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   <subfield code="a">eng</subfield>
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   <subfield code="a">LG 993.5 2023 P5 </subfield>
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  <datafield tag="100" ind1="1" ind2=" ">
   <subfield code="a">Gustillo, Stella Rowee</subfield>
   <subfield code="e">author </subfield>
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   <subfield code="a">In vitro assessment of the inhibitory effect of Chamaecostus cuspidatus herbal preparation on CYP2C9</subfield>
   <subfield code="c">Stella Rowee Gustillo ; Joana J. Arejola, adviser .</subfield>
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   <subfield code="a">Manila:</subfield>
   <subfield code="b">Department of Pharmacy, College of Pharmacy, University of the Philippines Manila</subfield>
   <subfield code="c">2023</subfield>
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   <subfield code="a">xxi, 213 leaves ;</subfield>
   <subfield code="c">28 cm.</subfield>
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   <subfield code="a">text</subfield>
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   <subfield code="a">volume</subfield>
   <subfield code="2">rdacarrier</subfield>
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   <subfield code="a">Thesis (Master of Science in Pharmacy)--University of the Philippines Manila, August 2023.</subfield>
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   <subfield code="a">Available only after consultation with author/thesis adviser</subfield>
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   <subfield code="a">Cytochrome P450 enzyme-mediated herb-drug interactions may pose considerable risk for critical clinical consequences when co-administered with prescribed medications. Oral hypoglycemic agents such as sulfonylureas, meglitinides, and thiazolidinediones are substrates of the most abundant CYP2C subfamily in the human liver-CYP2C9. Concomitant intake with herbal preparations which contain phytoconstituents that may potentially modulate drug metabolism could alter plasma drug concentrations, degree of drug efficacy and toxicity. Chamaecostus cuspidatus leaves traditional and commercial herbal preparations have been taken for diabetes mellitus in Southeast Asia with reports on combined use with allopathic medicine. The investigation of the risk of possible fatal outcomes such severe hypoglycemia through initial in vitro assessment of potential CYP2C9 inhibition by natural products may be of great importance for treatment optimization. The study assessed the ability of traditionally and commercially prepared Chamaecostus cuspidatus aqueous extracts to interfere with CYP2C9 activity via fluorescence-based enzyme assay. Among the aqueous extracts of Chamaecostus cuspidatus leaves, only the lyophilized leaf juice from Bacolod showed potential CYP2C9 inhibition. Flavonoids and alkaloids were detected via TLC and phytochemical screening which are the most likely class of metabolites in Chamaecostus cuspidatus responsible for the CYP2C9 inhibitory activity. Although none of the decoctions and tea preparations showed significant CYP2C9 percentage inhibition, further evidence is needed to determine the effect of heating on the CYP2C9-inhibiting compounds from Chamaecostus cuspidatus.</subfield>
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   <subfield code="a">Cytochrome P-450 Enzyme System.</subfield>
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   <subfield code="a">Drug Interactions.</subfield>
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   <subfield code="a">Herbal Medicine.</subfield>
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   <subfield code="a">Hypoglycemic agents.</subfield>
   <subfield code="x">Inhibition.</subfield>
   <subfield code="x">Diabetes Mellitus.</subfield>
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  <datafield tag="653" ind1="0" ind2="0">
   <subfield code="a">Chamaecostus cuspidatus.</subfield>
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   <subfield code="a">Cytochrome P450.</subfield>
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   <subfield code="a">Herb-Drug Interactions.</subfield>
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   <subfield code="a">Traditional Medicine.</subfield>
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   <subfield code="a">Phytoconstituents.</subfield>
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   <subfield code="a">Commercial Herbal Preparations.</subfield>
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   <subfield code="a">Arejola, Joana J. </subfield>
   <subfield code="e">adviser.</subfield>
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   <subfield code="h">LG 993.5 2023 P5</subfield>
   <subfield code="i">C85</subfield>
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