Comparing Hydroxypropyl Methylcellulose and Guar Gum on Sustained Release Effect of Metformin Hydrochloride Matrix Tablet

Publish Year: 1402
نوع سند: مقاله ژورنالی
زبان: English
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JR_PBRE-10-2_005

تاریخ نمایه سازی: 14 مرداد 1403

Abstract:

Background and Objectives: Limited diabetes drug availability and frequent adverse reactions to oral medications highlight the need for improved drug delivery. This study suggests optimizing drug efficiency through process modifications, focusing on anti-diabetic medications like metformin hydrochloride. Matrix-type formulations are utilized to overcome current drug targeting and dosage management limitations. Methods: This study aims to improve anti-diabetic drugs, focusing on metformin hydrochloride, via process modifications in drug delivery. We developed a sustainable drug release process with matrix-type formulations, comparing hydroxyl propyl methylcellulose (HPMC) and guar gum as rate-controlling polymers. The optimized formulation was then compared with Glyciphage SR ۵۰۰ to identify similarities and differences in drug release profiles. Results: We utilized matrix-type formulations to administer metformin hydrochloride. It develops a sustainable drug release process with HPMC and guar gum as rate-controlling polymers. Next, we conducted comparative drug release studies, systematically optimized the formulation, and compared it to Glyciphage SR ۵۰۰ using appropriate analytical methods. Results: Comparative dissolution data, including a high similarity factor (f۲) of ۷۵.۳۳ with Glyciphage SR ۵۰۰, emphasizes the promising resemblance between metformin hydrochloride tablet (MT۵) and the market sample, warranting further stability studies for potential upscaling. Conclusion: The study's novelty lies in successfully formulating sustained-release MT۵ using HPMC K۱۰۰M and guar gum via wet granulation, demonstrating a potential reduction in dosing frequency and adverse effects. MT۵'s optimal physical and chemical parameters and sustained drug release exceeded ۹۹% at ۱۲ hours.

Authors

Amlan Bishal

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Biplab DEbnath

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Bikash Gayen

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Bratati Bandyopadhyay

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Surjendu Payra

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Rishav Maji

Department of Pharmaceutical Technology, Bharat Technology, Howrah, India.

Kazi Asraf Ali

Division of Pharmaceutics, Department of Pharmaceutical Technology, Maulana Abul Kalam Azad University of Technology, Kolkata, India.

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