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基于白蛋白的水飞蓟宾纳米晶体靶向激活的肝星状细胞用于肝纤维化治疗。

Albumin-Based Silibinin Nanocrystals Targeting Activated Hepatic Stellate Cells for Liver Fibrosis Therapy.

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu610041, China.

Sichuan Institute for Drug Control NMPA Key Laboratory for Quality Control and Evaluation of Vaccines and Biological Products, Chengdu611731, China.

出版信息

ACS Appl Mater Interfaces. 2023 Feb 15;15(6):7747-7758. doi: 10.1021/acsami.2c19269. Epub 2023 Jan 31.

Abstract

Activated hepatic stellate cells (aHSCs) are critical during the development and progression of liver fibrosis. Once liver fibrosis occurs, aHSCs highly express secreted protein, acidic and rich in cysteine (SPARC), a typical albumin-binding protein. We designed a nano platform, silibinin albumin nanocrystals (SLB-HSA NCs), to target aHSCs for liver fibrosis therapy. The prepared SLB-HSA NCs showed uniform particle size distribution of approximately 60 nm with PDI < 0.15 and high loading efficiency up to 49.4%. Albumin coated on the surface of nanocrystals was demonstrated to increase cellular uptake by aHSCs through SPARC-mediated endocytosis. In addition, SLB-HSA NCs significantly improved the bioavailability compared with free SLB in pharmacokinetic study. Following tail-vein injection, SLB-HSA NCs were massively accumulated in the fibrotic liver and exhibited enhanced antifibrotic effects in hepatic fibrosis mice. Overall, our findings prove the great potential of SLB-HSA NCs in the targeted treatment of liver fibrosis.

摘要

活化的肝星状细胞(aHSCs)在肝纤维化的发生和发展中起着关键作用。一旦发生肝纤维化,aHSCs 会高度表达分泌蛋白、富含半胱氨酸的酸性蛋白(SPARC),这是一种典型的白蛋白结合蛋白。我们设计了一种纳米平台,即水飞蓟宾白蛋白纳米晶体(SLB-HSA NCs),用于针对肝星状细胞进行肝纤维化治疗。所制备的 SLB-HSA NCs 具有约 60nm 的均匀粒径分布,PDI<0.15,载药效率高达 49.4%。研究表明,白蛋白包覆在纳米晶体表面可通过 SPARC 介导的内吞作用增加 aHSCs 的细胞摄取。此外,与游离水飞蓟宾相比,SLB-HSA NCs 在药代动力学研究中显著提高了生物利用度。尾静脉注射后,SLB-HSA NCs 在纤维化肝脏中大量积聚,并在肝纤维化小鼠中表现出增强的抗纤维化作用。总的来说,我们的研究结果证明了 SLB-HSA NCs 在肝纤维化靶向治疗中的巨大潜力。

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