ArticleIranian journal of basic medical sciences2016
Pharmacokinetic study of furosemide incorporated PLGA microspheres after oral administration to rat.
Article in Iranian journal of basic medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
5 authors at 2 institutions in 1 country.
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Abstract
objectivesThe purpose of the current study was to assess the feasibility of microspheres from biocompatible polymer for oral bioavailability (BA) enhancement of potent sulfonamide- type loop diuretic- Furosemide - which used in the treatment of congestive heart failure, caused edema, cirrhosis, renal disease and as an adjunct in acute pulmonary edema. The comparatively poor and inconstant BA of furosemide, which occurs site-specifically in the stomach and upper small intestine, has been ascribed to the poor dissolution of furosemide. MATERIALS AND
methodsIn attempt to enhance the drug BA, poly (dl-lactic-co-glycolic acid) (PLGA) microspheres of furosemide were obtained using solvent-evaporation method and the carrier characteristics were investigated subsequently.
resultsThe
conclusionThe results showed that the prepared microspheres successfully improved BA of the poorly water-soluble drug effectively.
Indexed as
Identifiers
27872700PMC5110652W2545744901What OpenQuestion holds
Registered trials
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