Abstract
The supramolecular host–guest inclusion complex of Primaquine (PQ) with the nano-hydrophobic cavity of beta-cyclodextrin (β-CD) was prepared by physical mixing, kneading and co-precipitation methods. The formation of an inclusion complex in PQ with β-CD in the solution phase has been confirmed by UV–visible and fluorescence spectroscopy. The stoichiometry of the inclusion complex is 1:1; the Primaquine molecule is deeply entrapped in the cavity of β-cyclodextrin, which was confirmed by analysis of spectral shifts and corresponding absorbance and fluorescence intensities. The Benesi–Hildebrand plot was used to calculate the binding constant of the inclusion complex of PQ with β-CD at room temperature. The Gibbs energy change of the inclusion complex process has been calculated. The \( {\text{p}}K_{\text{a}} \) and \( {\text{p}}K_{\text{a}}^{*} \) for the monocation and neutral equilibrium of PQ in aqueous and β-CD media are discussed. The thermal stability for the inclusion complex of PQ with β-CD has been analyzed using differential scanning calorimetry. The modification of the crystal structure to amorphous for the solid inclusion complex was confirmed by powder X-ray diffraction. The structure of the complex is proposed by docking studies using the Patch-Dock server. A cytotoxic analysis was also carried out for the pure PQ and its solid complex on the MDA MB 231 cell line and showed that the activity is good for both substances. The cytotoxicity neither improved nor decreased with the formation of the inclusion complex with β-CD.
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Baird, K., Stephen, J., Hoffman, L.: Primaquine therapy for malaria. Clin. Infect. Dis. 39, 1336–1345 (2014)
Freudenberg, K., Cramer, F., Plieninger, H.: Inclusion Compounds of Physiologically Active Organic Compounds. German Pat. 895769 (1953)
Szejtli, J., Szente, L.: Elimination of bitter, disgusting tastes of drugs and foods by cyclodextrins. Eur. J. Pharm. Biopharm. 61, 115–125 (2005)
Shityakov, S., Broscheit, J., Förster, C.: α-Cyclodextrin dimer complexes of dopamine and levodopa derivatives to assess drug delivery to the central nervous system: ADME and molecular docking studies. Int. J. Nanomed. 7, 3211–3219 (2012)
Lee, C.W., Kim, S.J., Youn, Y.S., Widjojokusumo, E., Lee, Y.H., Kim, J., Lee, Y.W., Tjandrawinata, R.R.: Preparation of bitter taste masked cetirizine dihydrochloride/β-cyclodextrin inclusion complex by supercritical anti-solvent (SAS) process. J. Supercrit. Flu. 55, 348–357 (2010)
Charlton, A.J., Davis, A.L., Jones, D.P., Lewis, J.R., Davies, A.P., Haslam, E., Williamson, M.P.: The self-association of the black tea polyphenol theaflavin and its complexation with caffeine. J. Chem. Soc. Perkin Trans. 2, 317–322 (2000)
Al-Maaieh, A., Flanagan, D.R.: Salt effects on caffeine solubility, distribution, and self-association. J. Pharm. Sci. 91, 1000–1008 (2001)
Poltev, V.I., Grokhlina, T.I., González, A., Deriabina, Q., Cruz, L., Gor, J., Leszczynski, L.N., Djimant, A.N.: Veselkov.: the study of three-dimensional structure of caffeine associates using computational and experimental methods. J. Mol. Struct. 709, 123–128 (2004)
Dong, Z., Liang, Y.R., Fan, F.Y., Ye, J.H., Zheng, X.Q., Lu, J.L.: Adsorption behavior of the catechins and caffeine onto polyvinylpolypyrrolidone. J. Agric. Food Chem. 59, 4238–4247 (2011)
Murugan, M., Rajamohan, R., Sivakumar, K.: A study of host-guest complexation between amodiaquine and native cyclodextrin. Characterization in solid state and its in vitro anticancer activity. J. Macromol. Sci. A 53, 282–283 (2016)
Anitha, A., Murugan, M., Rajamohan, R.: Molecular encapsulation of amodiaquine in 2-hydroxypropyl β-cyclodextrin cavity. Spectros. Lett. (2018). https://doi.org/10.1080/00387010.2018.1448421
Bhardwaj, R., Dorr, R.T., Blanchard, J.: Approaches to reducing toxicity of parenteral anticancer drug formulations using cyclodextrins. J. Pharm. Sci. Technol. 54, 233–239 (2000)
Fujishima, N., Kusaka, K., Umino, T., Urushinata, T., Terumi, K.: Flour based foods containing highly branched cyclodextrins. Jpn. Patent JP 136, 898 (2001)
Holland, L., Rizzi, G., Malton, P.: Cosmetic compositions comprising cyclic oligosaccharides and fragrance. PCT Int. Appl. 67, 716 (1999)
Lezcano, M., Ai-Soufi, W., Novo, M., Rodriguez-Nunez, E., Tato, J.V.: Complexation of several benzimidazole-type fugicides with alpha and beta cyclodextrins. J. Agric. Food Chem. 50, 108–112 (2002)
Dufosse, J., Souchon, I., Feron, G., Latrasse, A., Spinnler, H.E.: In situ detoxification of the fermentation medium during γ-decalactone production with the yeast Sporidiobolus salmonicolor. Biotech. Prog. 15, 135–139 (1999)
Zhou, J., Ritter, H.: Cyclodextrin functionalized polymers as drug delivery systems. Pol. Chem. 1, 1552–1559 (2010)
Hedges, R.A.: Industrial applications of cyclodextrins. Chem. Rev. 98, 2035–2044 (1998)
Zhang, X., Wang, C.: Supramolecular amphiphiles. Chem. Soc. Rev. 40, 94–101 (2011)
Harada, A., Takashima, Y., Yamaguchi, H.: Cyclodextrin-based supramolecular polymers. Chem. Soc. Rev. 38, 875–882 (2009)
Chen, Y., Liu, Y.: Cyclodextrin-based bioactive supramolecular assemblies. Chem. Soc. Rev. 39, 495–505 (2010)
Nakahata, M., Takashima, Y., Yamaguchi, H., Harada, A.: Redox-responsive self-healing materials formed from host–guest polymers. Nat. Commun. 2, 511 (2011)
Chen, G., Jiang, M.: Cyclodextrin-based inclusion complexation bridging supramolecular chemistry and macromolecular self-assembly. Chem. Soc. Rev. 40, 2254–2266 (2011)
Hetzer, M., Schmidt, B.V.K.J., Barner-Kowollik, C., Ritter, H.: Limitations of cyclodextrin-mediated RAFT homo polymerization and block copolymer formation. J. Pol. Sci. Part A. 51, 2504–2517 (2013)
Schmidt, B.V.K.J., Hetzer, M., Ritter, H., Barner-Kowollik, C.: Cyclodextrin-complexed RAFT agents for the ambient temperature aqueous living/controlled radical polymerization of acrylamido monomers. Macromolecules 44, 7220–7232 (2011)
Schneidman-Duhovny, D., Inbar, Y., Nussinov, R., Wolfson, H.J.: PatchDock and Symm Dock: servers for rigid and symmetric docking. Nucl. Acids Res. 33, 363–367 (2005)
Connolly, M.L.: Solvent-accessible surfaces of proteins and nucleic acids. Science 221, 709–711 (1983)
Connolly, M.L.: Analytical molecular surface calculation. J. Appl. Crystallogr. 16, 548–558 (1983)
Zhang, C., Vasmatzis, G., Cornette, J.L., DeLisi, C.: Determination of atomic desolvation energies from the structures of crystallized proteins. J. Mol. Biol. 267, 707–726 (1997)
Prabu, S., Sivakumar, K., Swaminathan, M., Rajamohan, R.: Preparation and characterization of host–guest system between inosine and beta-cyclodextrin through inclusion mode. Spectrochim. Acta A 147, 151–157 (2015)
Schulman, S.G., Irene, P.: Dissociation constant of the 9-anthroic acidium cation in the lowest excited singlet state. J. Phys. Chem. 76, 1996–1999 (1972)
Misiuk, W.: Spectrofluorimetric study on inclusion interaction of beta-cyclodextrin with duloxetine and its analytical application. I. J. Chem. Sec A. 51, 1706–1710 (2012)
Rajamohan, R., Kothai Nayaki, S., Swaminathan, M.: Investigation on association behavior between 1-aminoisoquinoline and β-cyclodextrin in solution and solid state. J. Mol. Liq. 220, 918–925 (2016)
Enoch, M.V., Rajamohan, R., Swaminathan, M.: Fluorimetric and prototropic studies on the inclusion complexation of 3,3-diaminodiphenylsulphone with β-cyclodextrin and its unusual behavior. Spectrochim. Acta Part A 77, 473–474 (2010)
Farag, M.A., Altalba, W.Y., Sayed, E.L., Sherbini, A.L.: Spectrophotometric determination of acidity constant of 1-methyl-4-[4′-aminostyryl]quinolinium iodide in aqueous buffer and micellar solutions in the ground and excited states. Asian J. Chem. 25, 6181–6185 (2013)
Duhovny, D., Nussinov, R., Wolfson, H.J.: Efficient unbound docking of rigid molecules. In: Guigó, R., Gusfield, D. (eds.) Algorithms in Bioinformatics. WABI 2002. Lecture Notes in Computer Science. Springer, Berlin (2002)
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Murugan, M., Anitha, A., Sivakumar, K. et al. Supramolecular Interaction of Primaquine with Native β-Cyclodextrin. J Solution Chem 47, 906–929 (2018). https://doi.org/10.1007/s10953-018-0768-2
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DOI: https://doi.org/10.1007/s10953-018-0768-2