Impregnated silica-based layers in thin layer chromatography

References

• Gocan, S. Stationary Phases for Thin-Layer Chromatography. J. Chromatogr. Sci. 2002, 40, 538–549. DOI: 10.1093/chromsci/40.10.538.
   PubMed Web of Science ®Google Scholar
• Nichols, P. L. Coördination of Silver Ion with Methyl Esters of Oleic and Elaidic Acids. J. Am. Chem. Soc. 1952, 74, 1091–1092. DOI: 10.1021/ja01124a517.
   Web of Science ®Google Scholar
• Goering, H. L.; Closson, W. D.; Olson, A. C. Transannular Interactions. III. Synthesis and Assignment of Configurations in the Cis- and Trans-5-Cyclodecen-1-yl System. J. Am. Chem. Soc. 1961, 83, 3507–3511. DOI: 10.1021/ja01477a036.
   Web of Science ®Google Scholar
• Galli, G.; Paoletti, E. G. Separation of Cholesterol-Desmosterol Acetates by Thin-Layer and Column Chromatography on Silica Gel G-Silver Nitrate. Lipids 1967, 2, 72–75. DOI: 10.1007/BF02532004.
   PubMed Web of Science ®Google Scholar
• Morris, L. J. Separations of Lipids by Silver Ion Chromatography. J. Lipid Res. 1966, 7, 717–732.
   PubMed Web of Science ®Google Scholar
• Wilson, I. D. Encyclopedia of Separation Science III/Impregnation Techniques: Thin-Layer (Planar) Chromatography; Academic Press: Cambridge, MA, 2000; pp 3065–3071.
   Google Scholar
• Williams, C. M.; Mander, L. N. Chromatography with Silver Nitrate. Tetrahedron 2001, 57, 425–447. DOI: 10.1016/S0040-4020(00)00927-3.
   Web of Science ®Google Scholar
• Jardine, I.; McQuillin, F. J. Mechanisms of Hydrogenation. Part V. The Hydrogenation of Olefinic and Acetylenic Substances. The Influence of Stereochemistry and Substitution on Chemisorption and on Chromatography. J. Chem. Soc. C. 1966, 458–462. DOI: 10.1039/j39660000458.
   Google Scholar
• Nano, G. M.; Martelli, A. The Separation of Some Pairs of Allylic-Propenylic Isomers by TLC on Silica Impregnated with Silver Nitrate. J. Chromatogr. A. 1966, 21, 349. DOI: 10.1016/S0021-9673(01)91323-8.
   Web of Science ®Google Scholar
• Nikolova-Damyanova, B.; Momchilova, S. Silver Ion Thin-Layer Chromatography of Fatty Acids. A Survey. J. Liq. Chromatogr. Rel. Technol. 2001, 24, 1447–1466. DOI: 10.1081/JLC-100103922.
   Web of Science ®Google Scholar
• Tarandjiiska, R.; Marekov, I.; Nikolova-Damyanova, B.; Amidzhin, B. Determination of Molecular Species of Triacylglycerols from Highly Unsaturated Plant Oils by Successive Application of Silver Ion and Reversed Phase TLC. J. Liq. Chromatogr. 1995, 18, 859–872. DOI: 10.1080/10826079508010397.
   Web of Science ®Google Scholar
• Momchilova, S.; Nikolova‐Damyanova, B. Quantitative TLC and Gas Chromatography Determination of the Lipid Composition of Raw and Microwaved Roasted Walnuts, Hazelnuts, and Almonds. J. Liq. Chromatogr. Rel. Technol. 2007, 30, 2267–2285. DOI: 10.1080/10826070701451647.
   Web of Science ®Google Scholar
• Nikolova-Damyanova, B.; Velikova, R.; Kuleva, L. Quantitative TLC for Determination of the Triacylglycerol Composition of Sesame Seeds. J. Liq. Chromatogr. Rel. Technol. 2002, 25, 1623–1632. DOI: 10.1081/JLC-120005709.
   Web of Science ®Google Scholar
• Nikolova-Damyanova, B.; Chobanov, D.; Dimov, S. Separation of Isomeric Triacylglycerols by Silver Ion Thin-Layer Chromatography. J. Liq. Chromatogr. 1993, 16, 3997–4008. DOI: 10.1080/10826079308019682.
   Google Scholar
• Nikolova-Damyanova, B. Quantitative Thin-Layer Chromatography of Triacylglycerols. Principles and Application. J. Liq. Chromatogr. Rel. Technol. 1999, 22, 1513–1537. DOI: 10.1081/JLC-100101748.
   Web of Science ®Google Scholar
• Wilson, R.; Sargent, J. R. High-Resolution Separation of Polyunsaturated Fatty Acids by Argentation Thin-Layer Chromatography. J. Chromatogr. 1992, 623, 403–407. DOI: 10.1016/0021-9673(92)80385-8.
   Web of Science ®Google Scholar
• Wilson, R.; Sargent, J. R. Chain Separation of Monounsaturated Fatty Acid Methyl Esters by Argentation Thin-Layer Chromatography. J. Chromatogr. A. 2001, 905, 251–257. DOI: 10.1016/S0021-9673(00)01006-2.
   PubMed Web of Science ®Google Scholar
• Kramer, J. K.; Cruz-Hernandez, C.; Deng, Z.; Zhou, J.; Jahreis, G.; Dugan, M. E. Analysis of Conjugated Linoleic Acid and Trans 18:1 Isomers in Synthetic and Animal Products. Am. J. Clin. Nutr. 2004, 79, 1137S–1145S. DOI: 10.1093/ajcn/79.6.1137S.
   PubMed Web of Science ®Google Scholar
• Fournier, V.; Juanéda, P.; Destaillats, F.; Dionisi, F.; Lambelet, P.; Sébédio, J.-L.; Berdeaux, O. Analysis of Eicosapentaenoic and Docosahexaenoic Acid Geometrical Isomers Formed during Fish Oil Deodorization. J. Chromatogr. A. 2006, 1129, 21–28. DOI: 10.1016/j.chroma.2006.06.089.
   PubMed Web of Science ®Google Scholar
• Mohammad, A.; Zehra, A. Separation of Coexisting Tryptophan, Alanine, and Phenylalanine or Tyrosine by Silver Ion High-Performance Thin-Layer Chromatography. J. Planar Chromatogr. 2008, 21, 299–304. DOI: 10.1556/JPC.21.2008.4.14.
   Web of Science ®Google Scholar
• Dillon, J. T.; Aponte, J. C.; Tsai, Y.-J.; Huang, Y. Thin Layer Chromatography in the Separation of Unsaturated Organic Compounds Using Silver-Thiolate Chromatographic Material. J. Chromatogr. A. 2012, 1251, 240–243. DOI: 10.1016/j.chroma.2012.06.042.
   PubMed Web of Science ®Google Scholar
• Nikolova-Damyanova, B.; Christie, W. W.; Herslöf, B. Mechanistic Aspects of Fatty Acid Retention in Silver Ion Chromatography. J. Chromatogr. A. 1996, 749, 47–54. DOI: 10.1016/0021-9673(96)00365-2.
   Web of Science ®Google Scholar
• Momchilova, S.; Nikolova-Damyanova, B. Stationary Phases for Silver Ion Chromatography of Lipids: Preparation and Properties. J. Sep. Sci. 2003, 26, 261–270. DOI: 10.1002/jssc.200390032.
   Web of Science ®Google Scholar
• Spraggins, R. L. Transition Metal Ion Assisted Chromatography. Separation of Prostaglandins PGA2 and PGB2. J. Org. Chem. 1973, 38, 3661–3662. DOI: 10.1021/jo00960a063.
   PubMed Web of Science ®Google Scholar
• Shapiro, D. R.; Kuwahara, S. Ferric Chloridei - Impregnated Silica Gel for Thin-Layer Chromatography of Steroids. Clin. Chem. 1973, 19, 1305–1306. DOI: 10.1093/clinchem/19.11.1305.
   PubMed Web of Science ®Google Scholar
• Flieger, J.; Szumilo, H.; Gielzak-Koćwin, K. Optimizing Modification Conditions of Silica Gel with Metal Salts. J. Liq. Chromatogr. Rel. Technol. 1999, 22, 2879–2894. DOI: 10.1081/JLC-100102065.
   Web of Science ®Google Scholar
• Bhushan, R.; Reena ; Chauhan, R. S. Separation of Some Antihistamines on Impregnated TLC Silica Plates. Biomed. Chromatogr. 1989, 3, 46–47. DOI: 10.1002/bmc.1130030112.
   PubMed Web of Science ®Google Scholar
• Srivastava, S. P.; Reena , TLC Separation of Some Common Organic Phosphorous Pesticides on Metal-Salt as Well as on Phenol-Impregnated Layers. Anal. Lett. 1982, 15, 39–46. DOI: 10.1080/00032718208064361.
   Web of Science ®Google Scholar
• Mohammad, A.; Moheman, A.; El-Desoky, G. Amino Acid and Vitamin Determinations by TLC/HPTLC: Review of the Current State. Cent. Eur. J. Chem. 2012, 10, 731–750. DOI: 10.2478/s11532-012-0019-0.
   Web of Science ®Google Scholar
• Bhushan, R.; Martens, J. Separation of Amino Acids, Their Derivatives and Enantiomers by Impregnated TLC. Biomed. Chromatogr. 2001, 15, 155–165. DOI: 10.1002/bmc.56.
   PubMed Web of Science ®Google Scholar
• Mohammad, A.; Agrawal, V.; Kumar, S. Use of a Water-in-Oil Microemulsion as Mobile Phase in Complexation TLC of Amino Acids on Silica Layers Impregnated with Metal Cations. J. Planar Chromatogr. 2003, 16, 220–226. DOI: 10.1556/JPC.16.2003.3.10.
   Web of Science ®Google Scholar
• Grygierczyk, G.; Wasilewski, J.; Witkowska, M.; Kowalska, T. Use of Complexation TLC to Investigate Selected Monosulfides. Part I. Silica Impregnated with Cu(II), Co(II), Ni(II), Mn(II), Al(III), Cr(III), and Fe(III) Cations as Stationary Phase. J. Planar Chromatogr. 2003, 16, 11–14. DOI: 10.1556/JPC.16.2003.1.2.
   Web of Science ®Google Scholar
• Grygierczyk, G.; Wasilewski, J.; Łomankiewicz, D.; Klimczok, W.; Kowalska, T. Use of Complexation TLC to Investigate Monosulfides. II. Silica Impregnated with the Cd(II), Sr(II), Eu(III), and V(IV) Cations as Stationary Phase. J. Liq. Chromatogr. Rel. Technol. 2003, 26, 2651–2661. DOI: 10.1081/JLC-120024535.
   Web of Science ®Google Scholar
• Szumiło, H.; Flieger, J. TLC Separation of Carbohydrates on Silica Gel Modified with Copper (II) Salts. Acta Pol. Pharm. 2001, 58, 3–8.
   PubMedGoogle Scholar
• Bhushan, R.; Kaur, S. TLC Separation of Some Common Sugars on Silica Gel Plates Impregnated with Transition Metal Ions. Biomed. Chromatogr. 1997, 11, 59–60. DOI: 10.1002/(SICI)1099-0801(199701)11:1<59::AID-BMC632>3.0.CO;2-Q.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Thiong'o, G. T. Separation of Cephalosporins on Thin Silica Gel Layers Impregnated with Transition Metal Ions and by Reversed-Phase TLC. Biomed. Chromatogr. 2002, 16, 165–174. DOI: 10.1002/bmc.122.
   PubMed Web of Science ®Google Scholar
• Singh, D. K.; Maheshwari, G. Chromatographic Studies of Some Cephalosporins on Thin Layers of Silica Gel G-Zinc Ferrocyanide. Biomed. Chromatogr. 2010, 24, 1084–1088. DOI: 10.1002/bmc.1408.
   PubMed Web of Science ®Google Scholar
• Singh, D. K.; Maheshwari, G. Chromatographic Separation Studies of Penicillins, Cephalosporins and Carbapenems on Transition-Metal Silicate Modified Silica Layers. Anal. Sci. 2012, 28, 823–826. DOI: 10.2116/analsci.28.823.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Parshad, V. Improved Separation of Vitamin B Complex and Folic Acid Using Some New Solvent Systems and Impregnated TLC. J. Liq. Chromatogr. Rel. Technol. 1999, 22, 1607–1623. DOI: 10.1081/JLC-100101756.
   Web of Science ®Google Scholar
• Bhushan, R.; Parshad, V. Separation of Vitamin B Complex and Folic Acid Using TLC Plates Impregnated with Some Transition Metal Ions. Biomed. Chromatogr. 1994, 8, 196–198. DOI: 10.1002/bmc.1130080411.
   PubMed Web of Science ®Google Scholar
• Singh, D. K.; Srivastava, B.; Sahu, A. Thin Layer Chromatography of Purines on Silica Gel G Impregnated with Transition Metal Ions; Assay of Caffeine and Theophylline in Pharmaceutical Formulations. J. Chin. Chem. Soc. 2003, 50, 1031–1036. DOI: 10.1002/jccs.200300145.
   Web of Science ®Google Scholar
• Mezzetti, T.; Lato, M.; Rufini, S.; Ciuffini, G. Thin-Layer Chromatography of Oligosaccharides with Tungstic or Molybdic Acid as Impregnant. J. Chromatogr. 1971, 63, 329–342. DOI: 10.1016/S0021-9673(01)85646-6.
   Web of Science ®Google Scholar
• Ranganathan, T.; Kulkarni, P. R. A Simple Method for the Analysis of Trehalose Using HPTLC. Food Chem. 2002, 77, 263–265. DOI: 10.1016/S0308-8146(01)00324-7.
   Web of Science ®Google Scholar
• Jagannathan, S.; Vijayakumar, R.; Rahul Ghandhi, P.; Ananthi, M.; Chandra, C.; Premkumar, A.; Venkataramana, K. N. Analysis of Carbohydrates in Newly Developed Liquid State Rabies Vaccine. J. Microbial. Biochem. Technol. 2010, 02, 147–151. DOI: 10.4172/1948-5948.1000040.
   Google Scholar
• Panahi, H.; Rahimi, A.; Moniri, E.; Izadi, A.; Parvin, M. HPTLC Separation and Quantitative Analysis of Aspirin, Salicylic Acid, and Sulfosalicylic Acid. J. Planar Chromatogr. 2010, 23, 137–140. DOI: 10.1556/JPC.23.2010.2.10.
   Web of Science ®Google Scholar
• Panahi, H. A.; Kalal, H. S.; Rahimi, A. Separation of Vitamin B2 and B12 by Impregnate HPTLC Plates with Boric Acid. World Acad. Sci. Eng. Technol. 2008, 18, 193–195.
   Google Scholar
• Nezhati, M. N.; Panahi, H. A.; Ahmadian, M. Design and Synthesis of Bis(2-Hydroxy-4-Allyl)m-Phenylbenzamide as a Neutral Host and Its Complexation with Electrophilic Metal Cations. Middle-East J. Sci. Res. 2014, 19, 134–138.
   Google Scholar
• Pletnev, I. V.; Morosanova, E. I.; Zolotov, Y. A. Use of Mixed Stationary Phases for the Separation of Metal Ions. Anal. Sci. 1990, 6, 863–866. DOI: 10.2116/analsci.6.863.
   Web of Science ®Google Scholar
• Dutt Sharma, S.; Sharma, C. Reversed-Phase Thin-Layer Chromatography of Inorganic Anions on Tri-n-Butyl Amine Impregnated Silica Gel-G Layers: Separation of Coexisting I−, IO3− and IO4−, Fe(CN)64− and Fe(CN)43−. J. Planar Chromatogr. 2019, 32, 265–271. DOI: 10.1556/1006.2019.32.4.1.
   Google Scholar
• Sharma, S. D.; Sharma, C. Retention Behavior of Metal Ions on Tri-n-Butyl Phosphate and Tri-n-Butyl Amine-Impregnated Silica Gel G Layers: Quantitative Separation of Lead from Other Metal Ions and Synthetic Alloys. J. Planar Chromatogr. 2019, 32, 157–163. DOI: 10.1556/1006.2019.32.2.12.
   Web of Science ®Google Scholar
• Sharma, S. D.; Sharma, C.; Bhardwaj, R. Sorption Behavior of Metal Ions on Thiourea-Impregnated Silica Gel G and Alumina Stationary Phases in Aqueous HCl and Acetone—HCl Media: Quantitative Separation of Pb2+ and Hg2+ from Other Metal Ions. J. Planar Chromatogr. 2016, 29, 435–445. DOI: 10.1556/1006.2016.29.6.6.
   Web of Science ®Google Scholar
• Srivastava, S. P.; Gupta, V. K. Chromatographic Separation of Some Metal Ions on NTA-Impregnated Thin-Layer Plates. Chromatographia 1979, 12, 496–497. DOI: 10.1007/BF02302998.
   Web of Science ®Google Scholar
• Allan, D.; Cockcroft, S. A Modified Procedure for Thin-Layer Chromatography of Phospholipids. J. Lipid Res. 1982, 23, 1373–1374.
   PubMed Web of Science ®Google Scholar
• Becic, E.; Imamovic, B.; Dedic, M.; Sober, M. SPE Extraction and TLC Identification of Tetracycline and Fluoroquinolone in Surface Water. Bull. Chem. Technol. Bosnia Herzegovina. 2014, 43, 35–40.
   Google Scholar
• Bladek, J.; Neffe, S. Application of Thin‐Layer Chromatography in Clinical Chemistry. Sep. Purif. Rev. 2003, 32, 63–122. DOI: 10.1081/SPM-120025026.
   Web of Science ®Google Scholar
• Novakovic, J.; Nesmerak, K. Encyclopedia of Separation Science III/Sterols/Thin-Layer (Planar) Chromatography. Academic Press: Cambridge, MA, 2000; pp 4255–4261.
   Google Scholar
• Copius Peereboom, J. W.; Beekes, H. W. The Analysis of Mixtures of Animal and Vegetable Fats. J. Chromatogr 1962, 9, 316–320. DOI: 10.1016/S0021-9673(00)80791-8.
   Web of Science ®Google Scholar
• Grygierczyk, G. Chromatographic Analysis of Organic Compounds on Impregnated Chemically Bonded Stationary Phases. Acta Chromatogr. 2006, 17, 302–313.
   Web of Science ®Google Scholar
• Mohammad, A.; Gupta, R. Identification and Separation of Cationic and Non-Ionic Surfactants by Reversed Phase Thin Layer Chromatography. Ind. J. Chem. Technol. 2008, 15, 271–276.
   Web of Science ®Google Scholar
• Mohamad, A.; Sharma, S.; Bhawani, S. A. Reversed Phase Thin Layer Chromatography of Five Co-Administered Drugs with Surfactant Modified Solvent System. Ind. J. Chem. Technol. 2009,16, 344–350.
   Web of Science ®Google Scholar
• Abere, T. A.; Okeri, H. A.; Okafor, L. A. Comparative Evaluation of Selected Starches as Adsorbent for Thin-Layer Chromatography. Tropical J. Pharm. Res. 2007, 4, 331–339.
   Google Scholar
• Misra, A. K. Retention Behaviour of Synthetic Dyes on Coconut Oil Impregnated Egg Shell Layers in Pure and Mixed Solvent Systems. Ind. J. Chem. Technol. 2007, 14, 407–411.
   Web of Science ®Google Scholar
• Oros, G.; Cserháti, T. Relationship between the Calculated Physicochemical Parameters and Reversed Phase Thin-Layer Chromatographic Retention Behavior of Carboxamide Fungicides and Related Compounds. J. Liq. Chromatogr. Rel. Technol. 2010, 33, 880–893. DOI: 10.1080/10826071003766252.
   Web of Science ®Google Scholar
• Briciu, R. D.; Sârbu, C. Comparative Evaluation of Vegetable Oils-Impregnated Layers as Reversed-Phases for Thin-Layer Chromatography. J. Am. Oil Chem. Soc. 2010, 87, 1091–1102. DOI: 10.1007/s11746-010-1590-1.
   Web of Science ®Google Scholar
• Sârbu, C.; Briciu, R. D. Lipophilicity of Natural Sweeteners Estimated on Various Oils and Fats Impregnated Thin-Layer Chromatography Plates. J. Liq. Chromatogr. Rel. Technol. 2010, 33, 903–921. DOI: 10.1080/10826071003766021.
   Web of Science ®Google Scholar
• Briciu, R. D.; Sârbu, C. Lipophilicity of Flavonoids Estimated by Reversed-Phase High Performance Thin-Layer Chromatography: Chemically Bonded Plates vs. Impregnated Plates with Oils, Animal, and Human Fats. Sep. Sci. Technol. 2010, 45, 1275–1285. DOI: 10.1080/01496391003775907.
   Web of Science ®Google Scholar
• Perišić-Janjić, N.; Djaković-Sekulić, T.; Ušćumlić, G. Normal- and Reversed-Phase TLC of N-Phenylsuccinimide Derivatives. J. Planar Chromatogr. 2002, 15, 294–298. DOI: 10.1556/JPC.15.2002.4.10.
   Web of Science ®Google Scholar
• Mohammad, A.; Khatoon, S. Chromatographic Behavior of Cationic and Nonionic Surfactants on Silica Gel Impregnated with Paraffin Oil Using Aqueous Formamide Mobile Phase Systems. Acta Chim. Slov. 2009, 56, 997–1002.
   Web of Science ®Google Scholar
• Csermely, T.; Petroianu, G.; Kuca, K.; Fűrész, J.; Darvas, F.; Gulyás, Z.; Laufer, R.; Kalász, H. TLC of Quaternary Pyridinium Aldoximes, Antidotes of Organophosphorus Esterase Inhibitors. J. Planar Chromatogr. 2007, 20, 39–42. DOI: 10.1556/JPC.20.2007.1.5.
   Web of Science ®Google Scholar
• Djaković-Sekulić, T.; Sârbu, C.; Perišić-Janjić, N. A Comparative Study of the Lipophilicity of Benzimidazole and Benztriazole Derivatives by RPTLC. J. Planar Chromatogr. 2005, 18, 432–436. DOI: 10.1556/JPC.18.2005.6.6.
   Web of Science ®Google Scholar
• Pyka, A.; Babuśka, M.; Śliwiok, J. Use of Liquid Chromatography and Theoretical Computational Methods to Compare the Lipophilicity of Selected Cortisone Derivatives. J. Planar Chromatogr. 2006, 19, 432–437. DOI: 10.1556/JPC.19.2006.6.5.
   Web of Science ®Google Scholar
• Perišić-Janjić, N.; Djaković-Sekulić, T. Study of the Characteristics and Separation Properties of Unconventional TLC Supports. Part I. J. Planar Chromatogr. 2006, 19, 438–442. DOI: 10.1556/JPC.19.2006.6.6.
   Web of Science ®Google Scholar
• Djaković-Sekulić, T.; Perišić-Janjić, N. Study of the Characteristics and Separating Power of Unconventional TLC Supports. II. Principal-Components Analysis. J. Planar Chromatogr. 2007, 20, 7–11. DOI: 10.1556/JPC.20.2007.1.1.
   Web of Science ®Google Scholar
• Casoni, D.; Sârbu, C. The Lipophilicity of Parabens Estimated on Reverse Phases Chemically Bonded and Oil-Impregnated Plates and Calculated Using Different Computation Methods. J. Sep. Sci. 2009, 32, 2377–2384. DOI: 10.1002/jssc.200900037.
   PubMed Web of Science ®Google Scholar
• Livaja-Popovic, D.; Loncar, E.; Jevric, L.; Malbasa, R. Reversed-Phase Thin-Layer Chromatography Behavior of Aldopentose Derivatives. Hem. Ind. 2012, 66, 365–372. DOI: 10.2298/HEMIND111012099L.
   Web of Science ®Google Scholar
• Polak, B.; Traczuk, A.; Misztal, S. Separation of 9-Fluorenylmethyloxycarbonyl Amino Acid Derivatives in Micellar Systems of High-Performance Thin-Layer Chromatography and Pressurized Planar Electrochromatography. Sci. Reports. 2019, 9, 17103.
   PubMed Web of Science ®Google Scholar
• Kresta, J.; Kastner, P.; Klimeš, J.; Klimešová, V. Reversed-Phase Thin-Layer Chromatographic Determination of the Lipophilicity of Potential Antituberculotic Compounds. J. Planar Chromatogr. 2005, 18, 450–454. DOI: 10.1556/JPC.18.2005.6.9.
   Web of Science ®Google Scholar
• Mrkvičková, Z.; Kovaříková, P.; Klimeš, J.; Doležal, M. Determination of the Lipophilicity of Potential Antituberculotic Compounds by RP-TLC. J. Planar Chromatogr. 2006, 19, 422–426. DOI: 10.1556/JPC.19.2006.6.3.
   Web of Science ®Google Scholar
• Sharma, S. D.; Sharma, H.; Sharma, S. C. Retention Behavior of Amino Acids on Plain, Tri-n-Butylphosphate and Tri-n-Butylamine Impregnated Silica Gel-G Layers in Mixed Mobile Phases. J. Ind. Chem. Soc. 2002, 79, 743–746.
   Web of Science ®Google Scholar
• Pyka, A. New Method of Calculation of the Partition Coefficients of Selected Alkoxyphenols Investigated by RPTLC. J. Planar Chromatogr. 2004, 17, 58–60. DOI: 10.1556/JPC.17.2004.1.13.
   Web of Science ®Google Scholar
• Lepri, L.; Desideri, P. G.; Heimler, D. Soap Thin-Layer Chromatography of Some Primary Aliphatic Amines. J. Chromatogr. A. 1978, 153, 77–82. DOI: 10.1016/S0021-9673(00)89857-X.
   Web of Science ®Google Scholar
• Lepri, L.; Desideri, P. G., Heimler, D. Soap Thin-Layer Chromatography of Primary Aromatic Amines. J. Chromatogr. A. 1978, 155, 119–127. DOI: 10.1016/S0021-9673(00)83942-4.
   Web of Science ®Google Scholar
• Armstrong, D. W.; Terrill, R. Q. Thin Layer Chromatographic Separation of Pesticides, Decachlorobiphenyl, and Nucleosides with Micellar Solutions. Anal. Chem. 1979, 51, 2160–2163. DOI: 10.1021/ac50049a025.
   Web of Science ®Google Scholar
• Armstrong, D. W.; McNeely, M. Use of Micelles in the TLC Separation of Polynuclear Aromatic Compounds and Amino Acids. Anal. Lett. 1979, 12, 1285–1291. DOI: 10.1080/00032717908067919.
   Web of Science ®Google Scholar
• Armstrong, D. W.; Bui, K. H. Use of Aqueous Micellar Mobile Phases in Reverse Phase TLC. J. Liq. Chromatogr. 1982, 5, 1043–1050. DOI: 10.1080/01483918208067567.
   Web of Science ®Google Scholar
• Sumina, E. G.; Shtykov, S. N.; Tyurina, N. V. Surfactants in Thin Layer Chromatography. J. Anal. Chem. 2003, 58, 720–730. DOI: 10.1023/A:1025027409149.
   Web of Science ®Google Scholar
• Shtykov, S. N.; Sumina, E. G.; Smushkina, E. V.; Tyurina, N. V. Dynamic and Static Modifications of Stationary Phases with Surfactants in TLC: A Comparative Study. J. Planar Chromatogr. 2000, 13, 182–186.
   Web of Science ®Google Scholar
• Kovács-Hadady, K. A Systematic Study of the Desorption of Different Ion-Pairing Reagents on Reversed Phase Thin-Layers. Chromatographia. 1997, 45, 81–90. DOI: 10.1007/BF02505542.
   Web of Science ®Google Scholar
• Lukács, M.; Barcsa, G.; Kovács-Hadady, K. The Effects of PH, Ionic Strength and Buffer Concentration of Mobile Phase on RF of Acidic Compounds in Ion-Pair TLC. Chromatographia. 1998, 48, 511–516. DOI: 10.1007/BF02466642.
   Web of Science ®Google Scholar
• Lepri, L.; Desideri, P. G.; Heimler, D. Thin-Layer Chromatography of Amino Acids and Dipeptides on RP-2, RP-8 and RP-18 Plates Impregnated with Dodecylbenzenesulphonic Acid. J. Chromatogr. 1981, 209, 312–315. DOI: 10.1016/S0021-9673(00)81595-2.
   Web of Science ®Google Scholar
• Sherma, J.; Sleckman, B. P.; Armstrong, D. W. Chromatography of Amino Acids on Reversed Phase Thin Layer Plates. J. Liq. Chromatogr. 1983, 6, 95–108. DOI: 10.1080/01483918308066873.
   Web of Science ®Google Scholar
• Mohammad, A.; Zehra, A. A New TLC System for Specific Separation of L-Arginine from Other Non Essential Amino Acids. Acta Univ. Cibiniensis. Seria F Chemia. 2000, 9, 17–28.
   Google Scholar
• Mohammad, A.; Zehra, A. Surfactants Modified Silica Phase for Sorption Studies of Essential Amino Acids by Thin Layer Chromatography. Coll. Surf. A: Physicochem. Eng. Aspects. 2007, 301, 404–411. DOI: 10.1016/j.colsurfa.2007.01.004.
   Web of Science ®Google Scholar
• Mohammad, A.; Haq, N. TLC Separation of Amino Acids with a Green Mobile Phase. J. Planar Chromatogr. 2010, 23, 260–264. DOI: 10.1556/JPC.23.2010.4.4.
   Web of Science ®Google Scholar
• Mohammad, A.; Amin, A.; Moheman, A. Chromatographic Behavior and Separation of Pesticides on Thin Silica Gel Layers Impregnated with Cationic Micelles. J. Planar Chromatogr. 2012, 25, 101–107. DOI: 10.1556/JPC.25.2012.2.2.
   Web of Science ®Google Scholar
• Van Peteghem, C.; Bijl, J. Ion-Pair Extraction and Ion-Pair Adsorption Thin-Layer Chromatography for Rapid Identification of Ionic Food Dyes. J. Chromatogr. 1981, 210, 113–120. DOI: 10.1016/S0021-9673(00)91186-5.
   PubMed Web of Science ®Google Scholar
• Misra, A. K.; Gupta, U.; Langenfeld, J. J. Plain and Ion-Pair Thin-Layer Chromatography of Synthetic Dyes on an Admixture of Silica Gel G and Barium Sulfate in an Aqueous Ethanol System. J. Chromatogr. Sci. 2002, 40, 297–303. . DOI: 10.1093/chromsci/40.5.297.
   PubMed Web of Science ®Google Scholar
• Mohammad, A.; Zehra, A. Simultaneous Separation and Identification of Cyanocobalamin, Thiamine, and Ascorbic Acid on Polyoxyethylene Sorbitan Monooleate-Impregnated Silica Layers with Water as Mobile Phase. J. Planar Chromatogr. 2009, 22, 429–433. DOI: 10.1556/JPC.22.2009.6.8.
   Web of Science ®Google Scholar
• Mohammad, A.; Zehra, A. Anionic-Nonionic Surfactants Coupled Micellar Thin-Layer Chromatography: Synergistic Effect on Simultaneous Separation of Hydrophilic Vitamins. J. Chromatogr. Sci. 2010, 48, 145–149. DOI: 10.1093/chromsci/48.2.145.
   PubMed Web of Science ®Google Scholar
• Misra, A. K.; Pachauree, S.; Gupta, U. Plain and Ion Pair Thin Layer Chromatography of Some Herbicides and Related Compounds on a Mixture of Silica Gel G and Barium Sulphate in a Single Solvent System. Ind. J. Chem. Technol. 2001, 8, 408–412.
   Web of Science ®Google Scholar
• Mohammad, A.; Sharma, S.; Bhawani, S. A. Chromatographic Separation Studies of Cephalosporins on CTAB Modified Silica Layers with Different Buffer Solvent System. Int. J. ChemTech Res. 2009, 1, 591–595.
   Google Scholar
• Sumina, E. G.; Shtykov, S. N.; Dorofeeva, S. V. Ion-Pair Reversed-Phase Thin-Layer Chromatography and High-Performance Liquid Chromatography of Benzoic Acids. J. Anal. Chem. 2002, 57, 210–214.
   Web of Science ®Google Scholar
• Kovács-Hadady, K.; Szilágyi, J. Separation of Minoxidil and Its Intermediates by Overpressured Layer Chromatography Using a Stationary Phase Bonded with Tricaprylmethylammonium Chloride. J. Chromatogr. 1991, 553, 459–466. DOI: 10.1016/S0021-9673(01)88517-4.
   Web of Science ®Google Scholar
• Shalaby, A.; Khalil, H. Reversed-Phase Ion-Pair Thin Layer Chromatography of Some Alkaloids. J. Liq. Chromatogr. Rel. Technol. 1999, 22, 2345–2352. DOI: 10.1081/JLC-100101806.
   Web of Science ®Google Scholar
• Pandey, P.; Maheshwari, N.; Dave, A. Identification of Some Closely Related N-Carbamoyl-3,5-Dimethyl-4-Arylazopyrazoles by TLC. J. Liq. Chromatogr. Rel. Technol. 1991, 14, 3311–3315. DOI: 10.1080/01483919108049392.
   Web of Science ®Google Scholar
• Sobańska, A. W.; Brzezińska, E. Application of Planar and Column Micellar Liquid Chromatography to the Prediction of Physicochemical Properties and Biological Activity of Compounds. J. Liq. Chromatogr. Rel. Technol. 2019, 42, 227–237. DOI: 10.1080/10826076.2019.1585614.
   Web of Science ®Google Scholar
• Teixeira, J.; Tiritan, M. E.; Pinto, M. M. M.; Fernandes, C. Chiral Stationary Phases for Liquid Chromatography: Recent Developments. Molecules. 2019, 24, 865. DOI: 10.3390/molecules24050865.
   PubMed Web of Science ®Google Scholar
• Sajewicz, M.; Grygierczyk, G.; Gontarska, M.; Kowalska, T. Enantioseparation Of S,R‐(±)‐Ketoprofen on Plain Silica Gel Layers with Achiral Mobile Phase. J. Liq. Chromatogr. Rel. Technol. 2007, 30, 2185–2192. DOI: 10.1080/10826070701451522.
   Web of Science ®Google Scholar
• Lepri, L.; Coas, V.; Desideri, P. G. Planar Chromatography of Optical Isomers with Bovine Serum Albumin in the Mobile Phase. J. Planar Chromatogr. 1992, 5, 175–178.
   Google Scholar
• Lepri, L.; Coas, V.; Desideri, P. G.; Zocchi, A. Reversed Phase Planar Chromatography of Enantiomeric Typtophans with Bovine Serum Albumin in the Mobile Phase. J. Planar Chromatogr. 1992, 5, 234–238.
   Google Scholar
• Lepri, L.; Coas, V.; Desideri, P. G.; Santianni, D. Reversed Phase Planar Chromatography of Dansyl DL Amino Acids with Bovine Serum Albumin in the Mobile Phase. Chromatographia. 1993, 36, 297–301. DOI: 10.1007/BF02263881.
   Web of Science ®Google Scholar
• Lepri, L.; Coas, V.; Desideri, P. G.; Pettini, L. Reversed Phase Planar Chromatography of Enantiomeric Compounds with Bovine Serum Albumin in the Mobile Phase. J. Planar Chromatogr. 1992, 5, 364–367.
   Google Scholar
• Lepri, L.; Coas, V.; Desideri, P. G.; Pettini, L. Thin Layer Chromatographic Enantioseparation of Miscellaneous Compounds with Bovine Serum Albumin in the Eluent. J. Planar Chromatogr. 1993, 6, 100–104.
   Google Scholar
• Malik, P.; Bhushan, R. Thin Layer Chromatographic Resolution of Some β-Adrenolytics and a Β2-Agonist Using Bovine Serum Albumin as Chiral Additive in Stationary Phase. J. Chromatogr. Sci. 2018, 56, 92–98. DOI: 10.1093/chromsci/bmx082.
   PubMed Web of Science ®Google Scholar
• Singh, D.; Malik, P.; Bhushan, R. Superiority of Thin-Layer Chromatography over High-Performance Liquid Chromatography in Enantioseparation. J. Planar Chromatogr. 2019, 32, 7–12. DOI: 10.1556/1006.2019.32.1.1.
   Web of Science ®Google Scholar
• Bhushan, R.; Parshad, V. Resolution of (±)-Ibuprofen Using l-Arginine-Impregnated Thin-Layer Chromatography. J. Chromatogr. A. 1996, 721, 369–372. DOI: 10.1016/0021-9673(95)00772-5.
   Web of Science ®Google Scholar
• Bhushan, R.; Thuku Thiongo, G. Direct Enantioseparation of Some β-Adrenergic Blocking Agents Using Impregnated Thin-Layer Chromatography. J. Chromatogr. B. 1998, 708, 330–334. DOI: 10.1016/S0378-4347(97)00646-4.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Arora, M. Direct Enantiomeric Resolution of (±)-Atenolol, (±)-Metoprolol, and (±)-Propranolol by Impregnated TLC Using L-Aspartic Acid as Chiral Selector. Biomed. Chromatogr. 2003, 17, 226–230. DOI: 10.1002/bmc.216.
   PubMed Web of Science ®Google Scholar
• Mohammad, A.; Sharma, S.; Bhavani, S. A. Identification of Ketoprofen in Drug Formulation and Spiked Urine Samples by Micellar Thin Layer Chromatography and Its Quantitative Estimation by High Performance Liquid Chromatography. Int. J. PharmTech Res. 2010, 2, 89–96.
   Google Scholar
• Aboul-Enein, H. Y.; El-Awady, M. I.; Heard, C. M. Enantiomeric Resolution of Some 2-Arylpropionic Acids Using l-(−)-Serine-Impregnated Silica as Stationary Phase by Thin Layer Chromatography. J. Pharm. Biomed. Anal. 2003, 32, 1055–1059. DOI: 10.1016/S0731-7085(03)00208-5.
   PubMed Web of Science ®Google Scholar
• Patel, D.; Mashru, R. Enantiomeric Resolution of (±)Flurbiprofen Using L-(–)Serine Impregnated Silica as Stationary Phase by Thin Layer Chromatography. Int. J. Pharm. Pharmaceut. Sci. 2011, 3, 131–133.
   Google Scholar
• Bhushan, R.; Nagar, H. Resolution and Isolation of Enantiomers of (±)-Isoxsuprine Using Thin Silica Gel Layers Impregnated with L-Glutamic Acid, Comparison of Separation of Its Diastereomers Prepared with Chiral Derivatizing Reagents Having L-Amino Acids as Chiral Auxiliaries. Biomed. Chromatogr. 2015, 29, 357–365. DOI: 10.1002/bmc.3284.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Tanwar, S. Different Approaches of Impregnation for Resolution of Enantiomers of Atenolol, Propranolol and Salbutamol Using Cu(II)-L-Amino Acid Complexes for Ligand Exchange on Commercial Thin Layer Chromatographic Plates. J. Chromatogr. A. 2010, 1217, 1395–1398. DOI: 10.1016/j.chroma.2009.12.071.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Martens, J.; Wallbaum, S.; Joshi, S.; Parshad, V. TLC Resolution of Enantiomers of Amino Acids and Dansyl Derivatives Using (1R,3R,5R)-2-Azabicyclo[3,3,0]Octan-3-Carboxylic Acid as Impregnating Reagent. Biomed. Chromatogr. 1997, 11, 286–288. DOI: 10.1002/(SICI)1099-0801(199709)11:5 < 286::AID-BMC698 > 3.0.CO;2-9.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Arora, M. Resolution of Enantiomers of DL-Amino Acids on Silica Gel Plates Impregnated with Optically Pure (-)-Quinine. Biomed. Chromatogr. 2001, 15, 433–436. DOI: 10.1002/bmc.96.
   PubMed Web of Science ®Google Scholar
• Nagar, H.; Bhushan, R. Enantioresolution of Dl-Selenomethionine by Thin Silica Gel Plates Impregnated with (−) Quinine and Reversed-Phase TLC and HPLC Separation of Diastereomers Prepared with Difluorodinitrobenzene Based Reagents Having L-Amino Acids as Chiral Auxiliaries. Anal. Methods. 2014, 6, 4188. DOI: 10.1039/c3ay41893f.
   Web of Science ®Google Scholar
• Bhushan, R.; Tanwar, S. Direct TLC Resolution of Atenolol and Propranolol into Their Enantiomers Using Three Different Chiral Selectors as Impregnating Reagents. Biomed. Chromatogr. 2008, 22, 1028–1034. DOI: 10.1002/bmc.1025.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Parshad, V. Thin-Layer Chromatographic Separation of Enantiomeric Dansylamino Acids Using a Macrocyclic Antibiotic as a Chiral Selector. J. Chromatogr. A. 1996, 736, 235–238. DOI: 10.1016/0021-9673(95)01330-X.
   Web of Science ®Google Scholar
• Bhushan, R.; Agarwal, C. Resolution of Beta Blocker Enantiomers by TLC with Vancomycin as Impregnating Agent or as Chiral Mobile Phase Additive. J. Planar Chromatogr. 2010, 23, 7–13. DOI: 10.1556/JPC.23.2010.1.1.
   Web of Science ®Google Scholar
• Bhushan, R.; Martens, J.; Arora, M. Direct Resolution of (±)-Ephedrine and Atropine into Their Enantiomers by Impregnated TLC. Biomed. Chromatogr. 2001, 15, 151–154. DOI: 10.1002/bmc.55.
   PubMed Web of Science ®Google Scholar
• Bhushan, R.; Martens, J. Direct Resolution of Enantiomers by Impregnated TLC. Biomed. Chromatogr. 1997, 11, 280–285. DOI: 10.1002/(SICI)1099-0801(199709)11:5 < 280::AID-BMC697 > 3.0.CO;2-U.
   PubMed Web of Science ®Google Scholar
• 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: 10.1016/j.aca.2015.04.022.
   PubMed Web of Science ®Google Scholar
• Mohammad, A.; Mobin, R. Ionic Liquid as Separation Enhancer in Thin-Layer Chromatography of Biosurfactants: Mutual Separation of Sodium Cholate, Sodium Deoxycholate and Sodium Taurocholate. J. Anal. Sci. Technol. 2015, 6, 16.
   Google Scholar
• Mohammad, A.; Mobin, R. Ionic Liquid in Thin-Layer Chromatography of Anionic Surfactants: Selective Separation of Sodium Deoxycholate and Identification in Commercial Products. Tenside Surfact. Det. 2015, 52, 493–501. DOI: 10.3139/113.110402.
   Web of Science ®Google Scholar
• Sobańska, A. W. Application of Planar Chromatographic Descriptors to the Prediction of Physicochemical Properties and Biological Activity of Compounds. J. Liq. Chromatogr. Rel. Technol. 2018, 41, 255–271. DOI: 10.1080/10826076.2018.1447886.
   Web of Science ®Google Scholar
• Farkas, O.; Gere-Paszti, E.; Forgacs, E. Study of the Interaction of Structurally Similar Bioactive Compounds by Thin-Layer Chromatography. J. Chromatogr. Sci. 2003, 41, 169–172. DOI: 10.1093/chromsci/41.4.169.
   PubMed Web of Science ®Google Scholar
• Forgács, E.; Cserháti, T.; Farkas, O.; Eckhardt, A.; Miksik, I.; Deyl, Z. Interaction between Cholesterol and Non‐Ionic Surfactants Studied by Thin‐Layer Chromatography. J. Liq. Chromatogr. Rel. Technol. 2004, 27, 1981–1992. DOI: 10.1081/JLC-120039411.
   Web of Science ®Google Scholar
• Zajdel, P.; Bojarski, A. J.; Byrtus, H.; Chłoń-Rzepa, G.; Obniska, J.; Chevallet, P.; Martinez, J.; Pawłowski, M. Preliminary Study on Application of Impregnated Synthetic Peptide TLC Stationary Phases for the Pre-Screening of 5-HT1A Ligands. Biomed. Chromatogr. 2003, 17, 312–317. DOI: 10.1002/bmc.224.
   PubMed Web of Science ®Google Scholar
• Zajdel, P.; Bojarski, A. J.; Bugno, R.; Jurczyk, S.; Kołaczkowski, M.; Nowak, M.; Subra, G.; Martinez, J.; Pawłowski, M. A Study on Application of Impregnated Synthetic Peptide TLC Stationary Phases for the Screening of 5-HT1A Ligands. Part 2. Biomed. Chromatogr. 2004, 18, 542–549. DOI: 10.1002/bmc.354.
   PubMed Web of Science ®Google Scholar
• Brzezińska, E. An Application of TLC Chromatographic Data in QSAR Assay of TIQs Derivatives with Β2-Adrenergic Activity. Acta Pol. Pharm. Drug Res. 1996, 53, 383–388.
   Google Scholar
• Żydek, G.; Brzezińska, E. Development and Validation of Quantitative Structure-Activity Relationship Models for Compounds Acting on Serotoninergic Receptors. Sci. World J. 2012, 2012, 1–11. DOI: 10.1100/2012/157950.
   Google Scholar
• Żydek, G.; Brzezińska, E. Normal and Reversed Phase Thin Layer Chromatography Data in Quantitative Structure–Activity Relationship Study of Compounds with Affinity for Serotonin (5-HT) Receptors. J. Chromatogr. B. 2011, 879, 1764–1772. DOI: 10.1016/j.jchromb.2011.04.025.
   PubMed Web of Science ®Google Scholar
• Brzezińska, E.; Kośka, G.; Walczyński, K. Application of Thin-Layer Chromatographic Data in Quantitative Structure–Activity Relationship Assay of Thiazole and Benzothiazole Derivatives with H1-Antihistamine Activity. I. J. Chromatogr. A. 2003, 1007, 145–155. DOI: 10.1016/S0021-9673(03)00951-8.
   PubMed Web of Science ®Google Scholar
• Brzezińska, E.; Kośka, G.; Kłimczak, A. Application of Thin-Layer Chromatographic Data in Quantitative Structure–Activity Relationship Assay of Thiazole and Benzothiazole Derivatives with H1-Antihistamine Activity. II. J. Chromatogr. A. 2003, 1007, 157–164. DOI: 10.1016/S0021-9673(03)00961-0.
   PubMed Web of Science ®Google Scholar
• Brzezińska, E.; Kośka, G. TLC Data in QSAR Assay of Thiazole and Benzothiazole Derivatives with H1-Antihistamine Activity. Part 1. J. Planar Chromatogr. 2003, 16, 451–457. DOI: 10.1556/JPC.16.2003.6.9.
   Web of Science ®Google Scholar
• Brzezińska, E.; Kośka, G. TLC Data in QSAR Assay of Thiazole and Benzothiazole Derivatives with H1-Antihistamine Activity. Part 2. J. Planar Chromatogr. 2004, 17, 40–45. DOI: 10.1556/JPC.17.2004.1.9.
   Web of Science ®Google Scholar
• Żydek, G.; Brzezińska, E.; Stańczak, A.; Lewgowd, W. Application of Chromatographic Data in QSAR Studies of 3- [-(4-Arylpiperazin-1-yl)Alkyl]Pyrimido[5,4-c]Quinolin-4(3H)-One Derivatives as 5-HT1A Receptor Ligands. J. Chromatogr. Sci. 2013, 52, 596–603. DOI: 10.1093/chromsci/bmt082.
   PubMed Web of Science ®Google Scholar
• Brzezińska, E.; Kośka, G. A Structure–Activity Relationship Study of Compounds with Antihistamine Activity. Biomed. Chromatogr. 2006, 20, 1004–1016. DOI: 10.1002/bmc.621.
   PubMed Web of Science ®Google Scholar
• Żydek, G.; Brzezińska, E. NP TLC Data in Structure-Activity Relationship Study of Selected Compounds with Activity on Dopaminergic, Serotoninergic, and Muscarinic Receptors. J. Liq. Chromatogr. Rel. Technol. 2012, 35, 834–853. DOI: 10.1080/10826076.2011.613139.
   Web of Science ®Google Scholar