DOE在ELISA稳健性和耐用性评价中的应用。

IF 5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Thy Follmer, Seth Clark, Thorsten Verch
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引用次数: 0

摘要

复杂的测定,如免疫测定,可能受到健壮性和坚固性因素的影响。通过对关键因素进行系统的绩效评估,然后采取控制策略,可以减少相关风险。然而,大量的因素及其相互作用可以代表一个实验挑战。实验统计设计(DOE)除了评估潜在的因素相互作用外,还可以用更少的总分析次数有效地评估更多的因素。我们将do应用于疫苗效价ELISA的稳健性评估。测试因素的选择是基于对发展数据、科学经验和通常预期的变异性来源的审查和排序。与实验室限制的16-20趟比较不同的设计方案,根据总趟数、因素混杂程度和潜在投影特性,选择了16趟Resolution III设计。首先对DOE数据进行可视化分析,绘制参考曲线对DOE运行的浓度响应,然后建立最大荧光曲线信号和WRMSE拟合值的详细统计模型。通过从模型中消除没有影响的因素,以及在应用统计和科学专业知识后根据影响的可能性去除因素或相互作用,减少了因素及其相互作用之间的初始混淆。尽管最初存在混淆,但设计允许在15个因素中通过涂层浓度和时间的相互作用识别板制造商的影响,只有16次运行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of DOE to ELISA Robustness and Ruggedness Assessment.

Complex assays such as immunoassays can be affected by robustness and ruggedness factors. Associated risks can be reduced by a systematic performance assessment across key factors followed by control strategies. However, the large number of factors and their interactions can represent an experimental challenge. Statistical Design of Experiments (DOE) allows efficient evaluation of more factors with fewer total assay runs in addition to assessing potential factor interactions. We applied DOEs to the robustness evaluation of a vaccine potency ELISA. Test factors were selected based on a review and ranking of development data, scientific experience, and commonly expected sources of variability. Comparing different design options with 16-20 runs which was a laboratory limit, a 16-run Resolution III design was selected based on the total number of runs, the degree of factor confounding, and the potential projection properties. DOE data were first visually analyzed by plotting the concentration-responses of reference curves against DOE Runs followed by detailed statistical models of the maximum fluorescent curve signal and the WRMSE fit values. Initial confounding between factors and their interactions was reduced by eliminating factors with no impact from the models and by removing factors or interactions based on their likelihood of an impact after applying statistical and scientific expertise. Despite initial confounding, the designs allowed discerning an impact of plate manufacturer with interaction of coating concentration and time out of 15 factors with only 16 runs.

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来源期刊
AAPS Journal
AAPS Journal 医学-药学
CiteScore
7.80
自引率
4.40%
发文量
109
审稿时长
1 months
期刊介绍: The AAPS Journal, an official journal of the American Association of Pharmaceutical Scientists (AAPS), publishes novel and significant findings in the various areas of pharmaceutical sciences impacting human and veterinary therapeutics, including: · Drug Design and Discovery · Pharmaceutical Biotechnology · Biopharmaceutics, Formulation, and Drug Delivery · Metabolism and Transport · Pharmacokinetics, Pharmacodynamics, and Pharmacometrics · Translational Research · Clinical Evaluations and Therapeutic Outcomes · Regulatory Science We invite submissions under the following article types: · Original Research Articles · Reviews and Mini-reviews · White Papers, Commentaries, and Editorials · Meeting Reports · Brief/Technical Reports and Rapid Communications · Regulatory Notes · Tutorials · Protocols in the Pharmaceutical Sciences In addition, The AAPS Journal publishes themes, organized by guest editors, which are focused on particular areas of current interest to our field.
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