An intelligent method based on feed-forward artificial neural network and least square support vector machine for the simultaneous spectrophotometric estimation of anti hepatitis C virus drugs in pharmaceutical formulation and biological fluid

This study proposed simple and reliable spectrophotometry method for simultaneous analysis of hepatitis C antiviral binary mixture containing sofosbuvir (SOF) and daclatasvir (DAC). This technique is based on the use of feed-forward artificial neural network (FF-ANN) and least square support vector machine (LS-SVM). FF-NN with Levenberg-Marquardt (LM) and Cartesian genetic programming (CGP) algorithms was trained to determine the best number of hidden layers and the number of neurons. This comparison demonstrated that the LM algorithm had the minimum mean square error (MSE) for SOF (1.59 x 10(-28)) and DAC (4.71 x 10(-28)). In LS-SVM model, the optimum regularization parameter (gamma) and width of the function (sigma) were achieved with root mean square error (RMSE) of 0.9355 and 0.2641 for SOF and DAC, respectively. The coefficient of determination (R-2) value of mixtures containing SOF and DAC was 0.996 and 0.997, respectively. The percentage recovery values were in the range of 94.03-104.58 and 94.04-106.41 for SOF and DAC, respectively. Statistical test (ANOVA) was implemented to compare high-performance liquid chromatography (HPLC) and spectrophotometry, which showed no significant difference. These results indicate that the proposed method possesses great potential ability for prediction of concentration of components in pharmaceutical formulations. (C) 2021 Elsevier B.V. All rights reserved.

Automated summary

This study proposed a spectrophotometry method for simultaneous analysis of a binary mixture of hepatitis C antivirals containing sofosbuvir and daclatasvir. The method combines feed-forward artificial neural network and least square support vector machine algorithms, showing great potential in predicting component concentrations in pharmaceutical formulations. The proposed method was compared with high-performance liquid chromatography, with no significant difference observed.