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一种基于聚己内酯和聚乙烯亚胺的可生物降解聚(酯胺)作为基因载体。

A biodegradable poly(ester amine) based on polycaprolactone and polyethylenimine as a gene carrier.

作者信息

Arote Rohidas, Kim Tae-Hee, Kim You-Kyoung, Hwang Soon-Kyung, Jiang Hu-Lin, Song Ho-Hyun, Nah Jae-Woon, Cho Myung-Haing, Cho Chong-Su

机构信息

School of Agricultural Biotechnology, Seoul National University, Seoul 151-921, South Korea.

出版信息

Biomaterials. 2007 Feb;28(4):735-44. doi: 10.1016/j.biomaterials.2006.09.028. Epub 2006 Oct 10.

Abstract

The aim of research was to develop and optimize delivery systems for plasmid DNA (pDNA) based on biodegradable polymers, in particular, poly(ester amine)s (PEAs), suitable for non-viral gene therapy. Poly(ester amine)s were successfully synthesized by Michael addition reaction between polycaprolactone (PCL) diacrylate and low molecular weight polyethylenimine (PEI). PEA/DNA complexes showed effective and stable DNA condensation with the particle sizes below 200nm, implicating its potential for intracellular delivery. PEAs showed controlled degradation and were essentially non-toxic in all three cells (293T: Human kidney carcinoma, HepG2: Human hepatoblastoma and HeLa: Human cervix epithelial carcinoma cell lines) at higher doses in contrast to PEI 25K. PEAs also revealed much higher transfection efficiencies in three cell lines as compared to PEI 25K. The highest reporter gene expression was observed for PCL/PEI-1.2 (MW 1200) complex having transfection efficiency 15-25 folds higher than PEI 25K in vitro. Also PEA/DNA complexes successfully transfected cells in vivo after aerosol administration than PEI 25K. These PEAs can be used as most efficient polymeric vectors which provide a versatile platform for further investigation of structure property relationship along with the controlled degradation, significant low cytotoxicity and high transfection efficiency.

摘要

本研究的目的是开发并优化基于可生物降解聚合物(特别是聚(酯胺),PEA)的质粒DNA(pDNA)递送系统,该系统适用于非病毒基因治疗。通过聚己内酯(PCL)二丙烯酸酯与低分子量聚乙烯亚胺(PEI)之间的迈克尔加成反应成功合成了聚(酯胺)。PEA/DNA复合物显示出有效且稳定的DNA凝聚,粒径低于200nm,这表明其具有细胞内递送的潜力。与PEI 25K相比,PEA在较高剂量下表现出可控降解,并且在所有三种细胞(293T:人肾癌细胞、HepG2:人肝母细胞瘤细胞和HeLa:人宫颈上皮癌细胞系)中基本无毒。与PEI 25K相比,PEA在三种细胞系中也显示出更高的转染效率。对于PCL/PEI-1.2(分子量1200)复合物,观察到最高的报告基因表达,其体外转染效率比PEI 25K高15-25倍。此外,与PEI 25K相比,PEA/DNA复合物在气溶胶给药后在体内成功转染细胞。这些PEA可作为最有效的聚合物载体,为进一步研究结构-性质关系以及可控降解、显著的低细胞毒性和高转染效率提供一个通用平台。

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