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- W2890482330 abstract "Inclusion complexes were formed using β-cyclodextrin and hydroxypropyl-β-cyclodextrin to encapsulate a series of new non-steroidal drugs with antidiabetic properties presenting low water solubility. Complexes were thermodynamically characterized through Isothermal Titration Calorimetry (ITC). The 298 K complexation process turned out to be spontaneous in all cases, mainly because it was guided by entropy. It was found that the two main functional groups forming the studied drugs were able to interact with the cyclodextrin cavity, data suggest a 1:1 stoichiometry. Steric hindrance and host desolvation play a fundamental role in the drug’s cyclodextrin cavity incorporation. This study increases treatment possibilities for type 2 diabetes mellitus using FDA-approved biocompatible drug delivery systems, thus increasing solubility and application possibilities of the encapsulated active substance." @default.
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- W2890482330 date "2019-02-01" @default.
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- W2890482330 title "Thermodynamic characterization of the inclusion complexes formation between antidiabetic new drugs and cyclodextrins" @default.
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- W2890482330 doi "https://doi.org/10.1016/j.jct.2018.09.013" @default.
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