Lipids · 1983 · 80 citations · 9 references
PharmacyPharmaceuticsPharmacologyBioavailabilityDrug DeliveryOral Drug DeliveryLipid AnalysisLipid ChemistryLipid-based Drug Delivery SystemsLipid-protein InteractionsBile Salt InteractionsBinding CapacityChitosanHydrophobic InteractionsIonic StrengthIonic Strength DependenceIonic Strength EffectsMicellar Solutions
The lipid binding capacity of chitosan (partially deacetylated chitin) was determinined with respect to micellar solutions of bile salts, dodecyl sulfate, natural ox bile and an artificial mixed microemulsion. The stoichiometry was determined following the separation of the solid phase by filtration or centrifugation. The major variables in the extent of binding were the pH and ionic strength, suggesting that the interactions are mainly of ionic nature. It is noteworthy that under optimal conditions chitosan could bind, i.e., coprecipitate, with 4-5 times of its weight with all the lipid aggregates tested. These results have a bearing on the nutritional and pharmacological applications of chitosan. The analyses of the components from the precipitates with microemulsion and ox bile show a significant selectivily of binding caused by hydrophobic interactions.
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Studies of Intestinal Digestion and Absorption in the Human1
Bengt Borgström, Arne Dahlqvist, G Lundh et al. · Journal of Clinical Investigation · 1957 · 1.1K citations · Full text
Alan F. Hofmann, Bengt Borgström · Journal of Clinical Investigation · 1964 · 441 citations · Full text
Functional Properties of Chitin and Chitosan
Dietrich Knorr · Journal of Food Science · 1982 · 204 citations