开发用于评估药品冷冻干燥异质性的单瓶质量流量监测器

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Tiffany Yu, Richard Marx, Michael Hinds, Nicholas Schott, Emily Gong, Seongkyu Yoon, William Kessler
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引用次数: 0

摘要

在药物冻干过程中,药瓶间的干燥异质性仍然是一个重大障碍。由于冷冻干燥机中的药瓶位置不同,传热和传质也不同,因此边缘药瓶的冷冻方式不同,温度通常较高,干燥速度也比中心药瓶快。冷冻干燥机内这种与药瓶位置有关的异质性导致工艺开发过程中的取舍。在初级干燥过程中,工艺开发人员必须注意避免货架温度过高导致边缘小瓶过热,从而使产品升华界面温度高于临界(塌陷)温度。然而,在较低的货架温度下,中心瓶需要更长的时间才能完成初级干燥,从而有可能因干燥不完全而导致塌陷或回熔。这两种情况都可能导致产品质量不佳,影响药物稳定性、活性和复溶时间。我们提出了一种基于可调谐二极管激光吸收光谱(TDLAS)的监测药瓶特定位置水蒸气质量流量的新方法。单瓶监测器可测量升华冰的气体流速、水蒸气温度和气体浓度,从而计算出质量流量,结合传热和传质模型,可确定小瓶传热系数和产品抗干燥性。这些参数反过来又可用于稳健、快速的工艺开发和控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Single Vial Mass Flow Rate Monitor to Assess Pharmaceutical Freeze Drying Heterogeneity

During pharmaceutical lyophilization processes, inter-vial drying heterogeneity remains a significant obstacle. Due to differences in heat and mass transfer based on vial position within the freeze drier, edge vials freeze differently, are typically warmer and dry faster than center vials. This vial position-dependent heterogeneity within the freeze dryer leads to tradeoffs during process development. During primary drying, process developers must be careful to avoid shelf temperatures that would result in overheating of edge vials causing the product sublimation interface temperature to rise above the critical (collapse) temperature. However, at lower shelf temperatures, center vials require longer to complete primary drying, risking collapse or melt-back due to incomplete drying. Both situations may result in poor product quality affecting drug stability, activity, and reconstitution times. We present a new approach for monitoring vial location-specific water vapor mass flow based on Tunable Diode Laser Absorption Spectroscopy (TDLAS). The single vial monitor enables measurement of the gas flow velocity, water vapor temperature, and gas concentration from the sublimating ice, enabling the calculation of the mass flow rate which can be used in combination with a heat and mass transfer model to determine vial heat transfer coefficients and product resistance to drying. These parameters can in turn be used for robust and rapid process development and control.

Graphical Abstract

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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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