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pH-Sensitive Hydrogels Based on (Meth)Acrylates and Itaconic Acid

机译:基于(甲基)丙烯酸酯和衣康酸的pH敏感水凝胶

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Novel hydrogels based on 2-hydroxyethyl methacrylate (HEMA), itaconic acid (IA) and different poly (alkylene glycol) (meth)acrylates (PAGM) (P(HEMA/IA/PAGM)) were synthesized. We investigated the influence of different PAGM components, with acrylic or methacrylic acid residues in the main chain and ethylene glycol (EG) and/or propylene glycol (PG) units in pendant chains of varying length, on the nature and inherent properties of P(HEMA/IA/PAGM) copolymeric hydrogels. Swelling studies revealed pH sensitive behavior of P(HEMA/IA/PAGM) samples. Hydrogel structure and morphology were characterized by Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM), which corifirmed their chemical structure and differences in pore size. The shear modulus values for P(HEMA/IA/PAGM) hydrogels were close to that of PHEMA, but slightly lower than the value for P(HEMA/IA). Cephalexin (CEX) drug release profiles from P(HEMA/IA/PAGM) samples showed a marked dependence on the PAGM component. The presence of IA also influenced the release rate of CEX, leading to a faster release when IA was combined with the more hydrophilic PAGM component. An in vitro assay of P(HEMA/ IA/PAGM) cytotoxicity showed good cell viability. The results obtained indicate that P(HEMA/IA/PAGM) hydrogel properties were significantly dependent on the PAGM component, meaning that the type of side chains can be used to tune the characteristics of such biomaterials. These properties make P(HEMA/IA/PAGM) copolymeric hydrogels applicable in biomedical and biotechnological fields and controlled drag delivery.
机译:合成了基于甲基丙烯酸2-羟乙酯(HEMA),衣康酸(IA)和不同的聚(亚烷基二醇)(甲基)丙烯酸酯(PAGM)(P(HEMA / IA / PAGM))的新型水凝胶。我们研究了不同的PAGM组分,主链上的丙烯酸或甲基丙烯酸残基以及不同长度的侧链中的乙二醇(EG)和/或丙二醇(PG)单元对P( HEMA / IA / PAGM)共聚物水凝胶。溶胀研究表明P(HEMA / IA / PAGM)样品的pH敏感行为。通过傅立叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)表征了水凝胶的结构和形态,证实了它们的化学结构和孔径差异。 P(HEMA / IA / PAGM)水凝胶的剪切模量值接近PHEMA,但略低于P(HEMA / IA)的剪切模量。 P(HEMA / IA / PAGM)样品中的头孢氨苄(CEX)药物释放曲线显示出对PAGM成分的显着依赖性。 IA的存在也影响了CEX的释放速率,当IA与亲水性更高的PAGM组分结合使用时,释放速度更快。 P(HEMA / IA / PAGM)细胞毒性的体外测定显示出良好的细胞活力。获得的结果表明,P(HEMA / IA / PAGM)水凝胶的性能显着依赖于PAGM组分,这意味着侧链的类型可用于调整此类生物材料的特性。这些特性使P(HEMA / IA / PAGM)共聚物水凝胶可应用于生物医学和生物技术领域,并控制药物的传递。

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