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1. 2. 1. 2. 3. 4. 5. 6. 7. 3. 1. 4. 1. 00002-4 25 Copyright Ó 2013 Elsevier Inc. All rights reserved. 26 2. DERIVATIZATION IN LIQUID CHROMATOGRAPHY a compound or leads to more-robust results by enhancing the stability of the compound, reduces matrix interferences, improves the reproducibility of the method, or simplifies the operational steps in the method. Many compounds lack a suitable chromophore (UV-Visible detection), fluorophore (fluorescence and chemiluminescence detection), electrophore (electrochemical detection) or possess low ionization efficiently (mass spectrometric detection) for detection at anticipated sample concentrations.
In: Hage DS, editor. Handbook of affinity chromatography. 2nd ed. Boca Raton, FL: Taylor & Francis, CRC Press; 2006. p. 663e83. [104] Loun B, Hage DS. Chiral separation mechanisms in protein-based HPLC columns, II. Kinetic studies of R- and S-warfarin binding to immobilized human serum albumin. Anal Chem 1996;68:1218e25. [105] Schiel JE, Hage DS. Kinetic studies of biological interactions by affinity chromatography. J Sep Sci 2009;32:1507e22. [106] Schiel JE, Ohnmacht CM, Hage DS. Measurement of drug-protein dissociation rates by high-performance affinity chromatography and peak profiling.
In: Katz E, Eksteen R, Shoenmakers P, Miller N, editors. Handbook of HPLC. New York: Marcel Dekker; 1988. p. 483e98. [26] Friedberg F, Rhoads AR. Affinity chromatography of enzymes. In: Hage DS, editor. Handbook of affinity chromatography. 2nd ed. Boca Raton, FL: CRC Press; 2005. p. 313e46. [27] Parikh I, Cuatrecasas P. Affinity chromatography. Chem Eng News 1985;63:17e32. [28] Bourne Y, Astoul CH, Zamboni V, Peumans WJ, Menu-Bouaouiche I, Van Damme EJM, et al. Structural basis for the unusual carbohydrate-binding specificity of jacalin towards galactose and mannose.