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评估粉末流动性,确定片剂生产中理想的润滑剂混合时间。

Setting Ideal Lubricant Mixing Time for Manufacturing Tablets by Evaluating Powder Flowability.

机构信息

Department of Pharmaceutical Technology, School of Clinical Pharmacy, College of Pharmaceutical Sciences, Matsuyama University, 4-2 Bunkyo-cho, Matsuyama, Ehime, 790-8578, Japan.

出版信息

AAPS PharmSciTech. 2017 Oct;18(7):2832-2840. doi: 10.1208/s12249-017-0765-6. Epub 2017 Mar 29.

Abstract

We investigated the effectiveness of using Carr's flowability index (FI) and practical angle of internal friction (Φ) as indexes for setting the target Mg-St mixing time needed for preparing tablets with the target physical properties. We used FI as a measure of flowability under non-loaded conditions, and Φ as a measure of flowability under loaded conditions for pharmaceutical powders undergoing direct compression with varying concentrations of Mg-St and mixing times. We evaluated the relationship between Mg-St mixing conditions and pharmaceutical powder flowability, analyzed the correlation between the physical properties of the tablets (i.e., tablet weight variation, drug content uniformity, hardness, friability, and disintegration time of tablets prepared using the pharmaceutical powder), and studied the effect of Mg-St mixing conditions and pharmaceutical powder flowability on tablet properties. Mg-St mixing time highly correlated with pharmaceutical powder FI (R  = 0.883) while Mg-St concentration has low correlation with FI, and FI highly correlated with the physical properties of the tablet (R values: weight variation 0.509, drug content variation 0.314, hardness 0.525, friability 0.477, and disintegration time 0.346). Therefore, using pharmaceutical powder FI as an index could enable prediction of the physical properties of a tablet without the need for tableting, and setting the Mg-St mixing time by using pharmaceutical powder FI could enable preparation of tablets with the target physical properties. Thus, the FI of the intermediate product (i.e., pharmaceutical powder) is an effective index for controlling the physical properties of the finished tablet.

摘要

我们研究了使用 Carr 流度指数(FI)和实际内摩擦角(Φ)作为指标来设定目标 Mg-St 混合时间的有效性,以制备具有目标物理性质的片剂。我们使用 FI 作为非加载条件下流动性的衡量指标,使用 Φ 作为在直接压片过程中不同浓度的 Mg-St 和混合时间下的药用粉末在加载条件下的流动性的衡量指标。我们评估了 Mg-St 混合条件和药用粉末流动性之间的关系,分析了片剂物理性质(即片剂重量变化、药物含量均匀性、硬度、脆性和片剂崩解时间)之间的相关性,并研究了 Mg-St 混合条件和药用粉末流动性对片剂性质的影响。Mg-St 混合时间与药用粉末 FI 高度相关(R  = 0.883),而 Mg-St 浓度与 FI 相关性较低,FI 与片剂的物理性质高度相关(R 值:重量变化 0.509、药物含量变化 0.314、硬度 0.525、脆性 0.477 和崩解时间 0.346)。因此,使用药用粉末 FI 作为指标可以在不需要压片的情况下预测片剂的物理性质,并且通过使用药用粉末 FI 设定 Mg-St 混合时间可以制备具有目标物理性质的片剂。因此,中间产物(即药用粉末)的 FI 是控制成品片剂物理性质的有效指标。

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