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Quality control and drug-drug interactions between commercially available Metoprolol and Glimepiride tablets
Alqahtani, Saad Saeed; Ahmad, Sarfaraz; Banji, David; Sultan, Muhammad Hadi; Alam, Mohammad Sarfaraz; Alshahrani, Saeed; Alzarea, Abdulaziz I.
  • Alqahtani, Saad Saeed; Jazan University. College of Pharmacy. Pharmacy Practice Research Unit. SA
  • Ahmad, Sarfaraz; Jazan University. College of Pharmacy. Pharmacy Practice Research Unit. SA
  • Banji, David; Jazan University. College of Pharmacy. Pharmacy Practice Research Unit. SA
  • Sultan, Muhammad Hadi; Jazan University. College of Pharmacy. Department of Pharmaceutics. SA
  • Alam, Mohammad Sarfaraz; Jazan University. College of Pharmacy. Department of Pharmaceutics. SA
  • Alshahrani, Saeed; Jazan University. College of Pharmacy. Department of Pharmacology & Toxicology. SA
  • Alzarea, Abdulaziz I; Jouf University Sakaka. College of Pharmacy. Department of Clinical Pharmacy. SA
Braz. J. Pharm. Sci. (Online) ; 58: e20349, 2022. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1420459
ABSTRACT
Abstract Quality is paramount and needs to be maintained throughout the shelf life of pharmaceuticals. The current study aimed to evaluate the quality, potency, and drug-drug interaction in an in vivo animal model by using two drugs, namely, metoprolol and glimepiride. Tablets were selected for their physical characteristics, such as shape, size, and color. Quality control tests, such as weight variation, hardness, friability, and disintegration tests, and invitro drug release studies were performed as per USP. Drug-drug interaction and in vivo studies were carried out according to the standard protocol of the animal ethics committee. Quality control tests of both the tablets were within the specified range. The cumulative release percentages of the drugs were 81.12% and 85.36% for Metoprolol Tartrate and Glimepiride, respectively, in a physiological buffer solution within 1 h. The combination of metoprolol and Glimepiride also significantly decreased the blood glucose level in diabetic animals. However, the blood glucose level increased in the group receiving metoprolol only, but the difference was not significant. The result suggested that the formulations are safe. However, the chronic use of this combination requires frequent monitoring of blood glucose level to improve its efficacy and for the patient's safety.
Assuntos


Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Controle de Qualidade / Comprimidos / Interações Medicamentosas / Metoprolol Tipo de estudo: Estudo prognóstico Limite: Animais Idioma: Inglês Revista: Braz. J. Pharm. Sci. (Online) Assunto da revista: Farmacologia / Terapˆutica / Toxicologia Ano de publicação: 2022 Tipo de documento: Artigo País de afiliação: Arábia Saudita Instituição/País de afiliação: Jazan University/SA / Jouf University Sakaka/SA

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Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Controle de Qualidade / Comprimidos / Interações Medicamentosas / Metoprolol Tipo de estudo: Estudo prognóstico Limite: Animais Idioma: Inglês Revista: Braz. J. Pharm. Sci. (Online) Assunto da revista: Farmacologia / Terapˆutica / Toxicologia Ano de publicação: 2022 Tipo de documento: Artigo País de afiliação: Arábia Saudita Instituição/País de afiliação: Jazan University/SA / Jouf University Sakaka/SA