کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1229109 | 1495231 | 2015 | 9 صفحه PDF | دانلود رایگان |
• Determination of celecoxib in human serum using combination of PCA and ANN.
• Extraction and determination of celecoxib in human serum without any pretreatment.
• Good correlation between obtained results by PCA-ANN and HPLC.
This study describes a simple and rapid approach of monitoring celecoxib (CLX). Unfolded principal component analysis–radial basis function neural network (UPCA–RBFNN) and excitation–emission spectra were combined to develop new model in the determination of CLX in human serum samples. Fluorescence landscapes with excitation wavelengths from 250 to 310 nm and emission wavelengths in the range 280–450 nm were obtained. The figures of merit for the developed model were evaluated. High performance liquid chromatography (HPLC) technique was also used as a standard method. Accuracy of the method was investigated by analysis of the serum samples spiked with various concentration of CLX and a recovery of 103.63% was obtained. The results indicated that the proposed method is an interesting alternative to the traditional techniques normally used for determining CLX such as HPLC.
Unfolded principal component analysis–radial basis function neural network and excitation–emission spectra were combined to develop new model in the determination of celecoxib in human serum samples.Figure optionsDownload as PowerPoint slide
Journal: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy - Volume 138, 5 March 2015, Pages 675–683