Anastas PT, Warner JC (1998) Green chemistry: theory and practice. Oxford University Press, New York, NY

Google Scholar 

Sztanke M, Rzymowska J, Janicka M, Sztanke K (2020) Two novel classes of fused azaisocytosine-containing congeners as promising drug candidates: design, synthesis as well as in vitro, ex vivo and in silico studies. Bioorg Chem 95:103480. https://doi.org/10.1016/j.bioorg.2019.103480

CAS  Article  PubMed  Google Scholar 

Janicka M, Mycka A, Sztanke M, Sztanke K (2021) Predicting pharmacokinetic properties of potential anticancer agents via their chromatographic behavior on different reversed phase materials. Int J Mol Sci 22:4257. https://doi.org/10.3390/ijms22084257

CAS  Article  PubMed  PubMed Central  Google Scholar 

Hansch C (1993) Quantitative structure–activity relationships and the unnamed science. Acc Chem Res 26:147–153

CAS  Article  Google Scholar 

Kaliszan R (1987) Quantitative structure–chromatographic retention relationships. John Wiley & Sons, New York, NY

Google Scholar 

Héberger K (2007) Quantitative structure–(chromatographic) retention relationships. J Chromatogr A 1158:273–305

Article  Google Scholar 

Valkó K (2016) Lipophilicity and biomimetic properties measured by HPLC to support drug discovery. J Pharm Biomed Anal 130:35–54

Article  Google Scholar 

Ciura K, Dziomba S (2020) Application of separation methods for in vitro prediction of blood–brain barrier permeability—The state of the art. J Pharm Biomed Anal 177:112891. https://doi.org/10.1016/j.jpba.2019.112891

CAS  Article  PubMed  Google Scholar 

Ayouni L, Cazarola G, Chaillou D, Herbreteau B, Rudaz S, Lantéri P, Carrupt P-A (2005) Fast determination of lipophilicity by HPLC. Chromatographia 62:251–255

CAS  Article  Google Scholar 

Barbato FV, Cirocco L, Grumetto M, La Rotonda I (2007) Comparison between immobilized artificial membrane (IAM) HPLC data and lipophilicity in n-octanol for quinolone antibacterial agents. Eur J Pharm Sci 31:288–297

CAS  Article  Google Scholar 

Kempińska D, Chmiel T, Kot-Wasik A, Mróz A, Mazerska Z, Namieśnik J (2019) State of the art and prospects of methods for determination of lipophilicity of chemical compounds. Trends Anal Chem 113:54–73

Article  Google Scholar 

Ruiz-Angel MJ, Carda-Broch S, Torres-Lapasió JR, García-Alvarez-Coque MC (2009) Retention mechanisms in micellar liquid chromatography. J Chromatogr A 1216:1798–1814

CAS  Article  Google Scholar 

Tsopelas F, Panagiotis D, Pappa A, Tsantili-Kakoulidou A (2020) Biopartitioning micellar chromatography under different conditions: Insight into the retention mechanism and the potential to model biological processes. J Chromatogr A 1621:461027

CAS  Article  Google Scholar 

Escuder-Gilabert L, Molero-Monfort M, Villanueva-Camaňas RM, Sagrado S, Medina-Hernández MJ (2004) Potential of biopartitioning micellar chromatography as an in vitro technique for predicting drug penetration across the blood–brain barrier. J Chromatogr B 807:193–201

CAS  Article  Google Scholar 

Ciura K, Belka M, Kawczak P, Bączek T, Nowakowska J (2018) The comparative study of micellar TLC and RP-TLC as potential tools for lipophilicity assessment based on QSRR approach. J Pharm Biomed Anal 149:70–79. https://doi.org/10.1016/j.jpba.2017.10.034

CAS  Article  PubMed  Google Scholar 

Vuignier K, Schappler J, Veuthey J-L, Carrupt A (2010) Drug-protein binding: a critical review. Anal Bioanal Chem 398:53–66

CAS  Article  Google Scholar 

Waterbeemd H, Camenisch G, Folkers G, Chretien JR, Raevsky OA (1998) Estimation of blood–brain barrier crossing of drugs using molecular size and shape, and H-bonding descriptors. J Drug Target 6:151–165

Article  Google Scholar 

Feher M, Sourial E, Schmidt JM (2000) A simple model for the prediction of blood–brain partitioning. Int J Pharm 201:239–247

CAS  Article  Google Scholar 

Geldenhuys WJ, Mohammad AS, Adkins CE, Lockman PR (2015) Molecular determinants of blood–brain barrier permeation. Ther Deliv 6:961–971. https://doi.org/10.4155/tde.15.32

CAS  Article  PubMed  PubMed Central  Google Scholar 

Spangenberg B, Poole CF, Weins CH (2011) Quantitative thin-layer chromatography. A practical survey. Springer, Berlin

Book  Google Scholar 

Tandon H, Ranjan R, Chakraborty T, Suhag V (2021) Polarizability: a promising descriptor to study chemical-biological interactions. Mol Divers 25:249–262

CAS  Article  Google Scholar 

Hitchcok SA (2008) Blood-brain barrier permeability concentrations for CNS-targeted compound library design. Curr Opin Chem Biol 12:318–323

Article  Google Scholar 

Gramatica P (2013) On the development and validation of QSAR Models. In: Reisfeld B, Mayeno AN (eds) Computational toxicology. Springer Nature, Berlin

Google Scholar