Nano-sized solid dispersions based on hydrophobic-hydrophilic conjugates for dissolution enhancement of poorly water-soluble drugs.

导出原文传递

翻译打印收藏纠错

第一作者： Ha T T,Dinh

第一单位： International University, Vietnam National University, Ho Chi Minh City, Vietnam.

作者： Ha T T,Dinh ^[1] ; Phuong H L,Tran ^[2] ; Wei,Duan ^[2] ; Beom-Jin,Lee ^[3] ; Thao T D,Tran ^[4]

作者单位： International University, Vietnam National University, Ho Chi Minh City, Vietnam. ^[1] Deakin University, Geelong, School of Medicine, Australia. ^[2] Bioavailability Control Laboratory, College of Pharmacy, Ajou University, Republic of Korea. ^[3] Department for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City, Vietnam; Faculty of Pharmacy, Ton Duc Thang University, Ho Chi Minh City, Vietnam. Electronic address: trantruongdinhthao@tdt.edu.vn. ^[4]

关键词 hydrophilic-hydrophobic conjugate molecular interaction nano solid dispersion particle size

主题词药物载体(Drug Carriers);酯化(Esterification);亲水和疏水相互作用(Hydrophobic and Hydrophilic Interactions);溶解度(Solubility);悬液(Suspensions);玉米醇溶蛋白(Zein)

DOI 10.1016/j.ijpharm.2017.09.065

PMID 28951346

发布时间 2018-06-07

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交