ENHANCEMENT OF LORNOXICAM SOLUBILITY BY INCLUSION COMPLEXATION WITH CYCLODEXTRIN: PREPARATION AND CHARACTERIZATION

Authors

  • Shahira F. El-menshawe Pharmaceutics and industrial pharmacy department, Faculty of Pharmacy, Beni-suef University, Beni-suef, Egypt
  • Essam Eissa Pharmaceutics and industrial pharmacy department, Faculty of Pharmacy, Beni-suef University, Beni-suef, Egypt
  • Adel A. Ali Pharmaceutics and industrial pharmacy department, Faculty of Pharmacy, Beni-suef University, Beni-suef, Egypt
  • Ahmed A. Abderhman Pharmaceutics and industrial pharmacy department, Faculty of Pharmacy, Cairo University, Cairo, Egypt

DOI:

https://doi.org/10.22159/ijpps.2017v9i1.14848

Keywords:

Lornoxicam, Cyclodextrin, Lyophilization, Physical mixing, Inclusion complex

Abstract

Objective: Lornoxicam is a potent anti-inflammatory drug which has analgesic and antipyretic properties. It is water-insoluble powder. The inclusion complexes of lornoxicam (LOR) with β-cyclodextrin (βCD) and 2-hydroxypropyl-β-cyclodextrin (HPCD) were prepared and characterised in order to improve the solubility of the drug and enhance its bioavailability.

Methods: Complexes were prepared by physical mixing and freeze-drying in three different drug/polymer ratios (1:1, 1:2 and 3:2). The solid complexes were characterised through differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X-ray diffraction, nuclear magnetic resonance (NMR) spectroscopy, and Fourier transformed infrared (FTIR) spectroscopy.

Results: The data showed that LOR may be complexed with cyclodextrin (CD) forming soluble complexes. The lyophilized 1:2 LOR/HPCD complex is the most soluble.

Conclusion: Solubility increases with lyophilization than with physical mixing and by the use of HPCD than βCD in complexation.

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Published

01-01-2017

How to Cite

El-menshawe, S. F., E. Eissa, A. A. Ali, and A. A. Abderhman. “ENHANCEMENT OF LORNOXICAM SOLUBILITY BY INCLUSION COMPLEXATION WITH CYCLODEXTRIN: PREPARATION AND CHARACTERIZATION”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 9, no. 1, Jan. 2017, pp. 132-8, doi:10.22159/ijpps.2017v9i1.14848.

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