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Learn MoreLipid-based drug carriers can influence bioavailability through enhanced solubilization in the GI tract and reducing variability of systemic exposure. Understanding the digestion and absorption process of lipids is of great importance for interpretation of the biopharmaceutical properties of lipid-based formulations proposed for oral administration.3 Various lipid-based formulation approaches used to enhance oral drug bioavailability include 2:
Industry insiders claim that inclusion complex delivery systems make the magic possible for drug delivery by improving the safety and efficacy through control of rate, time, and place of drug release within the body.5
A common natural inclusion complex delivery system are cyclodextrin derivatives. Extensive studies have been performed on cyclodextrins and their complexes in the last 30 years. These starch derivatives have lipophilic inner cavities and a hydrophilic outer surface. Cyclodextrins create water-soluble inclusion complexes with hydrophobic drugs that exhibit low aqueous solubility.6 They have been shown to interact with a variety of molecules to form non-covalent inclusion complexes, resulting in decreased side effects and increased bioavailability.2
There are three types of cyclodextrins: α, β, and γ-cyclodextrins. β-Cyclodextrin is ideal for drug delivery due to the cavity size, efficient drug complexation and loading, availability, and relatively low cost.5
As presented in the examples above, your CDMO partner requires extensive knowledge and experience in oral solid dose development to help bring your drug to market. Pii’s experienced R&D team can assist in solving your formulation challenges, getting you quickly into the clinic, on time and on budget.
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