Inclusion of Paracetamol into β-cyclodextrin nanocavities in solution and in the solid state

Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy

Volumn 79, Issue 5, 2011, Pages 1904-1908

  El Kemary, Maged ^a   Sobhy, Saffaa ^a   El Daly, Samy ^b   Abdel Shafi, Ayman ^c  

^a Kafrelsheikh University   (Egypt)

^b Tanta University   (Egypt)

^c Ain Shams University   (Egypt)

Author keywords

Cyclodextrin; Hydroxypropyl cyclodextrin; Inclusion complex; Methyl CD; Paracetamol

Indexed keywords

ANTIPYRETIC AGENT; BINDING CONSTANT; CDS; CONFINEMENT EFFECTS; COPRECIPITATION METHOD; EMISSION CHARACTERISTICS; EMISSION INTENSITY; GUEST MOLECULES; INCLUSION COMPLEX; INCLUSION COMPOUNDS; METHYL GROUP; NANO-CAVITIES; NANOCAGES; NMR AND X-RAY; PARACETAMOL; PHOTOPHYSICAL BEHAVIOR; SPECTROSCOPIC FEATURES; STERIC EFFECT; UV-VISIBLE ABSORPTION;

CYCLODEXTRINS; FOURIER TRANSFORM INFRARED SPECTROSCOPY; FUNCTIONAL GROUPS; PRECIPITATION (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

WATER ABSORPTION;

BETA CYCLODEXTRIN DERIVATIVE; NANOMATERIAL; PARACETAMOL;

ARTICLE; CHEMISTRY; DIFFERENTIAL SCANNING CALORIMETRY; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SOLUTION AND SOLUBILITY; ULTRAVIOLET SPECTROPHOTOMETRY; X RAY DIFFRACTION;

ACETAMINOPHEN; BETA-CYCLODEXTRINS; CALORIMETRY, DIFFERENTIAL SCANNING; MAGNETIC RESONANCE SPECTROSCOPY; NANOSTRUCTURES; SOLUTIONS; SPECTROPHOTOMETRY, ULTRAVIOLET; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; X-RAY DIFFRACTION;

EID: 79960267455     PISSN: 13861425     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.saa.2011.05.084     Document Type: Article

References (23)

1. M. Davis, and M. Brewster Nat. Rev. Drug Discov. 3 2004 1023 1035
2. S. Monti, and S. Sortino Chem. Soc. Rev. 31 2002 287 300
3. N. Nandi, K. Bhattacharyya, and B. Bagchi Chem. Rev. 100 2000 2013 2045
4. M. El-Kemary, J. Organero, L. Santos, and A. Douhal J. Phys. Chem. B 110 2006 14128 14134
5. M. El-Kemary, and I. El-Mehasseb Talanta 62 2004 317 322
6. M. El-Kemary, H. El-Gezawy, H. El-Baradie, and R. Issa Spectrochim. Acta A 58 2002 495 502
7. A. Abdel-Shafi Spectrochim. Acta A 66 2007 732 738
8. A.A. Abdel-Shafi Spectrochim. Acta A 57 2001 1819 1828
9. M. El-Kemary, and A. Douhal A. Photochemistry and photophysics of cyclodextrin caged drugs A. Douhal, Cyclodextrin Materials Photochemistry, Photophysics and Photobiology 2006 Elsevier (Chapter 4)
10. P. Bortolus, and S. Monti Adv. Photochem. 21 1996 1 133
11. N.S. Moyon, T.S. Singh, and S. Mitra Biophys. Chem. 138 2008 55 62
12. K. Uekama, and T. Irie D. Duchêne, Cyclodextrins and Their Industrial Uses 1987 Editions de Santé Paris 395 439
13. C. Rosel, J. Carreno, M. Rodriguez-Baeza, and J. Alderetr Quim. Nova 23 2000 749 752
14. H. Benesi, and J. Hildebrand J. Am. Chem. Soc. 71 1949 2703 2707
15. A. Green, E. Miller, and J. Guillory J. Pharm. Sci. 1991 186 189
16. S.K. Mondal, D. Roy, K. Sahu, P. Sen, and K. Bhattacharyya J. Photochem. Photobiol. A 173 2005 334 339
17. T. Steiner, and W. Saenger Carbohydr. Res. 275 1995 73 82
18. C.J. Easton, and S.F. Lincoln Modified Cyclodextrins, Scaffolds and Templates for Supramolecular Chemistry 1999 Imperial College Press London
19. P. Mura, N. Zerrouck, M.T. Faucci, F. Maestrelli, and C. Chemtob Eur. J. Pharm. Biopharm. 54 2002 181 191
20. O. Abou-Zied, and A. Al-Hinai J. Phys. Chem. A 110 2006 7835 7840
21. J.E. Hansen, E. Pines, and G.R. Fleming J. Phys. Chem. 96 1992 6010 6904
22. A. Muñoz de la Peña, T. Ndou, J.B. Zung, and I.M. Warner J. Phys. Chem. 95 1991 3330 3334
23. S. Baboota, M. Dhaliwal, and K. Kohli AAPS Pharm. Sci. Technol. 6 2005 83 89