Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yi-Dong Yan"'
Autor:
Yi-Dong Yan, 顏貽棟
82
This thesis studies the formation of PtSi contacted p﹢n shallow junctions by ITS(implant-through-silicide)／ITM( implant- through-metal) BF2﹢ implantation and rapid thermal annealing ( RTA)technique. The experimental result shows that RT
This thesis studies the formation of PtSi contacted p﹢n shallow junctions by ITS(implant-through-silicide)／ITM( implant- through-metal) BF2﹢ implantation and rapid thermal annealing ( RTA)technique. The experimental result shows that RT
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/28140458847449898832
Publikováno v:
Chinese Journal of Luminescence. 42:1795-1803
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a63eb71eb73470b08d89d7659daff62f
https://doi.org/10.37188/cjl.20210217
https://doi.org/10.37188/cjl.20210217
Publikováno v:
Drug Development and Industrial Pharmacy. 40:172-177
A novel flurbiprofen-loaded nanoemulsion which gave uniform emulsion droplets with a narrow size distribution was previously reported to be prepared using membrane emulsification method. The purpose of this study is to develop a novel flurbiprofen-lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd1d7fdccb539446a9e9693417338e74
https://doi.org/10.3109/03639045.2012.752501
https://doi.org/10.3109/03639045.2012.752501
Publikováno v:
Journal of Pharmaceutical Sciences. 101:4584-4596
The aim of our study was to characterize and optimize a self-nanoemulsifying drug delivery system (SNEDDS) formulation by a three-factor, three-level Box-Behnken design (BBD) combined with a desirability function. The independent factors were the amo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5fe8ffc1574a4f985d76c91199da13
https://doi.org/10.1002/jps.23333
https://doi.org/10.1002/jps.23333
Autor:
Dong Wuk Kim, Chul Soon Yong, Yi-Dong Yan, Kun Kook Kim, Jun Ho Sung, Han-Gon Choi, Jong Oh Kim, Beom-Jin Lee
Publikováno v:
International Journal of Pharmaceutics. 422:202-210
With the aim of developing a novel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changes, various valsartan-loaded solid dispersions were prepared with water, hydroxypropyl methylcellulose (HPMC) and sodium lauryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e33a6f1b022db6f0cc527b4db02886cb
https://doi.org/10.1016/j.ijpharm.2011.10.053
https://doi.org/10.1016/j.ijpharm.2011.10.053
Autor:
Dong Won Lee, Jong Oh Kim, Jungsun Kim, Chul Soon Yong, Dong Wuk Kim, Jun Ho Sung, Eun-Mi Jeon, Dae-Duk Kim, Dong Xun Li, Han-Gon Choi, Yi-Dong Yan, Ming Guan Piao
Publikováno v:
International Journal of Pharmaceutics. 419:154-160
Various amide prodrugs of salicylic acid were synthesised, and their physicochemical properties including lipophilicity, chemical stability and enzymatic hydrolysis were investigated. In vivo skin permeation and accumulation profiles were also evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a8d7f58b1c5dba3194f5d61b6dc980c
https://doi.org/10.1016/j.ijpharm.2011.07.043
https://doi.org/10.1016/j.ijpharm.2011.07.043
Autor:
Doo Hyung Hwang, Chul Soon Yong, Jong Soo Woo, Srinivasan Shanmugam, Sang Cheol Chi, Won Seok Lyoo, Han-Gon Choi, Jae Hyun Park, Yi Dong Yan
Publikováno v:
Journal of Pharmacy and Pharmacology. 63:491-499
Objectives To avoid the major adverse effects induced by Cremophor EL formulated in the commercial paclitaxel products of Taxol. Methods An injectable paclitaxel solid dispersion free of Cremophor was prepared by a supercritical antisolvent process a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6a4a07b175257c3d3d66b54c7cac8a1
https://doi.org/10.1111/j.2042-7158.2010.01218.x
https://doi.org/10.1111/j.2042-7158.2010.01218.x
Publikováno v:
Biological and Pharmaceutical Bulletin. 34:1179-1186
In this study, a novel liquid self-emulsifying drug delivery system (SEDDS) containing curcumin was formulated and further developed into a solid form by a spray drying method using Aerosil 200 as the solid carrier. The optimum liquid SEDDS consisted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd5947e590e553043bb589f13f2d8022
https://doi.org/10.1248/bpb.34.1179
https://doi.org/10.1248/bpb.34.1179
Publikováno v:
Journal of Pharmaceutical Investigation. 40:277-283
− CoQ with low melting temperature was exploited to improve its solubility by preparing its solid dispersions(SDs) with a meltable polymer, poloxamer 407 (P 407). P407 can be utilized for a relatively simple, quick, inexpensive,reproducible and pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53a728717f1714e8da3fc5c146cabbb9
https://doi.org/10.4333/kps.2010.40.5.277
https://doi.org/10.4333/kps.2010.40.5.277
Autor:
Won Seok Lee, Chul-Soon Yong, Han-Gon Choi, Yi-Dong Yan, Han-Kyung Kim, Jong-Soo Woo, Ki-Heon Seo, Lee Gwan-Sun
Publikováno v:
Molecular Pharmaceutics. 7:2132-2140
EXP3174 is the major active metabolite of losartan, a drug currently widely used for the treatment of cardiovascular diseases. This study was designed to evaluate the physicochemical properties of EXP3174-pivoxil (a novel synthesized prodrug of EXP31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde1655c861890311eebdf8ca79bd813
https://doi.org/10.1021/mp100166c
https://doi.org/10.1021/mp100166c