Determination of Acid Dissociation Constant of Pravastatin under Degraded Conditions by Capillary Zone Electrophoresis
The acid dissociation constant of pravastatin was determined under degraded conditions. Pravastatin was degraded in an acidic solution (pH = 2.0) for 5 h, and the degradation solution was subjected to the measurement of the effective electrophoretic mobility by capillary zone electrophoresis. Althou...
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Published in | Analytical Sciences Vol. 31; no. 11; pp. 1193 - 1196 |
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Main Authors | , , , |
Format | Journal Article |
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The Japan Society for Analytical Chemistry
2015
Springer Nature Singapore Nature Publishing Group |
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Abstract | The acid dissociation constant of pravastatin was determined under degraded conditions. Pravastatin was degraded in an acidic solution (pH = 2.0) for 5 h, and the degradation solution was subjected to the measurement of the effective electrophoretic mobility by capillary zone electrophoresis. Although the amount of pravastatin decreased by the acid degradation, its acid dissociation constant was successfully determined with the residual pravastatin through its effective electrophoretic mobility. The determined acid dissociation constant value agreed well with the one obtained with freshly prepared solution and with some reported values. |
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AbstractList | The acid dissociation constant of pravastatin was determined under degraded conditions. Pravastatin was degraded in an acidic solution (pH = 2.0) for 5 h, and the degradation solution was subjected to the measurement of the effective electrophoretic mobility by capillary zone electrophoresis. Although the amount of pravastatin decreased by the acid degradation, its acid dissociation constant was successfully determined with the residual pravastatin through its effective electrophoretic mobility. The determined acid dissociation constant value agreed well with the one obtained with freshly prepared solution and with some reported values. The acid dissociation constant of pravastatin was determined under degraded conditions. Pravastatin was degraded in an acidic solution (pH = 2.0) for 5 h, and the degradation solution was subjected to the measurement of the effective electrophoretic mobility by capillary zone electrophoresis. Although the amount of pravastatin decreased by the acid degradation, its acid dissociation constant was successfully determined with the residual pravastatin through its effective electrophoretic mobility. The determined acid dissociation constant value agreed well with the one obtained with freshly prepared solution and with some reported values.The acid dissociation constant of pravastatin was determined under degraded conditions. Pravastatin was degraded in an acidic solution (pH = 2.0) for 5 h, and the degradation solution was subjected to the measurement of the effective electrophoretic mobility by capillary zone electrophoresis. Although the amount of pravastatin decreased by the acid degradation, its acid dissociation constant was successfully determined with the residual pravastatin through its effective electrophoretic mobility. The determined acid dissociation constant value agreed well with the one obtained with freshly prepared solution and with some reported values. |
Author | SHIMAKAMI, Natsumi TAKAYANAGI, Toshio AMIYA, Mika YABUTANI, Tomoki |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26561266$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1246/cl.2001.14 10.1111/j.1440-1746.1996.tb01706.x 10.1016/S0731-7085(00)00372-1 10.1002/jps.10087 10.2116/bunsekikagaku.64.105 10.1016/S0731-7085(03)00238-3 10.1002/jps.2600800905 10.1021/ac00017a029 10.2116/bunsekikagaku.63.643 |
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References_xml | – reference: 1. D. Mulvana, M. Jemal, and S. C. Pulver, J. Pharm. Biomed. Anal., 2000, 23, 851. – reference: 8. N. Shimakami, T. Yabutani, and T. Takayanagi, Bunseki Kagaku, 2014, 63, 643. – reference: 11. Y. Adachi, Y. Okuyama, H. Miya, H. Matsusita, M. Kitano, T. Kamisako, and T. Yamamoto, J. Gastroen. Hepatol., 1996, 11, 580. – reference: 5. T. Takayanagi, Bunseki Kagaku, 2015, 64, 105. – reference: 6. T. Takayanagi and S. Motomizu, Chem. Lett., 2001, 14. – reference: 4. M. G. Khaledi, S. C. Smith, and J. K. Strasters, Anal. Chem., 1991, 63, 1820. – reference: 2. B. Nigovic and I. Vegar, Croat. Chem. Acta, 2008, 81, 615. – reference: 10. A. T. M. Serajuddin, S. A. Ranadive, and E. M. Mahoney, J. Pharm. Sci., 1991, 80, 830. – reference: 9. The R Project for Statistical Computing, http://www.r-project.org/. – reference: 3. Y. Ishihama, M. Nakamura, T. Miwa, T. Kajima, and N. Asakawa, J. Pharm. Sci., 2002, 91, 933. – reference: 7. E. Örnskov, A. Linusson, and S. Folestad, J. Pharm. Biomed. Anal., 2003, 33, 379. – reference: ÖrnskovELinussonAFolestadSJ. Pharm. Biomed. Anal20033337910.1016/S0731-7085(03)00238-314550857 – reference: T. Takayanagi and S. Motomizu, Chem. Lett., 2001, 14. – reference: NigovićBVegarICroat. Chem. Acta200881615 – reference: KhalediM GSmithS CStrastersJ KAnal. Chem19916318201:CAS:528:DyaK3MXltVSitr0%3D10.1021/ac00017a0291789443 – reference: The R Project for Statistical Computing, http://www.r-project.org/. – reference: AdachiYOkuyamaYMiyaHMatsusitaHKitanoMKamisakoTYamamotoTJ. Gastroen. Hepatol1996115801:STN:280:DyaK28zosVChtA%3D%3D10.1111/j.1440-1746.1996.tb01706.x – reference: IshihamaYNakamuraMMiwaTKajimaTAsakawaNJ. Pharm. Sci2002919331:CAS:528:DC%2BD38XjtFKhtbg%3D10.1002/jps.1008711948531 – reference: MulvanaDJemalMPulverS CJ. Pharm. Biomed. Anal2000238511:CAS:528:DC%2BD3cXmtlGqu7Y%3D10.1016/S0731-7085(00)00372-111022911 – reference: SerajuddinA T MRanadiveS AMahoneyE MJ. Pharm. Sci1991808301:CAS:528:DyaK3MXms12qur8%3D10.1002/jps.26008009051800703 – reference: ShimakamiNYabutaniTTakayanagiTBunseki Kagaku2014636431:CAS:528:DC%2BC2cXhsVyrurvK10.2116/bunsekikagaku.63.643 – reference: TakayanagiTBunseki Kagaku2015641051:CAS:528:DC%2BC2MXktVGltr8%3D10.2116/bunsekikagaku.64.105 – ident: 31110015_CR6 doi: 10.1246/cl.2001.14 – volume: 11 start-page: 580 year: 1996 ident: 31110015_CR11 publication-title: J. Gastroen. Hepatol doi: 10.1111/j.1440-1746.1996.tb01706.x – volume: 23 start-page: 851 year: 2000 ident: 31110015_CR1 publication-title: J. Pharm. Biomed. Anal doi: 10.1016/S0731-7085(00)00372-1 – volume: 81 start-page: 615 year: 2008 ident: 31110015_CR2 publication-title: Croat. Chem. Acta – volume: 91 start-page: 933 year: 2002 ident: 31110015_CR3 publication-title: J. Pharm. Sci doi: 10.1002/jps.10087 – volume: 64 start-page: 105 year: 2015 ident: 31110015_CR5 publication-title: Bunseki Kagaku doi: 10.2116/bunsekikagaku.64.105 – volume: 33 start-page: 379 year: 2003 ident: 31110015_CR7 publication-title: J. Pharm. Biomed. Anal doi: 10.1016/S0731-7085(03)00238-3 – ident: 31110015_CR9 – volume: 80 start-page: 830 year: 1991 ident: 31110015_CR10 publication-title: J. Pharm. Sci doi: 10.1002/jps.2600800905 – volume: 63 start-page: 1820 year: 1991 ident: 31110015_CR4 publication-title: Anal. Chem doi: 10.1021/ac00017a029 – volume: 63 start-page: 643 year: 2014 ident: 31110015_CR8 publication-title: Bunseki Kagaku doi: 10.2116/bunsekikagaku.63.643 |
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SubjectTerms | acid degradation acid dissociation constant Analytical Chemistry Capillarity Capillary zone capillary zone electrophoresis Chemistry Constants Degradation Electrophoresis Electrophoresis, Capillary - methods Hydrogen-Ion Concentration Mathematical analysis micellar electrokinetic chromatography Pravastatin Pravastatin - chemistry Time Factors |
Title | Determination of Acid Dissociation Constant of Pravastatin under Degraded Conditions by Capillary Zone Electrophoresis |
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