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A transdermal delivery system was designed to release a drug through a rate - controlling membrane. The drug concentration in the reservoir was saturated and
A transdermal delivery system was designed to release a drug through a ratecontrolling membrane. The drug concentration in the reservoir was saturated and kept at mcgmL The membranereservoir partition coefficient is and drug diffusion coefficient in membrane is x cmsec The membrane thinness is mm and its crosssectional area is cmAssume sink condition without lag time. Calculate the Permeability coefficient cms: Continue from the question above, calculate the rate of diffusionmcgs: Continue from the question above, calculate for hours of constant controlled drug release, how much drug can be released across the membrane mcg:
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