Source:http://linkedlifedata.com/resource/pubmed/id/12115840
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2002-7-12
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pubmed:abstractText |
The objective of the current study was to develop and evaluate VLDL-resembling phospholipid-submicron emulsion (PSME) as a carrier system for new cholesterol-based compounds for targeted delivery to cancer cells. BCH, a boronated cholesterol compound, was originally developed in our laboratory to mimic the cholesterol esters present in the LDL and to follow a similar pathway of cholesterol transport into the rapidly dividing cancer cells. The VLDL-resembling system was then designed to solubilize BCH, facilitate the interaction with LDL, and thus assist the BCH delivery to cancer cells. BCH-containing PSME was prepared by sonication. Chemical compositions and particle sizes of different PSME fractions were determined. The lipid structure of PSME and location of BCH in the formulation were assessed based on experimental results. Density gradient ultracentrifugation fractionated the emulsion into three particle-size populations with structures and compositions resembling native VLDL. In vitro interaction between PSME and LDL was evident by agarose electrophoresis, as both formed a single band with an intermediate mobility. The transfer of BCH from PSME to LDL was also observed in the presence of other serum components including serum proteins. Cell culture data showed sufficient uptake of BCH in rat 9L glioma cells (> 50 microg boron/g cells). In conclusion, this system has the capability to incorporate the cholesterol-based compound, interact with native LDL, and assist the delivery of this compound into cancer cells in vitro.
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pubmed:grant | |
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 |
Jun
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pubmed:issn |
0022-3549
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2002 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
91
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1405-13
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12115840-Animals,
pubmed-meshheading:12115840-Biological Transport,
pubmed-meshheading:12115840-Chemistry, Pharmaceutical,
pubmed-meshheading:12115840-Cholesterol,
pubmed-meshheading:12115840-Drug Delivery Systems,
pubmed-meshheading:12115840-Drug Stability,
pubmed-meshheading:12115840-Electrophoresis, Agar Gel,
pubmed-meshheading:12115840-Emulsions,
pubmed-meshheading:12115840-Lipoproteins, VLDL,
pubmed-meshheading:12115840-Particle Size,
pubmed-meshheading:12115840-Phospholipids,
pubmed-meshheading:12115840-Rats,
pubmed-meshheading:12115840-Sonication,
pubmed-meshheading:12115840-Tumor Cells, Cultured
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pubmed:year |
2002
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pubmed:articleTitle |
VLDL-resembling phospholipid-submicron emulsion for cholesterol-based drug targeting.
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pubmed:affiliation |
Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, Univesity of Georgia, Athens 30602, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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