Nassim Belkacem1 , Mutaz Sheikh Salem2, Hatim Alkhatib3, Chiraz Soumia Amrine4
1Department of Physicochemical Biology, Laboratory of Plant Biotechnologies and Ethnobotany, Faculty of Natural and Life Sciences, Bejaia University, Algeria; 2Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology; 3Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, The University of Jordan, Jordan; 4Department of Physical and Earth Sciences, College of Science, Technology, Engineering, and Mathematics. Arkansas Tech University, USA.For correspondence:- Nassim Belkacem Email: nassim.belkacem@univ-bejaia.dz Tel:+213-782032193
Received: 1 March 2024 Accepted: 2 November 2024 Published: 28 November 2024
Citation: Belkacem N, Salem MS, Alkhatib H, Amrine CS. Dissolution enhancement of ketoprofen using melt-sonocrystallization technique. Trop J Pharm Res 2024; 23(11):1797-1806 doi: 10.4314/tjpr.v23i11.1
© 2024 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To investigate the effect of melt-sonocrystallization technique (MS) on the physicochemical characteristics and dissolution of a poorly soluble drug (ketoprofen). Methods: Ketoprofen was heated in paraffin oil bath at 97 °C and then poured into a beaker containing 25 mL deionized water at 25 oC and immediately treated using a probe ultrasonicator at different ultrasonic times, and varying amplitudes at frequency of 20 KHz. Prepared suspensions were evaluated for the effect of temperature and energy of production. Powders were characterized using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infra-red spectrophotometry (FTIR). The Heckle plot, Carr's compressibility index, and Hausner's ratio were used to determine compressibility properties. Furthermore, the angle of slide was used to evaluate flow characteristics. Results: There was a significant reduction in particle size characteristics following meltsonocrystallization (p < 0.05). The SEM micrographs revealed needle-shaped particles with smooth surfaces. There was no significant difference in DSC thermograms with peaks ranging from 97.3 to 98.1 °C (p < 0.05). The FT-IR spectra showed two specific sharp and symmetrical peaks at (1654.5 cm-1 ) and (1697.3 cm-1 ). Also, distinctive peaks of ketoprofen remained detectable in XRD patterns, indicating that the substance had not undergone structural modification. The solubility increased by 15 %. There was no improvement in flowability or compressibility. Dissolution was greatly improved from 67 to 85 %. Conclusion: Melt-sonocrystallization reduces particle size, solubility, and dissolution with no structural modification to ketoprofen. In vivo investigation of drug bioavailability from the generated powders would be required.
Archives
News Updates