Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/3592
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dc.date.accessioned2012-04-23T05:55:51Z-
dc.date.available2012-04-23T05:55:51Z-
dc.date.issued2012-04-23-
dc.identifier.urihttp://hdl.handle.net/10603/3592-
dc.description.abstractThe present investigation was aimed at studying the perse effect of herbal extracts containing alkaloids and coumarins (piper nigrum, Zingiber officinale, Angelica archengelica, Melilotus officinalis) and as well as their combination with chitosan (CTN) for possible use as percutaneous permeation enhancer. Overall, the results of the present investigation suggest a promising role of alkaloids and coumarins containing extracts in enhancing the percutaneous permeation of repaglinide (RGE). CTN was found to potentiate the permeation enhancing activity of these extracts. Further, the permeation enhancing activity of alkaloids and coumarins containing extracts and CTN was found to be mediated through their effect on microconstituents of epidermis which was manifested in the ultrastructure as evident in SEM and TEM photographs. The ultrastructural alterations and biochemical changes in rat skin after treatment with these extracts were correlated with the biophysical (transepidermal water loss) and thermotropic attributes (differential scanning calorimetric parameters). Hence, biochemical constitution and modification of epidermal ultrastructure seem to be inextricable aspects while understanding the percutaneous permeation activity of alkaloids and coumarins. Further, the normalization of contents of epidermal microconstituents after 48 h of application to viable rat skin rules out the possibility of irreversible damage by any of these agents. The application of patches containing mixture of alkaloids and coumarins containing extract and CTN resulted in sustained release of RGE which was able to control the blood glucose level in Streptozotocin-induced hyperglycemic rats through 24-36 h. Transdermal formulation containing Angelica archangelica extract-CTN mixture was observed to enhance the in vitro permeation of repaglinide by 8-fold as compared to control. Application of transdermal patch containing this formulation was able to control the increased blood glucose level in Steptozotocin-induced hypeglycemic rats for 36 hours as judged by pharmacokinetic and pharmacodynamic investigations. Further, treatment on HaCaT cell line by these extracts were observed to influence the TJ plaque protein zonula occludens (ZO383 1) as evidenced by reduced immunofluorescence of anti-TJP1 (ZO-1) antibody in confocal laser scanning microscopic studies. The results of the investigation revealed a promising role of coumarins (Angelica archangelica extract being the most effective) in formulating transdermal patches of repaglinide for once-a-day application.en_US
dc.format.extent381p.en_US
dc.languageEnglishen_US
dc.rightsuniversityen_US
dc.titleInvestigations on plant extracts for transdermal delivery of Repaglinideen_US
dc.creator.researcherNeeraj, Kaushalen_US
dc.subject.keywordSkin structureen_US
dc.subject.keywordPercutaneous Permeationen_US
dc.subject.keywordherbal extractsen_US
dc.subject.keywordPharmaceutical Sciencesen_US
dc.subject.keywordDrug Researchen_US
dc.description.noteReferences p.332-381en_US
dc.contributor.guideTiwary, A Ken_US
dc.contributor.guideJain, Subheeten_US
dc.publisher.placePatialaen_US
dc.publisher.universityPunjabi Universityen_US
dc.publisher.institutionDepartment of Pharmaceutical Sciences and Drug Researchen_US
dc.date.registered0en_US
dc.date.completed2010en_US
dc.format.accompanyingmaterialNoneen_US
dc.type.degreePh.D.en_US
dc.source.inflibnetINFLIBNETen_US
Appears in Departments:Department of Pharmaceutical Sciences & Drug Research

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01_title.pdfAttached File77.22 kBAdobe PDFView/Open
02_certificate.pdf91.43 kBAdobe PDFView/Open
03_declaration.pdf95.26 kBAdobe PDFView/Open
04_dedication.pdf2.07 MBAdobe PDFView/Open
05_acknowledgements.pdf70.55 kBAdobe PDFView/Open
06_index.pdf82.66 kBAdobe PDFView/Open
07_chapter 1.pdf280.33 kBAdobe PDFView/Open
08_chapter 2.pdf955.14 kBAdobe PDFView/Open
09_chapter 3.pdf153.78 kBAdobe PDFView/Open
10_chapter 4.pdf274.34 kBAdobe PDFView/Open
11_chapter 5.pdf40.83 MBAdobe PDFView/Open
12_summary.pdf95.9 kBAdobe PDFView/Open
13_referances.pdf425.87 kBAdobe PDFView/Open
14_abstract.pdf90.46 kBAdobe PDFView/Open


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