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Development and Quality evaluation of sustained release pellets of eperisone HCl.
Jawed, Syed Hameez; Muhammad, Iyad Naeem; Qazi, Faiza; Shoaib, Muhammad Harris; Arshad, Hafiz Muhammad; Siddiqui, Tuba.
Afiliación
  • Jawed SH; Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
  • Muhammad IN; Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
  • Qazi F; Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
  • Shoaib MH; Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
  • Arshad HM; Department of Pharmaceutics, Dow College of Pharmacy, DUHS, Karachi, Pakistan.
  • Siddiqui T; Department of Pharmaceutics, Faculty of Pharmacy, Federal Urdu University of Arts, Science and Technology, Karachi.
Pak J Pharm Sci ; 34(1(Supplementary)): 225-235, 2021 Jan.
Article en En | MEDLINE | ID: mdl-34275846
The objective was to develop eperisone HCl sustained-release pellets through extrusion spheronization technique and to determine the influence of different hydrophobic (polymeric based and wax-based) and hydrophilic (polymeric based) matrix former on the release of eperisone HCl (BCS class I drug) and on pellet sphericity. The pellet formulations consisted of different hydrophobic and hydrophilic matrix formers like HPMC K4M (10-20%) HPMC K15M (10%), EC (7cps) (10-20%), Carnauba wax (10-20%), Compritol ATO 888 (10-20%), Glyceryl monostearate (10%), lactose and microcrystalline cellulose. The initial burst release of the drug from matrix pellet formulations was effectively controlled by coating with 5% EC (ethylcellulose) dispersion. The dissolution profile and drug release kinetics of coated pellet formulations were determined at both acidic and basic pH medium. SEM (Scanning electron microscope) technique was used to determine the surface morphology and cross-section of F5 and F7 pellet formulation. The mechanism of drug release of coated formulation followed non-Fickian diffusion. FTIR spectroscopy was conducted and no drug and excipients interaction was observed. The results had shown that optimized coated formulation was F5 and F7 which effectively extend the drug release for 12 hours.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Propiofenonas / Preparaciones de Acción Retardada / Relajantes Musculares Centrales Idioma: En Revista: Pak J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: Pakistán
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Propiofenonas / Preparaciones de Acción Retardada / Relajantes Musculares Centrales Idioma: En Revista: Pak J Pharm Sci Asunto de la revista: FARMACIA / FARMACOLOGIA / QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Pakistán Pais de publicación: Pakistán