Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Ju-Hwan Park"'
Autor:
Ki-Taek Kim, Min-Hwan Kim, Ju-Hwan Park, Jae-Young Lee, Hyun-Jong Cho, In-Soo Yoon, Dae-Duk Kim
Publikováno v:
Journal of Ginseng Research, Vol 42, Iss 4, Pp 512-523 (2018)
Background: 20(S)-Protopanaxadiol (20S-PPD) is a fully deglycosylated ginsenoside metabolite and has potent dermal antiaging activity. However, because of its low aqueous solubility and large molecular size, a suitable formulation strategy is require
Externí odkaz:
https://doaj.org/article/3a44bbefb0224123b5f44c39efd904eb
Autor:
Jin Woo Choi, Ju-Hwan Park, Hye Rim Cho, Jin Wook Chung, Dae-Duk Kim, Hyo-Cheol Kim, Hyun-Jong Cho
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract Sorafenib (SOF; an angiogenesis inhibitor) and 2,3,5-triiodobenzoic acid (TIBA; a contrast agent for computed tomography imaging)-loaded poly(lactic-co-glycolic acid) (PLGA) microspheres (MSs) were fabricated. Embolization, drug delivery, an
Externí odkaz:
https://doaj.org/article/2c4cfbaaffa5439ebb75eb3830d7735d
Autor:
Ki-Taek Kim, Joon Lee, Min-Hwan Kim, Ju-Hwan Park, Jae-Young Lee, Joo-Hyun Song, Minwoong Jung, Myoung-Hoon Jang, Hyun-Jong Cho, In-Soo Yoon, Dae-Duk Kim
Publikováno v:
Drug Delivery, Vol 24, Iss 1, Pp 1204-1215 (2017)
Topical and transdermal drug delivery has great potential in non-invasive and non-oral administration of poorly bioavailable therapeutic agents. However, due to the barrier function of the stratum corneum, the drugs that can be clinically feasible ca
Externí odkaz:
https://doaj.org/article/4a95621d9a854b8ebcc489a223305883
Autor:
Nae-Won Kang, So-Yeon Yoon, Sungho Kim, Na-Young Yu, Ju-Hwan Park, Jae-Young Lee, Hyun-Jong Cho, Dae-Duk Kim
Publikováno v:
Pharmaceutics, Vol 13, Iss 6, p 864 (2021)
The daily oral administration of acetylcholinesterase (AChE) inhibitors for Alzheimer’s disease features low patient compliance and can lead to low efficacy or high toxicity owing to irregular intake. Herein, we developed a subcutaneously injectabl
Externí odkaz:
https://doaj.org/article/ab25444b0f904dab94a6ed330be23b64
Autor:
Min-Hwan Kim, Ju-Hwan Park, Duy-Thuc Nguyen, Sungyun Kim, Da In Jeong, Hyun-Jong Cho, Dae-Duk Kim
Publikováno v:
Pharmaceutics, Vol 13, Iss 2, p 170 (2021)
Hyaluronidase (HAase) inhibitor-incorporated hyaluronic acid (HA) hydrogel cross-linked with 1,4-butanediol diglycidyl ether (BDDE) was designed to reduce the toxicity risk induced by BDDE and its biodegradation rate in subcutaneous tissue. The formu
Externí odkaz:
https://doaj.org/article/4eca7a54c8894f0dbc678d937906c129
Autor:
Jin Woo Choi, Hyun-Jong Cho, Ju-Hwan Park, Song Yi Baek, Jin Wook Chung, Dae-Duk Kim, Hyo-Cheol Kim
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e115898 (2014)
In many studies for chemoembolization of hepatocellular carcinoma, the Lipiodol emulsion preparation protocols, especially the mixing steps, were unclear or even unrevealed at all. However, doxorubicin (DOX) release may depend on the composition and
Externí odkaz:
https://doaj.org/article/3f9b5bccf16d4d45a8e22860c98f83f8
Autor:
Yohan Park, Ju-Hwan Park, Suryeon Park, Song Yi Lee, Kwan Hyung Cho, Dae-Duk Kim, Won-Sik Shim, In-Soo Yoon, Hyun-Jong Cho, Han-Joo Maeng
Publikováno v:
Molecules, Vol 21, Iss 10, p 1272 (2016)
In this study, we synthesized the valine (Val)-conjugated amide prodrug of doxorubicin (DOX) by the formation of amide bonds between DOX and Val. The synthesis of the DOX-Val prodrug was identified by a proton nuclear magnetic resonance (1H-NMR) assa
Externí odkaz:
https://doaj.org/article/13f39169bb52414ab91fd8bcb8c4d470
Publikováno v:
JOURNAL OF SEMICONDUCTOR TECHNOLOGY AND SCIENCE. 22:387-394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f56229e871fd681cebe18d5a62d65fba
https://doi.org/10.5573/jsts.2022.22.6.387
https://doi.org/10.5573/jsts.2022.22.6.387
Publikováno v:
International journal of pharmaceutics. 628
Bentonite (BT) is a biocompatible clay mineral that has advantageous properties as a pharmaceutical excipient. However, the application of BT in controlled-release oral formulations has been challenging due to incomplete drug release from BT-drug com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f9e7e7495c4e471ae4943763974a95f
https://pubmed.ncbi.nlm.nih.gov/36349613
https://pubmed.ncbi.nlm.nih.gov/36349613
Autor:
Min-Jun Baek, Hyeon-Jong Shin, Ju-Hwan Park, Jaehwan Kim, Il-Mo Kang, Jangik I. Lee, Dae-Duk Kim
Publikováno v:
Applied Clay Science. 229:106677
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f310d3077112c7a7606fca70aae0fc6b
https://doi.org/10.1016/j.clay.2022.106677
https://doi.org/10.1016/j.clay.2022.106677