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To improve aqueous solubility and thus the therapeutic effectiveness of such compounds, a number of formulation strategies have been employed.
- Cyclodextrins are cyclic oligosaccharides with a bucket-like structure having a hydrophobic internal cavity and a hydrophilic exterior. This unique structure allows for the formation of inclusion complexes, where lipophilic compounds are non-covalently bound within the cavity.
- Cyclodextrins have been widely used in oral and parenteral drug delivery systems to improve the aqueous solubility and chemical stability of drugs. Topical applications of cyclodextrins have also been investigated.
- Cyclodextrins differ by the number of glucose units forming the ring structure as well as chemical substitutions on the exterior of the ‘bucket’. The influence of side chain substitutions of the cyclodextrin on the solubility of Ibuprofen, a BSC II model compound is essential to understand the complexation process.
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A consistent disintegration and dissolution profile is critical for the delivery of your medications’ active ingredients. Discover our solutions.