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Im trying to associate cumulative drug release profile with a mathematical model. How is this achieved?
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Does anyone have any recommendation on the best possible method? Or, the reason behind this? I have tried adjusting the pH of the aqueous phases but that hasn't changed anything. I look forward...
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I'm using water in oil in water (W/O/W) double emulsion. I was wondering what is the best method to encapsulate a hydrophilic compound? Should I dissolve the compound in the aqueous phase then...
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I want to quantify my drug using HPLC, but the the solvent im using (DCM) is interfering with my readings at 360nm. What is an alternative solvent to use that is not excited at 360 nm? Thanks.
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