Solubilizing properties of unmodified α-CD and per-6-thiolated α-CD for the model BCS Class IV drug FUR in aqueous solution were studied at room temperature according to an already established method.19 In detail, FUR was added (CD and FUR in molar ratio of 1:2) to an aqueous solution containing increasing amounts of α-CD and per-6-thiolated α-CD ranging from 0.5 to 5 mM. The suspension was homogenized at room temperature using a thermomixer (Thermomixer C, Eppendorf, Austria) at 750 rpm until equilibrium in solubility was reached (3–4 days). After filtration (polyvinylidene fluoride filter with pore size: 0.45 μm), the obtained clear solutions were diluted 10 times, and FUR was quantified photometrically at 276 nm. The apparent stability constant (KC) was determined from the slope of the straight line using eq 2
where S0 represents the solubility of FUR in water.
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