Bioavailability file: Amlodipine

dc.authorscopusid14032701900
dc.authorscopusid56094749300
dc.authorscopusid56095245300
dc.authorscopusid56666885900
dc.contributor.authorKaynak M.S.
dc.contributor.authorBogacz A.
dc.contributor.authorStelmasi?ski M.
dc.contributor.authorŞahin S.
dc.date.accessioned2024-08-04T20:01:01Z
dc.date.available2024-08-04T20:01:01Z
dc.date.issued2011
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAmlodipine (AML), a third-generation dihydropiridin, is a long-acting L-calcium channel blocker used in the treatment of hypertension and angina pectoris. It exerts its effects by blocking the voltage-dependent L-calcium channels and binding to both dihydropiridin and nondihydropiridin binding sites. AML is well absorbed (96%) after oral administration and its bioavailability is between 64-90%. Its volume of distribution is about 16 to 21 L/kg and protein binding is 98% after oral administration. AML is extensively metabolized in the liver and its elimination from the plasma is biphasic with a terminal half-life of 30 to 50 h. It is excreted by renal route about 60%. According to Biopharmaceutics Classification System, AML is classified as class I drug by WHO. In this review physicochemical properties, pharmacology, analytical methods, pharmacokinetics and bioavailability of amlodipine are discussed.en_US
dc.identifier.endpage222en_US
dc.identifier.issn1300-4182
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84897432947en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage207en_US
dc.identifier.urihttps://hdl.handle.net/11616/91196
dc.identifier.volume36en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherAnkara Universityen_US
dc.relation.ispartofFabad Journal of Pharmaceutical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmlodipineen_US
dc.subjectBioavailabilityen_US
dc.subjectBiopharmaceutics Classification System (BCS)en_US
dc.subjectPharmacokineticsen_US
dc.titleBioavailability file: Amlodipineen_US
dc.typeReview Articleen_US

Dosyalar