Liquid Chromatographic Determination of pKa Value of 1- (2-methylbenzonitrile)-3-benzylbenzimidazolium bromide as a Drug Candidate in Acetonitrile-Water Binary Mixtures

Liquid Chromatographic Determination of pKa Value of 1- (2-methylbenzonitrile)-3-benzylbenzimidazolium bromide as a Drug Candidate in Acetonitrile-Water Binary Mixtures

The ionization/protonation (pKa) constant, which is a physicochemical parameter that directly affects the pharmacokinetic properties of a drug such as absorption, distribution, metabolism, and excretion (ADME), is currently determined by analytical methods. The effect of pH of the mobile phase on the chromatographic behavior of 1-(2- methylbenzonitrile)-3-benzylbenzimidazolium bromide (2) which its synthesis, fully characterization, and antiproliferative activity properties were studied previously, and the protonation constant (pKa) value were determined in this study. The pKa value of compound 2, benzimidazolium salt, was determined by the reverse-phase liquid chromatographic (RPLC) method at 25 oC. ??! " " values were evaluated using retention time (tR) in acetonitrile-water binary mixtures with acetonitrile (ACN) percentages of 40%, 45%, 50% and 55% (v/v). The aqueous pKa ( ??! # # ) value of the synthesized compound was calculated from the ??! " " value using the macroscopic parameters (dielectric constant and mole fraction) which play an important role in the solvent properties. Obtained ??! # # values were found to be 11.290 and 11.241, respectively. In addition, the degree of ionization of the related compound was calculated using the ??! # # values.

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  • [1] Akkoç S, İlhan İÖ, Gök Y, Upadhyay PJ, Kayser V. In Vitro Cytotoxic Activities of New Silver and PEPPSI Palladium N-Heterocyclic Carbene Complexes Derived from Benzimidazolium Salts. Inorganica Chim Acta. 2016; 449: 75-81. [CrossRef]
  • [2] Espinosa S, Bosch E, Rosés M. Retention of Ionizable Compounds on HPLC. 5.Ph Scales and the Retention of Acids and Bases with Acetonitrile–Water Mobilephases. Anal. Chem. 2000; 72: 5193–5200. [CrossRef]
  • [3] Poturcu K, Demiralay EÇ. Determination of pKa Values for Some Benzimidazole and Imidazole Group Drugs Using the Reversed-Phase Liquid Chromatography Method. J. Chem. Eng. Data. 2020; 65: 5617−5626. [CrossRef]
  • [4] Barbosa J, Barrón D, Jiménez-Lozano E, Sanz-Nebot V. Comparison Between Capillary Electrophoresis, Liquid Chromatography, Potentiometric and Spectrophotometric Techniques for Evaluation of pKa Values of Zwitterionic Drugs in Acetonitrile-Water Mixtures. Anal. Chim. Acta. 2001; 437: 309-321. [CrossRef]
  • [5] Daldal YD, Demiralay EÇ. Chromatographic and UV–Visible Spectrophotometric pKa Determination of Some Purine Antimetabolites. J. Mol. Liq. 2020; 317: 1-8. [CrossRef]
  • [6] Tam KY, Hadley M, Patterson W. Multiwavelength Spectrophotometric Determination of Acid Dissociation Constants Part IV. Water-İnsoluble Pyridine Derivatives. Talanta. 1999; 49: 539–546. [CrossRef]
  • [7] Allen RI, Box KJ, Comer JEA, Peake C, Tam KY. Multiwavelength Spectrophotometric Determination of Acid Dissociation Constants of Ionizable Drugs. J. Pharm. Biomed. 1998; 17: 699–712. [CrossRef]
  • [8] Bocian S, Krzemińska K. The Separations Using Pure Water as A Mobile Phase in Liquid Chromatography Using Polarembedded Stationary Phases. Green Chem Lett Rev. 2019; 12(1): 69–78. [CrossRef]
  • [9] Kazakevich Y, Lobrutto Y. HPLC for Pharmaceutical Scientists, first ed., Wiley-Interscience, USA, 2007.
  • [10] Espinosa S, Bosch E, Rosés M. Retention of Ionizable Compounds on High-Performance Liquid Chromatography, XI. Global Linear Solvation Energy Relationships for Neutral and Ionizable Compounds. J. Chromatogr. A. 2002; 945: 83–96. [CrossRef]
  • [11] Bosch E, Espinosa S, Rose´s M. Retention of Ionizable Compounds on High-Performance Liquid Chromatography III. Variation of pk Values of Acids And ph Values of Buffers in Acetonitrile–Water Mobile Phases. J. Chromatogr. A. 1998; 824: 137–146. [CrossRef]
  • [12] Kazakevich YV, Lobrutto R. “HPLC For Pharmaceutical Scientists”. John Wiley & Sons, 2007.[CrossRef]
  • [13] Espinosa S, Bosch E, Rosés M. Retention of Ionizable Compounds in High-Performance Liquid Chromatography IX. Modelling Retention in Reversed-Phase Liquid Chromatography as A Function of ph and Solvent Composition with Acetonitrile–Water Mobile Phases. J. Chromatogr. A. 2002; 947: 47–58. [CrossRef]
  • [14] Ortak HY, Demiralay EÇ. Effect of Temperature on the Retention of Janus Kinase 3 Inhibitor Indifferent Mobile Phase Compositions Using Reversed-Phase Liquid Chromatography. J. Pharm. Biomed. 2019; 164: 706–712. [CrossRef]
  • [15] Sun N, Avdeef A. Biorelevant pKa (37 °C) Predicted from the 2D structure of the Molecule and its pKa at 25 °C. J. Pharm. Biomed. 2011; 56(2): 173-182. [CrossRef]
  • [16] Gagliardi LG, Castells CB, Rafols C, Roses M, Bosch E. Effect of Temperature on the Chromatographic Retention of Ionizable Compounds. III. Modelingretention of Pharmaceuticals as a Function of eluent pH and Column Temperature in RPLC. J. Sep. Sci. 2008; 31: 969 –980. [CrossRef]
  • [17] Mumcu, A, Küçükbay H. Determination of pKa Values of Some Novel Benzimidazole Salts by using a New Approach with 1H NMR Spectroscopy. Magn. Reson. Chem. 2015; 53: 1024–1030. [CrossRef]
  • [18] Konstandaras N, Dunn MH, Luis ET, Cole ML, Harper JB. The pKa Values of N-aryl Imidazolinium Salts, Their Higher Homologues, and Form Amidinium Salts in Dimethyl Sulfoxide. Org. Biomol. 2020; 10. [CrossRef]
  • [19] Tsukamoto M, Oyama K. Recent Application of Acidic 1,3-azolium Salts as Promoters in the Solution-Phase Synthesis of Nucleosides and Nucleotides. Tetrahedron Lett. 2018; 59(26): 2477-2484. [CrossRef]
  • [20] Amyes TL, Diver ST, Richard JP, Rivas FM, Toth K. Formation and Stability of N-heterocyclic Carbenes in Water: the Carbon Acid pKa of Imidazolium Cations in aqueous solution. J. Am. Chem. Soc. 2004; 126(13): 4366-74. [CrossRef]
  • [21] Mussini T, Covington AK, Longhi P, Rondinini S. Criteria for Standardization of pH Measurements in Organic Solvents and Water - Organic Solvent Mixtures of Moderate to High Permittivities. Pure Appl. Chem. 1985; 57: 865- 876. [CrossRef]
  • [22] Rondinini S, Mussini PR, Mussini T. Reference Value standards and Primary standards for pH Measurements in Organic Solvents and water - organic Solvent Mixtures of Moderate to High Permittivities. Pure Appl. Chem. 1987; 59: 1549-1560. [CrossRef]
  • [23] NLREG. Version 4.0. PH Sherrod, 1991. Available at: http://www.sandh.com/Sherrod (accessed 16 July 2013).
  • [24] Barbosa J, Barrón D, Bergés R, Buti S, Sanz-Nebot V. Evaluation of the Effect of Organic Modifier on pK Values of Diuretics in Mobile Phases Used in LC. Int J Pharm. 1998; 160: 173-185. [CrossRef]
  • [25] Barbosa J, Toro I, Sanz-Nebot V. Acid-base Behaviour of Tripeptides in Solvents Used in Liquid Chromatography. Correlation between pK values and solvatochromic parameters of acetonitrile-water mixtures. Anal Chim Acta. 1997; 347(3): 295-304. [CrossRef]
  • 26] Tallarida RJ, Murray RB. Henderson-Hasselbalch Equation, in: R.J. Tallarida, R.B. Murray (Ed.), Manual of Pharmacologic Calculations, Springer, New York. 1987; pp.74-75.
Journal of research in pharmacy (online)-Cover
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: Marmara Üniversitesi
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