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PLGA microspheres

Suarez, S., O hara, P., Kazantseva, M., et al. (2001a). Respirable PLGA microspheres containing rifampicin for the treatment of tuberculosis Screening in an infectious disease model. Pharmaceut. Res., 18, 1315-1319. [Pg.282]

Fu, K., Pack, D.W., Klibanov, A.M., and Langer, R. (2000). Visual evidence of acidic environment within degrading poly(lactic-co-glycolic acid) (PLGA) microspheres. Pharmaceut. Res., 17, 100-106. [Pg.304]

Jeyanthi, R., Mehta, R.C., Thanoo, B.C., and Deluca, P.P. (1997). Effect of processing parameters on the properties of peptide-containing PLGA microspheres. J. Microencapsulation, 14, 163-174. [Pg.304]

Shive MS, Anderson JM. Biodegradation and biocompatibility of PLA and PLGA microspheres. Adv Drug Deliv Rev 1997 28 5-24. [Pg.356]

TABLE 9.2 Physicochemical Characteristics of PLGA Microspheres Containing Leuprolide Acetate... [Pg.282]

Figure 9.2 Effect of drug load on the in vitro release of leuprolide acetate from PLGA microspheres. Figure 9.2 Effect of drug load on the in vitro release of leuprolide acetate from PLGA microspheres.
Ravivarapu, H. B., Lee, H., and DeLuca, P. P. Enhancing initial release of peptide from poly(D,L-lactide-co-glycolide) (PLGA) microspheres by addition of a porosigen and increasing drug load. Pharm. Dev. Techrwl. 5(2) 287-296, 2000. [Pg.302]

Hickey T, Kreutzer D, Burgess DJ, Moussy F. Dexamethasone/PLGA microspheres for continuous delivery of an anti-inflammatory drug for implantable medical devices. Biomaterials 2002, 23, 1649-1656. [Pg.84]

The Lupron Depot comprises a PLA/PLGA microsphere delivery system for the delivery of the GnRH analog, leuprolide, over a 1-, 3-, or 4-month period. The release rate is determined by the polymer composition and molecular weight (Table 4.5). [Pg.92]

PLGA microspheres can be prepared in rather narrow size ranges from 0.2 /mi up to > 100 /mi. The preparation, properties and degradation of these polymers have been discussed extensively in Chapter 4 (see Section 4.5.1). PLGA microspheres can now be prepared with surface oriented PEG-chains which improves in vivo circulation time ( stealth-effects ). [Pg.126]

Damgge G, Aprahamian M, Marchais H, Benoit JP, Pinget M (1996) Intestinal absorption of PLGA microspheres in the gut. J Anat 189 491 -501... [Pg.172]


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See also in sourсe #XX -- [ Pg.393 , Pg.404 ]

See also in sourсe #XX -- [ Pg.21 , Pg.31 ]




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