Interactive Mixture as a Rapid Drug Delivery System

REFERENCES

• Betageri G. V., Dipali S. R. Preparation and in vitro dissolution profiles of tolazamide-polyethylene glycol solid dispersions. Drug Dev. Ind. Pharm. 1995; 21: 1347–1352
   Web of Science ®Google Scholar
• Chiou W. L., Riegelman S. Pharmaceutical applications of solid dispersion systems. J. Pharm. Sci. 1971; 60: 1281–1302
   PubMed Web of Science ®Google Scholar
• Chutimaworapan S., Ritthidej G. C., Yonemochi E., Oguchi T., Yamamoto K. Effect of water-soluble carriers on dissolution characteristics of nifedipine solid dispersions. Drug Dev. Ind. Pharm. 2000; 26: 1141–1150
   PubMed Web of Science ®Google Scholar
• Doshi D. H., Ravis W. R., Betageri G. V. Carbamazepine and polyethylene glycol solid dispersions: Preparation, in vitro dissolution, and characterization. Drug Dev. Ind. Pharm. 1997; 23: 1167–1176
   Web of Science ®Google Scholar
• Goldberg A. H., Gibaldi M., Kanig J. L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures II: Experimental evaluation of eutectic mixture: Urea-acetaminophen system. J. Pharm. Sci. 1966a; 55: 482–487
   Web of Science ®Google Scholar
• Goldberg A. H., Gibaldi M., Kanig J. L. Increasing dissolution rates and gastrointestinal absorption of drugs via solid solutions and eutectic mixtures III: Experimental evaluation of griseofulvin-succinic acid solution. J. Pharm. Sci. 1966b; 55: 487–492
   Web of Science ®Google Scholar
• Hickey A. J., Ganderton D. Size reduction and classification. Pharmaceutical Process Engineering, A. J. Hickey, D. Ganderton. Marcel Dekker, New York 2001; 174–197
   Google Scholar
• Jachowicz R., Nürnberg E., Hoppe R. Solid dispersions of oxazepam. Int. J. Pharm. 1993; 99: 321–325
   Web of Science ®Google Scholar
• Jachowicz R., Nürnberg E., Hoppe R. Enhanced release of oxazepam from tablets containing solid dispersions. Int. J. Pharm. 1997; 159: 149–158
   Web of Science ®Google Scholar
• Joshi H. M., Tejwani R. W., Davidovich M., Sahasrabudhe V. P., Jemal M., Bathala M. S., Varia S. A., Serajuddin A. T. M. Bioavailability enhancement of a poorly water-soluble drug by solid dispersion in polyethylene glycol-polysorbate 80 mixture. Int. J. Pharm. 2004; 269: 251–258
   PubMed Web of Science ®Google Scholar
• Karavas E., Ktistis G., Xenakis A., Georgarakis E. Miscibility behavior and formation mechanism of stabilized felodipine-polyvinylpyrrolidone amorphous solid dispersions. Drug Dev. Ind. Pharm. 2005; 31: 473–489
   PubMed Web of Science ®Google Scholar
• Karavas E., Georgarakis E., Sigalas M. P., Avgoustakis K., Bikiaris D. Investigation of the release mechanism of a sparingly water-soluble drug from solid dispersions in hydrophilic carriers based on physical state of drug, particle size distribution and drug-polymer interactions. Eur. J. Pharm. Biopharm. 2007; 66: 334–347
   PubMed Web of Science ®Google Scholar
• Kerć J., Srćić S., Kofler B. Alternative solvent-free preparation methods for felodipine surface solid dispersions. Drug. Dev. Ind. Pharm. 1998; 24: 359–363
   PubMed Web of Science ®Google Scholar
• Lin C.-W., Cham T.-M. Effect of particle size on the available surface area of nifedipine from nifedipine-polyethylene glycol 6000 solid dispersions. Int. J. Pharm. 1996; 127: 261–272
   Web of Science ®Google Scholar
• Lin S. L., Menig J., Lachman L. Interdependence of physiological surfactant and drug particle size on the dissolution behavior of water-insoluble drugs. J. Pharm. Sci. 1968; 57: 2143–2148
   PubMed Web of Science ®Google Scholar
• Liu C., Wu J., Shi B., Zhang Y., Gao T., Pei Y. Enhancing the bioavailability of cyclosporine A using solid dispersion containing polyoxyethylene (40) stearate. Drug Dev. Ind. Pharm. 2006; 32: 115–123
   PubMed Web of Science ®Google Scholar
• Nilsson P., Westerberg M., Nyström C. Physicochemical aspects of drug release. V. The importance of surface coverage and compaction on drug dissolution from ordered mixtures. Int. J. Pharm. 1988; 45: 111–121
   Web of Science ®Google Scholar
• Nyström C., Westerberg M. The use of ordered mixtures for improving the dissolution rate of low solubility compounds. J. Pharm. Pharmacol. 1986; 38: 161–165
   PubMed Web of Science ®Google Scholar
• Parrott E. L. Milling in pharmaceutical solids. J. Pharm. Sci. 1974; 63: 813–829
   PubMed Web of Science ®Google Scholar
• Rabasco A. M., Ginés J. M., Fernández-Arévalo M., Holgado M. A. Dissolution rate of diazepam from polyethylene glycol 6000 solid dispersions. Int. J. Pharm. 1991; 67: 201–205
   Web of Science ®Google Scholar
• Ren F., Jing Q., Tang Y., Shen Y., Chen J., Gao F., Cui J. Characteristics of bicalutamide solid dispersions and improvement of the dissolution. Drug Dev. Ind. Pharm. 2006; 32: 967–972
   PubMed Web of Science ®Google Scholar
• Save T., Venkitachalam P. Studies on solid dispersions of nifedipine. Drug Dev. Ind. Pharm. 1992; 18: 1663–1679
   Web of Science ®Google Scholar
• Sekiguchi K., Obi N. Studies on absorption of eutectic mixture. I. A comparison of the behavior of eutectic mixture of sulfathiazole and that of ordinary sulfathiazole in man. Chem. Pharm. Bull. 1961; 9: 866–872
   Web of Science ®Google Scholar
• Serajuddin A. T. M. Solid dispersion of poorly water-soluble drugs: Early promises, subsequent problems, and recent breakthroughs. J. Pharm. Sci. 1999; 88: 1058–1066
   PubMed Web of Science ®Google Scholar
• Sheu M.-T., Yeh C.-M., Sokoloski T. D. Characterization and dissolution of fenofibrate solid dispersion systems. Int. J. Pharm. 1994; 103: 137–146
   Google Scholar
• Sjökvist E., Nyström C. Physicochemical aspects of drug release. VI. Drug dissolution rate from solid particulate dispersions and the importance of carrier and drug particle properties. Int. J. Pharm. 1988; 47: 51–66
   Web of Science ®Google Scholar
• Sjökvist E., Nyström C., Aldén M. Physicochemical aspects of drug release. XIII. The effect of sodium dodecyl sulphate additions on the structure and dissolution of a drug in solid dispersions. Int. J. Pharm. 1991; 69: 53–62
   Web of Science ®Google Scholar
• Sjökvist Saers E., Nyström C., Aldén M. Physicochemical aspects of drug release. XVI. The effect of storage on drug dissolution from solid dispersions and the influence of cooling rate and incorporation of surfactant. Int. J. Pharm. 1993; 90: 105–118
   Web of Science ®Google Scholar
• Sjökvist E., Nyström C., Aldén M., Caram-Lelham N. Physicochemical aspects of drug release. XIV. The effects of some ionic and non-ionic surfactants on properties of a sparingly soluble drug in solid dispersions. Int. J. Pharm. 1992; 79: 123–133
   Web of Science ®Google Scholar
• Sugimoto I., Kuchiki A., Nakagawa H., Tohgo K., Kondo S., Iwane I., Takahashi K. Dissolution and absorption of nifedipine from nifedipine-polyvinylpyrrolidone coprecipitate. Drug Dev. Ind. Pharm. 1980; 6: 137–160
   Web of Science ®Google Scholar
• Vippagunta S. R., Maul K. A., Tallavajhala S., Grant D. J. W. Solid-state characterization of nifedipine solid dispersions. Int. J. Pharm. 2002; 236: 111–123
   PubMed Web of Science ®Google Scholar
• Westerberg M., Jonsson B., Nyström C. Physicochemical aspects of drug release. IV. The effect of carrier particle properties on the dissolution rate from ordered mixtures. Int. J. Pharm. 1986; 28: 23–31
   Web of Science ®Google Scholar
• Westerberg M., Nyström C. Physicochemical aspects of drug release. XII. The effect of some carrier particle properties and lubricant admixture on drug dissolution from tableted ordered mixtures. Int. J. Pharm. 1991; 69: 129–141
   Web of Science ®Google Scholar
• Westerberg M., Nyström C. Physicochemical aspects of drug release. XVII. The effect of drug surface area coverage to carrier materials on drug dissolution from ordered mixtures. Int. J. Pharm. 1993; 90: 1–17
   Web of Science ®Google Scholar