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Figure 4: Perturbation plot showing the effect of all parameter on (a) Encapsulation efficiency (%) (b) drug release (μg GAE gbeads−1) (c) overlay plot of optimized values showing best response at optimized factors, where X1: Chitosan level, X2: Drug conc. of Saraca acosa microparticles A, B, C and D represents Chitosan: Polyethylene glycol ratio, Drug Conc.(w/v), sodium tripolyphosphate conc. (%) and crosslinking time (mins.) respectively |
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