Low density porous carrier. Drug adsorption and release study by response surface methodology using different solvents

International Journal of Pharmaceutics

Volumn 331, Issue 1, 2007, Pages 72-83

  Sher, Praveen ^a   Ingavle, Ganesh ^b   Ponrathnam, Surendra ^b   Pawar, Atmaram P ^a  

^a BHARATI VIDYAPEETH DEEMED UNIVERSITY   (India)

^b NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

32 factorial design; Carrier; Microporous polymer; Response surface methodology; Solvent evaporation

Indexed keywords

ACCUREL MP 1000; DICHLOROMETHANE; DRUG ADDITIVE; IBUPROFEN; METHANOL; POLYMER; POLYPROPYLENE; SOLVENT; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; DENSITY; DIFFERENTIAL SCANNING CALORIMETRY; DRUG ADSORPTION; DRUG DELIVERY SYSTEM; DRUG RELEASE; DRUG SOLUBILITY; EVAPORATION; FLOTATION; INFRARED SPECTROSCOPY; PARTICLE SIZE; PH; POROSITY; PRIORITY JOURNAL; SCANNING ELECTRON MICROSCOPY; SURFACE PROPERTY; THERMOGRAVIMETRY; X RAY DIFFRACTION;

ADSORPTION; CALORIMETRY, DIFFERENTIAL SCANNING; DRUG CARRIERS; IBUPROFEN; METHANOL; METHYLENE CHLORIDE; PARTICLE SIZE; POLYPROPYLENES; POROSITY; SOLUBILITY; SOLVENTS; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; SURFACE PROPERTIES; THERMOGRAVIMETRY; X-RAY DIFFRACTION;

EID: 33846571941     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2006.09.013     Document Type: Article

References (34)

1. Andersson J., Rosenholm J., Areva S., and Linden M. Influences of material characteristics on ibuprofen drug loading and release profiles from ordered micro- and mesoporous silica matrices. Chem. Mater. 16 (2004) 4160-4167
2. Berger J., Reist M., Mayer J.M., Felt O., and Gurny R. Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications. Eur. J. Pharm. Biopharm. 57 (2004) 35-52
3. Boer G.J., and Krusinbrink J. A polymeric controlled drug delivery device fro peptides based on a surface desorption/diffusion mechanism. Biomaterials 8 (1987) 265-274
4. Byrne R.S., and Deasy P.B. Use of commertial porous ceramic particles for sustained drug delivery. Int. J. Pharm. 246 (2002) 61-73
5. Civan Faruk. Scale effect on porosity and permeability: kinetics model and correlation. AIChE J. (2001) 47
6. Charnay C., Begu S., Tourney-Petelh C., Nicole L., Lerner D.A., and Devoisselle J.M. Inclusion of ibuprofen in mesoporous templated silica: drug loading and release property. Eur. J. Pharm. Biopharm. 57 (2004) 533-540
7. Chilkoti A., Dreher M.R., Meyer D.E., and Raucher D. Targeted drug delivery by thermally responsive polymers. Adv. Drug. Del. Rev. 54 (2002) 613-630
8. Germann P.F., and DiPietro L. When is porous-media flow preferential? A hydromechanical perspective. Geoderma 74 (1996) l-21
9. Gren T., Bjerre C., Camber O., and Ragnarsson G. In vitro drug release from porous cellulose matrices. Int. J. Pharm. 141 (1996) 53-62
10. Gurny R., Doelker E., and Peppas N.A. modeling of sustained release of water-soluble drugs fromporous, hydrophobic polymers. Biomaterial 3 (1982) 27-32
11. Gunko V.M., Mikhalovskii S.V., Melillo M., Voronin E.F., Nosach L.V., and Pakhlov E.M. The effect of the nature and structure of adsorbents on interaction with ibuprofen. Theor. Exp. Chem. (2004) 40
12. Ito Y., Arai H., Uchino K., Iwasaki K., Shibata N., and Takada K. Effect of adsorbents on the absorption of lansoprazole with surfactant. Int. J. Pharm. 289 (2005) 69-77
13. Janczuk B., Chibowski E., and Wojcik W. The Influence of n-alcohols on the wettability of hydrophobic solids. Powder Tech. 45 (1985) 1-6
14. Lemaire V., Belair J., and Hildgen P. Strutural modeling of drug release from biodegredable porous matrices based on a combined diffusion/erosion process. Int. J. Pharm. 258 (2003) 95-107
15. Li Z., Wen L., Shao L., and Chen J. Fabrication of porous hollow silica nanoparticles and their applications in drug release control. J. Control. Release 98 (2004) 24-254
16. Liu L., Fishman M.L., Kost J., and Hicks K.B. Pectin-based systems for colon-specific drug delivery via oral route. Biomaterials 24 (2003) 3333-3343
17. Lu Y., and Chen S.C. Micro and nano-fabrication of biodegradable polymers for drug delivery. Adv. Drug. Del. Rev. 56 (2004) 1621-1633
18. Müller R.H., Mäder K., and Gohla S. Solid lipid nanoparticles (SLN) for controlled drug delivery-a review of the state of the art. Eur. J. Pharm. Biopharm. 50 (2000) 161-177
19. Murakami T., and Yata N. Controlled drug release by the use of porous calcium silicate. Drug Del. Syst. 10 (1995) 159-166
20. Ohta K.M., Fuji M., Takei T., and Chikazawa M. development of a simple method for the prepration of a silica gel based controlled drug delivery system with a high drug content. Eur. J. Pharm. Sci. 26 (2005) 87-96
21. Otsuka M., Tokumitsu K., and Matsuda Y. Solid dosage form preparations from oily medicines and their drug release. Effect of degree of surface modification of silica gel on the drug release from phytonadione-loaded silica gels. J. Control. Release 67 (2000) 369-384
22. Packhaeuser C.B., Schnieders J., Oster C.G., and Kissel T. In situ forming parenteral drug delivery systems: an overview. Eur. J. Pharm. Biopharm. 58 (2004) 445-455
23. Salonen J., Laitinen L., Kaukonen A.M., Tuura J., Bjorkqvist M., Heikkila T., Vaha-Heikella K., Hirvonen J., and Lehto V.-P. Mesoporous silicon microparticles for oral drug delivery: loading and release of five model drugs. J. Control. Release 108 (2005) 362-374
24. Sarkisov L., and Monson P.A. modeling of adsorption and desorption in pores of simple geometry using molecular dynamics. Langmuir 17 (2001) 7600-7604
25. Scott D.C. An assessment of reasonable tortuosity values. Pharm. Res. 18 (2001) 1797
26. Shivanand P., and Sprockel O.L. A controlled porosity drug delivery system. Int. J. Pharm. 167 (1998) 83-96
27. Siegel R.A., Kost J., and Langer R. Mechanist studies of macromolecular drug release from macrporous polymers. I experiments and prelimnary theory concerning compleateness of drug release. J. Cont. Release. 8 (1990) 223-236
28. Siegel R.A., and Langer R. Mechanist studies of macromolecular drug release from macrporous polymers. II model for the slow kinetics of drug release. J. Cont. Release. 14 (1990) 153-167
29. Song S.-W., Hidajat K., and Kawi S. Functionalized SAB-15 material as carrier fro controlled drug delivery: influence of surface properties on matrix-drug interactions. Langmuir 21 (2005) 9568-9575
30. Streubel A., Sipemann J., and Bodmeier R. Floating microparticles based on low density foam powder. Int. J. Pharm. 241 (2002) 279-292
31. Streubel A., Sipemann J., and Bodmeier R. Multiple unit gastroretentive drug delivery systems: a new method for low density microparticles. J. Microencap. 20 (2003) 329-347
32. Tongta A., Liapis A.I., and Siehr D.J. Equilibrium and kinetic parameters of the adsorption of a -chymotrypsinogen A onto hydrophobic porous adsorbent particles. J. Chromatogr. A 686 (1994) 21-29
33. 3 microparticles and encapsulation by polyelectrolyte multilayer films for sustained drug delivery. Int. J. Pharm. 308 (2006) 160-167
34. Yiotis A.G., Stubos A.K., Boudouvis A.G., and Yortsos Y.C. A 2-D pore-network model of the drying of single-component liquids in porous media. Adv. Water Resourc. 24 (2001) 439-460