Equilibrium Analyses in Aqueous Solution under Accompanying Side Reactions by Capillary Zone Electrophoresis
Analysis methods of equilibrium in an aqueous solution have been developed by capillary zone electrophoresis (CZE) utilizing its separation principle. The equilibrium of interest has been analyzed by affinity capillary electrophoresis (ACE) through the change in the electrophoretic mobility. Coexist...
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Published in | BUNSEKI KAGAKU Vol. 64; no. 2; pp. 105 - 116 |
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Language | Japanese |
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The Japan Society for Analytical Chemistry
05.02.2015
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Abstract | Analysis methods of equilibrium in an aqueous solution have been developed by capillary zone electrophoresis (CZE) utilizing its separation principle. The equilibrium of interest has been analyzed by affinity capillary electrophoresis (ACE) through the change in the electrophoretic mobility. Coexisting substances including degraded compounds are resolved from the equilibrium species by CZE, and an acid dissociation constant of photo-degradable haloperidol was determined in the presence of the degraded substances. In addition to the classical CZE separation, it has been noticed that gradually generated substances during CZE are resolved from the equilibrium species, and that the generated substances are observed as a leading/tailing signal to the equilibrium species. Slowly generated species from phenolphthalein by the addition of OH− in an alkaline pH solution was resolved from the equilibrium species, and the side reaction to the objective acid-base equilibria was excluded. Thus, two steps of the acid dissociation constants of phenolphthalein were determined by ACE. The acid-base equilibrium of tetrabromophenolphthalein ethyl ester (TBPE) was also analyzed by CZE under the degrading conditions, although the hydrolysis of the ester moiety accompanies with TBPE in acidic pH conditions. The precipitation reaction as a side reaction can also be excluded in the CZE analysis. The low concentration of analyte below its solubility is detected as a usual CZE signal, and the equilibrium of interest can be analyzed. The ion-association constants of dipicrylaminate ion with pairing cations were determined by ACE. Even under precipitating conditions, the precipitate is resolved from the equilibrium species by CZE, and it is dissolved again in the separation buffer. Acid dissociation constants of tetrabromophenolphthalein are determined by ACE under precipitable conditions. It was demonstrated in this study that the utilization of the CZE separation is advantageous on equilibrium analysis by ACE to such reactions as to be degradable and precipitable ones, compared to the ordinary analysis in homogeneous solutions, including potentiometric and photometric titrations. |
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AbstractList | Analysis methods of equilibrium in an aqueous solution have been developed by capillary zone electrophoresis (CZE) utilizing its separation principle. The equilibrium of interest has been analyzed by affinity capillary electrophoresis (ACE) through the change in the electrophoretic mobility. Coexisting substances including degraded compounds are resolved from the equilibrium species by CZE, and an acid dissociation constant of photo-degradable haloperidol was determined in the presence of the degraded substances. In addition to the classical CZE separation, it has been noticed that gradually generated substances during CZE are resolved from the equilibrium species, and that the generated substances are observed as a leading/tailing signal to the equilibrium species. Slowly generated species from phenolphthalein by the addition of OH− in an alkaline pH solution was resolved from the equilibrium species, and the side reaction to the objective acid-base equilibria was excluded. Thus, two steps of the acid dissociation constants of phenolphthalein were determined by ACE. The acid-base equilibrium of tetrabromophenolphthalein ethyl ester (TBPE) was also analyzed by CZE under the degrading conditions, although the hydrolysis of the ester moiety accompanies with TBPE in acidic pH conditions. The precipitation reaction as a side reaction can also be excluded in the CZE analysis. The low concentration of analyte below its solubility is detected as a usual CZE signal, and the equilibrium of interest can be analyzed. The ion-association constants of dipicrylaminate ion with pairing cations were determined by ACE. Even under precipitating conditions, the precipitate is resolved from the equilibrium species by CZE, and it is dissolved again in the separation buffer. Acid dissociation constants of tetrabromophenolphthalein are determined by ACE under precipitable conditions. It was demonstrated in this study that the utilization of the CZE separation is advantageous on equilibrium analysis by ACE to such reactions as to be degradable and precipitable ones, compared to the ordinary analysis in homogeneous solutions, including potentiometric and photometric titrations. |
Author | TAKAYANAGI, Toshio |
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Copyright | The Japan Society for Analytical Chemistry 2015 |
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DOI | 10.2116/bunsekikagaku.64.105 |
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References_xml | – reference: 17) N. Iki, H. Hoshino, T. Yotsuyanagi : Anal. Chem., 72, 4812 (2000). – reference: 24) Z. Tamura, S. Abe, K. Ito, M. Maeda : Anal. Sci., 12, 927 (1996). – reference: 26) 本水昌二,磯崎昭徳,櫻川昭雄,伊原敏博,内山一美,善木道雄,寺前紀夫,中釜達朗,平山和雄,三浦恭之,南澤宏昭,森田孝節 : "基礎教育シリーズ 分析化学<基礎編>",p. 79 (2011), (東京教学社). – reference: 29) T. Takayanagi, A. Tabara, T. Kaneta : Anal. Sci., 29, 547 (2013). – reference: 3) T. Takayanagi : Anal. Sci., 20, 255 (2004). – reference: 15) R. Driouich, H. Trabelsi, K. A. Bouzouita : Chromatographia, 53, 629 (2001). – reference: 30) 酒井忠雄 : 分析化学 (Bunseki Kagaku), 24, 135 (1975). – reference: 2) T. Hirokawa, Y. Kiso : Anal. Sci., 8, 737 (1992). – reference: 31) T. Sakai, N. Ohno : Anal. Sci., 2, 275 (1986). – reference: 22) S. N. Krylov : Electrophoresis, 28, 69 (2007). – reference: 5) H. Jensen, S. W. Larsen, C. Larsen, J. Østergaard : J. Drug Deliv. Sci. Tec., 23, 333 (2013). – reference: 1) 木曽義之 : "ゾーン電気泳動",化学の領域選書3, (1972), (南江堂). – reference: 32) S. Motomizu, M. Oshima, Y.-H. Gao, S. Ishihara, K. Uemura : Analyst, 117, 1775 (1992). – reference: 20) M. Berezovski, S. N. Krylov : J. Am. Chem. Soc., 124, 13674 (2002). – reference: 13) E. Örnskov, A. Linusson, S. Folestad : J. Pharm. Biomed. Anal., 33, 379 (2003). – reference: 18) N. Iki, M. Takahashi, T. Takahashi, H. Hoshino : Anal. Chem., 81, 7849 (2009). – reference: 25) "分析化学反応の基礎─演習と実験─", 改訂版,日本分析化学会北海道支部・東北支部共編,p. 184 (1994), (培風館). – reference: 4) 高柳俊夫 : 化学と工業,55, 117 (2002). – reference: 33) T. Takayanagi, K. Ogura, T. Yabutani : Anal. Sci., 30, 919 (2014). – reference: 37) S. Eringathodi, P. Agnihotri, B. Ganguly, P. Bhatt, P. S. Subramanian, P. Paul, P. K. Ghosh : Eur. J. Inorg. Chem., 2005, 2198. – reference: 9) W. Friedl, J. C. Reijenga, E. Kenndler : J. Chromatogr. A, 709, 163 (1995). – reference: 6) M. H. A. Busch, L. B. Carels, H. F. M. Boelens, J. C. Kraak, H. Poppe : J. Chromatogr. A, 777, 311 (1997). – reference: 10) Y. Ishihama, Y. Oda, N. Asakawa : J. Pharm. Sci., 83, 1500 (1994). – reference: 14) 島上夏美,薮谷智規,高柳俊夫 : 分析化学 (Bunseki Kagaku), 63, 643 (2014). – reference: 38) T. Takayanagi : Anal. Sci., 29, 1067 (2013). – reference: 7) M. H. A. Busch, J. C. Kraak, H. Poppe : J. Chromatogr. A, 777, 329 (1997). – reference: 11) P. Janoš : J. Chromatogr. A, 1037, 15 (2004). – reference: 27) 原口紘旡 監訳 : "原書6版,クリスチャン分析化学 I. 基礎編", p. 301 (2005), (丸善). – reference: 8) 黒田幸弘,澁川明正,中川照眞 : CEアドバンス,4, 38 (2000). – reference: 36) S. Motomizu, M. Kobayashi : Anal. Sci., 10, 187 (1994). – reference: 16) A. Avdeef, O. Tsinman : Euro. J. Pharm. Sci., 28, 43 (2006). – reference: 21) S. N. Krylov, M. Berezovski : Analyst, 128, 571 (2003). – reference: 35) 木村道也,平山忠允,前島富美子 : 分析化学 (Bunseki Kagaku), 10, 1143 (1961). – reference: 39) Z. Tamura, R. Terada, K. Ohno, M. Maeda : Anal. Sci., 15, 339 (1999). – reference: 19) K. Ohtsuka, N. Iki, H. Hoshino, T. Takahashi : Anal. Sci., 29, 553 (2013). – reference: 23) T. Takayanagi, S. Motomizu : Chem. Lett., 2001, 14. – reference: 34) 石橋雅義,桐栄恭二 : 日本化学雑誌,76, 104 (1955). – reference: 28) "分析化学データブック", 改訂4版,日本分析化学会編,p. 82 (1994), (丸善). – reference: 12) S. K. Poole, S. Patel, K. Dehring, H. Workman, C. F. Poole : J. Chromatogr. A, 1037, 445 (2004). |
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Snippet | Analysis methods of equilibrium in an aqueous solution have been developed by capillary zone electrophoresis (CZE) utilizing its separation principle. The... |
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SubjectTerms | affinity capillary electrophoresis capillary zone electrophoresis equilibrium analysis side reaction |
Title | Equilibrium Analyses in Aqueous Solution under Accompanying Side Reactions by Capillary Zone Electrophoresis |
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