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are defined ratios of solubility and diffusion coefficient in the presence and absence of EPO. SE decreased in the order of indomethacin, mefenamic acid, warfarin, piroxicam, furosemide, bezafibrate, and tolbutamide. The solubilizing effect was attributed to both ionic and hydrophobic interactions between drugs and EPO. The excellent solubilizing properties of EPO are highly promising for pharmaceutical development, and the data set provides first steps toward an understanding of drug-excipient interaction mechanisms.
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Wiebke Saal
Roche (Switzerland)
Alfred Ross
Roche (Switzerland)
Nicole Wyttenbach
Roche (Switzerland)
Molecular Pharmaceutics
University of Basel
Roche (Switzerland)
FHNW University of Applied Sciences and Arts
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Saal et al. (Mon,) studied this question.
synapsesocial.com/papers/6a0165746be84a7ac885b21b — DOI: https://doi.org/10.1021/acs.molpharmaceut.6b01116