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药用级和不同批次黄原胶的生产厂家间和生产厂家内变异性。

Inter- and intra-manufacturer variability in pharmaceutical grades and lots of xanthan gum.

机构信息

Graduate School of Pharmaceutical Sciences, Duquesne University, 600 Forbes Avenue, Pittsburgh, Pennsylvania 15282, USA.

出版信息

AAPS PharmSciTech. 2010 Dec;11(4):1619-26. doi: 10.1208/s12249-010-9536-3. Epub 2010 Nov 18.

Abstract

A pharmaceutical formulation typically contains one or more excipients in addition to the active pharmaceutical ingredient(s). Though excipients have been considered inert components of a formulation, variability in their properties has been shown to affect the performance of drug dosage forms and delivery systems. This study investigates the inter- and intra-manufacturer variability among different NF grades and lots of xanthan gum made by two manufacturers. As many formulators rely on compendial standards to monitor and control the variability of excipients, this study focuses on the adequacy of the NF specifications, in particular the viscosity specification, to discern the variability in solution properties of different pharmaceutical grades and lots of xanthan gum. All the grades and lots in this study were NF grade materials. Xanthan gum solutions were prepared in accordance with NF test methodology and were rheologically evaluated using a rotational rheometer. Both steady shear measurements and small amplitude oscillatory measurements were carried out on 1% w/w xanthan gum solutions. Results showed significant inter- and intra-manufacturer variability among the NF grades and lots of xanthan gum that was not reflected in the NF viscosity test specifications.

摘要

药物制剂通常除了活性药物成分(s)之外还包含一种或多种赋形剂。尽管赋形剂被认为是制剂的惰性成分,但它们的性质变化已被证明会影响药物剂型和给药系统的性能。本研究调查了由两家制造商生产的不同 NF 等级和批次的黄原胶之间的制造商内和制造商间的可变性。由于许多制剂师依赖药典标准来监测和控制赋形剂的可变性,因此本研究侧重于 NF 规格的充分性,特别是粘度规格,以辨别不同制药等级和批次的黄原胶在溶液性质上的可变性。本研究中的所有等级和批次均为 NF 等级材料。黄原胶溶液按照 NF 测试方法制备,并使用旋转流变仪进行流变评估。在 1%w/w 的黄原胶溶液上进行了稳态剪切测量和小振幅振荡测量。结果表明,NF 等级和批次的黄原胶之间存在显著的制造商内和制造商间的可变性,而这在 NF 粘度测试规格中并未反映出来。

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