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de Bruin VM, Vieira MC, Rocha MN, Viana GS

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Initially the bioavailability of marker compounds was determined by administrating the pure marker compounds individually to Wistar rats by oral (dose 15 mg/kg b.w per oral) and parenteral (dose 1.5 mg/kg b.w i.v.) routes, followed by determination of content of the same in plasma at different time points by the HPTLC method