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

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Vahid Tayebi Khorrami, Mohammad Javad Raee, Samira Sadat Abolmaali, Mozhgan Abedanzadeh, Mina Shafiee, Ali Mohammad Tamaddon
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引用次数: 0

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.

用于装载和控释保肝剂 Silibinin 的红细胞膜伪装介孔二氧化硅复合纳米颗粒:A-合成与理化表征。
目的:奶蓟草一直被用于治疗肝胆疾病。本研究采用介孔二氧化硅复合纳米颗粒(NC)合成了具有抗氧化和保肝功能的水飞蓟素(SBN,水飞蓟种子的主要活性成分)长效递送系统,并在其表面包覆了 RBC 膜:方法:采用改良的 Stöber 法合成 NC,然后使用 FE-SEM、DLS、TEM、FTIR 和 EDAX 技术对其进行表征。使用合适的裂解缓冲液制备 RBC-ghost,并用超声涂覆 SBN-loaded NC(SBN-NC)。通过 SDS-PAGE、Bradford、TEM、EDAX 和 DLS 方法对包覆 RBC-ghost 的 SBN-NC(SBN-NC-RBCG)进行了评估。主要发现:与 SBN-NC 相比,SBN-NC-RBCG 涂层中的 RBC 膜蛋白得到了回收,SBN 的释放持续了 24 小时:总之,通过延长在血液中的循环时间和避开免疫系统,所开发的系统可提高 SBN 在肝脏炎症和纤维化条件下的生物利用率,有待进一步研究。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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