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pH-sensitive micelles self-assembled from star-shaped TPGS copolymers with ortho ester linkages for enhanced MDR reversal and chemotherapy
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作者 Yong Xu Shi Wang +4 位作者 Longshun Yang Yuhang Dong Yafang Zhang Guoqing Yan Rupei Tang 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2021年第3期363-373,共11页
TPGS approved by FDA can be used as a P-gp inhibitor to effectively reverse multi-drug resistance(MDR)and as an anticancer agent for synergistic antitumor effects.However,the comparatively high critical micelle concen... TPGS approved by FDA can be used as a P-gp inhibitor to effectively reverse multi-drug resistance(MDR)and as an anticancer agent for synergistic antitumor effects.However,the comparatively high critical micelle concentration(CMC),low drug loading(DL)and poor tumor target limit its further clinical application.To overcome these drawbacks,the pH-sensitive star-shaped TPGS copolymers were successfully constructed via using pentaerythritol as the initial materials,ortho esters as the pH-triggered linkages and TPGS active-ester as the terminated MDR material.The amphiphilic star-shaped TPGS copolymers could self-assemble into free and doxorubicin(DOX)-loaded micelles at neutral aqueous solutions.The micelles exhibited the lower CMC(8.2×10^(−5) mg/ml),higher DL(10.8%)and long-term storage and circulation stability,and showed enhanced cellular uptake,apoptosis,cytotoxicity,and growth inhibition for in vitro MCF-7/ADR and/or MCF-7/ADR multicellular spheroids and in vivo MCF-7/ADR tumors via efficiently targeted drug release at tumoral intracellular pH(5.0),MDR reversal of TPGS,and synergistic effect of DOX and TPGS.Therefore,the pH-sensitive micelles self-assembled from star-shaped TPGS copolymers with ortho ester linkages are potentially useful to clinically transform for enhanced MDR cancer treatment. 展开更多
关键词 TPGS Ortho esters Star-shaped copolymers mdr reversal
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Screening of Common Traditional Chinese Drugs for Reversing Multidrug Resistance of KBV200 In Vitro 被引量:1
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作者 张庆林 赵精华 +5 位作者 曹菊荣 宋京 毕建进 王小娜 龚萍 吴祖泽 《Journal of Chinese Pharmaceutical Sciences》 CAS 2002年第3期64-67,共4页
The ethanolic extracts of 100 common traditional Chinese drugs, which are widely used in many prescriptions in treatment of cancer in China, were screened for MDR of KBV200 cell line in vitro with MTT method. The ... The ethanolic extracts of 100 common traditional Chinese drugs, which are widely used in many prescriptions in treatment of cancer in China, were screened for MDR of KBV200 cell line in vitro with MTT method. The result showed 9 extracts having MDR reversal activity. They were the extracts of Fructus Lagenariae Sicerariae, Radix Glycyrrhizae, Poria, Herba Andrographitis, Radix Sophorae Tonkinensis, Caulis Mahoniae, Folium Artemisiae Argyi, Rhizoma Curcumae, Fructus Cnidii. Other 5 extracts showed cytotoxic on KBV200 cell line. $$$$ 展开更多
关键词 Traditional Chinese drugs Reversing mdr SCREENING In vitro
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Screening of Common Traditional Chinese Drugs for Reversing Multidrug Resistance of KBV200 In Vitro 被引量:4
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作者 张庆林 赵精华 +5 位作者 曹菊荣 宋京 毕建进 王小娜 龚萍 吴祖泽 《Journal of Chinese Pharmaceutical Sciences》 CAS 2002年第3期64-67,共页
The ethanolic extracts of 100 common traditional Chinese drugs, which are widely used in many prescriptions in treatment of cancer in China, were screened for MDR of KBV200 cell line in vitro with MTT method. The ... The ethanolic extracts of 100 common traditional Chinese drugs, which are widely used in many prescriptions in treatment of cancer in China, were screened for MDR of KBV200 cell line in vitro with MTT method. The result showed 9 extracts having MDR reversal activity. They were the extracts of Fructus Lagenariae Sicerariae, Radix Glycyrrhizae, Poria, Herba Andrographitis, Radix Sophorae Tonkinensis, Caulis Mahoniae, Folium Artemisiae Argyi, Rhizoma Curcumae, Fructus Cnidii. Other 5 extracts showed cytotoxic on KBV200 cell line. $$$$ 展开更多
关键词 Traditional Chinese drugs Reversing mdr SCREENING In vitro
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pH-sensitive polymeric micelles triggered drug release for extracellular and intracellular drug targeting delivery 被引量:11
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作者 Yanhua Liu Wenping Wang +2 位作者 Jianhong Yang Chengming Zhou Jin Sun 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2013年第3期159-167,共9页
Most of the conventional chemotherapeutic agents used for cancer chemotherapy suffer from multidrug resistance of tumor cells and poor antitumor efficacy.Based on physiological differences between the normal tissue an... Most of the conventional chemotherapeutic agents used for cancer chemotherapy suffer from multidrug resistance of tumor cells and poor antitumor efficacy.Based on physiological differences between the normal tissue and the tumor tissue,one effective approach to improve the efficacy of cancer chemotherapy is to develop pH-sensitive polymeric micellar delivery systems.The copolymers with reversible protonationedeprotonation core units or acid-liable bonds between the therapeutic agents and the micelle-forming copolymers can be used to form pH-sensitive polymeric micelles for extracellular and intracellular drug smart release.These systems can be triggered to release drug in response to the slightly acidic extracellular fluids of tumor tissue after accumulation in tumor tissues via the enhanced permeability and retention effect,or they can be triggered to release drug in endosomes or lysosomes by pH-controlled micelle hydrolysis or dissociation after uptake by cells via the endocytic pathway.The pH-sensitive micelles have been proved the specific tumor cell targeting,enhanced cellular internalization,rapid drug release,and multidrug resistance reversal.The multifunctional polymeric micelles combining extracellular pH-sensitivity with receptor-mediated active targeting strategies are of great interest for enhanced tumor targeting.The micelles with receptor-mediated and intracellular pH targeting functions are internalized via receptor-mediated endocytosis followed by endosomal-pH triggered drug release inside the cells,which reverses multidrug resistance.The pH sensitivity strategy of the polymeric micelles facilitates the specific drug delivery with reduced systemic side effects and improved chemotherapeutical efficacy,and is a novel promising platform for tumor-targeting drug delivery. 展开更多
关键词 pH-sensitive polymeric micelles Tumor extracellular pH targeting Tumor intracellular pH targeting Multifunctional polymeric micelles mdr reversion
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Design, Synthesis and Evaluation of Substituted N-(3-Arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides as Potent MDR Reversal Agents in Cancer 被引量:3
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作者 Velingkar, V. S. Dandekar, V. D. 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第3期504-510,共7页
A novel class of molecules with structure N-(3-arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides (20- 29) were designed by generating a pharmacophore for potent MDR reversal activity using phase drug design so... A novel class of molecules with structure N-(3-arylpropyl)-9,10-dihydro-9-oxoacridine-4-carboxamides (20- 29) were designed by generating a pharmacophore for potent MDR reversal activity using phase drug design software. The designed molecules were synthesized by a novel synthesis route and evaluated for their inhibitory effects on the transport activity of P-glycoprotein (P-gp) by standard Hoechst 33342 assay method. Based on the pIC50 values of ten title compounds screened, three compounds exhibited better activity as compared to Verapamil used as standard. 展开更多
关键词 N-(3-arylpropyl)-9 10-dihydro-9-oxo-acridine-4-carboxamides mdr reversal agents pharmacophore phase drug design software structure-activity relationships structure elucidation
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