W/O Pickering emulsion co-delivery systems stabilized by diacylglycerol nanocarriers and cellular uptake evaluation
Lipid nanoparticulate systems are efficient as active carriers with tailorable interfacial, crystallization profiles. In this study, medium−long chain diacylglycerol (MLCD)−based solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) were constructed for curcumin (Cur) delivery to...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | en |
| Published: |
Institution of Chemical Engineers
2026
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| Subjects: | |
| Online Access: | http://psasir.upm.edu.my/id/eprint/123027/1/123027.pdf http://psasir.upm.edu.my/id/eprint/123027/ https://www.sciencedirect.com/science/article/pii/S0960308526000131 |
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| Summary: | Lipid nanoparticulate systems are efficient as active carriers with tailorable interfacial, crystallization profiles. In this study, medium−long chain diacylglycerol (MLCD)−based solid lipid nanoparticles (SLNs) and nanostructured lipid carriers (NLCs) were constructed for curcumin (Cur) delivery to enhance its oral bioavailability and their Pickering stabilizing effects were evaluated. Cur−SLNs and NLCs stabilized by different surfactants, were prepared with particle sizes ranging from 148 to 305 nm. The nanoparticles were taken up by Caco-2 cells through clathrin and caveolae mediated endocytosis pathway, with the uptake efficiency of the NLCs being 2.25 −3.94 fold higher than that of free Cur. The nanoparticles effectively inhibited the LPS−induced inflammatory response in RAW 264.7 cells, resulting in a 60 % reduction in NO secretion. Furthermore, these SLNs/NLCs were utilized as Pickering stabilizers for water−in−oil (W/O) emulsions co−loaded with hydrophobic curcumin and hydrophilic NaCl. These emulsions demonstrated slow−release performance (78.23 −96.12 % retention) after 4 weeks storage and exhibited tunable rheological properties. The interfacial particles effectively acted as a solid shell, impeding the release of internal phase compounds. The Ritger−Peppas model offered the best fit for the release profiles of all Cur−loaded lipid formulations. This study provides a theoretical basis and technical support for the fabrication and application of lipid nanoparticles and Pickering emulsions as a multifunctional delivery system. |
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