Your browser doesn't support javascript.
loading
Formulation development and in-vitro evaluation of gastroretentive drug delivery system of loxoprofen sodium: A natural excipients based approach.
Zaman, Muhammad; Akhtar, Faiza; Baseer, Abdul; Hasan, Syed Muhammad Farid; Aman, Waqar; Khan, Amjad; Badshah, Munair; Majeedullah, -.
Afiliación
  • Zaman M; Faculty of Pharmacy, University of Central Punjab, Lahore, Pakistan.
  • Akhtar F; Faculty of Pharmacy, University of Lahore, Lahore, Pakistan.
  • Baseer A; Department of Pharmacy, Abasyn University Peshawar, Pakistan.
  • Hasan SMF; Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
  • Aman W; Department of Pharmacy, Kohat University of Science and Technology, Kohat, Pakistan.
  • Khan A; Department of Pharmacy, Kohat University of Science and Technology, Kohat, Pakistan.
  • Badshah M; Islam college of Pharmacy, Pasrur Road, Sialkot, Punjab Pakistan.
  • Majeedullah -; Department of Pharmacy, Kohat University of Science and Technology, Kohat, Pakistan.
Pak J Pharm Sci ; 34(1): 57-63, 2021 Jan.
Article en En | MEDLINE | ID: mdl-34248003
ABSTRACT
The limitations of conventional type delivery systems to retain drug (s) in the stomach has resulted in the development of novel gastroretentive drug delivery system. We developed single-layer effervescent floating tablets of loxoprofen sodium for prolong delivery in the stomach using natural polymers xanthan gum, guar gum and semisynthetic polymer HPMCK4M. All the formulations (F1-F9) were developed by varying concentrations of xanthan gum and HPMCK4M while guar gum concentration was kept constant. Two gas generating agent (s) incorporated were sodium bicarbonate and citric acid. All compendial pre and post-compression tests results were in the acceptable limits. FTIR analysis confirmed drug-polymer compatibility. The in-vitro drug release in simulated conditions i.e., 0.1 N HCl for 12 h revealed orderly increase in total floating time, i.e., less than 6 h for F1 over 12 h for F9. Formulations F1 to F4 were not capable to retard drug release up to 12 h, whereas F5-F7 for 12 h, while F8 and F9 for more than 12 h. Data fitting in various kinetic models showed that drug release best fit in first order kinetic model and F9 in zero order. Based on results data, F7 was the best among all.
Asunto(s)
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Química Farmacéutica / Sistemas de Liberación de Medicamentos / Composición de Medicamentos / Excipientes Idioma: En Revista: Pak J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Pakistán
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fármacos Gastrointestinales / Química Farmacéutica / Sistemas de Liberación de Medicamentos / Composición de Medicamentos / Excipientes Idioma: En Revista: Pak J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Pakistán