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Microspheres drug targeting

Hsu Y Y, Hao T, Hedley M L (1999). Comparison of process parameters for microencapsulation of plasmid DNA in poly(D,L-lactic-co-glycolic) acid microspheres. /. Drug Target. 7 313-323. [Pg.1055]

E. Norman, P. Williams and S. E. Dunn. 1993. Microspheres for targeting drugs to sped c body sites. J. Control. Rel24 157-163. [Pg.365]

Tomlinson, E., Burger, J., and Schoonderwoerd, E. Human serum albumin microspheres for intraarterial drug targeting of cytostatic compounds, pharmaceutical aspects and release characteristics, in Microspheres and Drug Therapy. Pharmaceutical, Immunological and Medical Aspects, ed. S. Davies et al. New York Elsevier Science Publishers, 1984, pp. 217-227. [Pg.303]

Moritera, T.-O., Y., Yoshimura, N., Kuriyama, S., Honda, Y., Tabata, Y. and Ikada, Y. (1994) Feasibility of drug targeting to the retinal pigment epithelium with biodegradable microspheres. Current Eye Research, 13 171-176. [Pg.318]

El-Shafy, M. A., Kellaway, I. W., Taylor, G, and Dickinson, P. A. (2000), Improved nasal bioavailability of FITC-dextran (Mw 4300) from mucoadhesive microspheres in rabbits, J. Drug Target., 7, 355-361. [Pg.681]

Tomlinson E. Microsphere delivery systems for drug targeting and controlled release. Int J Pharm Tech Prod Mfr 1983 4 49-57. [Pg.381]

A. E. Senyei and K. J. Widder. Drug targeting magnetically responsive albumin microspheres. A review of the system to date. Gynaecol. Oncol. 72 1-3 (1981). [Pg.36]

Menei P, Benoit JP, Boisdron-Celle M, Fournier D, Mercier P, Guy G. Drug targeting into the central nervous system by stereotactic implantation of biodegradable microspheres. Neurosurgery 1994 34 1058—1064. [Pg.369]

Jepson, M.A., Simmons, N.L., Hagan, D.T.O., Hirst, B.H. Comparison of poly(DL-lactide-co-glycolide) and polystyrene microsphere targeting to intestinal M cells. J. Drug Target., 1, 245, 1993. [Pg.1377]

Patashnik, S., Rabinovich, L., Golomb, G. (1997). Preparation and evaluation of chitosan microspheres containing bisphosphonates, 1. Drug Target. 4(6), 371-380. [Pg.581]

Ma, X.H., Santiago, N., Chen, Y.S., Chaudhary, K., Milstein, S.J., and Baughman, R.A., Stability study of dmg-loaded proteinoid microsphere formulations during freeze-drying, J. Drug Target., 1994, 2, 9-21. [Pg.997]

Drugs, cosmetic ingredients, and food additives are microencapsulated for a variety of reasons, which include reducing local side-effects, controlled release, site-specific (drug) delivery, and drug targeting. A tremendous amount of research work has been done in a search for suitable methods to achieve an effective eneapsulation of water-soluble active matter. The physical characteristics of the microspheres produced largely determine their suitability for use for different objectives. Microspheres are prepared from both natural and synthetic polymers. [Pg.396]

Khan, A. et al.. Site-specific administration of antisense oligonucleotides using biodegradable polymer microspheres provides sustained delivery and improved subcellular biodistribution in the neostriatum of the rat brain, /. Drug Target, 8,319,2000. [Pg.273]


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See also in sourсe #XX -- [ Pg.2334 ]




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