Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods
Entecavir (ETV), a guanosine analogue, can be rapidly phosphorylated to the active intracellular triphosphate form that inhibits replication of the hepatitis B virus (HBV). This work aims to develop useful methods to quantify the content of ETV-A in ETV-H and ETV-A binary mixtures. The integral enth...
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Language: | English |
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Elsevier
2021-10-01
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Series: | Arabian Journal of Chemistry |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1878535221003750 |
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doaj-079e12cdf5c74945950b1c3dc9ce27ab |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mingdi Liu Peng Shi Guangle Wang Gang Wang Ping Song Yumin Liu Songgu Wu Junbo Gong |
spellingShingle |
Mingdi Liu Peng Shi Guangle Wang Gang Wang Ping Song Yumin Liu Songgu Wu Junbo Gong Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods Arabian Journal of Chemistry Entecavir Anhydride impurity Quantification DSC PXRD ATR-FTIR |
author_facet |
Mingdi Liu Peng Shi Guangle Wang Gang Wang Ping Song Yumin Liu Songgu Wu Junbo Gong |
author_sort |
Mingdi Liu |
title |
Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
title_short |
Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
title_full |
Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
title_fullStr |
Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
title_full_unstemmed |
Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
title_sort |
quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methods |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2021-10-01 |
description |
Entecavir (ETV), a guanosine analogue, can be rapidly phosphorylated to the active intracellular triphosphate form that inhibits replication of the hepatitis B virus (HBV). This work aims to develop useful methods to quantify the content of ETV-A in ETV-H and ETV-A binary mixtures. The integral enthalpy value of the phase transformation in the DSC thermogram was selected to quantify the content of ETV-A in binary mixture. Different ranges (full spectrum and partial spectrum) of the PXRD and ATR-FTIR data versus ETV-A content were used to develop partial least squares (PLS) calibration curves with different pre-processing algorithms including multiplicative scatter correction (MSC), standard normal variate (SNV), wavelet transform (WT) or their combinations. The standard curve obtained for the DSC technique is Y = 100.455 + 7.255X, R2 = 0.997, in the ETV-A contents range of 0–100% w/w% in binary mixtures. Limit of detection (LOD) of ETV-A was 0.909% and limit of quantitation (LOQ) is 2.755%. The best correction models for PXRD and ATR-FTIR techniques, in the ETV-A contents range of 0–100% w/w% in binary mixtures, were Y = 0.346 + 0.999X, R2 = 0.999 in the 2θ range of 4-6° with 14-34° and Y = 0.767 + 0.991X, R2 = 0.991 in the range of 3500–2500 cm−1 with 2000–400 cm−1 pretreated by MSC + WT, respectively. Limit of detection (LOD) of ETV-A was 1.394% and limit of quantitation (LOQ) was 4.224% for PXRD technique. LOD and LOQ for ATR-FTIR technique were 9.124% and 27.648%. The results show that DSC, PXRD and ATR-FTIR techniques are precise and accurate, and could be used for the measurement of ETV-A content in the binary mixtures. |
topic |
Entecavir Anhydride impurity Quantification DSC PXRD ATR-FTIR |
url |
http://www.sciencedirect.com/science/article/pii/S1878535221003750 |
work_keys_str_mv |
AT mingdiliu quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT pengshi quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT guanglewang quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT gangwang quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT pingsong quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT yuminliu quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT songguwu quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods AT junbogong quantitativeanalysisofbinarymixturesofentecavirusingsolidstateanalyticaltechniqueswithchemometricmethods |
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spelling |
doaj-079e12cdf5c74945950b1c3dc9ce27ab2021-09-19T04:55:40ZengElsevierArabian Journal of Chemistry1878-53522021-10-011410103360Quantitative analysis of binary mixtures of entecavir using solid-state analytical techniques with chemometric methodsMingdi Liu0Peng Shi1Guangle Wang2Gang Wang3Ping Song4Yumin Liu5Songgu Wu6Junbo Gong7State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; College of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR ChinaState Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR ChinaState Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; College of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR ChinaCollege of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR ChinaCollege of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR ChinaState Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR ChinaState Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; College of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR China; Corresponding author at: School of Chemical Engineering and Technology, Tianjin University, PR China.State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; College of Chemistry and Chemical Engineering, Qinghai Nationalities University, Xining 810007, PR China; Collaborative Innovation Center of Chemistry Science and Engineering, Tianjin 300072, PR ChinaEntecavir (ETV), a guanosine analogue, can be rapidly phosphorylated to the active intracellular triphosphate form that inhibits replication of the hepatitis B virus (HBV). This work aims to develop useful methods to quantify the content of ETV-A in ETV-H and ETV-A binary mixtures. The integral enthalpy value of the phase transformation in the DSC thermogram was selected to quantify the content of ETV-A in binary mixture. Different ranges (full spectrum and partial spectrum) of the PXRD and ATR-FTIR data versus ETV-A content were used to develop partial least squares (PLS) calibration curves with different pre-processing algorithms including multiplicative scatter correction (MSC), standard normal variate (SNV), wavelet transform (WT) or their combinations. The standard curve obtained for the DSC technique is Y = 100.455 + 7.255X, R2 = 0.997, in the ETV-A contents range of 0–100% w/w% in binary mixtures. Limit of detection (LOD) of ETV-A was 0.909% and limit of quantitation (LOQ) is 2.755%. The best correction models for PXRD and ATR-FTIR techniques, in the ETV-A contents range of 0–100% w/w% in binary mixtures, were Y = 0.346 + 0.999X, R2 = 0.999 in the 2θ range of 4-6° with 14-34° and Y = 0.767 + 0.991X, R2 = 0.991 in the range of 3500–2500 cm−1 with 2000–400 cm−1 pretreated by MSC + WT, respectively. Limit of detection (LOD) of ETV-A was 1.394% and limit of quantitation (LOQ) was 4.224% for PXRD technique. LOD and LOQ for ATR-FTIR technique were 9.124% and 27.648%. The results show that DSC, PXRD and ATR-FTIR techniques are precise and accurate, and could be used for the measurement of ETV-A content in the binary mixtures.http://www.sciencedirect.com/science/article/pii/S1878535221003750EntecavirAnhydride impurityQuantificationDSCPXRDATR-FTIR |