Evaluation of microcolumn stability in ultrafast affinity extraction for binding and rate studies

Sazia Iftekhar1, David S. Hage1
1Department of Chemistry, University of Nebraska, Lincoln, NE 68588-0304, USA

Tài liệu tham khảo

Zheng, 2015, Analysis of hormone-protein binding in solution by ultrafast affinity extraction: interactions of testosterone with human serum albumin and sex hormone binding globulin, Anal. Chem., 87, 11187, 10.1021/acs.analchem.5b03007 Zheng, 2014, Analysis of free drug fractions by ultrafast affinity extraction: interactions of sulfonylurea drugs with normal or glycated human serum albumin, J. Chromatogr. A, 1371, 82, 10.1016/j.chroma.2014.10.092 Czub, 2019, Testosterone meets albumin - the molecular mechanism of sex hormone transport by serum albumins, Chem. Sci., 10, 1607, 10.1039/C8SC04397C Beeram, 2021, Characterization of drug binding with alpha1-acid glycoprotein in clinical samples using ultrafast affinity extraction, J. Chromatogr. A, 1649, 10.1016/j.chroma.2021.462240 Bi, 2016, Analysis of free drug fractions in serum by ultrafast affinity extraction and two-dimensional affinity chromatography using α1-acid glycoprotein microcolumns, J. Chromatogr. A, 1432, 49, 10.1016/j.chroma.2015.12.084 Beeram, 2017, Chromatographic studies of drug interactions with alpha1-acid glycoprotein by ultrafast affinity extraction and peak profiling, J. Chromatogr. A, 1497, 92, 10.1016/j.chroma.2017.03.056 Yang, 2018, Binding studies based on ultrafast affinity extraction and single- or two-column systems: interactions of second- and third-generation sulfonylurea drugs with normal or glycated human serum albumin, J. Chromatogr. B, 1102–1103, 8, 10.1016/j.jchromb.2018.10.015 Zheng, 2016, Analysis of free drug fractions in human serum by ultrafast affinity extraction and two-dimensional affinity chromatography, Anal. Bioanal. Chem., 408, 131, 10.1007/s00216-015-9082-7 Beeram, 2018, Characterization of solution-phase drug-protein interactions by ultrafast affinity extraction, Methods, 146, 46, 10.1016/j.ymeth.2018.02.021 Zheng, 2014, Determination of rate constants and equilibrium constants for solution-phase drug-protein interactions by ultrafast affinity extraction, Anal. Chem., 86, 6454, 10.1021/ac501031y Carter, 1989, Three-dimensional structure of human serum albumin, Science, 244, 1195, 10.1126/science.2727704 Kragh-Hansen, 1985, Relations between high-affinity binding sites of markers for binding regions on human serum albumin, Biochem. J., 225, 629, 10.1042/bj2250629 Kragh-Hansen, 2002, Practical aspects of the ligand-binding and enzymatic properties of human serum albumin, Biol. Pharm. Bull., 25, 695, 10.1248/bpb.25.695 Hage, 2005, Bioaffinity chromatography, 101 Yamasaki, 2013, Albumin-drug interaction and its clinical implication, Biochim. Biophys. Acta, 1830, 5435, 10.1016/j.bbagen.2013.05.005 Sleep, 2013, Albumin as a versatile platform for drug half-life extension, Biochim. Biophys. Acta, 1830, 5526, 10.1016/j.bbagen.2013.04.023 Rabbani, 2019, Structure, enzymatic activities, glycation and therapeutic potential of human serum albumin: a natural cargo, Int. J. Biol. Macromol., 123, 979, 10.1016/j.ijbiomac.2018.11.053 Moser, 2006, Stability of warfarin solutions for drug-protein binding measurements: spectroscopic and chromatographic studies, J. Pharm. Biomed. Anal., 41, 1101, 10.1016/j.jpba.2006.02.012 Kim, 2005, Immobilization methods for affinity chromatography, 36 O'Reilly, 1969, Interaction of the anticoagulant drug warfarin and its metabolites with human plasma albumin, J. Clin. Invest., 48, 193, 10.1172/JCI105968 Loun, 1994, Chiral separation mechanisms in protein-based HPLC columns. 1. Thermodynamic studies of (R)- and (S)-warfarin binding to immobilized human serum albumin, Anal. Chem., 66, 3814, 10.1021/ac00093a043 Yoo, 2011, Use of peak decay analysis and affinity microcolumns containing silica monoliths for rapid determination of drug-protein dissociation rates, J. Chromatogr. A, 1218, 2072, 10.1016/j.chroma.2010.09.070 Chen, 2009, Noncompetitive peak decay analysis of drug-protein dissociation by high-performance affinity chromatography, J. Sep. Sci., 32, 1632, 10.1002/jssc.200900074 Mallik, 2010, Analysis of drug-protein binding by ultrafast affinity chromatography using immobilized human serum albumin, J. Chromatogr. A, 1217, 2796, 10.1016/j.chroma.2010.02.026 Claessens, 2004, Review on the chemical and thermal stability of stationary phases for reversed-phase liquid chromatography, J. Chromatogr. A, 1060, 23, 10.1016/S0021-9673(04)01438-4 Kirkland, 1997, Stability of silica-based, endcapped columns with pH 7 and 11 mobile phases for reversed-phase high-performance liquid chromatography, J. Chromatogr. A, 762, 97, 10.1016/S0021-9673(96)00945-4 Hage, 1988, Non-linear elution effects in split-peak chromatography. I. Computer simulations for the cases of irreversible diffusion- and adsorption-limited kinetics, J. Chromatogr., 436, 111, 10.1016/S0021-9673(00)94574-6 Ravisankar, 2019, Fundamental chromatographic parameters, Int. J. Pharm. Sci. Rev. Res., 55, 46 Foley, 1983, Equations for calculation of chromatographic figures of merit for ideal and skewed peaks, Anal. Chem., 55, 730, 10.1021/ac00255a033 Hage, 2011, Chromatographic analysis of drug interactions in the serum proteome, Anal. Methods, 3, 1449, 10.1039/c1ay05068k