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chitosan and plga microspheres as drug delivery ... - UniCA Eprints

chitosan and plga microspheres as drug delivery ... - UniCA Eprints

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3. Aim of the WorkDuring the l<strong>as</strong>t three decades, therapeutic systems b<strong>as</strong>ed on polymers, both natural <strong>and</strong>synthetic, have shown to be effective in controlling rate or time of <strong>drug</strong> rele<strong>as</strong>e, in enhancing<strong>drug</strong> targeting specificity while lowering systemic <strong>drug</strong> toxicity, <strong>and</strong> providing protection forpharmaceuticals against degradation.An important consideration in the treatment of pulmonary infections is the fact that the MTB<strong>and</strong> MAC have the capability of surviving intra-cellulary in the host macrophages for longperiods of time (246). Therefore, the ability of the antibacterial agent to eradicate themicrorganisms within the macrophage is of key importance.However, most of the anti-mycobacteria <strong>drug</strong>s presently in use fail to penetrate macrophages.For this re<strong>as</strong>on, many researchers are considering the use of appropriately engineered <strong>delivery</strong>systems for these <strong>drug</strong>s, in order to make them therapeutically effective. It is well known thatmicro-encapsulation technology can be used to accomplish sustained rele<strong>as</strong>e of antibiotics,when they are formulated in larger sizes than 50 µm, or to target <strong>drug</strong> <strong>delivery</strong> systems tospecific cells (i.e., macrophages), when antibiotics are formulated in smaller sizes

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