Development and validation method for quantitative determination of rifampicin in human plasma and its application in bioequivalence test

• In: Poster presentation
• At: Seoul (South Korea) (2017)
• Type: Poster
• Poster code: POS-PAA-011
• By: LUKITANINGSIH, Endang (Gadjah Mada University, Pharmaceutical Chemistry Department, Yogyakarta, Indonesia)
• Co-author(s): Endang Lukitaningsih:
  Fathul Jannah: Advanced Pharmaceutical Sciences lab, Gadjah Mada University, Yogyakarta, Indonesia
  Arief Rahman Hakim: Pharmacology and Clinical Pharmacy, Gadjah Mada University, Yogyakarta, Indonesia
  Ratna Dewi Puspita: Gadjah Mada University Hospital, Gadjah Mada University, Yogyakarta, Indonesia
  Zullies Ikawati: Pharmacology and Clinical Pharmacy, Gadjah Mada University, Yogyakarta, Indonesia
  
• Abstract:

  Background

  Rifampicin has been used worldwide as first line drug-prescribed throughout tuberculosis therapy

  Purpose

  This study aims to develop and to validate an HPLC method couple with a UV detection for determination of rifampicin for bioequivalence study.

  Methods

  The chromatographic separation was achieved on a RP-C18 column (LachromHitachi, 250 x..

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