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作为DNA递送系统的胺化多糖微球。

Aminated polysaccharide microspheres as DNA delivery systems.

作者信息

Constantin M, Fundueanu G, Cortesi R, Esposito E, Nastruzzi C

机构信息

Department of Pharmaceutical Science, University of Ferrara, Ferrara, Italy.

出版信息

Drug Deliv. 2003 Jul-Sep;10(3):139-49.

Abstract

This article describes the production and characterization of cationic microparticles based on pullulan and starch for the delivery of nucleic acids. The microparticles were prepared by chemically cross-linkinking of a polymer solution dispersed in organic phase, followed by amination with N, N-diethyl-2-chloroethyl amine hydrochloride, or N-glycidyl-N,N-dimethyl-N-methylammonium chloride. The association of desoxyribonucleotide (DNA) with positively charged microparticles was determined. The association capacity and the affinity of microspheres for DNA were investigated as a function of type of polysaccharide, content and basicity of the amino groups. It was found that the both types of carriers synthetized display a high affinity for defibrotide due to the high porosity of polysaccharide microspheres (PMs). The in vitro release kinetics from microspheres showed an initial fast release of DNA (30 min) followed by slower release rate over 14 days. DNA release was influenced by the ionic strength of the receiving fluid. In addition, DNA release was slightly more rapid from pullulan than from starch complexes. DNA stability studies were performed by agarose gel, indicating no degradation even after 14 days. All the produced cationic microspheres were able to quantitatively load DNA. The release of DNA from PMs was strongly affected by the ionic strength of the receiving fluid. Finally, agarose gel electrophoresis of DNA released from microspheres indicated that no DNA degradation occurs even after 14 days of release from PMs.

摘要

本文描述了基于支链淀粉和淀粉的阳离子微粒用于核酸递送的制备及特性。微粒通过将分散在有机相中的聚合物溶液进行化学交联制备,随后用N,N - 二乙基 - 2 - 氯乙胺盐酸盐或N - 缩水甘油基 - N,N - 二甲基 - N - 甲基氯化铵进行胺化。测定了脱氧核糖核苷酸(DNA)与带正电荷微粒的结合情况。研究了微球对DNA的结合能力和亲和力与多糖类型、氨基含量和碱性的关系。发现由于多糖微球(PMs)的高孔隙率,合成的两种类型载体对去纤苷均显示出高亲和力。微球的体外释放动力学表明,DNA最初快速释放(30分钟),随后在14天内释放速率较慢。DNA释放受接收液离子强度的影响。此外,支链淀粉复合物中DNA的释放比淀粉复合物略快。通过琼脂糖凝胶进行DNA稳定性研究,结果表明即使在14天后也没有降解。所有制备的阳离子微球都能够定量负载DNA。PMs中DNA的释放受接收液离子强度的强烈影响。最后,从微球释放的DNA的琼脂糖凝胶电泳表明,即使从PMs释放14天后也没有发生DNA降解。

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