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Water-borne Polymeric Nanoparticles for Glutathione-Mediated Intracellular Delivery of Anticancer Drugs.

机译:谷胱甘肽介导的抗癌药物细胞内递送的水性聚合物纳米颗粒。

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摘要

A new family of water-borne, biocompatible and carboxyl- functionalized nanogels was developed for glutathione- mediated delivery of anticancer drugs. Poly(N-vinyl- pyrrolidone)-co-acrylic acid nanogels were generated by e- beam irradiation of aqueous solutions of a crosslinkable polymer, using industrial-type linear accelerators and set- ups. Nanogels physico-chemical properties and colloidal stability, in a wide pH range, were investigated. In vitro cell studies proved that the nanogels are fully biocompatible and able to quantitatively bypass cellular membrane. An anticancer drug, doxorubicin (DOX), was linked to the carboxyl groups of NGs through a spacer containing a disulphide cleavable linkage. In vitro release studies showed that glutathione is able to trigger the release of DOX through the reduction of the S-S linkage at a concentration comparable to its levels in the cytosol.
机译:开发了一种新型的水性,生物相容性和羧基官能化的纳米凝胶,用于谷胱甘肽介导的抗癌药物的递送。聚(N-乙烯基-吡咯烷酮)-共丙烯酸纳米凝胶是通过使用工业型线性促进剂和装置通过电子束辐照可交联聚合物的水溶液而生成的。研究了纳米凝胶在宽pH范围内的理化性质和胶体稳定性。体外细胞研究证明,纳米凝胶具有完全的生物相容性,能够定量绕过细胞膜。抗癌药阿霉素(DOX)通过含有二硫键可裂解键的间隔基与NG的羧基连接。体外释放研究表明,谷胱甘肽能够通过还原S-S键来触发DOX的释放,其浓度与其在细胞质中的水平相当。

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