strength and tensile modulus of the material. With the
PAI segment arrangement and reduced its crystallinity. PAI mainly provided mechanical
increase of the PEG content, the tensile strength and tensile modulus of the copolymer
strength for both
the copolymer, and PEG
showed a downward mainly
trend. provided
This might its toughness.
be because the additionTherefore, when PEG
of PEG destroyed
was added, the tensile
the PAI strength
segment and tensile
arrangement modulus
and reduced decreased,
its crystallinity. but theprovided
PAI mainly elongation
mechan-at break
and recovery icalrate increased
strength first and and
for the copolymer, thenPEG decreased with its
mainly provided the addition
toughness. of PEG,when
Therefore, reaching
the maximum PEG was added,
value in thetheS2tensile strength
material and tensile
group (252%modulus decreased,
and 97.5%, but the elongation
respectively, Figureat6B,D),
break and recovery rate increased first and then decreased with the addition of PEG,
while the values of the S1 material group were only 146% and 86%, respectively. When
reaching the maximum value in the S2 material group (252% and 97.5%, respectively, Fig-
the materialurewas stretched,
6B,D), physical
while the values of thecross-linking
S1 material group points would
were only 146% be
andformed between the
86%, respectively.
segments. TheWhen cross-linking
the material was point could
stretched, recover.
physical Therefore,
cross-linking pointswhen
wouldthe external
be formed force was
between
removed, the thematerial
segments. hadThe cross-linking point could recover.
recovery performance; when Therefore,
the amountwhen the
ofexternal
PEG addedforce was
was removed, the material had recovery performance; when the amount of PEG added
small, the regularity of the crystal region was less damaged, and the corresponding existing
was small, the regularity of the crystal region was less damaged, and the corresponding
physical cross-linking pointcross-linking
existing physical had higher pointrecovery rate. However,
had higher when
recovery rate. the amount
However, when oftheadded
PEG increased,
amount theofcrystallinity was severely
added PEG increased, damaged,
the crystallinity wasthe physical
severely cross-linking
damaged, the physicalpoints
were reduced, and the points
cross-linking recoverability
were reduced,thatandwould otherwisethat
the recoverability have
wouldbeen provided
otherwise naturally
have been
provided
decreased with naturally
it. This was whydecreased
the with it. Thisgroup
material was why the material
reached group reached
the maximum the max-
value in the S2
imum value in the S2 group and then showed a downward trend.
group and then showed a downward trend.

Figure 6. Analysis of mechanical properties of S1–S2; (A) Elastic strength; (B) Elastic modulus; (C)
Elongation at break; (D) Recovery rate.

3.5. Hydrophilic Performance Analysis


As shown in Figure 7, after the introduction of PEG into the polymer, the contact angle
of the polymer surface decreased from 90◦ to 52◦ , indicating that the introduction of PEG
Figure 6. Analysis of mechanical properties of S1–S2; (A) Elastic strength; (B) Elastic modulus; (C)
Elongation at break; (D) Recovery rate.

Polymers 2022, 14, 4694 3.5. Hydrophilic Performance Analysis 11 of 14


As shown in Figure 7, after the introduction of PEG into the polymer, the contact
angle of the polymer surface decreased from 90° to 52°, indicating that the introduction of
PEG effectively
effectively improved
improved the hydrophilic
the hydrophilic properties
properties of theofmaterial
the material surface.
surface. Compared
Compared with
with the degradable
the degradable polymers
polymers PLLAPLLA ◦
(85 )(85°) and PLGA
and PLGA ◦
(74.5 (74.5°)
) [22], [22], the PAI-PEG
the PAI-PEG copolymer
copolymer had a
had a better
better hydrophilic
hydrophilic property.
property. This might
This result result be
might be attributed
attributed to the
to the fact thatfact that
in an in an
aqueous
aqueous
medium,medium, the molecular
the molecular conformation
conformation of PEG ofwillPEG will change,
change, and theand thebond
ether ether(R-O-R)
bond (R- in
O-R) in the hydrophilic
the hydrophilic polyether
polyether chain segment
chain segment is distributed
is distributed on the
on the chain chain making
surface, surface, itmak-
easy
ing it easy towith
to combine combine
waterwith water
around thearound
polymer the[14].
polymer [14].

Figure 7. The water contact angle of the S1–S4.


Figure 7. The water contact angle of the S1–S4.
3.6. In Vitro Biocompatibility Analysis
3.6. In Vitro Biocompatibility Analysis
Figure 8A shows the live/dead staining of the BMSCs that were cultured for 5 days
on the S1–S4. It could be seen from the figure that there was no significant difference in
the results of live/dead staining in all material groups compared with the control group,
but it could be seen that S2 had the best live/dead cell staining. Studies have shown that
the growth rate of cells depends on the adhesion strength of cells on the surface of the
material [23,24]. Figure 8B is a cell adhesion map of S1–S4 and BMSCs cells co-cultured for
Polymers 2022, 14, 4694 12 of 14

3 days. From the figure, it could be seen that in all the material groups, the cells stretched
almost in the shape of a pseudo-foot on the surface of the material, which indicated that
the copolymer could provide a biocompatible surface environment for cell adhesion and
growth and good cell adhesion. Figure 8C is a graph of cell viability after co-culture of
S1–S4 and BMSCs. On the first day of co-cultivation, there was no significant difference in
the absorbance between the material group and the control group; on the third day, there
was no significant difference between the absorbance of S1 and the control group, and
the absorbance of the other groups were lower than that of the control group. There was
no significant difference in absorbance between the material group and the control group
on the fifth day. This indicated that all material groups could promote the growth and
proliferation of BMSCs. The results of in vitro biocompatibility tests showed that S1–S4
could promote the adhesion and proliferation of BMSCs in vitro.

Figure 8. (A): Live/dead staining of the BMSCs that were cultured for 5 days on the S1–S4, respec-
tively. (B): CLSM micrographs of the BMSCs adhesive on S1–S4 for 3 days. (C): Cell viabilities of the
BMSCs that were cultured on the S1–S4 for 1, 3, and 5 days, respectively.
Polymers 2022, 14, 4694 13 of 14

4. Conclusions
The main purpose of this study was to prepare a bone repair material with good
mechanical properties and biocompatibility. The PAI-PEG copolymer was successfully
prepared by solution polycondensation. The results showed that the S2 material exhibited
the most excellent physical and chemical properties. In vitro biocompatibility of the S1–S4
showed that all material groups were non-toxic and could support the proliferation and
adhesion of BMSCs. The S2 could potentially be used as bone repair implants in orthopedic
surgery in the future.

Author Contributions: Conceptualization, H.D.; methodology, R.Y., C.X. and X.W.; software, R.Y.;
validation, R.Y.; formal analysis, R.Y.; investigation, R.Y. and C.X.; resources, H.D.; data curation,
H.D.; writing—original draft preparation, R.Y.; writing—review and editing, R.Y., C.X., X.W. and
H.D.; visualization, R.Y. and H.D.; supervision, X.W. and H.D.; project administration, H.D.; funding
acquisition, H.D. All authors have read and agreed to the published version of the manuscript.
Funding: This work was supported by grants from the National Natural Science Foundation of
China (32201109 and 51772233), the Guangdong Basic and Applied Basic Research Foundation
(2021A1515110557) and Foshan Xianhu Laboratory of the Advanced Energy Science and Technology
Guangdong Laboratory (XHT2020-008).
Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.
Data Availability Statement: Not applicable.
Acknowledgments: This work was supported by grants from the National Natural Science Founda-
tion of China (32201109 and 51772233), the Guangdong Basic and Applied Basic Research Foundation
(2021A1515110557) and Foshan Xianhu Laboratory of the Advanced Energy Science and Technology
Guangdong Laboratory (XHT2020-008). The experimental studies were carried out using equipment
of Wuhan University of Technology (State Key Laboratory of Advanced Technology for Materials Syn-
thesis and Processing, Center for Materials Research and Analysis Wuhan University of Technology).
Conflicts of Interest: The authors declare no conflict of interest.

References
1. Simon, C.G.; Khatri, C.A.; Wight, S.A.; Wang, F.W. Preliminary report on the biocompatibility of a moldable, resorbable, composite
bone graft consisting of calcium phosphate cement and poly(lactide-co-glycolide) microspheres. J. Orthop. Res. 2002, 20, 473–482.
[CrossRef]
2. Sommerfeldt, D.; Rubin, C. Biology of bone and how it orchestrates the form and function of the skeleton. Eur. Spine J. 2001, 10,
S86–S95. [PubMed]
3. Rodan, A.G. Introduction to bone biology. Bone 1992, 13, S3–S6. [CrossRef]
4. Wang, B.; Zhang, Y.; Guo, Z.; Cheng, J.; Fang, Z. Biodegradable aliphatic/aromatic copoly(ester-ether)s: The effect of poly(ethylene
glycol) on physical properties and degradation behavior. J. Polym. Res. 2011, 18, 187–196. [CrossRef]
5. Yang, Y.; Pan, D.; Luo, K.; Li, L.; Gu, Z. Biodegradable and amphiphilic block copolymer–doxorubicin conjugate as polymeric
nanoscale drug delivery vehicle for breast cancer therapy. Biomaterials 2013, 34, 8430–8443. [CrossRef] [PubMed]
6. Guo, K.; Chu, C.C. Synthesis, characterization, and biodegradation of novel poly(ether ester amide)s based on L-phenylalanine
and oligoethylene glycol. biomacromolecules 2007, 8, 2851–2861. [CrossRef] [PubMed]
7. Yodoya, S.; Takagi, T.; Kurotani, M.; Hayashi, T.; Nagata, M.; Oka, M.; Hayashi, T. Preparation and properties of A–B–A tri-block
copolymer membranes consisting of N-hydroxypropyl-l-glutamine as the A component and l-alanine as the B component. Eur.
Polym. J. 2003, 39, 2059–2067. [CrossRef]
8. Horwitz, J.A.; Shum, K.M.; Bodle, J.C.; Deng, M.; Chu, C.-C.; Reinhart-King, C.A. Biological performance of biodegradable amino
acid-based poly(ester amide)s: Endothelial cell adhesion and inflammation in vitro. J. Biomed. Mater. Res. Part A 2010, 95A,
371–380. [CrossRef]
9. Scholl, M.; Kadlecova, Z.; Klok, H.-A. Dendritic and hyperbranched polyamides. Prog. Polym. Sci. 2009, 34, 24–61. [CrossRef]
10. Zhang, W.; Huang, Y. Biodegradable Copoly(Amino Acid)s Based on 6-Aminocaproic Acid andl-Leucine. J. Polym. Environ. 2011,
19, 177–181. [CrossRef]
11. Okada, M. Chemical syntheses of biodegradable polymers. Prog. Polym. Sci. 2002, 27, 87–133. [CrossRef]
12. Birchall, A.C.; Bush, S.M.; North, M. Copolymerization of peptide derived monomers and methyl methacrylate. Polymer 2001, 42,
375–389. [CrossRef]
Polymers 2022, 14, 4694 14 of 14

13. Zou, Q.; Zhou, Q.; Dai, H. Synthesis, mechanical properties and biocompatibility of novel biodegradable Poly(amide-imide)s for
spinal implant. Polym. Degrad. Stab. 2017, 135, 85–98. [CrossRef]
14. Zdyrko, B.; Klep, V.; Li, X.; Kang, Q.; Minko, S.; Wen, X.; Luzinov, I. Polymer brushes as active nanolayers for tunable bacteria
adhesion. Mater. Sci. Eng. C 2009, 29, 680–684. [CrossRef]
15. Lynn, A.D.; Kyriakides, T.R.; Bryant, S.J. Characterization of the in vitro macrophage response and in vivo host response to
poly(ethylene glycol)-based hydrogels. J. Biomed. Mater. Res. Part A 2010, 93A, 941–953.
16. Quan, S.; Huang, Y.; Chen, X.; Wu, M.; Sun, J.; Jing, X. Hemoglobin conjugated micelles based on triblock biodegradable polymers
as artificial oxygen carriers. biomaterials 2009, 30, 5077–5085.
17. Gref, R.; Miralles, G.; Dellacherie, É. Polyoxyethylene-coated nanospheres: Effect of coating on zeta potential and phagocytosis.
Polym. Int. 1999, 48, 251–256. [CrossRef]
18. Fang, W.; He, X.; Leng, Z. Bone Marrow-Derived Mesenchymal Stem Cells Transplantation for Spinal Cord Injury: A 13-Year
Bibliometric Analysis Based on the Web of Science. Am. J. Neuroprotection Neuroregeneration 2013, 5, 70–81. [CrossRef]
19. Jung, H.D.; Park, H.S.; Kang, M.H.; Li, Y.; Estrin, Y. Reinforcement of polyetheretherketone polymer with titanium for improved
mechanical properties and in vitro biocompatibility. J. Biomed. Mater. Res. Part B Appl. Biomater. 2015, 104, 141–148. [CrossRef]
20. Milla, P.; Dosio, F.; Cattel, L. Pegylation of proteins and liposomes: A powerful and flexible strategy to improve the drug delivery.
Curr Drug Metab 2012, 13, 105–119. [CrossRef]
21. Kohn, D.H.; Sarmadi, M.; Helman, J.I.; Krebsbach, P.H. Effects of ph on human bone marrow stromal cells in vitro: Implications
for tissue engineering of bone. J Biomed Mater Res 2002, 60, 292–299. [CrossRef] [PubMed]
22. Miller, W.M.; Blanch, H.W.; Wilke, C.R. A kinetic analysis of hybridoma growth and metabolism in batch and continuous
suspension culture: Effect of nutrient concentration, dilution rate, and pH. Biotechnol. Bioeng. 2000, 67, 853–871. [CrossRef]
23. Elwing, H. ChemInform Abstract: Protein Adsorption and Ellipsometry in Biomaterial Research. Cheminform 2010, 29. [CrossRef]
24. Singhvi, R.; Stephanopoulos, G.; Wang, D.I.C. Effects of substratum morphology on cell physiology. Biotechnol. Bioeng. 1994, 43,
764–771. [CrossRef] [PubMed]

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