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MicroRNA-216a: a potential therapeutic target for drug resistance and recurrent of liver cancer
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作者 Zhao-Lin Chen Tao-Tao Ma +3 位作者 Cheng Huang Tao Xu Ting-Ting Hu Jun Li 《Hepatobiliary & Pancreatic Diseases International》 SCIE CAS 2013年第6期661-661,共1页
The Editor welcomes submissions for possible publication in the Letters to the Editor section.Letters commenting on an article published in the Journal or other interesting pieces will be considered if they are receiv... The Editor welcomes submissions for possible publication in the Letters to the Editor section.Letters commenting on an article published in the Journal or other interesting pieces will be considered if they are received within 6 weeks of the time the article was published.Authors of the article being commented on will be given an opportunity to offer a timely response to the letter.Authors of letters will be notified that the letter has been received.Unpublished letters cannot be returned. 展开更多
关键词 HCC MicroRNA-216a a potential therapeutic target for drug resistance and recurrent of liver cancer
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Self-assembled Nanoparticles based on Folic Acid Modifi ed Carboxymethyl Chitosan Conjugated with Targeting Antibody 被引量:2
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作者 虎征宇 ZHENG Hua +6 位作者 LI Dan XIONG Xiong TAN Mingyuan HUANG Dan GUO Xing 张雪琼 严晗 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2016年第2期446-453,共8页
Nanoparticles conjugated with antibody were designed as active drug delivery system to reduce the toxicity and side effects of drugs for acute myeloid leukemia(AML).Moreover,methotrexate(MTX)was chosen as modeldru... Nanoparticles conjugated with antibody were designed as active drug delivery system to reduce the toxicity and side effects of drugs for acute myeloid leukemia(AML).Moreover,methotrexate(MTX)was chosen as modeldrug and encapsulate within folic acid modified carboxymethylchitosan(FACMCS)nanoparticles through self-assembling.The chemicalstructure,morphology,release and targeting of nanoparticles were characterized by routine detection.It is demonstrated that the mean diameter is about 150 nm,the release rate increases with the decreasing of p H,the binding rate of CD33 antibody and FA-CMCS nanoparticles is about 5:2,and nanoparticles can effectively bind onto HL60 cells in vitro.The experimentalresults indicate that the FA-CMCS nanoparticles conjugated with antibody may be used as a potentialp Hsensitive drug delivery system with leukemic targeting properties. 展开更多
关键词 chitosan nanoparticles targeted drug delivery cancer controlled release self-assembly pH-sensitive
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