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一种基于阻抗的方法来确定冻干药品的复溶时间。

An Impedance-Based Method to Determine Reconstitution Time for Freeze-Dried Pharmaceuticals.

作者信息

Werk Tobias, Huwyler Joerg, Hafner Mathias, Luemkemann Joerg, Mahler Hanns-Christian

机构信息

Pharmaceutical Development and Supplies, Pharma Technical Development Biologics EU, F. Hoffmann-La Roche Ltd, Basel, Switzerland.

Department of Pharmaceutical Technologies, University of Basel, Basel, Switzerland.

出版信息

J Pharm Sci. 2015 Sep;104(9):2948-55. doi: 10.1002/jps.24443. Epub 2015 Apr 8.

DOI:10.1002/jps.24443
PMID:25855314
Abstract

The reconstitution of freeze-dried products is usually determined by visual inspection with the naked eye. This can inevitably lead to significant variability in the ability to detect complete reconstitution of the dried solid. It was thus the goal of our study to assess an automated method to monitor reconstitution of a freeze-dried protein drug product in its primary packaging. A newly developed measuring device was used to measure impedance. This was achieved by detecting minor changes in impedance of the reconstitution medium, which occurred because of solid material dissolving during the dissolution process. This measurement system was capable of consistently detecting the dissolution of the last visible residues of freeze-dried lyophilisates. The endpoint of reconstitution was defined at an impedance change of less than 1 Ω for at least 7 s. Finally, we compared reconstitution times determined by the automated impedance method with results obtained by a visual method. In contrast to human operators, the new method delivered both accurate and precise results. Besides detection of the reconstitution endpoint, the impedance method and apparatus can monitor reconstitution endpoints as well as reconstitution kinetics. This standardized method can therefore advantageously be used for the determination of the reconstitution endpoint.

摘要

冻干产品的复溶情况通常通过肉眼目视检查来确定。这不可避免地会导致在检测干燥固体完全复溶的能力方面出现显著差异。因此,我们研究的目标是评估一种自动化方法,以监测处于其原始包装中的冻干蛋白药物产品的复溶情况。使用一种新开发的测量装置来测量阻抗。这是通过检测复溶介质阻抗的微小变化来实现的,这种变化是由于溶解过程中固体物质溶解而发生的。该测量系统能够持续检测冻干冻干物最后可见残留物的溶解情况。复溶终点定义为阻抗变化小于1Ω且持续至少7秒。最后,我们将自动阻抗法确定的复溶时间与目视法获得的结果进行了比较。与人工操作相比,新方法给出了准确且精确的结果。除了检测复溶终点外,阻抗法和仪器还可以监测复溶终点以及复溶动力学。因此,这种标准化方法可有利地用于确定复溶终点。

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Application of Magnetic Resonance to Assess Lyophilized Drug Product Reconstitution.应用磁共振评估冻干药物产品的复溶。
Pharm Res. 2019 Mar 22;36(5):71. doi: 10.1007/s11095-019-2591-x.