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1.
J Biopharm Stat ; 30(4): 721-733, 2020 07 03.
Artigo em Inglês | MEDLINE | ID: mdl-32163316

RESUMO

Potency determination via bioassay is a relative measure that requires an evaluation of parallelism between the dose-response relationships of a reference standard and a sample material. Typical approaches for assessing parallelism include difference ([Formula: see text]-value) and equivalence tests. These traditional methods rely on a statistical assessment of model parameters as opposed to direct evaluation of the similarity of the dose-response curves. We propose a simple curve similarity approach that tests the hypothesis that the sample material is a dilution or concentration of the reference standard. The test is achieved by quantifying and normalizing the total area between the two curves and provides a single composite measure of parallelism. Both a frequentist and a Bayesian approach to the test are provided. We show through a simulation study that the curve similarity approach overcomes the drawbacks of the traditional methods and is effective at detecting parallelism and non-parallelism for bioassays.


Assuntos
Bioensaio/estatística & dados numéricos , Projetos de Pesquisa/estatística & dados numéricos , Animais , Teorema de Bayes , Simulação por Computador , Interpretação Estatística de Dados , Relação Dose-Resposta a Droga , Humanos , Modelos Estatísticos , Método de Monte Carlo , Equivalência Terapêutica
2.
J Pharm Sci ; 103(8): 2278-86, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-24974956

RESUMO

Defining a suitable product presentation with an acceptable stability profile over its intended shelf-life is one of the principal challenges in bioproduct development. Accelerated stability studies are routinely used as a tool to better understand long-term stability. Data analysis often employs an overall mass action kinetics description for the degradation and the Arrhenius relationship to capture the temperature dependence of the observed rate constant. To improve predictive accuracy and precision, the current work proposes a least-squares estimation approach with a single nonlinear covariate and uses a polynomial to describe the change in a product attribute with respect to time. The approach, which will be referred to as Arrhenius time-scaled (ATS) least squares, enables accurate, precise predictions to be achieved for degradation profiles commonly encountered during bioproduct development. A Monte Carlo study is conducted to compare the proposed approach with the common method of least-squares estimation on the logarithmic form of the Arrhenius equation and nonlinear estimation of a first-order model. The ATS least squares method accommodates a range of degradation profiles, provides a simple and intuitive approach for data presentation, and can be implemented with ease.


Assuntos
Agregados Proteicos , Estabilidade Proteica , Simulação por Computador , Estabilidade de Medicamentos , Armazenamento de Medicamentos , Cinética , Análise dos Mínimos Quadrados , Modelos Químicos , Método de Monte Carlo , Temperatura
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