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作 者:Liqiong Sun Xinping Luo Chenxi Zhou Zhanwei Zhou Minjie Sun
机构地区:[1]College of Horticulture,Nanjing Agricultural University,Nanjing 210095,China [2]NMPA Key Laboratory for Research and Evaluation of Pharmaceutical Preparations and Excipients,State Key Laboratory of Natural Medicines,Department of Pharmaceutics,China Pharmaceutical University,Nanjing 210009,China
出 处:《Chinese Chemical Letters》2024年第2期341-346,共6页中国化学快报(英文版)
基 金:financially supported by the Jiangsu Agriculture Science and Technology Innovation Fund(No.CX(22)3174);the National Natural Science Foundation of China(No.82102202);Natural Science Foundation of Jiangsu Province(No.BK20210424);Postgraduate Research&Practice Innovation Program of Jiangsu Province(No.KYCX23_0849).
摘 要:Activated hepatic stellate cells(aHSCs),the main source of extracellular matrix deposition,are key targets in liver fibrosis.However,no effective drug specific to aHSCs has been clinically applied due to poor drug delivery efficiency.Herein,we designed a CXC chemokine receptor 4(CXCR4)-targeted reactive oxygen species(ROS)-responsive platform AMD-Dex-ROS-responsive-sorafenib(ARS)based on natural polysaccharide and thioctic acid frame,which can deliver anti-fibrosis drug represented by sorafenib specifically to aHSCs on account of CXCR4 over-expression on aHSCs,and smartly disassemble via ROS-responsive thioketal rupture relying on high intracellular ROS in HSCs,realized on-demand drug release and effective liver fibrosis reversion.Notably,in this platform,the CXCR4 antagonist AMD3100 not only enhanced aHSCs targeting efficiency of sorafenib but also effectively magnified the aHSCs elimination of sorafenib by blocking stroma cell derived factor-1(SDF-1)/CXCR4-induced aHSCs protection,resulting in synergistic anti-fibrosis effect.The platform provided a new approach for drug delivery system design and liver fibrosis treatment.
关 键 词:Nanoparticle CXCR4 antagonism ROS-responsive Hepatic stellate cells Liver fibrosis
分 类 号:TB383.1[一般工业技术—材料科学与工程] R575.2[医药卫生—消化系统]
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