A low-energy emulsification platform based on a Diet Coke–Mentos reaction-derived bubbly flow for formulating various emulsions as drug carriers

材料科学 乳状液 焦炭 药物输送 过饱和度 化学工程 玻璃管 流量(数学) 水溶液 管(容器) 纳米技术 复合材料 化学 有机化学 机械 冶金 物理 工程类
作者
Yu‐Jung Lin,Po-Kai Luo,Huei‐Rou Su,Hung-Yun Lu,Wei Ting Chang,Min-Chun Chiang,Hsin‐Lung Chen,Kai Chen,Hao-Ji Wei,Kun-Ju Lin,Hsing‐Wen Sung
出处
期刊:Biomaterials [Elsevier BV]
卷期号:301: 122264-122264
标识
DOI:10.1016/j.biomaterials.2023.122264
摘要

The formulation of a drug using high-energy emulsification commonly causes drug deterioration. Exploiting the well-known Diet Coke-Mentos reaction (DCMR), a U-shaped tube reactor that can generate an eruption of bubbly flow that can serve as a low-energy emulsification platform, is proposed. The liquid in the U-tube reactor is a supersaturated solution of aqueous CO2, which mimics Diet Coke. When glass beads with rough surfaces, mimicking Mentos, are dropped into the carbonated water, an eruptive bubbly flow is spontaneously created, mediating effective emulsification at a compound water-oil interface. Experimental results demonstrate that DCMR-mediated bubbly flow may provide a versatile platform for the production of "oil-in-water" or "water-in-oil" droplets and Pickering emulsion composite particles as drug carriers. The DCMR-derived bubbly flow is generated without significant temperature elevation, so the activity of the drug to be emulsified is unaffected. In vivo results reveal the feasibility of using this low-energy emulsification platform to formulate an emulsion system that contains catalase, a temperature-sensitive oxidoreductase, to mitigate an experimentally formed paw inflammation in mice. The as-proposed emulsification platform is attractive for formulating numerous drug delivery systems on a small-scale in a customized manner to meet the needs of each individual for personalized medicine.

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