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Water-soluble drugs immediate-release formulations

Zentner and coworkers [24,26] utilized this information in their development of a system that releases this drug over a 24 hr period. The use of NaCl to modulate the release of diltiazem presents an interesting problem in that the concentration of the solubility modifier must be maintained within certain limits and below its saturation solubility within the device. To solve this problem, core formulations were developed that contained both free and encapsulated NaCl. The encapsulated NaCl was prepared by placing a microporous coating of cellulose acetate butyrate containing 20 wt% sorbitol onto sieved NaCl crystals. The coated granules released NaCl over 12-14 hr period via an osmotic mechanism into either water or the core tablet formulation. The in vitro release profile for tablets (core I devices) containing 360 mg of diltiazem HC1 and 100 mg of NaCl equally divided between the immediate release and controlled release fractions... [Pg.441]


See other pages where Water-soluble drugs immediate-release formulations is mentioned: [Pg.922]    [Pg.822]    [Pg.656]    [Pg.363]    [Pg.381]    [Pg.398]    [Pg.822]    [Pg.499]    [Pg.160]    [Pg.239]    [Pg.374]    [Pg.888]    [Pg.1298]    [Pg.252]    [Pg.562]    [Pg.565]    [Pg.552]    [Pg.235]    [Pg.429]   
See also in sourсe #XX -- [ Pg.922 ]




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