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Microparticles controlled drug delivery

Kumar, M. (2000). Nano and microparticles as controlled drug delivery devices. Journal of Pharmacy and Pharmaceutical Sciences, Vol. 3, 2, (May-August 2000), pp. (234-258), ISSN 1482-1826... [Pg.81]

Nanoparticles show great promise as devices for the controlled release of drugs, provided that the choice of material for nanoparticle formation is made with the appropriate considerations of the drug cargo, administration route, and the desired site of action. The use of nano- and microparticles as controlled drug-delivery devices has recently been extensively reviewed [97]. [Pg.519]

The microparticle system has become an indispensable part of the controlled drug delivery fields for the past few decades since it can readily be adapted for various administration methods. In particular, biodegradable polymeric microparticles can provide a number of advantages over conventional parenteral formulations ... [Pg.2315]

Natural polymers such as proteins, carbohydrates, fats, and waxes constitute an important group of encapsulation materials however, microparticles for the controlled drug delivery purpose have been prepared... [Pg.2319]

Drug release from biodegradable polymer microparticles is determined by the polymer degradation kinetics, structural features of the microparticles, and distribution of the drugs within the particle matrix. The ultimate goal of microparticle systems in the controlled drug delivery is to achieve readily tunable release profiles, which has been pursued in various perspectives. [Pg.2322]

Brannon-Peppas, L. Recent advances on the use of biodegradable microparticles and nanoparticles in controlled drug delivery. Int. J. Pharm. 1995, 116, 1-9. [Pg.3256]

Ravi Kumar MN. Nano and microparticles as controlled drug delivery devices. J Pharm Pharm Sci 3(2) 234-258, 2000. [Pg.580]

Figure 1 Formulation of controlled drug delivery systems using the supercritical fluid-derived RESS process (A) films, (B) microparticles/nanoparticles/ liposomes, (C) coated products including microcapsules, and (D) microporous foams. Figure 1 Formulation of controlled drug delivery systems using the supercritical fluid-derived RESS process (A) films, (B) microparticles/nanoparticles/ liposomes, (C) coated products including microcapsules, and (D) microporous foams.
Particles in the nanometer size range often show burst release phenomena as a result of large surface area and short diffusion distance of the drug [48], Zur Miihlen showed a direct correlation between microparticle size range and the extent of burst release and the release profile for Compritol microparticles loaded with tetracaine [48], That is probably one reason why Domb demands that the particles to be greater than 1 pm for controlled drug delivery [1],... [Pg.13]

Q. Xu, M. Hashimoto, T. Dang, T. Hoare, D. Kohane, G. Whitesides, and R. Danger, Preparation of monodisperse biodegradable polymer microparticles using a microfluidic flow-focusing device for controlled drug delivery, Small, 5, 1575-1581, 2009. [Pg.378]

Almerfa, B., W. Deng, T.M. Fahmy, and A. Gomez. Controlling the morphology of electrospray-gen-erated PLGA microparticles for drug delivery. Journal of Colloid and Interface Science 343(1) (2010) 125-133. [Pg.436]

Srinivas, L. Preparation and evaluation of polyelectrolyte microparticles for controlled drug delivery. Asian J. Chem. 2012, 24 (3), 1282-1288. [Pg.1353]

Ficek BJ, Peppas NA (1993) Novel preparation of poly (vinyl alcohol) microparticles without crosslinking agent for controlled drug delivery of proteins. J Control Release 27 259... [Pg.196]

R. L. Cleek, K. C. Ting, S. G. Eskin, A. G. Mikos, Microparticles of poly(dWactic-co-glycolic acid)/poly(ethylene glycol) blends for controlled drug delivery, J. Control. Release 1997, 48, 259-268. [Pg.829]

Mclnnes S, Voelcker N (2012) Porous silicon-based nanostructured microparticles as degradable supports for solid-phase synthesis and release of oligonucleotides. Nanoscale Res Lett 7(1) 1-10 Mclnnes SJP, Szili EJ, Al-Bataineh SA, Xu J, Alf ME, Gleason KK, Short RD, Voelcker NH (2012) Combination of iCVD and porous silicon for the development of a controlled drug delivery system. ACS Appl Mater Interfaces 4(7) 3566-3574 Meade SO, Yoon MS, Ahn KH, Sailor MJ (2004) Porous silicon photonic crystals as encoded microcarriers. Adv Mater 16(20) 1811-1814... [Pg.644]

Aishwarya S, Mahalakshmi S, Sehgal PK. Collagen-coated polycaprolactone microparticles as a controlled drug delivery system. J Microencapsul 2008 25(5) 298—306. [Pg.258]

Native guar gum and its derivatives have found use in coatings, matrix tablets, hydrogels and nano/microparticles [4] and are investigated as potential carriers for targeted/ controlled drug delivery [4,54,56,68,69]. [Pg.500]


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See also in sourсe #XX -- [ Pg.2315 ]




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