In vitro and in vivo release properties of brilliant blue and tumour necrosis factor-alpha (TNF-alpha) from poly(D,L-lacticco-glycolic acid) multiphase microspheres

References

• COHEN, S., YOSHIOKA, T., LUCARELLI, M, HWANG; L. H., and LAN3ER, R., 1991, Controlled delivery system for proteins based on poly(lactic/glycolic acid) microspheres. Pharmaceutical Research, 8, 713–720.
   Google Scholar
• HERRMAN J., and BCEMEER, R., 1995, Somatostatin containing biodegradable microspheres prepared by a modified solvent evaporation method based on w/o/w-multiple emulsions. International Journal of Pharmaceutics, 126, 129–138.
   Web of Science ®Google Scholar
• HERRMAN J., and BCDIVITER, R., 1998, Biodegradable, somatostatin acetate containing microspheres prepared by various aqueous and non-aqueous solvent evaporation techniques. European Journal of Pharmaceutics and Biopharmaceutics, 45, 75–82.
   PubMed Web of Science ®Google Scholar
• HEYA T., OKADA, H, TANGWARA, Y., WM, Y., and TCGUCHI, H, 1991, Effects of counteranion of TRH and loading amount on control of TRH release from copoly(DL-lactic/glycolic acid) microspheres prepared by an in-water drying method. International Journal of Pharmaceutics, 69, 69–75.
   Google Scholar
• HORA, M. S., RANA, R. K., NUNBERG, J. H., TICE T. R., GILLEY, R. M., and FILESCN M. E, 1990, Release of human serum albumin from poly(lactide-co-glycolide) micro-spheres. Pharmaceutical Research, 7, 1190–1194.
   Google Scholar
• IWATA M, and McGthrry, J. W., 1992 Preparation of multi-phase microspheres of poly(PL-lactic acid) and poly(PL-lactic-co-glycolic acid) containing a W/O emulsion by a multiple emulsion solvent evaporation technique. Journal of Microencapsulation, 9, 201–214.
   PubMed Web of Science ®Google Scholar
• IWATA M., and MCGINTY, J. W., 1993, Dissolution, stability, and morphological properties of conventional and multiphase poly(m-lactic-co-glycolic acid) microspheres containing water-soluble compounds. Pharmaceutical Research, 10, 1219–1227.
   PubMed Web of Science ®Google Scholar
• IWATA, M, NAKAMURA, Y., and MCGINITY, J. W., 1999, Particle size and loading efficiency of poly(PL-lactic-co-glycolic acid) multiphase microspheres containing water soluble substances prepared by the hydrous and anhydrous solvent evaporation method. Journal of Microencapsulation, 16, 49–58.
   PubMed Web of Science ®Google Scholar
• IWATA M., TANAKA, T., NAKAMLRA Y., and MCGINTY, J. W, 1998, Selection of the solvent system for the preparation of poly(Phlactic-co-glycolic acid) microspheres containing tumor necrosis factor-alpha (TNF-alpha). International Journal of Pharmaceutics, 160, 145–156.
   Google Scholar
• JCHNSON R. E, LANASKE, L. A., GUPRA V., GRIFFIN M J., GLAD H T., NEMHAM T. E, and ZIA, H., 1991, Stability of atriopeptin III in poly(Et-lactic-co-glycolide) microspheres. Journal of Controlled Release; 17, 61–68.
   Web of Science ®Google Scholar
• LI, S., GARREAU H., and VERT, M., 1990, Structure-property relationships in the case of the degradation of massive poly(a-hydroxy acids) in aqueous media Part 2: Degradation of lactide-glycolide copolymers: PLA37.5GA25 and PLA75GA25. Journal of Materials Science: Materials in Medicine, 1, 131–139.
   Google Scholar
• MARCHAIS, H, BOURY, F., DAMS C., PRCCBT, J.-E, and BENar, J.-P., 1996, Formulation of bovine serum albumin loaded PLGA microspheres influence of the process variables on the loading and in vitro release. S.T T.P. Pharma Sciences, 6, 417–423.
   Google Scholar
• MCGINITY, J. W., and IWATA M, 1994, United States Patent No. 5,288,502.
   Google Scholar
• O’DONNELL, P. B., and MCGINTY, J. W., 1996, Properties of multiphase microspheres of poly(Et-lactic acid) or poly(m-lactic-co-glycolic acid) produced by mechanical agitation, sonication, or potentiometric dispersion. Journal of Microencapsulation, 13, 667–677.
   Google Scholar
• O’DONNELL, P. B., and MCGINTY, J. W, 1998, Influence of processing on the stability and release properties of biodegradable microspheres containing thioridazine hydro-chloride. European Journal of Pharmaceutics and Biopharmaceutics, 45, 83–94.
   Google Scholar
• O’DONNELL, P. B., IwATA M, and MCGINTY, J. W, 1995, Properties of multiphase microspheres of poly(PL-lactic-co-glycolic acid) prepared by a potentiometric dispersion technique. Journal of Microencapsulation, 12, 155–163.
   Google Scholar
• O’HAGAN D. T., JEHtRY, H, and DAVE S. S., 1994, The preparation and characterization of poly(lactide-co-glycolide) microparticles: III. Microparticle/polymer degradation rates and the in vitro release of a model protein. International Journal of Pharmaceutics, 103, 37–45.
   Google Scholar
• SAH T., TCDDYWALA, R., and CHLEN1 Y. W., 1994, The influence of biodegradable microcapsule formulations on the controlled release of a protein. Journal of Controlled Release, 30, 201–211.
   Google Scholar
• SANDER L. M., MCRAE, G. I., VITAL K M., and KM-, B. A., 1985, Controlled delivery of an LBRH analogue from biodegradable injectable microspheres. Journal of Controlled Release, 2, 187–195.
   Google Scholar
• UCHIDA, T., Yaii[DA, K, and GOFQ S., 1996, Preparation and characterization of polylactic acid microspheres containing water-soluble dyes using a novel w/o/w emulsion solvent evaporation method. Journal of Microencapsulation, 13, 219–228.
   Google Scholar
• UCHIDA, T., YCRIDA, K, NE\Cm[YA, A., and GOFQ S., 1995, Optimization of preparative conditions for polylactide (PLA) microspheres containing ovalbumin. Chemical Pharmaceutical Bulletin, 43, 1569–1573.
   Google Scholar
• VERT, M., LI, S., and GARREAL1 H., 1991, More about the degradation of LA/GA-derived matrices in aqueous media Journal of Controlled Release, 16, 15–26.
   Google Scholar
• YAMAKAWA, I., TSLISHINA Y., MACHEDN, R., and WATANABE, S., 1992, In vitro and in vivo release of poly(DL-lactic acid) microspheres containing neurotensin analogue prepared by novel oil-in-water solvent evaporation method. Journal of Pharmaceutical Sciences, 81, 808–811.
   Google Scholar