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含琥珀酸美托洛尔缓释片和苯磺酸氨氯地平速释片的薄膜包衣双层片的可扩展工艺开发。

Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate.

作者信息

Tuyen Nguyen Thi Linh, Nghiem Le Quan, Tuan Nguyen Duc, Le Phuoc Huu

机构信息

Faculty of Pharmacy, Can Tho University of Medicine and Pharmacy, 179 Nguyen Van Cu, Can Tho City 94000, Vietnam.

Faculty of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, 41 Dinh Tien Hoang Street, District 1, Ho Chi Minh City 760000, Vietnam.

出版信息

Pharmaceutics. 2021 Oct 27;13(11):1797. doi: 10.3390/pharmaceutics13111797.

Abstract

The development of new drugs that combine active ingredients for the treatment hypertension is critically essential owing to its offering advantages for both patients and manufacturers. In this study, for the first time, detailed development of a scalable process of film-coated bi-layer tablets containing sustained-release metoprolol succinate and immediate-release amlodipine besylate in a batch size of 10,000 tablets is reported. The processing parameters of the manufacturing process during dry mixing-, drying-, dry mixing- completion stages were systematically investigated, and the evaluation of the film-coated bi-layer tablet properties was well established. The optimal preparation conditions for metoprolol succinate layer were 6 min- dry mixing with a high-speed mixer (120 rpm and 1400 rpm), 30-min drying with a fluid bed dryer, and 5-min- mixing completion at 25 rpm. For the preparation of amlodipine besylate layer, the optimal dry-mixing time using a cube mixer (25 rpm) was found to be 5 min. The average weight of metoprolol succinate layers and bi-layer tablets were controlled at 240-260 mg and 384-416 mg, respectively. Shewhart R chart and X¯ charts of all three sampling lots were satisfactory, confirming that the present scalable process was stable and successful. This study confirms that the manufacturing process is reproducible, robust; and it yields a consistent product that meets specifications.

摘要

开发将活性成分结合用于治疗高血压的新药至关重要,因为这对患者和制造商都有好处。在本研究中,首次报告了批量为10000片的含琥珀酸美托洛尔缓释片和苯磺酸氨氯地平速释片的薄膜包衣双层片可扩展工艺的详细开发情况。系统研究了干混、干燥、干混完成阶段制造过程的工艺参数,并建立了薄膜包衣双层片性能的评估方法。琥珀酸美托洛尔层的最佳制备条件为:用高速混合器(120转/分和1400转/分)干混6分钟,用流化床干燥器干燥30分钟,以25转/分完成混合5分钟。对于苯磺酸氨氯地平层的制备,发现使用立方混合器(25转/分)的最佳干混时间为5分钟。琥珀酸美托洛尔层和双层片的平均重量分别控制在240 - 260毫克和384 - 416毫克。所有三个抽样批次的休哈特R图和X¯图均令人满意,证实了目前的可扩展工艺稳定且成功。本研究证实该制造工艺具有可重复性、稳健性;并且能生产出符合规格的一致产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17c6/8618854/a7d68be2baad/pharmaceutics-13-01797-g001.jpg

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