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Validation of HPLC quantity determination procedure of "ibumol" suppositories

  • In: Laboratory and Medicines Control Services Posters
  • At: Hyderabad (India) (2011)
  • Type: Poster
  • Poster code: LMCS-P-02
  • By: TILLAEVA, Gulnora (Head Dept. of Drug And Med. Equip. Quality Control, Tashkent, Uzbekistan)
  • Co-author(s): Ganieva, Khilola (Tashkent Pharmaceutical Inst., Tashkent, Uzbekistan)
  • Abstract:

    Aim: validation of HPLC quantity control procedure of "Ibumol" suppositories is determined on validative characteristic: Method: for HPLC validation procedure of "Ibumol" suppositories the extraction of investigated substances from forming substances has been preliminary conducted. For extraction hexan, 5% solutions of sodium carbonate were used.


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Last update 4 October 2019

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