Enhanced Emulsifying Ability of Deoxycholate through Dynamic Interaction with Layered Double Hydroxide - PubMed
- ️Sun Jan 01 2023
Enhanced Emulsifying Ability of Deoxycholate through Dynamic Interaction with Layered Double Hydroxide
Jing Xie et al. Nanomaterials (Basel). 2023.
Abstract
The emulsifying ability of the naturally occurring surfactant deoxycholic acid (DCA) was improved by dynamic interaction with nanometric layered particles, layered double hydroxide (LDH). As DCA molecules are rigid due to the facial configuration of hydrophobic-hydrophilic groups, they tend to form molecular aggregation in an acidic condition or imbalanced water-lipid ratios. In this study, the homogeneous hybrids of DCA and LDH were obtained by the in situ growth of LDH at a DCA molecule. The DCA-LDH hybrid successfully prevented the molecular aggregation of DCA at an acidic pH and imbalanced water-to-oil ratio. The dynamic light scattering showed that the hydrodynamic radius of micelle in the emulsion made with DCA-LDH maintained its small size (<500 nm), while upon pH change and dilution with water, that made with DCA only uncontrollably increased up to ~3000 nm. The polydispersity index value of the DCA-LDH emulsion remained constant (<0.3) after the pH change and dilution with water, indicating the high stability of the formulation. Furthermore, time-dependent turbidity monitoring revealed that the DCA-only formulation suffered from serious coalescence and creaming compared with the DCA-LDH formulation. It is suggested that the dynamic interaction between LDH layers and DCA prevented molecular aggregation under unfavorable conditions for the oil-in-water emulsion.
Keywords: deoxycholic acid; emulsifier; emulsifying ability; emulsion formulation; layered double hydroxide.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
![Figure 1](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/2151d15f2ebc/nanomaterials-13-00567-g001.gif)
Chemical structures of the materials used in this experimental work: (a) sodium deoxycholic acid (DCA), (b) layered double hydroxide (LDH), (c) DCA adsorbed on LDH (DCA-LDH), (d) Caprylic/capric triglyceride (CCT), (e) polysorbate 60 (PS 60), (f) hydrogenated lecithin (HL).
![Scheme 1](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/6367361b511e/nanomaterials-13-00567-sch001.gif)
Schematic of the dispersion systems consisting of DCA only or DCA with LDH, before and after stimulation.
![Figure 2](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/1f1eda41e0b4/nanomaterials-13-00567-g002.gif)
(a) X-ray diffraction pattern, and (b) FT−IR for DCA and DCA−LDH.
![Figure 3](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/4ea9b380ed07/nanomaterials-13-00567-g003.gif)
Photos of the different formulations at lowered pH (~5.5) for 24 h.
![Figure 4](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/ba758a8c2545/nanomaterials-13-00567-g004.gif)
(A) Z-average, and (B) polydispersity index (PDI, plotted as black squares), of emulsions with respect to dilution factor for (a) F1 and F1′, (b) F2 and F2′, and (c) F3 and F3′.
![Figure 5](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/354784371c0e/nanomaterials-13-00567-g005.gif)
Histograms for zeta potentials of the prepared emulsions: F1, F1′, F2, F2′, F3, and F3′.
![Figure 6](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/c7ab8cfc1e17/nanomaterials-13-00567-g006.gif)
Turbiscan profiles of (a,b) transmission, and (c,d) backscattering, for F1 and F1′ over 7 h.
![Figure 7](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69ce/9920619/0a70f4ed4f3c/nanomaterials-13-00567-g007.gif)
Turbiscan profiles of backscattering for (a) F2, (b) F2′, (c) F3, and (d) F3′, over 7 h.
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