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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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5. RFP Loaded Chitosan Microspheres Prepared by Spray-Drying MethodAs can be seen in Figure 5.4, cross-linked formulations A-D showed better NE% thanuncrossed linked formulations: almost 80% of rifampicin w<strong>as</strong> recovered after nebulizationfrom formulations A-C. On the contrary, NE% w<strong>as</strong> quite low for the uncross-linkedformulations E-H, thus confirming their stability is lower than that of the corresponding GAcontaining formulations.10080% RFP6040200A B C D E F G HNebulizarion Efficiency (NE%)Figure 5.4: Nebulization Efficiency (NE%) of Spray-Dryed MicrospheresSince nebulization can lead to <strong>drug</strong> leakage, it is also important to evaluate how much of theaerosolized <strong>drug</strong> is still encapsulated after the nebulization (NEED%). Best results in terms ofNEED% were obtained from the cross-linked formulations A-D that were able to retain up to70% of the encapsulated <strong>drug</strong>. NEED values were affected by <strong>chitosan</strong> concentration: theydecre<strong>as</strong>ed <strong>as</strong> <strong>chitosan</strong> concentration incre<strong>as</strong>ed. Once again, uncross-linked formulations E-Hshowed very poor nebulization properties since NEED values ranged from 5 to 20%. Resultsobtained in this analysis seem to point out that the most important factor affecting NEED ispolymer cross-linkage, <strong>as</strong> can be seen by the comparison of NEED values from formulationsobtained using the same amount of <strong>chitosan</strong> in Figure 5.5. Cross-linkage contributes toimprove <strong>chitosan</strong> microsphere stability by immobilizing the encapsulated <strong>drug</strong>80

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