DETERMINATION OF OPTIMAL DISSOLUTION TEST CONDITIONS FOR “NAVESTO” CAPSULES

Auteurs

  • F.Kh. Maksudova 1 Автор
  • N.M. Vakhidova 1 Автор
  • Z.B. Bakhtiyorova 1 Автор

Résumé

The therapeutic efficacy of antihypertensive drugs is closely associated with their biopharmaceutical characteristics, particularly the solubility and dissolution behavior of the active pharmaceutical ingredients (APIs). Therefore, the evaluation of in vitro biopharmaceutical performance, including dissolution testing, represents a critical component of pharmaceutical quality assessment. Since the solubility of valsartan and sacubitril is highly dependent on the pH of the dissolution medium, the scientific justification of optimal dissolution test conditions for “Navesto” capsules containing these active ingredients is of particular importance. Establishing appropriate dissolution conditions and evaluating the in vitro biopharmaceutical characteristics of the formulation are essential for ensuring its quality, performance, and potential therapeutic efficacy. 

 

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Publiée

2026-08-01

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Comment citer

Maksudova, F., Vakhidova, N., & Bakhtiyorova, Z. (2026). DETERMINATION OF OPTIMAL DISSOLUTION TEST CONDITIONS FOR “NAVESTO” CAPSULES . International Conference on Social Sciences & Humanities, 2(7), 67-68. https://uniconflix.com/index.php/ICSH/article/view/5596