Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system
碩士 === 國立臺灣大學 === 化學工程學研究所 === 87 === The polymer membranes for colon-specific drug delivery system were prepared by phase inversion method. The physical and chemical properties change was discussed in this study. The dense E2 membranes made of EVAL with dry process and IPA/Water as co-so...
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ndltd-TW-087NTU000630452016-02-01T04:12:24Z http://ndltd.ncl.edu.tw/handle/99610940869396265174 Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system 聚乙烯乙烯醇薄膜於藥物制放之應用 Yen-Shih Huang 黃彥士 碩士 國立臺灣大學 化學工程學研究所 87 The polymer membranes for colon-specific drug delivery system were prepared by phase inversion method. The physical and chemical properties change was discussed in this study. The dense E2 membranes made of EVAL with dry process and IPA/Water as co-solvent were suitable for the application. The drug, 5-ASA, had little transport through the E2 membranes at pH 2.00. However, 5-ASA released more at pH 7.40. The permeability was risen from 0.034*10-3 at pH 2.00 to 0.184*10-3 cm2/hr at pH 7.40. There would be an electro-repulsion between 5-ASA and membranes at pH 2.00. Therefore, it might inhibit the release. However, the swelling properties of PVA membranes dominate the drug delivery. The electro-repulsion effects might be ignored and there was no difference between the drug releases at two pH values. In addition, the Lysine-modified E2 membranes had better drug release. The permeabilities were lager both at pH 2.00 (0.139*10-3 cm2/hr) and pH 7.40 (0.312*10-3 cm2/hr) than original. The study shows that the EVAL membranes are promising candidates for providing a colon-specific drug delivery. Leo-Wang Chen 陳劉旺 1999 學位論文 ; thesis 84 zh-TW |
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碩士 === 國立臺灣大學 === 化學工程學研究所 === 87 === The polymer membranes for colon-specific drug delivery system were prepared by phase inversion method. The physical and chemical properties change was discussed in this study.
The dense E2 membranes made of EVAL with dry process and IPA/Water as co-solvent were suitable for the application. The drug, 5-ASA, had little transport through the E2 membranes at pH 2.00. However, 5-ASA released more at pH 7.40. The permeability was risen from 0.034*10-3 at pH 2.00 to 0.184*10-3 cm2/hr at pH 7.40. There would be an electro-repulsion between 5-ASA and membranes at pH 2.00. Therefore, it might inhibit the release.
However, the swelling properties of PVA membranes dominate the drug delivery. The electro-repulsion effects might be ignored and there was no difference between the drug releases at two pH values.
In addition, the Lysine-modified E2 membranes had better drug release. The permeabilities were lager both at pH 2.00 (0.139*10-3 cm2/hr) and pH 7.40 (0.312*10-3 cm2/hr) than original.
The study shows that the EVAL membranes are promising candidates for providing a colon-specific drug delivery.
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author2 |
Leo-Wang Chen |
author_facet |
Leo-Wang Chen Yen-Shih Huang 黃彥士 |
author |
Yen-Shih Huang 黃彥士 |
spellingShingle |
Yen-Shih Huang 黃彥士 Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
author_sort |
Yen-Shih Huang |
title |
Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
title_short |
Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
title_full |
Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
title_fullStr |
Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
title_full_unstemmed |
Poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
title_sort |
poly(ethylene-co-vinyl alcohol) membranes for drug delivery system |
publishDate |
1999 |
url |
http://ndltd.ncl.edu.tw/handle/99610940869396265174 |
work_keys_str_mv |
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