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一种高效、低毒、基于磷脂的相分离凝胶,用于肽的长期递送。

A high-efficiency, low-toxicity, phospholipids-based phase separation gel for long-term delivery of peptides.

机构信息

Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Key Laboratory of Drug Targeting and Drug Delivery Systems, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

出版信息

Biomaterials. 2015 Mar;45:1-9. doi: 10.1016/j.biomaterials.2014.12.042. Epub 2015 Jan 13.

Abstract

Peptide and protein drugs are currently under rapid development attributed to their high potency and efficacy in therapy. Their successful delivery, however, is highly limited by their short half-life, fast degradation and rapid clearance. Here, we present a high content phospholipids-based phase separation gel (PPSG), which is readily injectable due to its low initial viscosity and can rapidly transform into an in situ implant after injection upon exposure to an aqueous environment. A selected model peptide, octreotide acetate, is loaded into PPSG and achieves sustained release profiles for one month in rats. In addition, the local irritation caused by ethanol contained in PPSG is ethanol content-dependent and the irritation of PPSG with 70% phospholipids content can be eliminated by partially replacing ethanol with medium chain triglyceride. The mechanisms underlying phase transition of PPSG are based on water-insolubility of phospholipids. Our findings demonstrate that PPSG is a readily injectable, highly safe and efficient in situ forming implant for sustained delivery of peptides.

摘要

肽类和蛋白质类药物由于在治疗方面具有高效力和高特异性,目前正处于快速发展阶段。然而,由于它们的半衰期短、降解快、清除快,其成功传递受到高度限制。在这里,我们介绍了一种基于高含量磷脂的相分离凝胶(PPSG),由于其初始粘度低,可轻易注射,并且在暴露于水相环境后可迅速转化为原位植入物。选择一种模型肽,醋酸奥曲肽,负载到 PPSG 中,在大鼠体内可实现一个月的持续释放。此外,PPSG 中所含乙醇引起的局部刺激与乙醇含量有关,并且通过部分用中链甘油三酯代替乙醇,可以消除 70%磷脂含量的 PPSG 的刺激。PPSG 的相转变机制基于磷脂的不溶于水。我们的研究结果表明,PPSG 是一种可轻易注射、高度安全且高效的原位形成植入物,可用于肽类的持续释放。

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