Thermochemical Analysis of the Interaction between Pyridoxine and L-Carnosine, L-Histidine, and L-Asparagine in Aqueous Solutions
- Autores: Tyunina E.Y.1, Krutova O.N.2, Barannikov V.P.1
-
Afiliações:
- Krestov Institute of Solution Chemistry, Russian Academy of Sciences
- Ivanovo State University of Chemistry and Technology
- Edição: Volume 97, Nº 3 (2023)
- Páginas: 397-403
- Seção: ФИЗИЧЕСКАЯ ХИМИЯ РАСТВОРОВ
- ##submission.dateSubmitted##: 27.02.2025
- ##submission.datePublished##: 01.03.2023
- URL: https://vestnikugrasu.org/0044-4537/article/view/668808
- DOI: https://doi.org/10.31857/S0044453723030287
- EDN: https://elibrary.ru/EAXQBF
- ID: 668808
Citar
Resumo
Calorimetry is used to study the interaction between dipeptide L-carnosine (Car) and amino acids L-histidine (His) and L-asparagine (Asn) with pyridoxine (PN) in an aqueous solution. Experimental values of the enthalpy of dissolution of amino acids and peptide in an aqueous PN solution at T = 298.15 K are obtained for the first time. The thermodynamic characteristics and stoichiometry of the formation of molecular complexes between the reactants are determined. It is found that the stability of the resulting complexes depends on the structure of the reactants and falls in the order Car > Asn > His. It is shown that the main contribution to the stabilization of the resulting complexes comes from the entropy component of the Gibbs energy of complexation.
Sobre autores
E. Tyunina
Krestov Institute of Solution Chemistry, Russian Academy of Sciences
Email: tey@isc-ras.ru
153045, Ivanovo, Russia
O. Krutova
Ivanovo State University of Chemistry and Technology
Email: tey@isc-ras.ru
153000, Ivanovo, Russia
V. Barannikov
Krestov Institute of Solution Chemistry, Russian Academy of Sciences
Autor responsável pela correspondência
Email: tey@isc-ras.ru
153045, Ivanovo, Russia
Bibliografia
- Kihal A., Rodriguez-Prado M., Godoy C. et al. // J. Dairy Sci. 2020. V. 103. P. 3125. https://doi.org/10.3168/jds.2019-17561
- Koczoń P., Piekut J., Borawska M. et al. // Spectrochim. Acta. Part A. 2005. V. 61. P. 1917. https://doi.org/10.1016/j.saa.2004.07.022
- Hellmann H., Mooney S. // Molecules. 2010. V. 15. P. 442. https://doi.org/10.3390/molecules15010442
- Li W., Yang X., Song Q. et al. // Bioorg. Chem. 2020. V. 97. P. 103707. https://doi.org/10.1016/j.bioorg.2020.103707
- Komasa A., Babijczuk K., Dega-Szafran Z. et al. // J. Mol. Struct. 2022. V. 1254. P. 131773. https://doi.org/10.1016/j.molstruc.2021.131773
- Ristilä M., Matxain J.M., Strid Ă. et al. // J. Phys. Chem. B. 2006. V. 110. P. 16774. https://doi.org/10.1021/jp062800n
- Гамов Г.А., Александрийский В.В., Шарнин В.А. // Журн. структур. химии. 2017. Т. 58. № 2. С. 293. https://doi.org/10.15372/JSC20170208
- Takács-Novák K., Tam K.Y. // J. Pharm. Biomed. Anal. 2000. V. 21. P. 1171.
- Noszál B. Acid-Base Properties of Pioligands in Piocoordination Chemistry. Ellis-Horwood, Chichester, UK, 1990.
- Tyunina E.Y., Badelin V.G., Mezhevoi I.N. et al. // J. Mol. Liq. 2015. V. 211. P. 494. https://doi.org/10.1016/j.molliq.2015.07.024
- Sharma M., Banipal T.S., Banipal P.K. // J. Chem. Eng. Data. 2018. V. 63. No. 5. P. 1325. https://doi.org/10.1021/acs.jced.7b00937
- Slifkin Von M.A. Charge Transfer Interaction in Biomolecules. London – New York: Acad. Press, 1971. https://doi.org/10.1002/ardp.19723050815
- Kimura T., Matubayasi N., Sato H. et al. // J. Phys. Chem. B. 2002. V. 106. P. 12336. https://doi.org/10.1021/jp021246o
- Krall A.S., Xu Sh., Geraeber Th.G. et al. // Nut. Commun. 2016. V. 7. P. 11457. https://doi.org/10.1038/ncomms11457
- Bretti C., Cigala R.M., Giuffrè O. et al. // Fluid Phase Equilibr. 2018. V. 459. P. 51. https://doi.org/10.1016/j.fluid.2017.11.030
- Tyunina E.Yu., Badelin V.G., Mezhevoi I.N. // J. Mol. Liq. 2019. V. 278. P. 505. https://doi.org/10.1016/j.molliq.2019.01.092
- Cleland W.W. // Arch. Biochem. Biophys. 2000. V. 382. P. 1.
- Tyunina E.Yu., Mezhevoi I.N., Dunaeva V.V. // J. Chem. Thermodynamic. 2020. V. 150. P. 106206. https://doi.org/10.1016/j.jct.2020.106206
- Abdelkader H., Swinden J., Pierscionek B.K. et al. // J. Pharm. Biomed. Analysis. 2015. V. 114. P. 241. https://doi.org/10.1016/j.jpba.2015.05.025
- Guiotto A., Calderan A., Ruzza P. et al. // Curr. Med. Chem. 2005. V. 12. P. 2293. https://doi.org/10.2174/0929867054864796
- Bertinaria M., Rolando B., Giorgis M. et al. // J. Med. Chem. 2011. V. 54. P. 611. https://doi.org/10.1021/jm101394n
- Tyunina E.Yu., Krutova O.N., Lytkin A.I. // Thermochim. Acta. 2020. V. 690. P. 178704. https://doi.org/10.1016/j.tca.2020.178704
- Barannikov V.P., Badelin V.G., Venediktov E.A. et al. // Russ. J. Phys. Chem. A. 2011. V. 85. № 1. P. 16.https://doi.org/10.1134/S003602441101002X
- Krutova O.N., Usacheva T.R., Myshenkov M.S. et al. // J. Therm. Anal. Cal. 2021. No.7. https://doi.org/10.1007/s10973-021-10982-1
- Kochergina L.A., Grosheva S.G., Krutova O.N. // Russ. J. Inorg. Chem. 2011. V. 56. P. 1481. https://doi.org/10.1134/S0036023611090129
- Vasil'ev V.P., Kochergina L.A., Garavin V.Yu. // Russ. J. Gen. Chem. 1985. V. 55. P. 2780.
- Lytkin A.I., Barannikov V.P., Badelin V.G. et al. // J. Therm. Anal. Cal. 2020. V. 139. P. 3683. https://doi.org/10.1007/s10973-019-08604-y
- Lytkin A.I., Krutova O.N., Tyunina E.Yu. et al. // Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. [Russ. J. Chem. & Chem. Tech.] 2020. V. 63. № 6. P. 25. https://doi.org/10.6060/ivkkt.20206306.6183
- Badelin V.G., Tyunina E.Yu., Mezhevoi I.N. // Russ. J. Appl. Chem. 2007. V. 80. P. 711. https://doi.org/10.1134/S1070427207050047
- Smirnov V.I., Badelin V.G. // Thermochim. Acta. 2015. V. 606. P. 41. https://doi.org/10.1016/j.tca.2015.03.007
- Wadsö I., Goldberg R.N. // Pure Appl. Chem. 2001. V. 73. P. 1625.
- Archer D.G. // Phys. Chem. Ref. Data. 1999. V. 28. P. 1. https://doi.org/10.1063/1.556034
- Badelin V.G., Smirnov V.I., Mezhevoi I.N. // Russ. J. Phys. Chem. 2002. V. 76. P. 1168.
- Badelin V.G., Smirnov V.I. // Russ. J. Phys. Chem. 2010. V. 84. P. 1163. https://doi.org/10.1134/S0036024410070150
- Palecz B. // J. Therm. Anal. Calorim. 1998. V. 54. P. 257.
- Piekarski H., Nowicka B. // J. Therm. Anal. Calorim. 2010. V. 102. P. 31.
- Palecz B., Piekarski H., Romanowski S. // J. Mol. Liq. 2000. V. 84. P. 279.
- Бородин В.А., Васильев В.П., Козловский Е.В. Математические задачи химической термодинамики. Новосибирск: Наука, 1985. С. 219–226.
- Palecz B. // J. Am. Chem. Soc. 2005. V. 127. No. 50. P. 17768. https://doi.org/10.1021/ja054407l
- Refat M.S., Al-Azab F.M., Al-Maydama H.M.A. et al. // Spectrochim. Acta. Part A: Mol. Biomol. Spectroscopy. 2014. V. 127. P. 196. https://doi.org/10.1016/j.saa.2014.02.043
- Ross P.D., Subramanian S. // Biochemistry. 1981. V. 20. № 11. P. 3096. https://doi.org/10.1021/bi00514a017
Arquivos suplementares
