- 期刊Food research international (Ottawa, Ont.)(Food Res Int)
- 发表时间2026-08-18
- 作者Zhang J, Tang Q, Han Y, Wang Y, Mi S, Rakariyatham K, McClements DJ, Cao C, Xu X, Yuan B
- 卷期页码V244 : 120440
- DOI10.1016/j.foodres.2026.120440
- PMID42858977
摘要机译
姜黄素等疏水保健品在功能性食品中应用前景广阔,但它们的水分散性差、胃肠稳定性有限和口服生物利用度低极大地限制了它们的功效。因此,开发食品级输送系统以改善其胃肠命运和消化后功能非常重要。
本研究采用甜菜碱-乳酸深共晶溶剂辅助抗溶剂自组装策略制备木质素纳米颗粒,所得木质素纳米颗粒随后作为颗粒乳化剂形成并稳定载姜黄素的Pickering乳液,优化后的LNP-7.5颗粒表现出良好的胶体性能,SPAN值为0.812,ze-电位为-54.47 mV。
相应的姜黄素负载Pickering乳液的包封率为81.65%,负载量为7.03%。它还表现出良好的抗氧化性能,ABTS和DPPH自由基清除活性分别超过90%和60%。
模拟消化显示了gastrointestinal-responsive释放特征,6小时后胃部条件下姜黄素释放有限(31.1%),但在小肠条件下释放明显较高(69.8%)。在体外粪便发酵过程中,消化的Cur-LNP-PE促进短链脂肪酸的产生。小鼠重复口服给药耐受性良好,调节结肠氧化还原和inflammation-related基因表达。
此外,16S rRNA基因测序揭示了五组之间肠道微生物群落组成的显著总体差异。总体而言,优化的给药系统表现出良好的包封特性、pH和消化依赖性释放以及formulation-dependent的肠道和微生物反应,支持其口服给药疏水保健品的潜力。
展开英文摘要原文
Hydrophobic nutraceuticals such as curcumin are highly promising for functional food applications, but their poor aqueous dispersibility, limited gastrointestinal stability, and low oral bioavailability greatly restrict their efficacy. Thus, it is important to develop food-grade delivery systems that can improve their gastrointestinal fate and post-digestion functionality. In this study, lignin nanoparticles were fabricated using betaine-lactic acid deep eutectic solvent-assisted anti-solvent self-assembly strategy. The resulting lignin nanoparticles were then used as particulate emulsifiers to form and stabilize curcumin-loaded Pickering emulsions. The optimized LNP-7.5 particles showed favorable colloidal properties, with a SPAN value of 0.812 and a ζ-potential of -54.47 mV. The corresponding curcumin-loaded Pickering emulsion achieved an encapsulation efficiency of 81.65% and loading capacity of 7.03%. It also exhibited favorable antioxidant performance, with ABTS and DPPH radical scavenging activities exceeding 90% and 60%, respectively. Simulated digestion revealed the gastrointestinal-responsive release profile, with limited curcumin release under gastric conditions after 6 h (31.1%) but markedly higher release under small intestinal conditions (69.8%). During in vitro fecal fermentation, digested Cur-LNP-PEs promoted short-chain fatty acid production. Repeated oral administration in mice was well tolerated and modulated colonic redox- and inflammation-related gene expression. Moreover, 16S rRNA gene sequencing revealed a significant overall difference in gut microbial community composition among the five groups. Overall, the optimized delivery system exhibited good encapsulation properties, pH- and digestion-dependent release, and formulation-dependent intestinal and microbial responses, supporting its potential for oral delivery of hydrophobic nutraceuticals.
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