Two modes of associations of curcumin with pre- and nanoaggregated chitosan oligosaccharide lactate: Ionic strength and hydrophobic bile salt modulate partition of drug and self-assembly process

dc.contributor.authorChebl, Mazhar
dc.contributor.authorAbiad, Mohamad G.
dc.contributor.authorMoussa, Zeinab
dc.contributor.authorPatra, Digambara
dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentDepartment of Nutrition and Food Sciences
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.facultyFaculty of Agricultural and Food Sciences (FAFS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:21:47Z
dc.date.available2025-01-24T11:21:47Z
dc.date.issued2016
dc.description.abstractChitosan oligosaccharide lactate (COL) has been modified to improve water solubility of chitosan, especially for the uses in drug delivery and biomedical applications. The present study reveals that self-assembly of COL in solution forms nanoaggregates of size 10-30 nm with a critical aggregation concentration (cac) of ∼5 μM. Fluorescence quenching of pyrene establishes that one COL chain may form around five independent hydrophobic microdomains during self-assembly in solution that are crucial to drug-polymer contact. Interaction of COL with a representative hydrophobic drug molecule, curcumin, implies two different kinds of binding mechanisms of curcumin with the pre- and nanoaggregated forms of COL, respectively. A strong ground state interaction between curcumin and nanoaggregated COL has been noted with an association constant of 3.91 × 104 L/mol at 298 K. This association has been found to be diffusion controlled, enthalpy driven, and as consequences of hydrophobic effects due to van der Waals interactions. Increase in ionic strength, such as NaCl concentration, in the medium pushes the hydrophobic chain of COL and curcumin out from the solution by marginally lowering the cac and increasing the size (∼30-60 nm) of the nanoaggregate; thus, it also exponentially boosts the partition of curcumin into COL nanoaggregates. However, similar increase in NaCl concentration in the medium discourages contact of curcumin with preaggregated COL, confirming an electrostatic interaction between curcumin and preaggregated form of COL. This is further supported by FT-IR spectra. On the other hand, hydrophobic bile salt surges both the cac and size of nanoaggregates (∼100 nm), indicating bulky and hydrophobic cholate/deoxycholate group cooperatively binds with COL and curcumin for which higher concentration of COL is needed to accommodate bulky size of cholate/deoxycholate and form large nanoaggregates. The present study also reports that water vapor permeability of COL film declines linearly with curcumin concentration under investigation due to blocking of the hydrophilic part of COL by curcumin and hydrophobic nature of curcumin. © 2016 American Chemical Society.
dc.identifier.doihttps://doi.org/10.1021/acs.jpcc.6b01486
dc.identifier.eid2-s2.0-84971430844
dc.identifier.urihttp://hdl.handle.net/10938/25317
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.relation.ispartofJournal of Physical Chemistry C
dc.sourceScopus
dc.subjectChitosan
dc.subjectWater solubility
dc.titleTwo modes of associations of curcumin with pre- and nanoaggregated chitosan oligosaccharide lactate: Ionic strength and hydrophobic bile salt modulate partition of drug and self-assembly process
dc.typeArticle

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