References
- Kirkland, J. Development of Some Stationary Phases for Reversed-Phase HPLC. J. Chromatogr. A 2004, 1060, 9–21. DOI: https://doi.org/10.1016/S0021-9673(04)01892-8.
- Majors, R.; Przybyciel, M. Columns for Reversed-Phase LC Separations in Highly Aqueous Mobile Phases. LC-GC Eur. Column Watch 2002, 1–7.
- Przybyciel, M. Novel Phases for HPLC Separations. LC-GC Column Technol. Suppl. 2004, 26–29.
- Przybyciel, M. Novel Phases for HPLC Separations. LC-GC Column Technol. Suppl. 2006, 49–52.
- Bocian, S.; Krzemińska, K. The Separations Using Pure Water as a Mobile Phase in Liquid Chromatography Using Polar-Embedded Stationary Phases. Green Chem. Lett. Rev. 2019, 12, 69–78. DOI: https://doi.org/10.1080/17518253.2019.1576775.
- Ojha, S.; Kale, S.; Gadwe, S.; Mulgund, S. Newer Stationary Phases for Reverse Phase-Liquid Chromatographic Analysis. Int. J. Pharm. Biol. Sci. Arch. 2013, 1, 98–109.
- Farsa, O. Chromatographic Behaviour Predicts the Ability of Potential Nootropics to Permeate the Blood-Brain Barrier. Sci. Pharm. 2013, 81, 81–91. DOI: https://doi.org/10.3797/scipharm.1208-19.
- Vinas, P.; Balsalobre, N.; Hernandezcordoba, M. Liquid Chromatography on an Amide Stationary Phase with Post-Column Derivatization and Fluorimetric Detection for the Determination of Streptomycin and Dihydrostreptomycin in Foods. Talanta 2007, 72, 808–812. DOI: https://doi.org/10.1016/j.talanta.2006.12.006.
- Borges-Muñoz, A. C.; Colón, L. A. Evaluation of an Amide-Based Stationary Phase for Supercritical Fluid Chromatography. J. Sep. Sci. 2016, 39, NA–3476. DOI: https://doi.org/10.1002/jssc.201600530.
- Rafferty, J. L.; Siepmann, J. I.; Schure, M. R. Molecular-Level Comparison of Alkylsilane and Polar-Embedded Reversed-Phase Liquid Chromatography Systems. Anal. Chem. 2008, 80, 6214–6221. DOI: https://doi.org/10.1021/ac8005473.
- Bocian, S.; Krzemińska, K.; Buszewski, B. A Study of Separation Selectivity Using Embedded Ester-Bonded Stationary Phases for Liquid Chromatography. Analyst 2016, 141, 4340–4348. DOI: https://doi.org/10.1039/C6AN00139D.
- Dietrich, B.; Holtin, K.; Bayer, M.; Friebolin, V.; Kühnle, M.; Albert, K. Synthesis, Characterization, and High-Performance Liquid Chromatographic Evaluation of C14 Stationary Phases Containing Branched and Unbranched Alkyl Groups. Anal. Bioanal. Chem. 2008, 391, 2627–2633. DOI: https://doi.org/10.1007/s00216-008-2183-9.
- Bocian, S.; Buszewski, B. Synthesis and Characterization of Phosphodiester Stationary Bonded Phases for Liquid Chromatography. Talanta 2015, 143, 35–41. DOI: https://doi.org/10.1016/j.talanta.2015.04.079.
- O'Gara, J. E.; Walsh, D. P.; Alden, B. A.; Casellini, P.; Walter, T. H. Systematic Study of Chromatographic Behavior vs Alkyl Chain Length for HPLC Bonded Phases Containing an Embedded Carbamate Group. Anal. Chem. 1999, 71, 2992–2997. DOI: https://doi.org/10.1021/ac9900331.
- Liu, X.; Bordunov, A.; Tracy, M.; Slingsby, R.; Avdalovic, N.; Pohl, C. Development of a Polar-Embedded Stationary Phase with Unique Properties. J. Chromatogr. A 2006, 1119, 120–127. DOI: https://doi.org/10.1016/j.chroma.2005.12.097.
- Silva, C. R.; Bachmann, S.; Schefer, R. R.; Albert, K.; Jardim, I. C. S. F.; Airoldi, C. Preparation of a New C18 Stationary Phase Containing Embedded Urea Groups for Use in High-Performance Liquid Chromatography. J. Chromatogr. A 2002, 948, 85–95. DOI: https://doi.org/10.1016/S0021-9673(01)01263-8.
- Li, Y.; Dai, P.; Ke, Y.; Jin, Y.; Liang, X. Preparation of a Stationary Phase with s-Triazine Ring Embedded Group for Reversed Phase High-Performance LC. J. Sep. Sci. 2010, 33, 2998–3004. DOI: https://doi.org/10.1002/jssc.201000056.
- Qiu, H.; Mallik, A. K.; Takafuji, M.; Liu, X.; Jiang, S.; Ihara, H. A New Imidazolium-Embedded C18 Stationary Phase with Enhanced Performance in Reversed-Phase Liquid Chromatography. Anal. Chim. Acta. 2012, 738, 95–101. DOI: https://doi.org/10.1016/j.aca.2012.06.018.
- Bocian, S.; Paca, M.; Buszewski, B. Characterization of New N,O-Dialkyl Phosphoramidate-Bonded Stationary Phases for Reversed-Phase HPLC – Retention and Selectivity. Analyst 2013, 138, 5221. DOI: https://doi.org/10.1039/c3an00371j.
- Sobanska, A. W.; Brzezinska, E. Phospholipid-Based Immobilized Artificial Membrane (IAM) Chromatography: A Powerful Tool to Model Drug Distribution Processes. Curr. Pharm. Des. 2017, 23, 6784–6794. DOI: https://doi.org/10.2174/1381612823666171018114331.
- Sander, L. C.; Sharpless, K. E.; Craft, N. E.; Wise, S. A. Development of Engineered Stationary Phases for the Separation of Carotenoid Isomers. Anal. Chem. 1994, 66, 1667–1674. DOI: https://doi.org/10.1021/ac00082a012.
- Gupta, P.; Sreelakshmi, Y.; Sharma, R. A Rapid and Sensitive Method for Determination of Carotenoids in Plant Tissues by High Performance Liquid Chromatography. Plant Methods. 2015, 11, 5. DOI: https://doi.org/10.1186/s13007-015-0051-0.
- Turcsi, E.; Nagy, V.; Deli, J. Study on the Elution Order of Carotenoids on Endcapped C18 and C30 Reverse Silica Stationary Phases. A Review of the Database. J. Food Compos. Anal. 2016, 47, 101–112. DOI: https://doi.org/10.1016/j.jfca.2016.01.005.
- Saha, S.; Walia, S.; Sharma, K.; Banerjee, K. Suitability of Stationary Phase for LC Analysis of Biomolecules. Crit. Rev. Food Sci. Nutr. 2019, 1–18. DOI: https://doi.org/10.1080/10408398.2019.1665494.
- Zhang, M.; Mai, W.; Zhao, L.; Guo, Y.; Qiu, H. A Polar-Embedded C30 Stationary Phase: Preparation and Evaluation. J. Chromatogr. A 2015, 1388, 133–140. DOI: https://doi.org/10.1016/j.chroma.2015.02.023.
- Zhang, Y.; Zhong, H.; Cao, Z.; Zhou, S.; Zhang, D.; Lu, R.; Han, H.; Zhang, M.; Qiu, H. Design and Evaluation of Polar-Embedded Stationary Phases Containing Triacontyl Group for Liquid Chromatography. J. Chromatogr. A 2020, 461035. (in press) . DOI: https://doi.org/10.1016/j.chroma.2020.461035.
- Needham, S. R.; Brown, P. R.; Duff, K. Phenyl Ring Structures as Stationary Phases for the High Performance Liquid Chromatography Electrospray Ionization Mass Spectrometric Analysis of Basic Pharmaceuticals. Rapid Commun. Mass Spectrom. 1999, 13, 2231–2236. https://doi.org/10.1002/. (sici)1097-0231(19991130)13:22 < 2231::aid-rcm779 > 3.0.co;2-4. DOI: https://doi.org/10.1002/(SICI)1097-0231(19991130)13:22<2231::AID-RCM779>3.0.CO;2-4.
- Stevenson, P. G.; Mayfield, K. J.; Soliven, A.; Dennis, G. R.; Gritti, F.; Guiochon, G.; Shalliker, R. A. π-Selective Stationary Phases: (I) Influence of the Spacer Chain Length of Phenyl Type Phases on the Aromatic and Methylene Selectivity of Aromatic Compounds in Reversed Phase High Performance Liquid Chromatography. J. Chromatogr. A 2010, 1217, 5358–5364. DOI: https://doi.org/10.1016/j.chroma.2010.06.002.
- Petruczynik, A.; Wróblewski, K.; Dzioba, K.; Waksmundzka-Hajnos, M. Retention, Separation Selectivity and System Efficiency of Selected Basic Psychotropic Drugs on Different RPLC Columns. Open Chem. 2015, 13, 943–950. https://doi.org/10.1515/chem-2015-0106.
- Lindner, J. M.; Vogeser, M.; Grimm, S. H. Biphenyl Based Stationary Phases for Improved Selectivity in Complex Steroid Assays. J. Pharm. Biomed. Anal. 2017, 142, 66–73. DOI: https://doi.org/10.1016/j.jpba.2017.04.020.
- Wongyai, S. Synthesis and Characterization of Phenylpropanolamine Bonded Silica for Multimode Liquid Chromatography of Small Molecules. Chromatographia 1994, 38, 485–490. DOI: https://doi.org/10.1007/BF02269841.
- Jezorek, J. R.; Tang, J.; Cook, W. L.; Obie, R.; Ji, D.; Rowe, J. M. Aspects of the Synthesis, Characterization and Metal–Ligand Stoichiometry of Aminopropyl, Nitrobenzamide, and 8-Quinolinol Silica Gels. Anal. Chim. Acta 1994, 290, 303–315. https://doi.org//10.1016/0003-2670(94)80117-7. DOI: https://doi.org/10.1016/0003-2670(94)80117-7.
- Takeuchi, T.; Kawasaki, T.; Lim, L. W. Separation of Inorganic Anions on a Pyridine Stationary Phase in Ion Chromatography. Anal. Sci. 2010, 26, 511–514. DOI: https://doi.org/10.2116/analsci.26.511.
- Auler, L. M. L. A.; Silva, C. R.; Collins, K. E.; Collins, C. H. New Stationary Phase for Anion-Exchange Chromatography. J. Chromatogr. A 2005, 1073, 147–153. DOI: https://doi.org/10.1016/j.chroma.2004.10.012.
- Sun, M.; Feng, J.; Luo, C.; Liu, X.; Jiang, S. Benzimidazole Modified Silica as a Novel Reversed-Phase and Anion-Exchange Mixed-Mode Stationary Phase for HPLC. Talanta 2013, 105, 135–141. DOI: https://doi.org/10.1016/j.talanta.2012.11.077.
- Qiu, H.; Jiang, S.; Liu, X. N-Methylimidazolium Anion-Exchange Stationary Phase for High-Performance Liquid Chromatography. J. Chromatogr. A 2006, 1103, 265–270. DOI: https://doi.org/10.1016/j.chroma.2005.11.035.
- Qiu, H.; Jiang, S.; Liu, X.; Zhao, L. Novel Imidazolium Stationary Phase for High-Performance Liquid Chromatography. J. Chromatogr. A 2006, 1116, 46–50. DOI: https://doi.org/10.1016/j.chroma.2006.03.016.
- Zhang, P.; Chen, J.; Jia, L. N-Methylimidazolium-Functionalized Monolithic Silica Column for Mixed-Mode Chromatography. J. Chromatogr. A 2011, 1218, 3459–3465. DOI: https://doi.org/10.1016/j.chroma.2011.03.062.
- Wang, T.; Yang, H.; Qiu, R.; Huang, S. Synthesis of Novel Chiral Imidazolium Stationary Phases and Their Enantioseparation Evaluation by High-Performance Liquid Chromatography. Anal. Chim. Acta. 2016, 944, 70–77. DOI: https://doi.org/10.1016/j.aca.2016.09.018.
- Kiseleva, M. G.; Nesterenko, P. N. Phenylaminopropyl Silica – A New Specific Stationary Phase for High-Performance Liquid Chromatography of Phenols. J. Chromatogr. A 2000, 898, 23–34. DOI: https://doi.org/10.1016/S0021-9673(00)00872-4.
- Kiseleva, M. G.; Nesterenko, P. N. Novel Stationary Phase with Regulated Anion-Exchange Capacity. J. Chromatogr. A 2001, 920, 87–93. DOI: https://doi.org/10.1016/S0021-9673(01)00694-X.
- Sun, M.; Feng, J.; Liu, S.; Xiong, C.; Liu, X.; Jiang, S. Dipyridine Modified Silica—a Novel Multi-Interaction Stationary Phase for High Performance Liquid Chromatography. J. Chromatogr. A 2011, 1218, 3743–3749. DOI: https://doi.org/10.1016/j.chroma.2011.04.036.
- Nagai, K.; Shibata, T.; Shinkura, S.; Ohnishi, A. Poly(4-Vinylpyridine) Based Novel Stationary Phase Investigated under Supercritical Fluid Chromatography Conditions. J. Chromatogr. A 2018, 1572, 119–127. DOI: https://doi.org/10.1016/j.chroma.2018.08.038.
- Yu, A.; Peng, D.; Hu, K.; Cao, A.; Chang, J.; Wu, Y.; Zhang, S. A New 4-Ferrocenylbenzoyl Chloride-Bonded Stationary Phase for High Performance Liquid Chromatography. J. Chromatogr. A 2013, 1283, 75–81. DOI: https://doi.org/10.1016/j.chroma.2013.01.090.
- Waksmundzka-Hajnos, M.; Petruczynik, A.; Hawrył, A. Comparison of Chromatographic Properties of Cyanopropyl-, Diol- and Aminopropyl- Polar-Bonded Stationary Phases by the Retention of Model Compounds in Normal-Phase Liquid Chromatography Systems. J. Chromatogr. A 2001, 919, 39–50. DOI: https://doi.org/10.1016/S0021-9673(01)00796-8.
- Greco, G.; Letzel, T. Main Interactions and Influences of the Chromatographic Parameters in HILIC Separations. J. Chromatogr. Sci. 2013, 51, 684–693. DOI: https://doi.org/10.1093/chromsci/bmt015.
- Aturki, Z.; D'Orazio, G.; Rocco, A.; Si-Ahmed, K.; Fanali, S. Investigation of Polar Stationary Phases for the Separation of Sympathomimetic Drugs with Nano-Liquid Chromatography in Hydrophilic Interaction Liquid Chromatography Mode. Anal. Chim. Acta. 2011, 685, 103–110. DOI: https://doi.org/10.1016/j.aca.2010.11.017.
- McCalley, D. V. Comparison of the Performance of Conventional C18 Phases with Others of Alternative Functionality for the Analysis of Basic Compounds by Reversed-Phase High-Performance Liquid Chromatography. J. Chromatogr. A 1999, 844, 23–38. DOI: https://doi.org/10.1016/S0021-9673(99)00250-2.
- Ciura, K.; Belka, M.; Kawczak, P.; Bączek, T.; Nowakowska, J. The Comparative Study of Micellar TLC and RP-TLC as Potential Tools for Lipophilicity Assessment Based on QSRR Approach. J. Pharm. Biomed. Anal. 2018, 149, 70–79. DOI: https://doi.org/10.1016/j.jpba.2017.10.034.
- Pesek, J. J.; Matyska, M. T.; Williamser, E. J.; Tam, R. Variable-Temperature, Solid-State NMR Studies of Bonded Liquid Crystal Stationary Phases for HPLC. Chromatographia 1995, 41, 301–310. DOI: https://doi.org/10.1007/BF02688044.
- Delaurent, C.; Tomao, V.; Siouffi, A. M. Synthesis and Characterization of a Chemically-Bonded Cholesteric Stationary Phase for High-Performance Liquid Chromatography. Chromatographia 1997, 45, 355–363. DOI: https://doi.org/10.1007/BF02505584.
- Al-Haj, M. A.; Haber, P.; Kaliszan, R.; Buszewski, B.; Jezierska, M.; Chilmonzyk, Z. Mechanism of Separation on Cholesterol–Silica Stationary Phase for High-Performance Liquid Chromatography as Revealed by Analysis of Quantitative Structure–Retention Relationships. J. Pharm. Biomed. Anal. 1998, 18, 721–728. DOI: https://doi.org/10.1016/S0731-7085(98)00287-8.
- Catabay, A.; Okumura, C.; Jinno, K.; Pesek, J. J.; Williamsen, E.; Fetzer, J. C.; Biggs, W. R. Retention Behavior of Large Polycyclic Aromatic Hydrocarbons on Cholesteryl 10-Undecenoate Bonded Phase in Microcolumn Liquid Chromatography. Chromatographia 1998, 47, 13–20. DOI: https://doi.org/10.1007/BF02466780.
- Courtois, C.; Allais, C.; Constantieux, T.; Rodriguez, J.; Caldarelli, S.; Delaurent, C. Cholesteric Bonded Stationary Phases for High-Performance Liquid Chromatography: Synthesis, Physicochemical Characterization, and Chromatographic Behavior of a Phospho–Cholesteric Bonded Support. A New Way to Mimic Drug/Membrane Interactions? Anal. Bioanal. Chem. 2008, 392, 1345–1354. DOI: https://doi.org/10.1007/s00216-008-2385-1.
- Bocian, S.; Matyska, M.; Pesek, J.; Buszewski, B. Study of the Retention and Selectivity of Cholesterol Bonded Phases with Different Linkage Spacers. J. Chromatogr. A 2010, 1217, 6891–6897. DOI: https://doi.org/10.1016/j.chroma.2010.08.064.
- Buszewski, B.; Bocian, S.; Matyska, M.; Pesek, J. Study of Solvation Processes on Cholesterol Bonded Phases. J. Chromatogr. A 2011, 1218, 441–448. DOI: https://doi.org/10.1016/j.chroma.2010.11.052.
- Pesek, J. J.; Matyska, M. T.; Brent Dawson, G.; Wilsdorf, A.; Marc, P.; Padki, M. Cholesterol Bonded Phase as a Separation Medium in Liquid Chromatography. J. Chromatogr. A 2003, 986, 253–262. DOI: https://doi.org/10.1016/S0021-9673(02)01958-1.
- Soukup, J.; Bocian, S.; Jandera, P.; Buszewski, B. Comparison of Four Cholesterol-Based Stationary Phases for the Separation of Steroid Hormones. J. Sep. Sci. 2014, 37, 345–351. DOI: https://doi.org/10.1002/jssc.201301088.
- Bocian, S.; Soukup, J.; Matyska, M.; Pesek, J.; Jandera, P.; Buszewski, B. The Influence of the Organic Modifier in Hydro-Organic Mobile Phase on Separation Selectivity of Steroid Hormones Separation Using Cholesterol-Bonded Stationary Phases. J. Chromatogr. A 2012, 1245, 90–97. DOI: https://doi.org/10.1016/j.chroma.2012.05.038.
- Studzińska, S.; Krzemińska, K.; Szumski, M.; Buszewski, B. Application of a Cholesterol stationary phase in the Analysis of Phosphorothioate Oligonucleotides by Means of Ion Pair Chromatography Coupled with Tandem Mass Spectrometry. Talanta 2016, 154, 270–277. DOI: https://doi.org/10.1016/j.talanta.2016.03.082.
- Flieger, J.; Tatarczak-Michalewska, M.; Kowalska, A.; Rządkowska, M.; Szacoń, E.; Kaczor, A. A.; Matosiuk, D. Fragmental Method KowWIN as the Powerful Tool for Prediction of Chromatographic Behavior of Novel Bioactive Urea Derivatives. J. Brazil. Chem. Soc. 2016, 27, 2312–2321. DOI: https://doi.org/10.5935/0103-5053.20160128.
- Yeman, H.; Nicholson, T. M.; Friebolin, V.; Steinhauser, L.; Matyska, M. T.; Pesek, J. J.; Albert, K. Time-Dependent Column Performance of Cholesterol-Based Stationary Phases for HPLC by LC Characterization and Solid-State NMR Spectroscopy. J. Sep. Sci. 2012, 35, 1582–1588. DOI: https://doi.org/10.1002/jssc.201200079.
- Shundo, A.; Sakurai, T.; Takafuji, M.; Nagaoka, S.; Ihara, H. Molecular-Length and Chiral Discriminations by β-Structural Poly(l-Alanine) on Silica. J. Chromatogr. A 2005, 1073, 169–174. DOI: https://doi.org/10.1016/j.chroma.2004.08.062.
- Shundo, A.; Mallik, A. K.; Sakurai, T.; Takafuji, M.; Nagaoka, S.; Ihara, H. Controllable Shape Selectivity Based on Highly Ordered Carbonyl and Methyl Groups in Simple β-Structural Polypeptide on Silica. J. Chromatogr. A 2009, 1216, 6170–6176. DOI: https://doi.org/10.1016/j.chroma.2009.06.075.
- Rahman, M. M.; Takafuji, M.; Ansarian, H. R.; Ihara, H. Molecular Shape Selectivity through Multiple Carbonyl − π Interactions with Noncrystalline Solid Phase for RP-HPLC. Anal. Chem. 2005, 77, 6671–6681. DOI: https://doi.org/10.1021/ac050851v.
- Li, Y.; Xu, Z.; Feng, Y.; Liu, X.; Chen, T.; Zhang, H. Preparation and Evaluation of Poly-l-Lysine Stationary Phase for Hydrophilic Interaction/Reversed-Phase Mixed-Mode Chromatography. Chromatographia 2011, 74, 523–530. DOI: https://doi.org/10.1007/s10337-011-2120-5.
- Guo, H.; Liu, R.; Yang, J.; Yang, B.; Liang, X.; Chu, C. A Novel Click Lysine Zwitterionic Stationary Phase for Hydrophilic Interaction Liquid Chromatography. J. Chromatogr. A 2012, 1223, 47–52. DOI: https://doi.org/10.1016/j.chroma.2011.12.033.
- Shen, A.; Guo, Z.; Yu, L.; Cao, L.; Liang, X. A Novel Zwitterionic HILIC Stationary Phase Based on “Thiol-Ene” Click Chemistry between Cysteine and Vinyl Silica. Chem. Commun. (Camb). 2011, 47, 4550–4552. DOI: https://doi.org/10.1039/c1cc10421g.
- Shen, A.; Guo, Z.; Cai, X.; Xue, X.; Liang, X. Preparation and Chromatographic Evaluation of a Cysteine-Bonded Zwitterionic Hydrophilic Interaction Liquid Chromatography Stationary Phase. J. Chromatogr. A 2012, 1228, 175–182. DOI: https://doi.org/10.1016/j.chroma.2011.10.086.
- Wu, S.; Li, X.; Zhang, F.; Jiang, G.; Liang, X.; Yang, B. An Arginine-Functionalized Stationary Phase for Hydrophilic Interaction Liquid Chromatography. Analyst 2015, 140, 3921–3924. DOI: https://doi.org/10.1039/C5AN00570A.
- Xue, M.; Huang, H.; Ke, Y.; Chu, C.; Jin, Y.; Liang, X. Click Dipeptide”: a Novel Stationary Phase Applied in Two-Dimensional Liquid Chromatography. J. Chromatogr. A 2009, 1216, 8623–8629. DOI: https://doi.org/10.1016/j.chroma.2009.10.019.
- Shen, A.; Li, X.; Dong, X.; Wei, J.; Guo, Z.; Liang, X. Glutathione-Based Zwitterionic Stationary Phase for Hydrophilic Interaction/Cation-Exchange Mixed-Mode Chromatography. J. Chromatogr. A 2013, 1314, 63–69. DOI: https://doi.org/10.1016/j.chroma.2013.09.002.
- Ray, S.; Takafuji, M.; Ihara, H. Multi-Mode Chromatographic Evaluation of a New Lysine-Silica Stationary Phase for High-Performance Liquid Chromatography. Anal. Methods 2014, 6, 7674–7680. DOI: https://doi.org/10.1039/C4AY01214C.
- Ray, S.; Takafuji, M.; Ihara, H. A New Peptide-Silica Bio-Inspired Stationary Phase with an Improved Approach for Hydrophilic Interaction Liquid Chromatography. Analyst 2012, 137, 4907–4909. DOI: https://doi.org/10.1039/c2an36024a.
- Ray, S.; Takafuji, M.; Ihara, H. Chromatographic Evaluation of a Newly Designed Peptide-Silica Stationary Phase in Reverse Phase Liquid Chromatography and Hydrophilic Interaction Liquid Chromatography: Mixed Mode Behavior. J. Chromatogr. A 2012, 1266, 43–52. DOI: https://doi.org/10.1016/j.chroma.2012.10.004.
- Teixeira, J.; Tiritan, M. E.; Pinto, M. M. M.; Fernandes, C. Chiral Stationary Phases for Liquid Chromatography: Recent Developments. Molecules 2019, 24, 865. DOI: https://doi.org/10.3390/molecules24050865.
- Moslavac Forjan, D.; Vinković, V.; Kontrec, D. Performance of a New HPLC Chiral Stationary Phase Derived from N-(3,5-Dinitrobenzoyl)-D-α-Phenylglycine with a Quinoxaline Branching Unit. Acta Chromatogr. 2006, 17, 97–107.
- Aral, H. Synthesis and Characterisation of a New Hydrophilic Interaction/Reversed Phase Mixed-Mode Chromatographic Stationary Phase. HJBC. 2018, 1, 43–52. DOI: https://doi.org/10.15671/HJBC.2018.213.
- Zheng, Y.; Wang, X.; Ji, Y. Monoliths with Proteins as Chiral Selectors for Enantiomer Separation. Talanta 2012, 91, 7–17. DOI: https://doi.org/10.1016/j.talanta.2012.01.039.
- Turowski, M.; Kaliszan, R. Keratin Immobilized on Silica as a New Stationary Phase for Chromatographic Modelling of Skin Permeation. J. Pharm. Biomed. Anal. 1997, 15, 1325–1333. DOI: https://doi.org/10.1016/S0731-7085(96)02009-2.
- Turowski, M.; Kaliszan, R. Collagen Immobilised on Silica Derivatives as a New Stationary Phase for HPLC. Biomed. Chromatogr. 1998, 12, 187–192. DOI: https://doi.org/10.1002/(SICI)1099-0801(199807/08)12:4<187::AID-BMC727>3.0.CO;2-2.
- Domenici, E.; Bertucci, C.; Salvadori, P.; Félix, G.; Cahagne, I.; Motellier, S.; Wainer, I. W. Synthesis and Chromatographic Properties of an HPLC Chiral Stationary Phase Based upon Human Serum Albumin. Chromatographia 1990, 29, 170–176. DOI: https://doi.org/10.1007/BF02268706.
- Noctor, T.; Wainer, I. The in Situ Acetylation of an Immobilized Human Serum Albumin Chiral Stationary Phase for High-Performance Liquid Chromatography in the Examination of Drug-Protein Binding Phenomena. Pharm. Res. 1992, 9, 480–484. DOI: https://doi.org/10.1023/a:1015884112039.
- Kim, H. S.; Wainer, I. W. Rapid Analysis of the Interactions between Drugs and Human Serum Albumin (HSA) Using High-Performance Affinity Chromatography (HPAC). J. Chromatogr. B 2008, 870, 22–26. DOI: https://doi.org/10.1016/j.jchromb.2008.05.029.
- Chrysanthakopoulos, M.; Giaginis, C.; Tsantili-Kakoulidou, A. Retention of Structurally Diverse Drugs in Human Serum Albumin Chromatography and Its Potential to Simulate Plasma Protein Binding. J. Chromatogr. A 2010, 1217, 5761–5768. DOI: https://doi.org/10.1016/j.chroma.2010.07.023.
- Ishii, T.; Minoda, K.; Bae, M.-J.; Mori, T.; Uekusa, Y.; Ichikawa, T.; Aihara, Y.; Furuta, T.; Wakimoto, T.; Kan, T.; Nakayama, T. Binding Affinity of Tea Catechins for HSA: Characterization by High-Performance Affinity Chromatography with Immobilized Albumin Column. Mol. Nutr. Food Res. 2009, 54, 816–822. DOI: https://doi.org/10.1002/mnfr.200900071.
- Mallik, R.; Yoo, M. J.; Briscoe, C. J.; Hage, D. S. Analysis of Drug–Protein Binding by Ultrafast Affinity Chromatography Using Immobilized Human Serum Albumin. J. Chromatogr. A 2010, 1217, 2796–2803. DOI: https://doi.org/10.1016/j.chroma.2010.02.026.
- Valkó, K. L. Lipophilicity and Biomimetic Properties Measured by HPLC to Support Drug Discovery. J. Pharm. Biomed. Anal. 2016, 130, 35–54. DOI: https://doi.org/10.1016/j.jpba.2016.04.009.
- Valko, K. Application of Biomimetic HPLC to Estimate in Vivo Behavior of Early Drug Discovery Compounds. Future Drug Discov. 2019, 1, 1–14. https://doi.org/https://doi.org/10.4155/fdd-2019-0004.
- Wanat, K.; Brzezińska, E.; Sobańska, A. W. Aspects of Drug-Protein Binding and Methods of Analyzing the Phenomenon. Curr. Pharm. Des. 2018, 24, 2974–2985. DOI: https://doi.org/10.2174/1381612824666180808145320.
- Hage, D. S. Analysis of Biological Interactions by Affinity Chromatography: Clinical and Pharmaceutical Applications. Clin. Chem. 2017, 63, 1083–1093. DOI: https://doi.org/10.1373/clinchem.2016.262253.
- Sobansky, M. R.; Hage, D. S. Identification and Analysis of Stereoselective Drug Interactions with Low-Density Lipoprotein by High-Performance Affinity Chromatography. Anal. Bioanal. Chem. 2012, 403, 563–571. DOI: https://doi.org/10.1007/s00216-012-5816-y.
- Chen, S.; Sobansky, M. R.; Hage, D. S. Analysis of Drug Interactions with High-Density Lipoprotein by High-Performance Affinity Chromatography. Anal. Biochem. 2010, 397, 107–114. DOI: https://doi.org/10.1016/j.ab.2009.10.017.
- Xuan, H.; Hage, D. S. Immobilization of α1-Acid Glycoprotein for Chromatographic Studies of Drug–Protein Binding. Anal. Biochem. 2005, 346, 300–310. DOI: https://doi.org/10.1016/j.ab.2005.08.025.
- Mallik, R.; Wa, C.; Hage, D. S. Development of Sulfhydryl-Reactive Silica for Protein Immobilization in High-Performance Affinity Chromatography. Anal. Chem. 2007, 79, 1411–1424. DOI: https://doi.org/10.1021/ac061779j.
- Bi, C.; Jackson, A.; Vargas-Badilla, J.; Li, R.; Rada, G.; Anguizola, J.; Pfaunmiller, E.; Hage, D. S. Entrapment of Alpha1-Acid Glycoprotein in High-Performance Affinity Columns for Drug-Protein Binding Studies. J. Chromatogr. B 2016, 1021, 188–196. DOI: https://doi.org/10.1016/j.jchromb.2015.11.021.
- Zhang, Q.; Zou, H.; Wang, H.; Ni, J. Synthesis of a Silica-Bonded Bovine Serum Albumin s-Triazine Chiral Stationary Phase for High-Performance Liquid Chromatographic Resolution of Enantiomers. J. Chromatogr. A 2000, 866, 173–181. DOI: https://doi.org/10.1016/S0021-9673(99)01112-7.
- Anguizola, J.; Bi, C.; Koke, M.; Jackson, A.; Hage, D. S. On-Column Entrapment of Alpha1-Acid Glycoprotein for Studies of Drug-Protein Binding by High-Performance Affinity Chromatography. Anal. Bioanal. Chem. 2016, 408, 5745–5756. DOI: https://doi.org/10.1007/s00216-016-9677-7.
- Mohammadzadeh Kakhki, R. Application of Crown Ethers as Stationary Phase in the Chromatographic Methods. J. Incl. Phenom. Macrocycl. Chem. 2013, 75, 11–22. DOI: https://doi.org/10.1007/s10847-012-0158-0.
- Hyun, M. H. Liquid Chromatographic Enantioseparations on Crown Ether-Based Chiral Stationary Phases. J. Chromatogr. A 2016, 1467, 19–32. DOI: https://doi.org/10.1016/j.chroma.2016.07.049.
- Dotsevi, G.; Sogah, Y.; Cram, D. J. Chromatographic Optical Resolution through Chiral Complexation of Amino Ester Salts by a Host Covalently Bound to Silica Gel. J. Am. Chem. Soc. 1975, 97, 1259–1261. DOI: https://doi.org/10.1021/ja00838a059.
- Kimura, K.; Hayata, E.; Shono, T. Convenient, Efficient Crown Ether-Containing Stationary Phases for Chromatographic Separation of Alkali Metal Ions: Dynamic Coating of Highly Lipophilic Crown Ethers on Octadecylsilanized Silica. J. Chem. Soc, Chem. Commun. 1984, 271. DOI: https://doi.org/10.1039/c39840000271.
- Makino, Y.; Ohta, S.; Hirobe, M. Enantiomeric Separation of Amphetamine by High-Performance Liquid Chromatography Using Chiral Crown Ether-Coated Reversed-Phase Packing: Application to Forensic Analysis. Forensic Sci. Int. 1996, 78, 65–70. DOI: https://doi.org/10.1016/0379-0738(95)01865-4.
- Shinbo, T.; Yamaguchi, T.; Nishimura, K.; Sugiura, M. Chromatographic Separation of Racemic Amino Acids by Use of Chiral Crown Ether-Coated Reversed-Phase Packings. J. Chromatogr. A 1987, 405, 145–153. DOI: https://doi.org/10.1016/S0021-9673(01)81756-8.
- Adhikari, S.; Lee, W. Chiral Separation Using Chiral Crown Ethers as Chiral Selectors in Chirotechnology. J. Pharm. Investig.. 2018, 48, 225–231. DOI: https://doi.org/10.1007/s40005-017-0348-2.
- Hyun, M. H. Preparation and Application of HPLC Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-Tetracarboxylic Acid. J. Sep. Sci. 2006, 29, 750–761. DOI: https://doi.org/10.1002/jssc.200500431.
- Hyun, M. H. Development of HPLC Chiral Stationary Phases Based on (+)-(18-Crown-6)-2,3,11,12-Tetracarboxylic Acid and Their Applications. Chirality 2015, 27, 576–588. DOI: https://doi.org/10.1002/chir.22484.
- Kim, B.-H.; Jung, J.; Han, Y.-K. Liquid Chromatographic Enantiomer Separation of Racemic Amine Using Chiral Crown Ether Stationary Phase. J. Chromatogr. Sci. 2006, 44, 27–31. DOI: https://doi.org/10.1093/chromsci/44.1.27.
- Steffeck, R. J.; Zelechonok, Y.; Gahm, K. H. Enantioselective Separation of Racemic Secondary Amines on a Chiral Crown Ether-Based Liquid Chromatography Stationary Phase. J. Chromatogr. A 2002, 947, 301–305. DOI: https://doi.org/10.1016/S0021-9673(01)01604-1.
- Hyun, M. H.; Han, S. C.; Lipshutz, B. H.; Shin, Y.-J.; Welch, C. J. New Chiral Crown Ether Stationary Phase for the Liquid Chromatographic Resolution of α-Amino Acid Enantiomers. J. Chromatogr. A 2001, 910, 359–365. DOI: https://doi.org/10.1016/S0021-9673(00)01230-9.
- Machida, Y.; Nishi, H.; Nakamura, K. Separation of the Enantiomers of Amino and Amide Compounds on Novel Chiral Stationary Phases Derived from a Crown Ether. Chromatographia 1999, 49, 621–627. DOI: https://doi.org/10.1007/BF02466903.
- Li, Y.; Sheng, Z.; Zhu, C.; Yin, W.; Chu, C. Silica Based Click-Dibenzo-18-Crown-6-Ether High Performance Liquid Chromatography Stationary Phase and Its Application in Separation of Fullerenes. Talanta 2018, 178, 195–201. DOI: https://doi.org/10.1016/j.talanta.2017.07.037.
- Kupai, J.; Lévai, S.; Antal, K.; Balogh, G. T.; Tóth, T.; Huszthy, P. Preparation of Pyridino-Crown Ether-Based New Chiral Stationary Phases and Preliminary Studies on Their Enantiomer Separating Ability for Chiral Protonated Primary Aralkylamines. Tetrahedron: Asymmetry 2012, 23, 415–427. DOI: https://doi.org/10.1016/j.tetasy.2012.04.008.
- Lévai, S.; Németh, T.; Fődi, T.; Kupai, J.; Tóth, T.; Huszthy, P.; Balogh, G. T. Studies of a Pyridino-Crown Ether-Based Chiral Stationary Phase on the Enantioseparation of Biogenic Chiral Aralkylamines and α-Amino Acid Esters by High-Performance Liquid Chromatography. J. Pharm. Biomed. Anal. 2015, 115, 192–195. DOI: https://doi.org/10.1016/j.jpba.2015.07.011.
- Németh, T.; Lévai, S.; Kormos, A.; Kupai, J.; Tóth, T.; Balogh, G. T.; Huszthy, P. Preparation and Studies of Chiral Stationary Phases Containing Enantiopure Acridino-18-Crown-6 Ether Selectors. Chirality 2014, 26, 651–654. DOI: https://doi.org/10.1002/chir.22361.
- Cho, H. S.; Choi, H. J.; Hyun, M. H. Preparation of a New Crown Ether-Based Chiral Stationary Phase Containing Thioester Linkage for the Liquid Chromatographic Separation of Enantiomers. J. Chromatogr. A 2009, 1216, 7446–7449. DOI: https://doi.org/10.1016/j.chroma.2009.04.026.
- Hu, K.; Zhao, W.; Wen, F.; Liu, J.; Zhao, X.; Xu, Z.; Niu, B.; Ye, B.; Wu, Y.; Zhang, S. Investigation on the Preparation and Chromatographic Behavior of a New Para-Tert-Butylcalix[4]Arene-1,2-Crown-4 Stationary Phase for High Performance Liquid Chromatography. Talanta 2011, 85, 317–324. DOI: https://doi.org/10.1016/j.talanta.2011.03.068.
- Li, L.-S.; Da, S.-L.; Feng, Y.-Q.; Liu, M. Preparation and Characterization of a New p-Tert-Butyl-Calix[8]Arene-Bonded Stationary Phase for High-Performance Liquid Chromatography. Anal. Sci. 2004, 20, 561–564. DOI: https://doi.org/10.2116/analsci.20.561.
- Erdemir, S.; Yilmaz, M. Preparation of a New 1,3-Alternate-Calix[4]Arene-Bonded HPLC Stationary Phase for the Separation of Phenols, Aromatic Amines and Drugs. Talanta 2010, 82, 1240–1246. DOI: https://doi.org/10.1016/j.talanta.2010.06.063.
- Glennon, J. D.; O′Connor, K.; Srijaranai, S.; Manley, K.; Harris, S. J.; McKervey, M. A. Enhanced Chromatographic Selectivity for Na + Ions on a Calixarene-Bonded Silica Phase. Anal. Lett. 1993, 26, 153–162. DOI: https://doi.org/10.1080/00032719308016803.
- Brindle, R.; Albert, K.; Harris, S. J.; Tröltzsch, C.; Horne, E.; Glennon, J. D. Silica-Bonded Calixarenes in Chromatography. J. Chromatogr. A 1996, 731, 41–46. DOI: https://doi.org/10.1016/0021-9673(95)01079-3.
- Glennon, J. D.; Horne, E.; Hall, K.; Cocker, D.; Kuhn, A.; Harris, S. J.; McKervey, M. A. Silica-Bonded Calixarenes in Chromatography. J. Chromatogr. A 1996, 731, 47–55. DOI: https://doi.org/10.1016/0021-9673(95)01080-7.
- Friebe, S.; Gebauer, S.; Krauss, G. J.; Goermar, G.; Krueger, J. HPLC on Calixarene Bonded Silica Gels. I. Characterization and Applications of the p-Tert-Butyl-Calix[4]Arene Bonded Material. J. Chromatogr. Sci. 1995, 33, 281–284. DOI: https://doi.org/10.1093/chromsci/33.6.281.
- Gebauer, S.; Friebe, S.; Gubitz, G.; Krauss, G.-J. High Performance Liquid Chromatography on Calixarene-Bonded Silica Gels. II. Separations of Regio-and Stereoisomers on p-Tert-Butylcalix[n]Arene Phases. J. Chromatogr. Sci. 1998, 36, 383–387. DOI: https://doi.org/10.1093/chromsci/36.8.383.
- Śliwka-Kaszyńska, M.; Jaszczołt, K.; Kołodziejczyk, A.; Rachoń, J. 1,3-Alternate 25,27-Dibenzoiloxy-26,28-Bis-[3-Propyloxy]-Calix[4]Arene-Bonded Silica Gel as a New Type of HPLC Stationary Phase. Talanta 2006, 68, 1560–1566. https://doi.org/10.1016/j.talanta.2005.08.014.
- Zadmard, R.; Tabar-Heydar, K.; Imani, M. Separation of Amino Acids by High Performance Liquid Chromatography Based on Calixarene-Bonded Stationary Phases. J. Chromatogr. Sci. 2015, 53, 702–707. DOI: https://doi.org/10.1093/chromsci/bmu107.
- Sliwka-Kaszynska, M.; Karaszewski, S. Preparation and HPLC Evaluation of a New1,3-Alternate25,27-Bis-[p-Chlorobenzyloxy]-26,28-Bis-[3-Propyloxy]-Calix[4]Arene Silica Bonded Stationary Phase. J. Sep. Sci. 2008, 31, 926–934. DOI: https://doi.org/10.1002/jssc.200700504.
- Taghvaei-Ganjali, S.; Zadmard, R.; Saber-Tehrani, M. Immobilization of Chlorosulfonyl-Calix[4]Arene onto the Surface of Silica Gel through the Directly Estrification. Appl. Surf. Sci. 2012, 258, 5925–5932. DOI: https://doi.org/10.1016/j.apsusc.2011.09.019.
- Barc, M.; Sliwka-Kaszyńska, M. Preparation and Evaluation of 1,3-Alternate 25,27-Bis-(Pentafluorobenzyloxy)-26,28-Bis-(3-Propyloxy)-Calix[4]Arene-Bonded Silica Gel High Performance Liquid Chromatography Stationary Phase. J. Chromatogr. A 2009, 1216, 3954–3960. DOI: https://doi.org/10.1016/j.chroma.2009.03.008.
- Zhang, W.; Zhang, Y.; Zhang, Y.; Lan, C.; Miao, Y.; Deng, Z.; Ba, X.; Zhao, W.; Zhang, S. Tetra-Proline Modified Calix[4]Arene Bonded Silica Gel: A Novel Stationary Phase for Hydrophilic Interaction Liquid Chromatography. Talanta 2019, 193, 56–63. DOI: https://doi.org/10.1016/j.talanta.2018.09.083.
- Yaghoubnejad, S.; Tabar Heydar, K.; Ahmadi, S. H.; Zadmard, R. Preparation and Evaluation of a Chiral HPLC Stationary Phase Based on Cone Calix[4]Arene Functionalized at the Upper Rim with L-Alanine Units. Biomed. Chromatogr. 2018, 32, e4122. DOI: https://doi.org/10.1002/bmc.4122.
- Jaszczołt, K.; Śliwka-Kaszyńska, M. Preparation and Evaluation of 1,3-Alternate 25,27-Bis-[p-Nitrobenzyloxy]-26,28-Bis-[3-Propyloxy]-Calix[4]Arene-Bonded Silica Gel Stationary Phase for LC. Chroma. 2007, 66, 837–845. DOI: https://doi.org/10.1365/s10337-007-0419-z.
- Thamarai Chelvi, S. K.; Yong, E. L.; Gong, Y. Preparation and Evaluation of Calix[4]Arene-Capped β-Cyclodextrin-Bonded Silica Particles as Chiral Stationary Phase for High-Performance Liquid Chromatography. J. Chromatogr. A 2008, 1203, 54–58. DOI: https://doi.org/10.1016/j.chroma.2008.07.021.
- Chelvi, S. K. T.; Zhao, J.; Chen, L.; Yan, S.; Yin, X.; Sun, J.; Yong, E. L.; Wei, Q.; Gong, Y. Preparation and Characterization of 4-Isopropylcalix[4]Arene-Capped (3-(2-O-β-Cyclodextrin)-2-Hydroxypropoxy)-Propylsilyl-Appended Silica Particles as Chiral Stationary Phase for High-Performance Liquid Chromatography. J. Chromatogr. A 2014, 1324, 104–108. DOI: https://doi.org/10.1016/j.chroma.2013.11.025.
- Lu, J.; Zhang, W.; Zhang, Y.; Zhao, W.; Hu, K.; Yu, A.; Liu, P.; Wu, Y.; Zhang, S. A New Stationary Phase for High Performance Liquid Chromatography: Calix[4]Arene Derivatized Chitosan Bonded Silica Gel. J. Chromatogr. A 2014, 1350, 61–67. DOI: https://doi.org/10.1016/j.chroma.2014.05.021.
- Yaghoubnejad, S.; Tabar Heydar, K.; Ahmadi, S. H.; Zadmard, R.; Ghonouei, N. Preparation and Evaluation of a Deoxycholic-Calix[4]Arene Hybrid-Type Receptor as a Chiral Stationary Phase for HPLC. J. Sep. Sci. 2018, 41, 1903–1912. DOI: https://doi.org/10.1002/jssc.201701348.
- Hu, K.; Yu, A.; Zhang, J.; Wen, F.; Liang, S.; Zhao, X.; Ye, B.; Wu, Y.; Zhang, S. Development of Three End-Capped Para-Benzoyl Calix[4,6, or 8]Arene Bonded Stationary Phases for HPLC. J. Chromatogr. Sci. 2012, 50, 123–130. DOI: https://doi.org/10.1093/chromsci/bmr041.
- Zhao, W.; Hu, K.; Wang, C.; Liang, S.; Niu, B.; He, L.; Lu, K.; Ye, B.; Zhang, S. New Oxo-Bridged Calix[2]Arene[2]Triazine Stationary Phase for High Performance Liquid Chromatography. J. Chromatogr. A 2012, 1223, 72–78. DOI: https://doi.org/10.1016/j.chroma.2011.12.031.
- Zhao, W.; Wang, W.; Chang, H.; Cui, S.; Hu, K.; He, L.; Lu, K.; Liu, J.; Wu, Y.; Qian, J.; Zhang, S. Tetraazacalix[2]Arene[2]Triazine Modified Silica Gel: A Novel Multi-Interaction Stationary Phase for Mixed-Mode Chromatography. J. Chromatogr. A 2012, 1251, 74–81. DOI: https://doi.org/10.1016/j.chroma.2012.06.030.
- Sokoliess, T.; Schönherr, J.; Menyes, U.; Roth, U.; Jira, T. Characterization of Calixarene- and Resorcinarene-Bonded Stationary Phases. J. Chromatogr. A 2003, 1021, 71–82. DOI: https://doi.org/10.1016/j.chroma.2003.09.014.
- Tan, H. M.; Soh, S. F.; Zhao, J.; Yong, E. L.; Gong, Y. Preparation and Application of Methylcalix[4]Resorcinarene-Bonded Silica Particles as Chiral Stationary Phase in High-Performance Liquid Chromatography. Chirality 2011, 23, E91–E97. DOI: https://doi.org/10.1002/chir.20983.
- Ma, M.; Wei, Q.; Meng, M.; Yin, J.; Shan, Y.; Du, L.; Zhu, X.; Soh, S. F.; Min, M.; Zhou, X.; et al. Preparation and Application of Aza-15-Crown-5-Capped Methylcalix[4]Resorcinarene-Bonded Silica Particles for Use as Chiral Stationary Phase in HPLC. Chromatographia 2017, 80, 1007–1014. DOI: https://doi.org/10.1007/s10337-017-3312-4.
- Shinbo, T.; Shimabukuro, Y.; Kanamori, T.; Iwatsubo, T.; Nagawa, Y.; Hiratani, K. Separation of Aromatic Isomers on Cyclophane-Bonded Stationary Phases. J. Chromatogr. A 2000, 877, 61–69. DOI: https://doi.org/10.1016/S0021-9673(00)00159-X.
- He, L.; Zhang, J.; Sun, Y.; Liu, J.; Jiang, X.; Qu, L. A Multiple-Function Stationary Phase Based on Perhydro-26-Membered Hexaazamacrocycle for High-Performance Liquid Chromatography. J. Chromatogr. A 2010, 1217, 5971–5977. DOI: https://doi.org/10.1016/j.chroma.2010.07.064.
- He, L.; Zhang, M.; Zhao, W.; Liu, J.; Jiang, X.; Zhang, S.; Qu, L. A New 14-Membered Tetraazamacrocycle-Bonded Silica Stationary Phase for Reversed-Phase High-Performance Liquid Chromatography. Talanta 2012, 89, 433–440. DOI: https://doi.org/10.1016/j.talanta.2011.12.057.
- Zhao, W.; Liu, L.; Jia, Y.; Yuan, H.; Pan, L.; He, L.; Xiang, G.; Jiang, X.; Zhang, S. Investigation of the Retention Characteristics of a 26-Membered Aromatic-Aliphatic Azamacrocycle Bonded Silica Gel Stationary Phase for High Performance Liquid Chromatography. New J. Chem. 2018, 42, 1682–1689. DOI: https://doi.org/10.1039/C7NJ03648E.
- He, L.; Zhang, M.; Liu, L.; Jiang, X.; Mao, P.; Qu, L. Two New Azamacrocycle-Based Stationary Phases for High-Performance Liquid Chromatography: Preparation and Comparative Evaluation. J. Chromatogr. A 2012, 1270, 186–193. DOI: https://doi.org/10.1016/j.chroma.2012.11.007.
- Chen, X.; Yamamoto, C.; Okamoto, Y. Polysaccharide Derivatives as Useful Chiral Stationary Phases in High-Performance Liquid Chromatography. Pure App. Chem. 2007, 79, 1561–1573. DOI: https://doi.org/10.1351/pac200779091561.
- Ali, I.; Saleem, K.; Hussain, I.; Gaitonde, V. D.; Aboul‐Enein, H. Y. Polysaccharides Chiral Stationary Phases in Liquid Chromatography. Sep. Purif. Rev. 2009, 38, 97–147. DOI: https://doi.org/10.1080/15422110802589916.
- Chankvetadze, B. Recent Developments on Polysaccharide-Based Chiral Stationary Phases for Liquid-Phase Separation of Enantiomers. J. Chromatogr. A 2012, 1269, 26–51. DOI: https://doi.org/10.1016/j.chroma.2012.10.033.
- Ikai, T.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Immobilized Polysaccharide-Based Chiral Stationary Phases for HPLC. Polym. J. 2006, 38, 91–108. DOI: https://doi.org/10.1295/polymj.38.91.
- Ribeiro, J.; Tiritan, M.; Pinto, M.; Fernandes, C. Chiral Stationary Phases for Liquid Chromatography Based on Chitin- and Chitosan-Derived Marine Polysaccharides. Symmetry 2017, 9, 190. DOI: https://doi.org/10.3390/sym9090190.
- Francotte, E.; Huynh, D.; Zhang, T. Photochemically Immobilized 4-Methylbenzoyl Cellulose as a Powerful Chiral Stationary Phase for Enantioselective Chromatography. Molecules 2016, 21, 1740. DOI: https://doi.org/10.3390/molecules21121740.
- Guo, Y.; Gaiki, S. Retention and Selectivity of Stationary Phases for Hydrophilic Interaction Chromatography. J. Chromatogr. A 2011, 1218, 5920–5938. DOI: https://doi.org/10.1016/j.chroma.2011.06.052.
- Qiao, L.; Shi, X.; Xu, G. Recent Advances in Development and Characterization of Stationary Phases for Hydrophilic Interaction Chromatography. Trends Anal. Chem. 2016, 81, 23–33. DOI: https://doi.org/10.1016/j.trac.2016.03.021.
- Kawaguchi, Y.; Tanaka, M.; Nakae, M.; Funazo, K.; Shono, T. Chemically Bonded Cyclodextrin Stationary Phases for Liquid Chromatographic Separation of Aromatic Compounds. Anal. Chem. 1983, 55, 1852–1857. DOI: https://doi.org/10.1021/ac00262a005.
- Xiao, Y.; Ng, S.-C.; Tan, T. T. Y.; Wang, Y. Recent Development of Cyclodextrin Chiral Stationary Phases and Their Applications in Chromatography. J. Chromatogr. A 2012, 1269, 52–68. DOI: https://doi.org/10.1016/j.chroma.2012.08.049.
- Fujimura, K.; Ueda, T.; Ando, T. Retention Behavior of Some Aromatic Compounds on Chemically Bonded Cyclodextrin Silica Stationary Phase in Liquid Chromatography. Anal. Chem. 1983, 55, 446–450. DOI: https://doi.org/10.1021/ac00254a009.
- Fujimura, K.; Suzuki, S.; Hayashi, K.; Masuda, S. Retention Behavior and Chiral Recognition Mechanism of Several Cyclodextrin-Bonded Stationary Phases for Dansyl Amino Acids. Anal. Chem. 1990, 62, 2198–2205. DOI: https://doi.org/10.1021/ac00219a009.
- Zhong, Q.; He, L.; Beesley, T. E.; Trahanovsky, W. S.; Sun, P.; Wang, C.; Armstrong, D. W. Optimization of the Synthesis of 2,6-Dinitro-4-Trifluoromethylphenyl Ether Substituted Cyclodextrin Bonded Chiral Stationary Phases. Chroma. 2006, 64, 147–155. DOI: https://doi.org/10.1365/s10337-006-0014-8.
- Wang, Y.; Chen, H.; Xiao, Y.; Ng, C. H.; Oh, T. S.; Tan, T. T. Y.; Ng, S. C. Preparation of Cyclodextrin Chiral Stationary Phases by Organic Soluble Catalytic “Click” Chemistry. Nat. Protoc. 2011, 6, 935–942. DOI: https://doi.org/10.1038/nprot.2011.340.
- Wang, Y.; Ong, T.-T.; Li, L.-S.; Tan, T. T. Y.; Ng, S.-C. Enantioseparation of a Novel “Click” Chemistry Derived Native β-Cyclodextrin Chiral Stationary Phase for High-Performance Liquid Chromatography. J. Chromatogr. A 2009, 1216, 2388–2393. DOI: https://doi.org/10.1016/j.chroma.2009.01.039.
- Armstrong, D. W.; Stalcup, A. M.; Hilton, M. L.; Duncan, J. D.; Faulkner, J. R.; Chang, S. C. Derivatized Cyclodextrins for Normal-Phase Liquid Chromatographic Separation of Enantiomers. Anal. Chem. 1990, 62, 1610–1615. DOI: https://doi.org/10.1021/ac00214a014.
- Zhong, Q.; He, L.; Beesley, T. E.; Trahanovsky, W. S.; Sun, P.; Wang, C.; Armstrong, D. W. Development of Dinitrophenylated Cyclodextrin Derivatives for Enhanced Enantiomeric Separations by High-Performance Liquid Chromatography. J. Chromatogr. A 2006, 1115, 19–45. DOI: https://doi.org/10.1016/j.chroma.2006.02.065.
- Lin, C.; Luo, W.; Zhang, S.; Zhang, Z.; Zhang, W.; Zheng, S.; Fan, J.; Li, W.; Qin, Q.; Guo, Z. Phenylcarbamoylated β-CD: π-Acidic and π-Basic Chiral Selectors for HPLC. J. Sep. Sci. 2010, 33, 1558–1562. DOI: https://doi.org/10.1002/jssc.200900826.
- Si-Ahmed, K.; Tazerouti, F.; Badjah-Hadj-Ahmed, A. Y. Preparation and Enantioseparation Characteristics of Three Chiral Stationary Phases Based on Modified β-Cyclodextrin for Liquid Chromatography. Anal. Bioanal. Chem. 2009, 395, 507–518. DOI: https://doi.org/10.1007/s00216-009-2972-9.
- Fan, Q.; Zhang, K.; Tian, L.; Fan, J.; Zheng, S.; Zhang, W.-G. Preparation and Enantioseparation of a New Click Derived β-Cyclodextrin Chiral Stationary Phase. J. Chromatogr. Sci. 2014, 52, 453–459. DOI: https://doi.org/10.1093/chromsci/bmt060.
- Zhou, J.; Pei, W.; Zheng, X.; Zhao, S.; Zhang, Z. Preparation and Enantioseparation Characteristics of a Novel β-Cyclodextrin Derivative Chiral Stationary Phase in High-Performance Liquid Chromatography. J. Chromatogr. Sci. 2015, 53, 676–679. DOI: https://doi.org/10.1093/chromsci/bmu099.
- Tang, J.; Zhang, S.; Lin, Y.; Zhou, J.; Pang, L.; Nie, X.; Zhou, B.; Tang, W. Engineering Cyclodextrin Clicked Chiral Stationary Phase for High-Efficiency Enantiomer Separation. Sci. Rep. 2015. DOI: https://doi.org/10.1038/srep11523.
- Zhou, Z.-M.; Li, X.; Chen, X.-P.; Fang, M.; Dong, X. Separation Performance and Recognition Mechanism of Mono(6-Deoxy-Imino)-β-Cyclodextrins Chiral Stationary Phases in High-Performance Liquid Chromatography. Talanta 2010, 82, 775–784. DOI: https://doi.org/10.1016/j.talanta.2010.05.052.
- Zhao, B.; Li, L.; Wang, Y.; Zhou, Z. Preparation of Polar Group Derivative β-Cyclodextrin Bonded Hydride Silica Chiral Stationary Phases and Their Chromatography Separation Performances. Chinese Chem. Lett. 2019, 30, 643–649. DOI: https://doi.org/10.1016/j.cclet.2018.10.013.
- Zhang, M.; Mallik, A. K.; Takafuji, M.; Ihara, H.; Qiu, H. Versatile Ligands for High-Performance Liquid Chromatography: An Overview of Ionic Liquid-Functionalized Stationary Phases. Anal. Chim. Acta. 2015, 887, 1–16. DOI: https://doi.org/10.1016/j.aca.2015.04.022.
- Rahim, N. Y.; Tay, K. S.; Mohamad, S. Chromatographic and Spectroscopic Studies on β-Cyclodextrin Functionalized Ionic Liquid as Chiral Stationary Phase: Enantioseparation of Flavonoids. Chromatographia 2016, 79, 1445–1455. DOI: https://doi.org/10.1007/s10337-016-3169-y.
- Rahim, N. Y.; Tay, K. S.; Mohamad, S. Chromatographic and Spectroscopic Studies on β-Cyclodextrin Functionalized Ionic Liquid as Chiral Stationary Phase: Enantioseparation of NSAIDs. Adsorpt. Sci. Technol. 2018, 36, 130–148. DOI: https://doi.org/10.1177/0263617416686798.
- Rahim, N. Y.; Tay, K. S.; Mohamad, S. β-Cyclodextrin Functionalized Ionic Liquid as Chiral Stationary Phase of High Performance Liquid Chromatography for Enantioseparation of β-Blockers. J. Incl. Phenom. Macrocycl. Chem. 2016, 85, 303–315. DOI: https://doi.org/10.1007/s10847-016-0629-9.
- Qiu, H.; Loukotková, L.; Sun, P.; Tesařová, E.; Bosáková, Z.; Armstrong, D. W. Cyclofructan 6 Based Stationary Phases for Hydrophilic Interaction Liquid Chromatography. J. Chromatogr. A 2011, 1218, 270–279. DOI: https://doi.org/10.1016/j.chroma.2010.11.027.
- Jiang, C.; Tong, M.-Y.; Breitbach, Z. S.; Armstrong, D. W. Synthesis and Examination of Sulfated Cyclofructans as a Novel Class of Chiral Selectors for CE. Electrophoresis 2009, 30, 3897–3909. DOI: https://doi.org/10.1002/elps.200900215.
- Kozlík, P.; Šímová, V.; Kalíková, K.; Bosáková, Z.; Armstrong, D. W.; Tesařová, E. Effect of Silica Gel Modification with Cyclofructans on Properties of Hydrophilic Interaction Liquid Chromatography Stationary Phases. J. Chromatogr. A 2012, 1257, 58–65. DOI: https://doi.org/10.1016/j.chroma.2012.08.004.
- Padivitage, N. L.; Smuts, J. P.; Breitbach, Z. S.; Armstrong, D. W.; Berthod, A. Preparation and Evaluation of HPLC Chiral Stationary Phases Based on Cationic/Basic Derivatives of Cyclofructan 6. J. Liq. Chromatogr. Rel. Technol. 2015, 38, 550–560. DOI: https://doi.org/10.1080/10826076.2014.917668.
- Wang, Y.; Wahab, M. F.; Breitbach, Z. S.; Armstrong, D. W. Carboxylated Cyclofructan 6 as a Hydrolytically Stable High Efficiency Stationary Phase for Hydrophilic Interaction Liquid Chromatography and Mixed Mode Separations. Anal. Methods 2016, 8, 6038–6045. DOI: https://doi.org/10.1039/C6AY01246A.
- Huang, H.; Jin, Y.; Xue, M.; Yu, L.; Fu, Q.; Ke, Y.; Chu, C.; Liang, X. A Novel Click Chitooligosaccharide for Hydrophilic Interaction Liquid Chromatography. Chem. Commun. 2009, 6973–6975. DOI: https://doi.org/10.1039/b911680j.
- Chen, T.; Zhu, L.; Lu, H.; Song, G.; Li, Y.; Zhou, H.; Li, P.; Zhu, W.; Xu, H.; Shao, L. Preparation and Application of Covalently Bonded Polysaccharide-Modified Stationary Phase for per Aqueous Liquid Chromatography. Anal. Chim. Acta. 2017, 964, 195–202. DOI: https://doi.org/10.1016/j.aca.2017.02.013.
- dos Santos Pereira, A.; David, F.; Vanhoenacker, G.; Sandra, P. The Acetonitrile Shortage: Is Reversed HILIC with Water an Alternative for the Analysis of Highly Polar Ionizable Solutes?. J. Sep. Sci. 2009, 32, 2001–2007. DOI: https://doi.org/10.1002/jssc.200900272.
- Ward, T. J.; Farris, A. B. III, Chiral Separations Using the Macrocyclic Antibiotics: A Review. J. Chromatogr. A 2001, 906, 73–89. DOI: https://doi.org/10.1016/S0021-9673(00)00941-9.
- Ilisz, I.; Pataj, Z.; Aranyi, A.; Péter, A. Macrocyclic Antibiotic Selectors in Direct HPLC Enantioseparations. Sep. Purif. Rev. 2012, 41, 207–249. DOI: https://doi.org/10.1080/15422119.2011.596253.
- Zhang, X.; Bao, Y.; Huang, K.; Barnett-Rundlett, K. L.; Armstrong, D. W. Evaluation of Dalbavancin as Chiral Selector for HPLC and Comparison with Teicoplanin-Based Chiral Stationary Phases. Chirality 2010, 22, 495–513. DOI: https://doi.org/10.1002/chir.20771.
- Hroboňová, K.; Lehotay, J.; Čižmárik, J. HPLC Enantioseparation of Phenylcarbamic Acid Derivatives by Using Macrocyclic Chiral Stationary Phases. Nova Biotechnol. Chim. 2016, 15, 12–22. DOI: https://doi.org/10.1515/nbec-2016-0002.
- Lämmerhofer, M.; Lindner, W. Liquid Chromatographic Enantiomer Separation and Chiral Recognition by Cinchona Alkaloid-Derived Enantioselective Separation Materials. Adv. Chromatogr. 2009, 46, 1–107.
- Ilisz, I.; Bajtai, A.; Lindner, W.; Péter, A. Liquid Chromatographic Enantiomer Separations Applying Chiral Ion-Exchangers Based on Cinchona Alkaloids. J. Pharm. Biomed. Anal. 2018, 159, 127–152. DOI: https://doi.org/10.1016/j.jpba.2018.06.045.
- Kumano, D.; Iwahana, S.; Iida, H.; Shen, C.; Crassous, J.; Yashima, E. Enantioseparation on Riboflavin Derivatives Chemically Bonded to Silica Gel as Chiral Stationary Phases for HPLC. Chirality 2015, 27, 507–517. DOI: https://doi.org/10.1002/chir.22452.
- Zhou, D.; Zeng, J.; Fu, Q.; Gao, D.; Zhang, K.; Ren, X.; Zhou, K.; Xia, Z.; Wang, L. Preparation and Evaluation of a Reversed-Phase/Hydrophilic Interaction/Ion-Exchange Mixed-Mode Chromatographic Stationary Phase Functionalized with Dopamine-Based Dendrimers. J. Chromatogr. A 2018, 1571, 165–175. DOI: https://doi.org/10.1016/j.chroma.2018.08.018.