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Preparation, Characterization and Evaluation of Flavonolignan Silymarin Effervescent Floating Matrix Tablets for Enhanced Oral Bioavailability.
Ahmad, Sher; Khan, Jamshaid Ali; Kausar, Tabassum Naheed; Mahnashi, Mater H; Alasiri, Ali; Alqahtani, Abdulsalam A; Alqahtani, Thamer S; Walbi, Ismail A; Alshehri, Osama M; Elnoubi, Osman A; Mahmood, Fawad; Sadiq, Abdul.
Afiliación
  • Ahmad S; Department of Pharmacy, University of Peshawar, Peshawar 25120, KP, Pakistan.
  • Khan JA; Department of Pharmacy, University of Peshawar, Peshawar 25120, KP, Pakistan.
  • Kausar TN; Mumtaz Maternity Hospital, Hashtnagri, Peshawar 25220, KP, Pakistan.
  • Mahnashi MH; Department of Pharmaceutical Chemistry, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Alasiri A; Department of Pharmaceutics, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Alqahtani AA; Department of Pharmaceutics, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Alqahtani TS; Department of Pharmaceutics, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Walbi IA; Department of Clinical Pharmacy, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Alshehri OM; Department of Clinical Pharmacy, College of Pharmacy, Najran University, Najran 55461, Saudi Arabia.
  • Elnoubi OA; College of Applied Medical Sciences, Najran University, Najran 55461, Saudi Arabia.
  • Mahmood F; Department of Pharmacy, University of Peshawar, Peshawar 25120, KP, Pakistan.
  • Sadiq A; Department of Pharmacy, University of Malakand, Chakdara 18000, KP, Pakistan.
Molecules ; 28(6)2023 Mar 13.
Article en En | MEDLINE | ID: mdl-36985575
ABSTRACT
The convenient and highly compliant route for the delivery of active pharmaceutical ingredients is the tablet. A versatile platform of tablets is available for the delivery of therapeutic agents to the gastrointestinal tract. This study aimed to prepare gastro retentive drug delivery floating tablets of silymarin to improve its oral bioavailability and solubility. Hydroxypropyl methylcellulose (HPMCK4M and HPMCK15), Carbopol 934p and sodium bicarbonate were used as a matrix, floating enhancer and gas generating agent, respectively. The prepared tablets were evaluated for physicochemical parameters such as hardness, weight variation, friability, floating properties (floating lag time, total floating time), drug content, stability study, in vitro drug release, in vivo floating behavior and in vivo pharmacokinetics. The drug-polymer interaction was studied by Differential Scanning Calorimetry (DSC) thermal analysis and Fourier transform infrared (FTIR). The floating lag time of the formulation was within the prescribed limit (<2 min). The formulation showed good matrix integrity and retarded the release of drug for >12 h. The dissolution can be described by zero-order kinetics (r2 = 0.979), with anomalous diffusion as the release mechanism (n = 0.65). An in vivo pharmacokinetic study showed that Cmax and AUC were increased by up to two times in comparison with the conventional dosage form. An in vivo imaging study showed that the tablet was present in the stomach for 12 h. It can be concluded from this study that the combined matrix system containing hydrophobic and hydrophilic polymers min imized the burst release of the drug from the tablet and achieved a drug release by zero-order kinetics, which is practically difficult with only a hydrophilic matrix. An in vivo pharmacokinetic study elaborated that the bioavailability and solubility of silymarin were improved with an increased mean residence time.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Silimarina Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Silimarina Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Pakistán