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实验室与生产冻干周期的相关性

Correlation of laboratory and production freeze drying cycles.

作者信息

Kuu Wei Y, Hardwick Lisa M, Akers Michael J

机构信息

BioPharma Solutions, Baxter Healthcare Corporation, Round Lake, IL 60073, USA.

出版信息

Int J Pharm. 2005 Sep 30;302(1-2):56-67. doi: 10.1016/j.ijpharm.2005.06.022.

Abstract

The purpose of this study was to develop the correlation of cycle parameters between a laboratory and a production freeze-dryer. With the established correlation, key cycle parameters obtained using a laboratory dryer may be converted to those for a production dryer with minimal experimental efforts. In order to develop the correlation, it was important to consider the contributions from the following freeze-drying components: (1) the dryer, (2) the vial, and (3) the formulation. The critical parameters for the dryer are the shelf heat transfer coefficient and shelf surface radiation emissivity. The critical parameters for the vial are the vial bottom heat transfer coefficients (the contact parameter Kcs and separation distance lv), and vial top heat transfer coefficient. The critical parameter of the formulation is the dry layer mass transfer coefficient. The above heat and mass transfer coefficients were determined by freeze-drying experiments in conjunction with mathematical modeling. With the obtained heat and mass transfer coefficients, the maximum product temperature, Tbmax, during primary drying was simulated using a primary drying subroutine as a function of the shelf temperature and chamber pressure. The required shelf temperature and chamber pressure, in order to perform a successful cycle run without product collapse, were then simulated based on the resulting values of Tbmax. The established correlation approach was demonstrated by the primary drying of the model formulation 5% mannitol solution. The cycle runs were performed using a LyoStar dryer as the laboratory dryer and a BOC Edwards dryer as the production dryer. The determined normalized dried layer mass transfer resistance for 5% mannitol is expressed as RpN=0.7313+17.19l, where l is the receding dry layer thickness. After demonstrating the correlation approach using the model formulation 5% mannitol, a practical comparison study was performed for the actual product, the lactate dehydrogenase (LDH) formulation. The determined normalized dried layer mass transfer resistance for the LDH formulation is expressed as RpN=4.344+10.85l. The operational templates Tbmax and primary drying time were also generated by simulation. The cycle run for the LDH formulation using the Edwards production dryer verified that the cycle developed in a laboratory freeze-dryer was transferable at the production scale.

摘要

本研究的目的是建立实验室冻干机和生产型冻干机循环参数之间的相关性。利用已建立的相关性,通过最少的实验工作,就可以将使用实验室冻干机获得的关键循环参数转换为生产型冻干机的参数。为了建立这种相关性,考虑以下冻干组件的贡献很重要:(1)冻干机,(2)小瓶,以及(3)制剂。冻干机的关键参数是搁板传热系数和搁板表面辐射发射率。小瓶的关键参数是小瓶底部传热系数(接触参数Kcs和分离距离lv)以及小瓶顶部传热系数。制剂的关键参数是干燥层传质系数。上述传热和传质系数通过冻干实验结合数学建模来确定。利用获得的传热和传质系数,使用一次干燥子程序模拟了一次干燥过程中产品的最高温度Tbmax,它是搁板温度和腔室压力的函数。然后根据Tbmax的结果值模拟出为成功完成循环运行且产品不塌陷所需的搁板温度和腔室压力。通过对模型制剂5%甘露醇溶液的一次干燥,证明了所建立的相关性方法。使用LyoStar冻干机作为实验室冻干机,BOC Edwards冻干机作为生产型冻干机进行循环运行。5%甘露醇的归一化干燥层传质阻力表示为RpN = 0.7313 + 17.19l,其中l是后退干燥层厚度。在使用模型制剂5%甘露醇证明了相关性方法后,对实际产品乳酸脱氢酶(LDH)制剂进行了实际对比研究。LDH制剂的归一化干燥层传质阻力表示为RpN = 4.344 + 10.85l。还通过模拟生成了操作模板Tbmax和一次干燥时间。使用Edwards生产型冻干机对LDH制剂进行的循环运行验证了在实验室冻干机中开发的循环可以在生产规模上进行转换。

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