Source:http://linkedlifedata.com/resource/pubmed/id/14744480
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rdf:type | |
lifeskim:mentions |
umls-concept:C0004434,
umls-concept:C0013227,
umls-concept:C0026336,
umls-concept:C0085104,
umls-concept:C0185023,
umls-concept:C0237497,
umls-concept:C0332307,
umls-concept:C0369963,
umls-concept:C0439855,
umls-concept:C1314972,
umls-concept:C1522492,
umls-concept:C1707689,
umls-concept:C1947904,
umls-concept:C1999228,
umls-concept:C2825781
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pubmed:issue |
2-3
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pubmed:dateCreated |
2004-1-27
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pubmed:abstractText |
Recent studies have focused on the active targeting of drug delivery by combining a homing device and antitumor drug. For this purpose, synthesis of a well-designed vehicle (such as polymer/drug conjugates or nanoparticles) carrying a drug and a homing device requires many steps. We propose a new type of drug delivery system (DDS) by formation of a complex containing avidin (Av) plus biotinyl drug with a biotinyl homing device, which easily accommodates the combination of various drugs and homing devices. The targetable drug complex can be prepared by selecting an appropriate biotinyl drug derivative and a biotinyl homing device and mixing them with avidin. Fluorescent dye with 5-(and-6)-carboxytetramethylrhodamine (TAMRA) was used as a drug model, and galactose (Gal) recognized by liver parenchymal cells was used as a homing device. TAMRA and galactose were attached to biotin (Bio) through a triethyleneglycol (TEG) spacer group to give Bio-TEG-TAMRA conjugate and Bio-TEG-Gal conjugate, respectively. Confocal laser scanning microscopic studies suggest that the complexes prepared by mixing Bio-TEG-Gal conjugate and fluorescein isothiocyanate (FITC)-labeled Av (feed molar ratio 4:1), and mixing Bio-TEG-Gal conjugate, Bio-TEG-TAMRA conjugate and FITC-labeled Av are internalized into the hepatoma cells through a receptor-mediated endocytosis mechanism.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0168-3659
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
94
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
281-91
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading | |
pubmed:year |
2004
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pubmed:articleTitle |
Design of attachment type of drug delivery system by complex formation of avidin with biotinyl drug model and biotinyl saccharide.
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pubmed:affiliation |
Department of Applied Chemistry, Faculty of Engineering, Kansai University, Suita Osaka 564-8680, Japan. touchi@ipcku.kansai-u.ac.jp
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pubmed:publicationType |
Journal Article
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