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\ndeacetylation. The release of prednisolone (PS), as a model drug, from the CS gel beads was sustained signifi-
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\nincrement of NaOH concentration in the solution employed for the preparation of CS gel beads. We also investi-
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\ntern was not affected by the treatment time. The time to 50% drug release was about 5 min with PS powder,
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\nGly (pH 9.0) treated with Cho. Thus CS gel beads appear promising as a vehicle for sustained drug delivery, and
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