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红细胞膜伪装的介孔硅复合纳米载药系统用于水飞蓟宾的装载和控制释放:A-合成与理化性质表征。

Erythrocyte membrane-camouflaged mesoporous silica composite nanoparticles for loading and controlled release of the hepatoprotective agent silibinin: A-synthesis and physicochemical characterization.

机构信息

Center for Nanotechnology in Drug Delivery, Shiraz University of Medical Sciences, Shiraz 7146864685, Iran.

Student Research Committee, Shiraz University of Medical Sciences, Shiraz 7146864685, Iran.

出版信息

J Pharm Pharmacol. 2024 Aug 2;76(8):995-1005. doi: 10.1093/jpp/rgae046.

DOI:10.1093/jpp/rgae046
PMID:38762907
Abstract

OBJECTIVES

Milk thistle has long been used in the treatment of liver and biliary disorders. In the present study, to make a long-acting delivery system for silibinin (SBN, a major active constituent of milk thistle seeds with antioxidant and hepatoprotective function), mesoporous silica composite nanoparticles (NC) were synthesized and coated with RBC membrane.

METHODS

A modified Stöber method was used for NC synthesis, which was then characterized using FE-SEM, DLS, TEM, FTIR, and EDAX techniques. A suitable lysis buffer was used to prepare RBC-ghost, and sonication was used to coat SBN-loaded NC (SBN-NC). The RBC-ghost coated SBN-NC (SBN-NC-RBCG) was evaluated by SDS-PAGE, Bradford, TEM, EDAX, and DLS methods. SBN release was then compared for the SBN-NC and SBN-NC-RBCG samples.

KEY FINDINGS

the RBC membrane proteins were recovered from the coating of SBN-NC-RBCG, and SBN release was sustained over 24 h when compared with the SBN-NC.

CONCLUSIONS

Overall, through prolonging circulation in the bloodstream and evading the immune system, the developed system can improve SBN bioavailability in liver inflammation and fibrosis conditions that need further research.

摘要

目的

水飞蓟素长期以来一直被用于治疗肝脏和胆道疾病。在本研究中,为了制备水飞蓟宾(SBN,一种具有抗氧化和保肝作用的水飞蓟种子的主要活性成分)的长效递药系统,合成了介孔硅复合纳米粒(NC)并包覆红细胞膜。

方法

采用改良的Stöber 法合成 NC,并用 FE-SEM、DLS、TEM、FTIR 和 EDAX 技术进行表征。使用合适的裂解缓冲液制备 RBC-ghost,并用超声处理包覆载有 SBN 的 NC(SBN-NC)。通过 SDS-PAGE、Bradford、TEM、EDAX 和 DLS 方法评价包覆 RBC-ghost 的 SBN-NC(SBN-NC-RBCG)。然后比较 SBN-NC 和 SBN-NC-RBCG 样品的 SBN 释放情况。

主要发现

从 SBN-NC-RBCG 的包覆中回收了 RBC 膜蛋白,与 SBN-NC 相比,SBN 的释放可持续 24 小时以上。

结论

总之,通过延长在血液中的循环时间并逃避免疫系统,开发的系统可以提高在需要进一步研究的肝脏炎症和纤维化情况下 SBN 的生物利用度。

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