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用于抗肿瘤药物递送的脂质体表面修饰策略 被引量:2
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作者 伊帕尔古丽·阿皮孜 王昭志 +2 位作者 贺宏吉 李喆喆 王梅 《华西药学杂志》 CAS CSCD 2023年第2期207-213,共7页
脂质体作为一种传统的药物传递系统,因其在药物及蛋白质、基因、核酸等生物活性物质的高效传递方面的应用而备受研究领域的关注。脂质体给药系统在抗肿瘤药物研究领域经历了常规脂质体、长循环脂质体、配体功能脂质体、刺激响应型脂质体... 脂质体作为一种传统的药物传递系统,因其在药物及蛋白质、基因、核酸等生物活性物质的高效传递方面的应用而备受研究领域的关注。脂质体给药系统在抗肿瘤药物研究领域经历了常规脂质体、长循环脂质体、配体功能脂质体、刺激响应型脂质体等4个阶段。现结合相关文献,综述了这4种脂质体给药系统常用的表面修饰靶向策略和研究进展,以期为脂质体的进一步研究和基本靶向修饰提供参考。 展开更多
关键词 脂质体 抗肿瘤 靶向策略 表面修饰 研究进展 综述 传统脂质体 新型脂质体
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Exploring the mechanism of Peganum harmala L.seeds on hepatocellular carcinoma based on network pharmacology and molecular docking 被引量:1
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作者 ipargul hafiz Zhaozhi Wang +2 位作者 Hongji He Zhezhe Li Mei Wang 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2022年第7期517-529,共13页
Peganum harmala L.is a medicinal plant,and its seeds have been used to treat gastrointestinal cancer and malaria for a long time in North-Western China.In the present study,we aimed to probe the potential molecular ta... Peganum harmala L.is a medicinal plant,and its seeds have been used to treat gastrointestinal cancer and malaria for a long time in North-Western China.In the present study,we aimed to probe the potential molecular targets and pharmacological mechanisms of Peganum harmala L.seeds(PHS)on hepatocellular carcinoma(HCC)using network analysis and molecular docking.First,the chemical ingredients of PHS were obtained from TCMID and BATMAN-TCM databases,and the effective ingredients were screened by SwissADME.Furthermore,the target information of the effective ingredients was acquired from PharmMapper and SwissTargetPrediction databases.Secondly,HCC-related targets were obtained from Liverome,DisGeNET,and GeneCards databases.The intersection with the PHS was obtained.The“compounds-targets”was drawn using Cytoscape software,and PPI network diagrams were drawn using their intersection targets.GO analysis and KEGG enrichment analysis were carried out using the DAVID database.Finally,molecular docking was conducted between protein receptors and the active components using AutoDockTools.Our results showed 105 intersection targets of PHS with HCC.Moreover,10 core targets included ALB,AKT1,EGFR,CASP3,SRC,ESR1,MAPK3,MMP9,ANXA5,and MAPK1.Besides,404 GO functional annotations were obtained,including 287 biological processes,37 cell compositions,and 80 molecular functions.In addition,110 signaling molecules and pathways,including chemical oncogene receptors,PI3K-Akt pathway,HCC,and hepatitis B,were identified.The molecular docking results showed that the binding energies of the 10 core targets and the 12 active components were all less than–5 kcal/mol.In conclusion,this study expounded on the“component-target-pathway”interaction mechanism of PHS for the treatment of HCC,and it also provided a scientific basis for the clinical application of PHS. 展开更多
关键词 Peganum harmala L.seeds Hepatocellular carcinoma Network pharmacology Molecular docking MECHANISM
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