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一种新型脂质体包裹血红蛋白/二氧化硅纳米颗粒作为氧载体。

A novel liposome-encapsulated hemoglobin/silica nanoparticle as an oxygen carrier.

机构信息

Department of Chemistry, Tongji University, 1239 Siping Road, Shanghai 200092, PR China.

出版信息

Int J Pharm. 2012 May 10;427(2):354-7. doi: 10.1016/j.ijpharm.2012.02.019. Epub 2012 Feb 18.

Abstract

A novel liposome-encapsulated hemoglobin/silica nanoparticle (LEHSN) was fabricated by a water-in-oil-in-water (W/O/W) double emulsion approach. Bovine hemoglobin (Hb) was first adsorbed onto the surfaces of silica nanoparticles (SNs), and then the complex of Hb/SNs was encapsulated by liposome to form LEHSN which has a core-shell supramolecular structure. On the one hand, liposomes built a cell membrane-like environment for the controlled release of Hb. On the other hand, SNs which act as rigid core provide a supported framework for lecithin membrane, and enhance the stability of liposomes. In comparison with liposome-encapsulated Hb (LEH), LEHSN shows substantially enhanced stability and improved release property of Hb in vitro. This study highlights the potential of the novel LEHSN as an oxygen carrier for pharmaceutical applications.

摘要

一种新型的脂质体包裹血红蛋白/二氧化硅纳米粒子(LEHSN)是通过水包油包水(W/O/W)双重乳液法制备的。牛血红蛋白(Hb)首先被吸附到二氧化硅纳米粒子(SNs)的表面,然后血红蛋白/SNs 复合物被脂质体包裹形成具有核壳超分子结构的 LEHSN。一方面,脂质体为 Hb 的控制释放构建了类似于细胞膜的环境。另一方面,SNs 作为刚性核为卵磷脂膜提供了支撑框架,增强了脂质体的稳定性。与包封血红蛋白的脂质体(LEH)相比,LEHSN 在体外显示出 Hb 稳定性显著提高和释放性能改善。这项研究突出了新型 LEHSN 作为药物应用中氧载体的潜力。

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