Poly epsilon-caprolactone nanoparticles containing a poorly soluble pesticide: formulation and stability study

References

• ADAmSON A. W., 1990, Adsorption of gases and vapors on solids. In Physical Chemistry of Surfaces, 5th edn, edited by Wiley-Interscience, New York) pp. 591–681.
   Google Scholar
• ALCNSC:t M. J., IDEA, C, CALArq R, and VILA-JATQ J. L, 1991, Approaches to improve the association of amikacin sulfate to poly(alkylcyanoacrylate) nanoparticles. Inter-national Journal of Pharmacy, 68, 69–76.
   Web of Science ®Google Scholar
• ALCNSQ M J., SANCHEZ, A., TCRRES, D., SEUQ B., and VILA JATQ J. L, 1990, Joint effects of monomer and stabilizer concentration on physico-chemical characteristics of poly(buty1-2-cyanoacrylate) nanoparticles. Journal of Microencapsulation, 7, 517–526.
   Google Scholar
• BAPAT, N., and BCROUJERDI, M, 1992, Uptake capacity and adsorption isotherms of doxorubicin on polymeric nanoparticles: effect of methods of preparation. Drug Developments in Industrial Pharmacy, 18, 65–77.
   Web of Science ®Google Scholar
• DOUGLAS, S. J., num, L, and DAVIS, S. S., 1985, Particle size and size distribution of poly(butyl 2-cyanoacrylate) nanoparticles. II. Influence of stabilizers. Journal of Colloid Interface Science, 103, 154–163.
   Web of Science ®Google Scholar
• FESSI, H., PuISIEux, F., DEVISSAGUET, J. R, AMMOURY, N., and BENITA, S., 1989, Nanocapsule formation by interfacial polymer deposition following solvent displacement. International Journal of Pharmacy, 55, R1—R4.
   Google Scholar
• GILES, C 11, D'SHNA, A. P., and EASTCN J. A., 1974b, A general treatment and classification of the solute adsorption isotherm. Part II. Experimental interpretation, Journal of Colloid Science, 47, 766–778.
   Google Scholar
• GILES, C H., SMITH, D., and HUITSCN A., 1974a, A general treatment and classification of the solute adsorption isotherm. Part I. Theoritical, Journal of Colloid Science, 47, 755–765.
   Google Scholar
• GUTERRES, S. S., FESSI, 11., BARRATT, G., DEVISSAGUET, J. R, and RASIEux, F., 1995, Poly(DL-lactide) nanocapsules containing diclofenac I. Formulation and stability study, International Journal of Pharmacy, 113, 57–63.
   Google Scholar
• HARMIA, T., SPEISER, R, and KREUTER, J., 1987, Nanoparticles as drug carriers in ophtalmology. Pharmacetica. Acta Helvetica, 62, 322–331.
   PubMed Web of Science ®Google Scholar
• ILUMM, KHAN M A., MARK, E, and DAVIS, S. S., 1986, Evaluation of carrier capacity and release characteristics for poly (butyl-2-cyanoacrylate) nanoparticles. Inter-national Journal of Pharmacy, 30, 17–28.
   Google Scholar
• JEFFERY, H., DAVIS, S. S., and 0 HAGAN D. T., 1991, The preparation and characterization of poly(lactide-co-glycolide) microparticles. I: Oil-in-water emulsion solvent evaporation. International Journal of Pharmacy, 77, 169–175.
   Google Scholar
• JULIENNE, M. C, ALONSCA M. J., GOMEZ AmCgA, J. L, and BENOIT, J. P., 1992, Preparation of poly (D,L-lactide/glycolide) nanoparticles of controlled particle size distribution: application of experimental designs, Drug Developments in Industrial Pharmacy, 10, 1063–1077.
   Google Scholar
• KREUTER, J., 1992, Technics in Microcapsules and Nanoparticles in Medicine and Pharmacy, edited by M. Donbrow (Boca Raton, CRC Press Inc.), pp. 126–143.
   Google Scholar
• MOLPECERE, S. J., GuzmAN M., ABERTURAS, M. R., CHAOCN, M., and BERGES, L, 1996, Application of central composite designs to the preparation of polycaprolactone nanoparticles by solvent displacement, Journal of Pharmaceutical Science, 85, 206–213.
   Google Scholar
• MURAKAM1, 11., KAWASHIMA, Y., NIWA, T., limp T., TAKEuaii, H., and KOBAYASHI, M., 1997, Influences of the degrees of hydrolyzation and polymerization of poly(vinylalcohol) on the preparation and properties of poly(DL-lactide-co-glycolide) nanoparticles. International Journal of Pharmacy, 149, 43–49.
   Google Scholar
• NIWA, T., TAKEUCHI, H., HiNq T., KUNOU, N., and KAWASHIMA, Y., 1993, Preparations of biodegradable nanospheres of water-soluble and insoluble drugs with DL-lactide/ glycolide copolymer by a novel spontaneous emulsification solvent diffusion method and the drug release behavior. Journal of Controlled Release, 25, 89–98.
   Google Scholar
• PITT, C G, GRATZL, M M., JEFFCOAT, A. R., ZWEIDINGER, R. A., and SCHINDLER, A., 1979b, Sustained drug delivery systems. II factors affecting release rates from poly(e-caprolactone) and related biodegradable polyesters. Journal of Pharmaceutical Science, 68, 1534–1538.
   PubMed Web of Science ®Google Scholar
• PITT, C G., JEFFCOAT, A. R., ZWEIDINGER, R. A., and SC:HINDLFR, A., 1979a, Sustained drug delivery systems. I the permeability of poly(e-caprolactone), poly(DL-lactic acid) and their copolymers, Journal of Biomedical Materials Research, 13, 497–507.
   Google Scholar
• SANTCS MAGALHAES, N. S., FESSI, N. S., PUISIEUX, F. BENITA, S., and SEILLER, M., 1995, An in vitro release kinetic examination between submicron emulsion and polylactic acid nanocapsules of clofibride. Journal of Microencapsulation, 12, 195–205.
   Google Scholar
• STAINMESSE S., ORECCHHIONI, A. M., and NAKAC:HE, E, 1992, Modeling of an original process to obtain biocompatible polymeric NS, 6th International Conference on Pharmaceutical Technology, I, 89–97.
   Google Scholar
• VANSNICK, L, CCUVREUR, P., CHRISTIAENS- LEYH, D., and ROLAND M, 1985, Molecular weights of free and drug-loaded nanoparticles. Pharmaceutical Research, 1, 36–41.
   Google Scholar