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包载小干扰 RNA 的明胶水凝胶的制备及其控制释放。

Preparation of gelatin hydrogels incorporating small interfering RNA for the controlled release.

机构信息

Department of Biomaterials, Field of Tissue Engineering, Institute for Frontier Medical Sciences, Kyoto University, Sakyo-ku, Japan.

出版信息

J Drug Target. 2012 Dec;20(10):864-72. doi: 10.3109/1061186X.2012.725170. Epub 2012 Sep 26.

Abstract

The objective of this study is to design biodegradable hydrogels of gelatin for the controlled release of bioactive small interfering RNA (siRNA). Gelatin was cationized by chemically introducing ethylene diamine into the carboxyl groups in different conditions to obtain cationized gelatins (CGs). The CG was mixed with siRNA at various mixing ratios of amino groups of gelatin to the phosphate groups of siRNA in aqueous solution to form the siRNA-CGnano-complex. Gelatin together with the complex of siRNA and CG was chemically crosslinked to prepare the gelatin hydrogel incorporating the complex. The hydrogel incorporating the siRNA-CG complex was hardly degraded in phosphate-buffered saline solution (PBS) at 37°C and did not release the siRNA complex after initial siRNA release. When placed in PBS containing collagenase, the hydrogel was enzymatically degraded to release the siRNA complex. In this release system, the siRNA was released as a result of hydrogel degradation. The siRNA released showed an activity to specifically suppress the expression of the corresponding gene. The hydrogel is promising to release siRNA and also elicit biological activity for a longer time.

摘要

本研究旨在设计用于生物活性小干扰 RNA(siRNA)控制释放的明胶可生物降解水凝胶。通过在不同条件下将乙二胺化学引入到羧基中,使明胶阳离子化,得到阳离子化明胶(CG)。将 CG 与 siRNA 以明胶氨基与 siRNA 磷酸基团不同的混合比例在水溶液中混合,形成 siRNA-CGnano-复合物。通过化学交联明胶和 siRNA 与 CG 的复合物来制备掺入复合物的明胶水凝胶。掺入 siRNA-CG 复合物的水凝胶在 37°C 的磷酸盐缓冲盐水(PBS)中几乎不降解,初始 siRNA 释放后也不会释放 siRNA 复合物。当置于含有胶原酶的 PBS 中时,水凝胶会被酶解以释放 siRNA 复合物。在该释放系统中,siRNA 的释放是由于水凝胶的降解。释放的 siRNA 表现出特异性抑制相应基因表达的活性。该水凝胶有望在更长时间内释放 siRNA 并引发生物活性。

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