Structure and Dynamics of Curcumin Encapsulated Lecithin Micelles: A Molecular Dynamics Simulation Study

Abstract

Curcumin is a natural product with potential pharmaceutical applications that can be augmented by drug delivery technology such as nano emulsion. Our study focuses on microscopic structural and dynamics response of curcumin encapsulation in micellar system with lecithin as a natural surfactant under variations of composition and temperature using molecular dynamics (MD) simulations. The results highlight the self-assembly of lecithin micelle, with curcumin encapsulated inside, from initial random configurations in the absence of external field. The variation of composition shows that lecithin can aggregate into spherical and rod-like micelle with the second critical micelle concentration lies between 0.17-0.22 mol dm−3. The radial local density centering at the micelle center of mass shows that the effective radius of micelle is indeed defined by the hydrophilic groups of lecithin molecule and theencapsulated curcumin molecules are positioned closer to these hydrophilic groups than the innermost part of the micelle. The spherical micelle is shown to be thermally stable within the temperature range of 277-310 K without a perceivable change in the spherical eccentricity. The dynamics of micelle are enhanced by the temperature, but it is shown to be insensitive to the variation of lecithin-curcumin composition within the studied range. Simulation results are in agreement with the pattern obtained from experimental results based on particle size, polydispersity index, and encapsulation efficiency.

Increasing the Solubility and Anti-Inflammatory Activity of Curcumin by Cocrystallization

“…Therefore, CUR is considered one of the natural compounds with tremendous potential in treating diseases (Peng et al, 2021) . However, until now, the use of CUR as a therapeutic drug is still constrained by pharmacokinetics (Sohn et al, 2021;Tabanelli et al, 2021;Hakim et al, 2021). CUR given orally is very little absorbed in the gastrointestinal tract, so its bioavailability to achieve pharmacological effects is less than 1% (Suresh and Nangia, 2018;Peng et al, 2021).…”