Xu Liang, Qiu Linzi, Sheng Yang, Sun Yixin, Deng Linhong, Li Xinqing, Bradley Mark, Zhang Rong
Jiangsu Key Laboratory of Environmentally Friendly Polymeric Materials, School of Materials Science and Engineering, Changzhou University, Changzhou 213164, China.
J Mater Chem B. 2018 Jan 21;6(3):510-517. doi: 10.1039/c7tb01851g. Epub 2018 Jan 5.
Dual-drug loaded pH-responsive hydrogels were prepared as a delivery system carrying, as exemplars, both anti-cancer and anti-bacterial agents for pH controlled drug release. The hydrogels were composed of poly(l-lactide)-co-polyethyleneglycol-co-poly(l-lactide) dimethacrylates (with various molecular weights of l-lactide oligomers) as a macromolecular crosslinker and copolymerized with acrylic acid and N-isopropylacrylamide. The biodegradability, biocompatibility and mechanical properties of the hydrogels were characterized with the hydrogels being nontoxic to cells, while showing a reversible >80% reduction in volume at pH 1.2 compared to pH 7.4. Drug release profiles showed differential release of tetracycline over doxorubicin at pH 1.2, with both drugs being released equally at pH 7.4. Biodegradability was tunable by altering the crosslinking density and pH, with the total degradation of the best gels observed within 2 weeks at pH 7.4.
制备了负载双药的pH响应水凝胶作为一种递送系统,作为示例,该系统携带抗癌和抗菌药物以实现pH控制的药物释放。水凝胶由聚(L-丙交酯)-共-聚乙二醇-共-聚(L-丙交酯)二甲基丙烯酸酯(具有不同分子量的L-丙交酯低聚物)作为大分子交联剂,并与丙烯酸和N-异丙基丙烯酰胺共聚而成。对水凝胶的生物降解性、生物相容性和机械性能进行了表征,结果表明水凝胶对细胞无毒,同时在pH 1.2时与pH 7.4相比体积可逆减少>80%。药物释放曲线显示,在pH 1.2时四环素的释放与阿霉素不同,而在pH 7.4时两种药物释放相同。通过改变交联密度和pH值可调节生物降解性,在pH 7.4条件下,最佳凝胶在2周内可观察到完全降解。
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