Kinetic study of anti-HIV drugs by thermal decomposition analysis: a multilayer artificial neural network propose
Carregando...
Data
Título da Revista
ISSN da Revista
Título de Volume
Editor
Universidade Federal de Minas Gerais
Descrição
Tipo
Artigo de periódico
Título alternativo
Primeiro orientador
Membros da banca
Resumo
Kinetic study by thermal decomposition of antiretroviral drugs, efavirenz (EFV) and lamivudine (3TC), usually present in the HIV cocktail, can be done by individual adjustment of the solid decomposition models. However, in some cases, unacceptable errors are found using this methodology. To circumvent this problem, here is proposed to use a multilayer perceptron neural network, with an appropriate algorithm, which constitutes a linearization of the network by setting weights between the input layer and the intermediate one and the use of kinetic models as activation functions of neurons in the hidden layer. The interconnection weights between that intermediate layer and output layer determine the contribution of each model in the overall fit of the experimental data. Thus, the decomposition is assumed to be a phenomenon that can occur following different kinetic processes. In investigated data, the kinetic thermal decomposition process was best described by R1 and D4 models for all temperatures to EFV and 3TC, respectively. The residual error of adjustment over the network is on average 10³ times lower for EFV and 10² times lower for 3TC compared to the best individual kinetic model. These improvements in physical adjustment allow detailed study of the process and therefore a more accurate calculation of the kinetic parameters such as the activation energy and frequency factor.
Abstract
Assunto
Farmacocinética, Físico-química, Química analítica, Análise térmica, Calorimetria, Redes neurais (Computação), HIV (Virus), Medicamentos
Palavras-chave
Efavirenz, Lamivudine, Thermal decomposition analysis, Artificial neural network multilayer
Citação
Departamento
Curso
Endereço externo
https://link.springer.com/article/10.1007/s10973-016-5855-2