Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Zhenmin Mao"'
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 2, Pp 373-382 (2015)
The purpose of this study was to develop a reservoir-type transdermal delivery system for isosorbide dinitrate (ISDN). The developed patch consisted of five layers from bottom to top, namely, a temporary liner, an adhesive layer, a rate-controlling m
Externí odkaz:
https://doaj.org/article/18ba520d5ace4aa3a7ac50a9c5283722
Publikováno v:
e-Polymers, Vol 21, Iss 1, Pp 466-475 (2021)
Snus is one of the types of smokeless tobaccos, which is popular in many countries and regions. The nicotine level in the plasma samples obtained from snus users is similar to the nicotine level obtained from cigarette smokers; hence, the snus users
Publikováno v:
International Journal of Pharmaceutics. 528:47-54
A novel ultrasound-responsive liposomal system for tumor targeting was prepared in order to increase the antitumor efficacy and decrease serious side effects. In this paper, PLGA nanoparticles were used ultrasound-responsive agents instead of convent
Autor:
Jian Chen, Shuai Wang, Kai Zhao, Yuxuan Xin, Yuankui Zhang, Zhenmin Mao, Xiaoping Zhan, Lan Lan
Publikováno v:
Bulletin of the Korean Chemical Society. 37:200-206
A new series of 3-substituted 4-(4-methyloxy phenyl)-1H-pyrrole derivatives were synthesized and biologically evaluated for potential anticancer activity. Fifteen targeted compounds showed high selectivity toward normal cells and cancer cells: that i
Publikováno v:
e-Polymers. 16:83-89
The aims of this paper are to investigate the inherent relationship between the structures of the polyacrylates and release behaviors as drug carriers in the transdermal drug delivery systems. Three model polyacrylates compounds were synthesized by r
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 51, Iss 2, Pp 373-382 (2015)
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 No. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 Núm. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences; v. 51 n. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Volume: 51, Issue: 2, Pages: 373-382, Published: JUN 2015
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 No. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences; Vol. 51 Núm. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences; v. 51 n. 2 (2015); 373-382
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Volume: 51, Issue: 2, Pages: 373-382, Published: JUN 2015
The purpose of this study was to develop a reservoir-type transdermal delivery system for isosorbide dinitrate (ISDN). The developed patch consisted of five layers from bottom to top, namely, a temporary liner, an adhesive layer, a rate-controlling m
Publikováno v:
e-Polymers. 15:55-63
A film-like copolymer composed of 2-hydroxy-3-phenoxypropylacrylate, 4-hydroxybutyl acrylate and cyclohexyl methacrylate was synthesized and exploited as a rate-controlling membrane in the transdermal drug delivery systems (TDDs). A series of acrylat
Publikováno v:
Bulletin of the Korean Chemical Society. 35:1337-1342
A novel and convenient route for the synthesis of a series of thalidomide derivatives is described. Compound 2 was cyclized with different amines under alkaline condition to obtain 4-nitro substituted phthalimidines 3a-d. Hydroxylactams 4a-d were pro
Publikováno v:
Anti-Cancer Agents in Medicinal Chemistry. 14:994-1002
A novel series of 3-substituted-4-(4-methylthio phenyl)-1H-pyrrole derivatives were synthesized via Van Leusen pyrrole synthesis. The in vitro anticancer activity against a panel of 16 cancer cell lines and 2 normal cell lines was investigated by MTT
Autor:
Yuxuan Xin, Xiaoping Zhan, Kai Zhao, Zhenmin Mao, Jian Chen, Lan Lan, Yuankui Zhang, Shuai Wang
Publikováno v:
ChemInform. 47
A new series of 3-substituted 4-(4-methyloxy phenyl)-1H-pyrrole derivatives were synthesized and biologically evaluated for potential anticancer activity. Fifteen targeted compounds showed high selectivity toward normal cells and cancer cells: that i