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摘要:
Although surface PEGylation of nanomedicines can decrease serum protein adsorption in vivo,it also blocks uptake by tumor cells.This dilemma could be overcome by employing detachably PEGylated strategy at tumoral extracellular microenvironment to achieve improved cellular uptake while prolonged circulation times.Herein,the amphiphilic graft copolymers with p H-sensitive ortho ester-linked m PEG in side chains and polyurethanes in backbone,can self-assemble into the free and doxorubicin(DOX)-loaded micelles.The p H-sensitive micelles could undergo several characteristics as follows:(i)PEGylated shells for stability in sodium dodecyl sulfonate(SDS)solution;(ii)De PEGylation via degradation of ortho ester linkages at tumoral extracellular pH(6.5)for gradually dynamic size changes and effective release of DOX;and(iii)enhanced cellular uptake and cytotoxicity via positive DOX.Moreover,the dynamic micelles with detachable PEGylation could quickly penetrate the centers of SH-SY5 Y multicellular spheroids(MCs)and strongly inhibit tumor growth in vitro and in vivo,and might be considered as promising and effective drug carriers in tumor therapy.
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篇名 Dynamic micelles with detachable PEGylation at tumoral extracellular pH for enhanced chemotherapy
来源期刊 亚洲药物制剂科学(英文) 学科 医学
关键词 Micelles Ortho ester PEGYLATION Size transition ANTITUMOR
年,卷(期) 2020,(6) 所属期刊栏目
研究方向 页码范围 728-738
页数 11页 分类号 R73
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Micelles
Ortho
ester
PEGYLATION
Size
transition
ANTITUMOR
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期刊影响力
亚洲药物制剂科学(英文)
双月刊
1818-0876
21-1608/R
中国沈阳市文化路103号107号信箱
8-624
出版文献量(篇)
70
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0
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0
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