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用于监管政策考量的酒石酸美托洛尔缓释骨架片制剂的研发

Development of metoprolol tartrate extended-release matrix tablet formulations for regulatory policy consideration.

作者信息

Nellore R V, Rekhi G S, Hussain A S, Tillman L G, Augsburger L L

机构信息

Department of Pharmaceutical Sciences, University of Maryland, School of Pharmacy, Baltimore 21201-1180, USA.

出版信息

J Control Release. 1998 Jan 2;50(1-3):247-56. doi: 10.1016/s0168-3659(97)00141-7.

DOI:10.1016/s0168-3659(97)00141-7
PMID:9685891
Abstract

This research study was designed to develop model extended-release (ER) matrix tablet formulations for metoprolol tartrate (100 mg) sufficiently sensitive to manufacturing variable and to serve as the scientific basis for regulatory policy development on scale-up and post approval changes for modified-release dosage forms (SUPAC-MR). Several grades and levels of hydroxypropyl methylcellulose (Methocel K4M, K15M, K100M and K100LV), fillers and binders and studied. Three granulation processes were evaluated; direct compression, fluid-bed or high-shear granulation. Lubrication was performed in a V-blender and tablets were compressed on an instrumented rotary tablet press. Direct compression formulations exhibited poor flow, picking and sticking problems during tableting. High-shear granulation resulted in the formation of hard granules that were difficult to mill but yielded good tablets. Fluid-bed granulations were made using various binders and appeared to be satisfactory in terms of flow and tableting performance. In vitro drug release testing was performed in pH 6.8 phosphate buffer using USP apparatus 2 (paddle) at 50 rpm. At a fixed polymer level, drug release from the higher viscosity grades (K100M) was slower as compared to the lower viscosity grades (K100LV). In addition, release from K100LV was found to be more sensitive to polymer level changes. Increased in polymer level from 10 to 40% and/or filler change from lactose to dicalcium phosphate resulted in about 25-30% decrease in the amount of metoprolol release after 12 h. The results of this study led to the choice of Methocel K100LV as the hydrophilic matrix polymer and fluid-bed granulation as the process of choice for further evaluation of critical and non-critical formulation and processing variables.

摘要

本研究旨在开发对制造变量足够敏感的酒石酸美托洛尔(100毫克)的模型缓释(ER)骨架片制剂,并作为制定缓释剂型放大生产和批准后变更(SUPAC-MR)监管政策的科学依据。研究了几种不同等级和水平的羟丙基甲基纤维素(Methocel K4M、K15M、K100M和K100LV)、填充剂和粘合剂。评估了三种制粒工艺;直接压片、流化床制粒或高剪切制粒。在V型混合器中进行润滑,并在装有仪器的旋转压片机上压片。直接压片制剂在压片过程中表现出流动性差、裂片和黏冲问题。高剪切制粒导致形成难以研磨的硬颗粒,但能得到良好的片剂。流化床制粒使用了各种粘合剂,在流动性和压片性能方面似乎令人满意。在pH 6.8磷酸盐缓冲液中使用美国药典装置2(桨板)以50转/分钟的速度进行体外药物释放测试。在聚合物水平固定的情况下,与较低粘度等级(K100LV)相比,较高粘度等级(K100M)的药物释放较慢。此外,发现K100LV的释放对聚合物水平变化更敏感。聚合物水平从10%增加到40%和/或填充剂从乳糖改为磷酸氢钙导致12小时后酒石酸美托洛尔释放量减少约25-30%。本研究结果导致选择Methocel K100LV作为亲水性骨架聚合物,并选择流化床制粒作为进一步评估关键和非关键制剂及工艺变量的首选工艺。

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