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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/13864
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dc.contributor.authorSundriyal, Sandeep-
dc.date.accessioned2024-01-17T09:08:50Z-
dc.date.available2024-01-17T09:08:50Z-
dc.date.issued2006-
dc.identifier.urihttps://www.ingentaconnect.com/contentone/asp/jnn/2006/00000006/F0020009/art00080-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/13864-
dc.description.abstractGlitazones are PPARγ agonistic insulin sensitizers used clinically for the treatment of type-2 diabetes. The delivery of these compounds with the help of dendrimers is possible. Ab initio MO calculations and MESP analysis indicate that the dendrimers with complementary electrostatic potential to glitazones can be designed. The estimated binding strength between one arm of dendrimer and thiazolidinedione is about 15–20 kcal/mol. This binding strength originates from three hydrogen bonds between the dendrimer and each molecule of glitazone. This binding strength is quite suitable for drug encapsulation on the dendrimer based nanoparticles and can be employed for drug delivery.en_US
dc.language.isoenen_US
dc.publisherAmerican Scientific Publishersen_US
dc.subjectPharmacyen_US
dc.subjectGlitazonesen_US
dc.subjectDendrimersen_US
dc.subjectDrug Deliveryen_US
dc.titleMolecular Electrostatic Potentials in the Design of Dendrimers for the Delivery of Glitazonesen_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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