References
- BISWAS, M., A KOGYERAM, C. 0., SCOTT, K. R., POTTI, G. K., GALLELLI, J. F., and H ABIB, M. J., 1993, Development of carbamazepine:phospholipid dispersion formulations. Journal of Controlled Release, 23, 239.
- CHIOU, W. L., and R IEGELMAN, S., 1971, Preparation and dissolution characteristics of several fast-release solid dispersions of griseofulvin. Journal of Pharmaceutical Sciences, 60, 1281.
- COLPAERT, F. C., KOEK, W., L EHMANN, J., RIVET, J. M., L EJEUNE, F., CANTON, H., B ERVOET S, K., MHLAN, M. J., LAumE, M., and LAviELLE, G., 1992, S14506: A novel, potent, high-efficacy 5-HT lA agonist and potential anxiolytic agent Drug Development Research, 26, 21.
- DOHERTY, C., and YORK, P., 1989, Microenvironmental pH control of drug dissolution. International Journal of Pharmacy, 50, 223.
- GARCIA S AGRADO, F., GUZMAN, M POLPECERES, J., and A PERTURAS, M. R., 1994, Pluronic copolymers, characteristics, properties and pharmaceutical applications II. Pharmaceutical Technology in Europe, 6, 38.
- GAUT IER, S., 1995, Hydrophobisation du vecteur poly(L-lysine citramide): Comportement physico-chimique et aptitude A solubiliser des molecules lipophiles dans l'eau. These de doctorat, Universite de Montpellier, France.
- HABIB, M. J., A KOGYERAM, C. 0., and A HMADI, B., 1993, Improved dissolution of indomethacin in coprecipitates with phospholipids-I. Drug Developments in Industrial Pharmacy, 19, 499.
- HUGUET, J., and VERT, M., 1985, Partially quaternized poly(tertiary amine) as pH-dependent drug carrier for solubilization and temporary trapping of lipophilic drugs in aqueous media Journal of Controlled Release, 1, 217.
- LAVIELLE, G., L AUBIE, M., and CoLPAERT, F., 1991, 1-Naphthylpiperazine derivatives, process for their preparation and pharmaceutical compositions containing them. European Patent Application EP 434,561 (Cl. C07D295/12).
- MALLARD, C., COUDANE, J., R AULT, I., and VERT, M., 1999, Attempts to adjust the in vitro delivery of a sparingly water soluble compound from PLA50 microparticles. Journal of Microencapsulation, in press.
- MARIETTE, B., COUDANE, J., VERT, M., GAUTIER, J. C., and MONETON, P., 1993, Release of the GRF29NH2 analog of human GRF44NH2 from a PLA/GA matrix. Journal of Controlled Release, 24, 237.
- POIRIER-LITTRE, M. F., 1989, Systeme sdrotoninergique et depression. Conference de l'Institut Pasteur (Paris: 3, Masson publisher).
- POTTI, G. K., GALLELLI, J. F., AKOGYERAM, C. 0., AHMADI, B., and HABIB, M. J., 1993, Improved dissolution of indomethacin in coprecipitates with phospholipids-II. Drug Developments in Industrial Pharmacy, 19, 1221.
- PUISIEUX, F., and DELATTRE, J., 1985, Physico-chimie des phospholipides in 'Les liposomes', Technique et Documentation, Lavoisier Ed. (Paris), chap 1, 1.
- SAVE, T., and VENKITACHALAK P., 1992, Studies on solid dispersions of nifedipine. Drug Devices in Pharmacy, 18, 1663.
- SCHWACH, G., COUDANE, J., ENGEL, R., and VERT, M., 1994, Stannous octoate versus zinc initiated polymerization of racemic lactide. Effects on configurational structures. Polymer bulletin, 32, 617–623.
- SERAJUDDIN, A. T. M., and JAROWSKI, C., 1985, Effect of diffusion layer pH and solubility on the dissolution rates of pharmaceutical acids and their sodium salts. II. Salicylic acid, theophylline and benzoic acid. Journal of Pharmaceutical Sciences, 74, 148.
- SPENLEHAUER, G., VEILLARD, M., and BENOIT, J. P., 1986, Formation and characterization of cisplatin loaded poly(D,L-lactide) microspheres for chemoembolization. Journal of Pharmaceutical Sciences, 75, 750.
- VANDERVEEN, C., BUITENDIJK, H., and LERK, C. F., 1991, The effect of acidic excipients on the release of wealdy basic drugs from the programmed release megaloporous system. European Journal of Pharmacy and Biopharmacy, 37, 238.
- VENKATARAM, S., and ROGERS, J. A., 1984, Characteristics of drug-phospholipid coprecipitates I: Physical properties and dissolution behavior of griseofulvin-dimyristoylphosphatidylcholine systems. Journal of Pharmaceutical Sciences, 73, 757.
- VENKARARAM, S., and ROGERS, J. A., 1985, Controlled release of griseofulvin from coprecipitates with phospholipids. Drug Developments in Industrial Pharmacy, 11 (2 & 3), 223.
- VUDATHALA, G. K., and ROGERS, J. A., 1992a, Dissolution of fluorocortisone from phospholipid coprecipitates. Journal of Pharmaceutical Sciences, 81, 282.
- VUDATHALA, G. K., and ROGERS, J. A., 1992b, Microencapsulation of solid dispersions: Release of griseofulvin from griseofulvin:phospholipid coprecipitates in micro-spheres, Pharmaceutical Research, 9, 759.