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Macromolecules, controlled release

Machluf M, Regev O, Peled Y, et al. Characterization of microencapsulated liposome systems for the controlled delivery of liposome-associated macromolecules. / Control Release 1997 43 35 5. [Pg.23]

M. Thanou, S. Henderson, A. Kydonieus, and C. Elson, N-sulfonato-N, O-carboxy-methylchitosan A novel polymeric absorption enhancer for the oral delivery of macromolecules,/. Control. Release, 117 (2), 171-178,2007. [Pg.294]

H. Zhao, K. Yang, A. Martinez, A. Basu, R. Chintala, H.C. Liu, A. Janjua, M. Wang, D. Filpula, Linear and branched bicin hnkers for releasable PEGylation of macromolecules controlled release in vivo and in vitro from mono- and multi-PEGylated proteins. [Pg.95]

Payne LG, Jenkino SA, Adrianov A, Langer R, and Robert BE. Xenobiotic pol3nners as vaccine vehicles. In Mestecky J (ed). Advances in Mucosal Immunology. New York Plenum Press, pp. 1475-1480. Ibim SM, Ambrosio AA, Larrier D, Allcock HR, and Laurencin CT. Controlled macromolecule release from poly(phosphazene) matrices. J Control Release, 1996, 40, 31-39. [Pg.253]

Robert Langer, Polymer Systems for Controlled Release of Macromolecules, Immobilized Enzyme Medical Bioreactors, and Tissue Engineering J. J. Linderman, P. A. Mahama, K. E. Forsten, and D, A. Lauffenburger, Diffusion and Probability in Receptor Binding and Signaling Rakesh K. Jain, Transport Phenomena in Tumors... [Pg.345]

YH Bae, IC Kwon, CM Pai, SW Kim. Controlled release of macromolecules from electrical and chemical stimuli-sensitive hydrogels. Makromol Chem, Macromol Symp 70 173-177, 1993. [Pg.585]

Langer, R. 1994. Polymer systems for controlled release of macromolecules, immobilized enzyme medical bioreactors, and tissue engineering. In Advances in Chemical Engineering, vol. 19. San Diego, CA Academic Press 1-50. [Pg.349]

Robert Langer, Polymer Systems for Controlled Release of Macromolecules, Immobilized Enzyme Medical Bioreactors, and Tissue Engineering... [Pg.184]

R.Langer, Controlled release of macromolecules, Chemtech, 3 (February), 98-105 (1982). [Pg.191]

D.S.T.Hsieh, C.C.Chiang, D.S.Desai, Controlled release of macromolecules from silicone elatomer, Pharm. Technol., 6,39-49 (1985). [Pg.191]

Bernkop-Schnurch, A., C.E. Kast, and D. Guggi. 2003. Permeation enhancing polymers in oral delivery of hydrophilic macromolecules Thiomer/GSH systems. J Control Release 93 95. [Pg.52]

Choksakulnimitr S, Masuda S, Tokuda H et al (1995) In vitro cytotoxicity of macromolecules in different cell culture systems. J Control Release 34(3) 233—241... [Pg.186]

N. S. Patil, J. S. Dordick, and D. G. Rethwisch, Macroporous poly(sucrose acrylate) hydrogel for controlled release of macromolecules, Biomaterials, 17 (1996) 2343-2350. [Pg.291]

The controlled release of macromolecules from non-erodible, hydrophobic polymeric matrices is modelled as a discrete diffusion process with the release of solute occuring through distinct pores in the polymer which are formed as solid particles of molecule dissolve. In order to formulate predictive models of the release behavior of these devices, quantitative information on the microgeometry of the system is required. We present a computer-based system for obtaining estimates of the system porosity, isotropy, particle shape, and particle size distribution from observations on two-dimensional sections from the polymer matrix. [Pg.16]

Schacht, E. "Polysaccharide Macromolecules as Drug Carriers" In "Controlled Release of Drugs from Polymer Particles and Macromolecules" Ilium, L. Davis, S.S. Eds. John Wright Bristol, in press. [Pg.199]

Bernkop-Schnurch A, Gockel NC (1997) Development and analysis of a polymer protecting from luminal enzymatic degradation caused by a-chymotrypsin. Drug Dev Ind Pharm 23 733-740 Bernkop-Schnurch A, Kast CE, Guggi D (2003) Permeation enhancing polymers in oral delivery of hydrophilic macromolecules thiomer / GSH systems. J Control Release. 2003 Dec 5 93(2) 95-103. [Pg.80]

Dendrimers Well-defined, nanosized, monodispersing macromolecules with hyperbranched structures Loading all kinds of active agents for good bioavailability, targeted delivery, and controlled release 23... [Pg.1253]

Figure 5.31. Network (megamer) formation through the hydrolysis/crosslinMng of neighboring PAMAMOS dendrimer units. Hydrolysis of the C-O-Si bond may also be exploited for the controlled-release of entrained agents (e.g, cancer drugs, etc.). It should be noted that subsequent thermal annealing to remove the PAMAM cores results in a nanoporous network that has a dielectric constant (k) of ca. 1.5 - of extreme interest for next-generation IC interconnect applications. Reproduced with permission from Dvornic, P. R. Li, J. de Leuze-Jallouli, A. M. Reeves, S. D. Owen, M. J. Macromolecules, 2002, 35, 9323. Copyright 2002 American Chemical Society. Figure 5.31. Network (megamer) formation through the hydrolysis/crosslinMng of neighboring PAMAMOS dendrimer units. Hydrolysis of the C-O-Si bond may also be exploited for the controlled-release of entrained agents (e.g, cancer drugs, etc.). It should be noted that subsequent thermal annealing to remove the PAMAM cores results in a nanoporous network that has a dielectric constant (k) of ca. 1.5 - of extreme interest for next-generation IC interconnect applications. Reproduced with permission from Dvornic, P. R. Li, J. de Leuze-Jallouli, A. M. Reeves, S. D. Owen, M. J. Macromolecules, 2002, 35, 9323. Copyright 2002 American Chemical Society.

See other pages where Macromolecules, controlled release is mentioned: [Pg.137]    [Pg.137]    [Pg.33]    [Pg.117]    [Pg.104]    [Pg.244]    [Pg.422]    [Pg.399]    [Pg.396]    [Pg.84]    [Pg.17]    [Pg.162]    [Pg.148]    [Pg.115]    [Pg.1652]    [Pg.2391]    [Pg.2710]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.6 , Pg.7 , Pg.8 , Pg.9 , Pg.10 ]




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