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곽상규

Kwak, Sang Kyu
Kyu’s MolSim Lab @ UNIST
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dc.citation.conferencePlace KO -
dc.citation.conferencePlace Daejeon -
dc.citation.number 2 -
dc.citation.startPage 1467 -
dc.citation.title 한국화학공학회 2016년도 가을총회 -
dc.citation.volume 22 -
dc.contributor.author Go, Eun Min -
dc.contributor.author Shin, Eun Hye -
dc.contributor.author Kwak, Sang Kyu -
dc.date.accessioned 2023-12-19T20:06:32Z -
dc.date.available 2023-12-19T20:06:32Z -
dc.date.created 2017-01-06 -
dc.date.issued 2016-10-20 -
dc.description.abstract Drug encapsulation and release are directly related to the efficiency of biological therapy. In this work, dynamics of vesicle for encapsulating and releasing the anti-cancer drug were studied by coarse-grained molecular dynamics; amphiphilic block-copolymer (i.e. polyethylene glycol (PEG) and polylactic acid (PLA)) for vesicle and gemcitabine for anti-cancer drug. In particular, the self-assembly of vesicle covering drug and the shape control of the vesicle were investigated. First, we observed that the self-assembly occurred only if the volume ratio of PEG-PLA became 3:7, where the optimal area per the number of polymer chain was 0.3 nm2. Controlling the inner and outer surface areas of the membrane of vesicle induced anisotropic shape of vesicle with the aspect ratio of 1.1. Second, the effective mole ratio of block-copolymer and drug was found to be 100 to 1, which worked for loading drug into vesicle. Finally, the rupture of the vesicle in low pH environments (i.e. pH 3 ~ pH 7) mimicking the inside of cancer cell, was studied for the drug release. Hydrolysis of PEG and crystalline PLA were heavily involved in the drug release -
dc.identifier.bibliographicCitation 한국화학공학회 2016년도 가을총회, v.22, no.2, pp.1467 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/40179 -
dc.language 영어 -
dc.publisher 한국화학공학회 -
dc.title Theoretical Study on Encapsulation and Release of Anti-cancer Drug in PEG-PLA Vesicle -
dc.type Conference Paper -
dc.date.conferenceDate 2016-10-19 -

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