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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 9 · IF 1.64

Salt and pH sensitive semi-interpenetrating polyelectrolyte hydrogels poly(HEMA-co-METAC)/PEG and its BSA adsorption behavior

Yan-Yan Hu,Jing Zhang,Qi-Chen Fang,Dong-Mei Jiang,Chu-Cheng Lin,Yi Zeng,Ji-Sen Jiang

A novel semi-interpenetrating poly(2-hydroxyethyl methacrylate) (pHEMA) based polyelectrolyte hydrogel [p(HEMA- co -METAC)/PEG] was prepared by copolymerizing HEMA with the cationic monomer 2-methacryloyloxyethyltrimethyl ammonium chloride (METAC) in the presence of polyethylene glycol (PEG) with different content and molecular weight (MW 4000 and 400). The chemical structure of the gels was confirmed by FT-IR spectroscopy, morphology study was performed by scanning electron microscope (SEM), thermal stability was revealed by thermogravimetric analysis (TGA), and the mechanical properties were determined by electronic universal testing machine. Swelling studies showed introduction of cationic monomer METAC led to high water content, and the obvious salt and pH sensitive properties were observed which proved the smart behavior of the semi-interpenetrating polymer networks (IPNs) gels. In addition, the effect of temperature and some important biological solution on swelling behavior were reported. Cytotoxicity test demonstrated that synthesized gels owned satisfactory cytocompatibility and were convenient for the application as biomaterials. Finally, the weak bovine serum albumin (BSA) adsorption on semi-IPNs by introducing METAC and controlling the content of PEG in gels demonstrated that they were of good protein resistance effect in biomedical applications. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41537.

CAS / MDL: 868-77-9 25322-68-3
研究领域: 材料科学 · 生物医学工程
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CHEMICAL ENGINEERING JOURNAL · 2014 · IF 4.058

Preparation of one-dimensional La2−xGdx(MoO4)3−y(WO4)y: Eu3+ amorphous materials by multiple irradiations and in polymeric gels

Jiansheng Huo,Yuhui Zheng,Qianming Wang

Novel red-emitting Eu 3+ -activated La 2 − x Gd x (MoO 4 ) 3 − y (WO 4 ) y phosphors with well-defined one-dimensional nanostructures were synthesized via a supersonic microwave co-assistance (SMC) method for the first time at very low temperature (60   °C). Scanning electron microscopy studies substantiated that these phosphors are very uniform. The crystal structure and luminescent properties were characterized by powder X-ray diffraction patterns (XRD) and photoluminescence measurements (PL) respectively. An intense red emission at 615   nm ( 5 D 0   →   7 F 2 ) was detected under the excitation at 280   nm. The PL properties of La 2 − x Gd x (MoO 4 ) 3 − y (WO 4 ) y : Eu 3+ with different ratio of La/Gd or MoO 4 /WO 4 have also been investigated in detail. Furthermore, the optimized phosphor was embedded into the poly-hydroxyethylmethacrylate(HEMA) gel and the corresponding luminescent gel was achieved.

研究领域: 材料科学 · 光学
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JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION · 2017 · IF 1.9

Iodine-responsive poly (HEMA–PVP) hydrogel for self-regulating burst-free extended release

Jinku Xu,Peili Zhao,Yongchun Zhang

Swollen hydrogels with extended iodine release kinetics is highly desirable for burn and scald treatment. In this paper semi-interpenetrating poly (HEMA–PVP) hydrogels were prepared by radical polymerization followed by thermo-treatment to crosslink its PVP component. Incorporation of PVP component endows the hydrogels responsive to loaded iodine undergoing a reversible shrunken/swollen volume transition. This resulted in a self-regulating iodine release model, in which shrunken hydrogel at high iodine loading decreased drug diffusion thereby reducing burst release, and then gradually swollen hydrogel as drug release ensures rapid release of dissociated drug from strong affinity sites on hydrogel backbone, achieving a burst-free extended release. The hydrogels demonstrated 11.5-fold higher iodine loading than pure pHEMA hydrogel and showed a highest 40% volume shrink. Initial burst release of iodine was efficiently decreased from 12,894 μg/day of pure pHEMA hydrogel to 2570 μg/day of pHEMA/PVP hydrogel with 37% PVP content. Iodine-loaded hydrogels showed zero-order release at three time periods of 0–15 h, 15 h–3.5 days and 3.5–23.5 days corresponding to release rate of 2570, 776 and 493 μg/day. The work gained a new insight into swollen hydrogel drug delivery system with burst-free extended drug release kinetics.

研究领域: 材料科学 · 药学 · 生物医学工程
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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS · 2020 ·Vol. 109 ·期 1 ·50-59 · IF 2.831

A convenient approach by using poly-(HEMA-co-NIPAM)/Cu2+ solution sol–gel transition for wound protection and healing

Yansong Wang,Xin Chu,Yu Sun,Peng Teng,Tianzhi Xia,Yisheng Chen

Rapid and convenient wound healing is crucial for reducing potential post-traumatic wound complications. In this study, a temperature-sensitive polymer of poly-(HEMA-co-NIPAM) (PHN) was synthesized by free-radical polymerization, in which the solution quickly underwent a sol–gel transition above 29°C, thus responding to a typical body temperature and facilitating wound sealing. PHN solution incorporated with copper ions (PHN-Cu) not only exhibited excellent antibacterial properties, but also expedited wound closure and facilitated tissue angiogenesis. The in vivo and in vitro experiments showed that the PHN-Cu had a higher wound closure rate and demonstrated an ability to promote skin tissue angiogenesis. Such a versatile, convenient aqueous solution could enable nonprofessionals to promptly treat wounds in a short time after injury, thus providing suitable conditions for later treatment, and can be used as a convenient method to clean wounds.

研究领域: 材料科学 · 生物医学工程 · 伤口护理
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Biomaterials Advances · 2022 · IF 0

Poly(2-hydroxyethyl methacrylate-co-quaternary ammonium salt chitosan) hydrogel: A potential contact lens material with tear protein deposition resistance and antimicrobial activity

Xilin Lin,Jinqiang Liu,Fei Zhou,Yangtao Ou,Jianhua Rong,Jianhao Zhao

Tear protein deposition resistance and antimicrobial property are two challenges of conventional poly(2-hydroxyethyl methacrylate) (pHEMA) contact lenses. In this work, we developed a poly(2-hydroxyethyl methacrylate- co -quaternary ammonium salt chitosan) hydrogel, named as p(HEMA-co-mHACC) hydrogel, using acryloyl HACC (mHACC) as a macromolecular crosslinker. With increasing the acryloyl substitution degree (14–29%) or mHACC content (2–11%), the hydrogel showed an enhanced tensile strength (432–986 kPa) and Young's modulus (360–1158 kPa), a decreased elongation at break (242–84%), and an increased visible light transmittance (0–95%). At an optimal acryloyl substitution degree of 26%, with the increase of mHACC content from 2% to 11%, p(HEMA-co-mHACC) hydrogel presented a decreased water contact angle from 84.6 to 55.3 degree, an increased equilibrium water content from 38% to 45%, and an enhanced oxygen permeability from 8.5 to 13.5 barrer. Due to the enhancement in surface hydrophilicity and electropositivity, p(HEMA-co-mHACC) hydrogel remarkably reduced the deposition of lysozyme, but little affected the adsorption of BSA, depending on the hydrophilic/hydrophobic and electrostatic interactions . The antimicrobial test against Staphylococcus aureus and Escherichia coli showed that p(HEMA-co-mHACC) hydrogel presented an 8–32 times higher germicidal ability than pHEMA hydrogel, indicative of a better antimicrobial activity. The in vitro cell culture of mouse NIH3T3 fibroblasts and immortalized human keratinocytes showed that p(HEMA-co-mHACC) hydrogel was non-toxic. Thus, p(HEMA-co-mHACC) hydrogel with tear protein deposition resistance and antimicrobial activity is a potential candidate for contact lenses.

研究领域: 生物材料学 · 眼科医学 · 高分子化学
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IRANIAN POLYMER JOURNAL · 2019 ·Vol. 28 ·期 11 ·957-967 · IF 1.707

Multi-stimuli-responsive poly(hydroxyethyl methacrylate-co-N-vinyl pyrrolidone-co-methacrylic acid-co-N-isopropylacryl amide) hydrogel: synthesis, characterization and application in drug release

Yang Xiaoli,Wang Kunyan,Yan Lei,Yu QiNing,Xia Hongxia,Liu Yanbo,Yan Chengjun

Multi-stimuli-responsive hydrogels are being increasingly studied due to their sensitive response to small stimuli and wide applications in biosensors and drug delivery. In this study, a multi-stimuli-responsive hydrogel, poly(hydroxyethyl methacrylate- co - N -vinyl pyrrolidone- co -methacrylic acid- co - N -isopropylacryl amide) [poly(HEMA- co -NVP- co -MAA- co -NIPA)], was synthesized by radical polymerization and characterized by Fourier transform infrared (FTIR) and 13 C NMR spectroscopy techniques. With the aids of scanning electron microscopy (SEM) characterization, it was confirmed that the sensitive stimuli-responsive behavior of the hydrogel stemmed from its microstructure variation with those external stimulus. Rheological study showed that the hydrogel had rheological feature of typical elastomer. Compression tests revealed that the poly(hydroxyethyl methacrylate- co - N -vinyl pyrrolidone) [poly(HEMA- co -NVP)] played an important role in enhancing the compressive modulus of such hydrogel. More interestingly, the equilibrium swelling ratio (ESR) studies further confirmed that the composite hydrogel displayed response sensitively to the stimulus of temperature, pH, and ionic strength. Herein, theophylline as a drug model was adopted due to the multi-stimulus properties of hydrogels, which were a potential candidate for drug loading and delivering. Releasing drug continuously in a given period was dependent on the characteristics of solution and loading time. The mechanisms for drug release from the hydrogels were studied by Ritger–Peppas model.

CAS / MDL: 110-26-9
研究领域: 材料科学 · 生物医学工程 · 药剂学
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