Biopharmaceutical Characterization and Stability of Nabumetone–Cyclodextrins Complexes Prepared by Grinding
<b>Background:</b> Nabumetone (NAB) is a poorly soluble nonsteroidal anti-inflammatory prodrug (BCS class II drug) whose solubility is significantly improved by complexation with cyclodextrins (CDs). <b>Methods</b>: The solid complexes, in a 1:1 molar ratio, were prepared by mechanochemical activation by grinding, using β-cyclodextrin (β-CD) and its derivatives, hydroxypropyl- and sulfobutylether-β-cyclodextrin (HP-β-CD and SBE-β-CD). The complexation was confirmed by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), and attenuated total reflectance Fourier-transformed infrared spectroscopy (ATR-FTIR). Obtained products were further characterized regarding their solubility, in vitro dissolution, permeability and chemical stability. <b>Results</b>: Co-grinding with HP-β-CD and SBE-β-CD yielded products that showed in vitro dissolution profiles in hydrochloric acid medium (pH 1.2) that were substantially different from that of pure NAB, yielding dissolution efficiency enhancements of 34.86 ± 1.64 and 58.30 ± 0.28 times, respectively, for the optimized products. Their in vitro dissolution and gastrointestinal permeability were also studied in a low-volume environment at pH 6.8, corresponding to the intestinal environment. Both β-CD derivatives increased NAB dissolution rate and NAB mass transport across the biomimetic membrane. The effect of β-CD derivatives on NAB chemical stability was studied under the stress conditions by the developed and validated UHPLC-DAD-HRMS method. In acidic conditions, pure and complexed NAB was prone to hydrolytic degradation, yielding one degradation product-pharmacologically inactive NAB metabolite. However, under the oxidative conditions at elevated temperatures, 10 NAB degradation products were identified from co-ground samples. All systems were stable during photo- and long-term stability studies. <b>Conclusions</b>: NAB complexes with HP-β-CD and SBE-β-CD are promising candidates for pharmaceutical product development.
Authors
- Nives Galić (ORCID: https://orcid.org/0000-0002-0958-1791)
- Anna Vincze (ORCID: https://orcid.org/0000-0002-9756-574X)
- György Tibor Balogh (ORCID: https://orcid.org/0000-0001-8273-1760)
- Mario Jug (ORCID: https://orcid.org/0000-0002-7473-9807)
- Rita Szolláth
- David Klarić (ORCID: https://orcid.org/0000-0003-0109-6393)
- Željka Soldin
Institutions
- Semmelweis University (HU)
- University of Zagreb (HR)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2024-11-21
- DOI
- https://doi.org/10.3390/pharmaceutics16121493
- Citations
- 2
- Primary Topic
- Drug Solubulity and Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.42
Funders
- Hrvatska Zaklada za Znanost
- CEEPUS
- European Regional Development Fund