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迈向稳定冻干脂质体开发的一步:质量源于设计方法(QbD)。

A step forward towards the development of stable freeze-dried liposomes: a quality by design approach (QbD).

作者信息

Sylvester Bianca, Porfire Alina, Achim Marcela, Rus Lucia, Tomuţă Ioan

机构信息

a Department of Pharmaceutical Technology and Biopharmaceutics , University of Medicine and Pharmacy 'Iuliu Haţieganu' , Cluj-Napoca , Romania.

b Department of Drug Analysis , University of Medicine and Pharmacy 'Iuliu Haţieganu', Cluj-Napoca , Romania.

出版信息

Drug Dev Ind Pharm. 2018 Mar;44(3):385-397. doi: 10.1080/03639045.2017.1395457. Epub 2017 Nov 8.

DOI:10.1080/03639045.2017.1395457
PMID:29098869
Abstract

This study highlights the advantages of using a Quality by Design (QbD) approach in order to gain a more comprehensive understanding of the freeze-drying process of pravastatin-loaded long-circulating liposomes (LCL-PRAV). Within the QbD paradigm, the present study aimed to establish the design space for the optimization of freeze-dried LCL-PRAV by means of Design of Experiment (DOE). The encapsulated solute retention (ESR), the average particle size, and zeta potential after freeze-drying, the residual moisture content, the macroscopic cake appearance, the glass transition temperature (T) of the freeze-dried cake, and the primary drying time were defined as critical quality attributes (CQAs) for the freeze-dried final product. Further on, the influence of lyoprotectant type, freezing rate, shelf temperature during primary drying, and the presence of an annealing step on the CQAs was investigated through a 21-run D-optimal experimental design. Three-dimensional response surfaces were generated to complete the statistical analysis and for a better understanding of the influence of variables and their interactions on the responses. The developed model was then used to build the design space for the freeze-dried liposomes, within which the product quality was assured and the process variability was minimized.

摘要

本研究突出了采用质量源于设计(QbD)方法的优势,以便更全面地了解载有普伐他汀的长循环脂质体(LCL-PRAV)的冻干过程。在QbD范式内,本研究旨在通过实验设计(DOE)建立冻干LCL-PRAV优化的设计空间。冻干后的包封溶质保留率(ESR)、平均粒径、zeta电位、残留水分含量、宏观饼状外观、冻干饼的玻璃化转变温度(T)以及一次干燥时间被定义为冻干最终产品的关键质量属性(CQA)。此外,通过21次运行的D最优实验设计,研究了冻干保护剂类型、冷冻速率、一次干燥期间的搁板温度以及退火步骤的存在对CQA的影响。生成了三维响应面以完成统计分析,并更好地理解变量及其相互作用对响应的影响。然后使用所开发的模型构建冻干脂质体的设计空间,在此空间内产品质量得到保证,且过程变异性最小化。

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