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Mussel inspired protein-mediated surface functionalization of electrospun nanofibers for pH-responsive drug delivery

机译:贻贝启发了电纺纳米纤维的蛋白质介导的表面功能化可用于pH响应药物递送

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摘要

pH-responsive drug delivery systems could mediate drug releasing rate by changing pH values at specific time as per the pathophysiological need of the disease. Herein, we demonstrated a mussel inspired protein polydopamine coating can tune the loading and releasing rate of charged molecules from electrospun poly (ε-caprolactone) (PCL) nanofibers in solutions with different pH values. In vitro release profiles showed that the positive charged molecules released significantly faster in acidic than those in neutral and basic environments within the same incubation time. The results of fluorescein diacetate staining and 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays showed the viability of cancer cells after treatment with doxorubicin released media at different pH values qualitatively and quantitatively, indicating the media contained doxorubicin which was released in solutions at low pH values could kill significantly higher number of cells than that released in solutions at high pH values. Together, the pH-responsive drug delivery systems based on polydopamine-coated PCL nanofibers could have potential applications in oral delivery of anticancer drugs for treating gastric cancer and vaginal delivery of anti-viral drugs or anti-inflammatory drugs, which could raise their efficacy, deliver them to the specific target, and minimize their toxic side effects.
机译:pH响应型药物输送系统可以根据疾病的病理生理需要,通过在特定时间改变pH值来介导药物释放速率。在这里,我们证明了贻贝启发的蛋白质聚多巴胺涂层可以调节具有不同pH值的溶液中电纺聚(ε-己内酯)(PCL)纳米纤维带电分子的负载和释放速率。体外释放曲线表明,在相同的孵育时间内,带正电的分子在酸性条件下的释放速度明显快于中性和碱性环境。荧光素双乙酸盐染色和3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)分析的结果表明,用阿霉素释放的培养基在不同pH值下定性和定量地分析了癌细胞的活力,表明含有在低pH值溶液中释放的阿霉素的培养基比在高pH值溶液中释放的阿霉素能杀死更多的细胞。总之,基于聚多巴胺涂层的PCL纳米纤维的pH响应药物传递系统可能在口服传递抗胃癌药物以治疗胃癌和阴道传递抗病毒药或抗炎药方面具有潜在的应用,从而提高其疗效,将它们递送到特定目标,并最大程度地减少其毒副作用。

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