Faster biodegradation, immunogenicity and lack of cell penetrative capabilities are hurdles in development of peptidyl drugs for cancer therapy. Polymeric carriers can be used to overcome these problems. The present study is focused on the use of polyhydroxybutyrate as a potential nanovehicle for the delivery of anticancer peptides. PHB (72kDa) was produced by thermal treatment of high molecular weight PHB (300kDa) under melt conditions and then conjugated with PEG (4kDa) by Steglich esterification reaction. Anticancer peptide NuBCP-9 (FSRSLHSLL) encapsulated PHB(72K)-PEG(4K) NPs were prepared by double emulsion solvent evaporation method. PHB(72K)-PEG(4K) NPs showed encapsulation efficiency of 61% and exhibited sustained release of peptide over a period of 26days at physiological pH. NuBCP-9 loaded PHB(72K)-PEG(4K) NPs showed an IC50 value of 2.2μM & 1.6μM in MCF-7 cells in 48h and 72h respectively. Confocal laser microscopy confirmed efficient cellular uptake and induction of apoptosis by peptide loaded NPs in a time dependent manner. In vivo intraperitonial administration of 20mg/kg NuBCP-9/NPs twice a week for three weeks triggered 90% tumor regression in Ehrlich syngeneic mouse model. Our results illustrated the potential of PHB(72K)-PEG(4K) based nanoformulation as a tool for targeting intracellular proteins.

译文

更快的生物降解,免疫原性和缺乏细胞渗透能力是开发用于癌症治疗的肽基药物的障碍。聚合物载体可以用来克服这些问题。本研究的重点是将聚羟基丁酸酯用作递送抗癌肽的潜在纳米载体。通过在熔融条件下对高分子量PHB (300kDa) 进行热处理,然后通过Steglich酯化反应与PEG (4kDa) 缀合,制得PHB (72kDa)。采用双乳液溶剂蒸发法制备了抗癌肽NuBCP-9 (FSRSLHSLL) 封装的PHB(72K)-PEG(4K) NPs。PHB(72K)-PEG(4K) NPs显示出61% 的包封效率,并且在生理pH下在26天的时间内显示出肽的持续释放。NuBCP-9负载的PHB(72K)-PEG(4K) NPs在48h和72h的MCF-7细胞中分别显示出2.2 μ m和1.6 μ m的IC50值。共聚焦激光显微镜证实了肽负载的NPs以时间依赖性方式有效地吸收了细胞并诱导了凋亡。在Ehrlich同基因小鼠模型中,每周两次体内施用20mg/kg NuBCP-9/NPs,持续三周,可触发90% 肿瘤消退。我们的结果说明了基于PHB(72K)-PEG(4K) 的纳米制剂作为靶向细胞内蛋白质的工具的潜力。

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