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Inventi Impact: Pharmaceutical Process Development

Articles

  • Inventi:ppd/33616/20
    Enhancing the Solubility of Curcumin Using a Solid Dispersion System with Hydroxypropyl- Beta-Cyclodextrin Prepared by Grinding, Freeze-Drying, and Common Solvent Evaporation Methods
    Research 2021 : January - March
    Nguyen Ngoc Sao Mai, Riko Nakai, Yayoi Kawano, Takehisa Hanawa

    Cyclodextrins (CDs) and their derivatives significantly increase drug solubility by forming\ndrug/CD complexes known as solid dispersions (SDs), which consist of an inclusion complex (IC),\nwhere the drug is entrapped within the CD cavity, and a non-IC. Here, the SDs of curcumin (CUR).......................

    How to Cite this Article
    Attribution/ CC Compliant Citation: Mai, Nguyen Ngoc Sao, et al. \"Enhancing the Solubility of Curcumin Using a Solid\nDispersion System with Hydroxypropyl-Beta-Cyclodextrin Prepared by Grinding, Freeze-Drying, and Common Solvent\nEvaporation Methods.\" Pharmacy 8.4 (2020): 203.\nhttps://doi:10.3390/pharmacy8040203\nhttp://creativecommons.org/licenses/by/4.0/\nSome formatting elements, header, footer, logos, dates and pagination were modified while adapting this article.
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