Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix

碩士 === 國立陽明大學 === 醫學工程研究所 === 87 === Methotrexate(MTX), the most widely used antimetabolite, is a folic acid antagonist. It has an essential role in the treatment of solid tumor and suppression of graft—versus—host disease. However, oral or intravenous treatment may lead to serve adverse effects. Al...

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Main Authors: Heng-Hui, Su, 蘇恆輝
Other Authors: Yng-Jiin, Wang
Format: Others
Language:zh-TW
Published: 1999
Online Access:http://ndltd.ncl.edu.tw/handle/57458413185760368925
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spelling ndltd-TW-087YM0005300162015-10-13T11:50:26Z http://ndltd.ncl.edu.tw/handle/57458413185760368925 Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix 含胺基甲基葉酸微脂粒在膠原蛋白基材內之製備與應用 Heng-Hui, Su 蘇恆輝 碩士 國立陽明大學 醫學工程研究所 87 Methotrexate(MTX), the most widely used antimetabolite, is a folic acid antagonist. It has an essential role in the treatment of solid tumor and suppression of graft—versus—host disease. However, oral or intravenous treatment may lead to serve adverse effects. Alternative drug delivery system has been developed, including conjugation and encapsulation. Liposomes are microscopic particles consisting of one or more spheres of phospholipid bilayers separated by aqueous compartment. Drug molecules can either be encapsulated in the aqueous phase or intercalated into the lipid bilayer depending on their own hydro— or lipophilicity. Liposome have great properties for drug delivery but is too largely cleared by the reticuloendothelial system, so we have to coat some bioadhesive to locate the liposomes. Collagen is a natural polymer purified from biological tissue. It has excellent biocompatibility and biodegradability, and is essential for tissue adhesion, which is a good liposome—composite material. In this study, Liposomes were prepared by ether injection and membrane extrusion method, and with diameters about 200 nm. Liposome encapsulated MTX (liposome—MTX) is dispersed in collagen matrix as a drug delivery system, and the encapsulation ratio is 10%. The release property of liposome—MTX and liposome—MTX ¤ collagen is first order with equations ln (1—Q) = —0.000234t — 0.265 and ln (1—Q) = —0.000135—0.148, respectively, and release 80% drug in seven days. Osteosarcoma cell line is selected to be In vitro model, and the 50% inhibitory dose (ID50) is assayed. Although the ID50 of liposome—MTX and liposome—MTX ¤ collagen are higher than free MTX, the difference is slightly and as a controlled release drug delivery system, the liposome—MTX ¤ collagen is an expectable bioadhesive controlled—release carriers. Yng-Jiin, Wang 王盈錦 1999 學位論文 ; thesis 119 zh-TW
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description 碩士 === 國立陽明大學 === 醫學工程研究所 === 87 === Methotrexate(MTX), the most widely used antimetabolite, is a folic acid antagonist. It has an essential role in the treatment of solid tumor and suppression of graft—versus—host disease. However, oral or intravenous treatment may lead to serve adverse effects. Alternative drug delivery system has been developed, including conjugation and encapsulation. Liposomes are microscopic particles consisting of one or more spheres of phospholipid bilayers separated by aqueous compartment. Drug molecules can either be encapsulated in the aqueous phase or intercalated into the lipid bilayer depending on their own hydro— or lipophilicity. Liposome have great properties for drug delivery but is too largely cleared by the reticuloendothelial system, so we have to coat some bioadhesive to locate the liposomes. Collagen is a natural polymer purified from biological tissue. It has excellent biocompatibility and biodegradability, and is essential for tissue adhesion, which is a good liposome—composite material. In this study, Liposomes were prepared by ether injection and membrane extrusion method, and with diameters about 200 nm. Liposome encapsulated MTX (liposome—MTX) is dispersed in collagen matrix as a drug delivery system, and the encapsulation ratio is 10%. The release property of liposome—MTX and liposome—MTX ¤ collagen is first order with equations ln (1—Q) = —0.000234t — 0.265 and ln (1—Q) = —0.000135—0.148, respectively, and release 80% drug in seven days. Osteosarcoma cell line is selected to be In vitro model, and the 50% inhibitory dose (ID50) is assayed. Although the ID50 of liposome—MTX and liposome—MTX ¤ collagen are higher than free MTX, the difference is slightly and as a controlled release drug delivery system, the liposome—MTX ¤ collagen is an expectable bioadhesive controlled—release carriers.
author2 Yng-Jiin, Wang
author_facet Yng-Jiin, Wang
Heng-Hui, Su
蘇恆輝
author Heng-Hui, Su
蘇恆輝
spellingShingle Heng-Hui, Su
蘇恆輝
Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
author_sort Heng-Hui, Su
title Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
title_short Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
title_full Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
title_fullStr Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
title_full_unstemmed Preparation and Applications of Methotrexate-Liposomes in Collagen Matrix
title_sort preparation and applications of methotrexate-liposomes in collagen matrix
publishDate 1999
url http://ndltd.ncl.edu.tw/handle/57458413185760368925
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