Browse > Article
http://dx.doi.org/10.4333/KPS.2007.37.1.001

Preparation and Characterization of Piroxicam/Poloxamer Solid Dispersion Prepared by Melting Method and Solvent Method  

Yu, Hang (BK21 Project Team, College of Pharmacy, Chosun University)
Chun, Myung-Kwan (BK21 Project Team, College of Pharmacy, Chosun University)
Choi, Hoo-Kyun (BK21 Project Team, College of Pharmacy, Chosun University)
Publication Information
Journal of Pharmaceutical Investigation / v.37, no.1, 2007 , pp. 1-5 More about this Journal
Abstract
Solid dispersions of piroxicam were prepared by melting method using poloxamer as a carrier. The results of DSC and XRD studies showed that the amorphous farm of piroxicam coexisted with the crystalline form in the solid dispersions. However, the ratio of crystalline form of piroxicam in the solid dispersion prepared by melting method decreased in comparison with the same ratio of the solid dispersion prepared by solvent method. As the ratio of poloxamer in the solid dispersion increased, the ratio of the amorphous form of piroxicam in the solid dispersion increased. The dissolution rate of piroxicam from the solid dispersions was significantly higher than that from piroxicam powder. In comparison to the solid dispersion prepared by solvent method, the dissolution rate of piroxicam from the solid dispersion prepared by melting method was higher. As the ratio of poloxamer in the solid dispersion prepared by melting method increased, the initial dissolution rate decreased, however, the total amount dissolved at the end of the study increased.
Keywords
Piroxicam; Solid dispersion; Melting method; Poloxamer; Dissolution rate;
Citations & Related Records
연도 인용수 순위
  • Reference
1 P.A Insel, Analgesic-antipyretic and anti-inflammatory agents and drugs employed in the treatment of gout. In: Goodman & Gilman s The pharmacological basis of therapeutics, 9th Edition, J.G Hardman,L.E. Limbird, P.B. Molinoff, R.W Ruddon and A.G. Gilman (eds.), McGraw-Hill, New York, USA, pp. 617-657 (1996)
2 A. Karata,N. Yuksel and T. Baykara,Improved solubility and dissolution rate of piroxicam using gelucire44/14 and labrasol, Il Farmaco, 60, 777-782 (2005)   DOI   ScienceOn
3 M. Fernandez, I. C. Rodriguez, M. V. Margaritand A. Cerezo, Characterization of solid dispersions of piroxicam/polyethylene glycol 4000, Int. J. Pharm., 84, 197-202 (1992)
4 V. Tantishaiiyakul, N. Kaewnopparat and S. Ingkatawomwong, Properties of solid dispersions of piroxicam in polyvinyl- pyrrolidone, Int. J Pharm., 181, 143-151 (1999)   DOI   ScienceOn
5 H.-S. Gwak, J.-S. Choi and H.-K. Choi, Enhancedbioavailability of piroxicam via salt formation with ethanolamines, Int. J Pharm., 297, 156-161 (2005)
6 S. M. Wong, I. W Kellaway and S. Murdan, Enhancement of the dissolution rate and oral absorption of a poorly water soluble drug by formation of surfactant-containing micro- particles, Int. J Pharm., 317, 61-68 (2006)   DOI   ScienceOn
7 S.-C. Shin and C.-W Cho, Physicochemical characterizations of piroxicam-poloxamer solid dispersion, Pharm. Dev. Technol., 2, 403-407 (1997)   DOI
8 M. Fathy and M. El-Badry, Preparation and evaluation of piroxicam-pluronic solid dispersions, Bull. Pharm. Sci., 26, 97-108 (2003)
9 E.-J. Kim, M.-K. Chun,J.-S. Jang, I.-H. Lee,K.-R.Lee and H.K. Choi, Preparation of a solid dispersion of felodipine using a solvent wetting method,Eur. J Pharm. Biopharm., 64, 200-205 (2006)   DOI   ScienceOn
10 J. H. Collettand H. Popli, Poloxamer. In: Handbook of Pharmaceutical Excipients, 3rd Edition, A H. Kibbe, (ed.), American Pharmaceutical Association, Washington DC, USA, pp. 386-388 (2000)
11 C. Leuner and J. Dressman, Improving drug solubility for oral deliveryusing solid dispersions, Eur. J Pharm. Biopharm., 50, 47-60 (2000)   DOI   ScienceOn
12 M. Jug and M. Beirevi-Laan, Influence of hydroxypropyl-l3cyclodextrin complexation on piroxicam release from buccoadhesive tablets, Eur. J Pharm. Sci., 21, 251-260 (2004)   DOI   ScienceOn
13 S. Prabhu, M. Ortega and C. Ma, Novel lipid-based formulations enhancing the in vitro dissolution and permeability characteristics of a poorly water-soluble model drug, piroxi- cam, Int. J Pharm., 301, 209-216 (2005)   DOI   ScienceOn