This study examined how the triblock structure of poloxamers and the choice of ripening inhibitors influence the Ostwald ripening stability of n-decane-in-water emulsions. Emulsions were stabilized using three poloxamers (P188, P338, and P407) that differed in the lengths of polyethylene oxide (PEO) and polypropylene oxide (PPO) blocks. All emulsions showed rapid droplet growth during storage, but the P407-stabilized emulsion ripened the fastest, while the P188- and P338-stabilized emulsions ripened at only about half of this rate. The results revealed that the stability was not linearly correlated with the length of PEO and PPO blocks. Instead, the findings suggest that the molecular structure influences stability through a coupled effect: while the PPO blocks determine interfacial tension, the entanglement of the hydrophilic PEO blocks modifies interfacial rheology, which plays a critical role in retarding droplet growth. Long-chain hydrocarbons (n-tetradecane, n-hexadecane, and n-octadecane) were tested as ripening inhibitors. n-Tetradecane only slowed droplet growth and did not completely inhibit ripening, whereas n-hexadecane exhibited a typical inhibitor effect and fully inhibited droplet growth once its concentration passed poloxamer-specific threshold levels. n-Octadecane needed much higher concentrations and showed more complex, formulation-dependent behavior. In contrast, corn oil, a triacylglycerol oil commonly used as a ripening inhibitor in food emulsions, accelerated droplet growth, likely due to conformational changes in the PPO blocks induced by alterations in the oil phase environment. Overall, these findings show how poloxamer structure and ripening inhibitor type jointly control Ostwald ripening and provide guidance for designing more stable poloxamer-based emulsions for food applications.
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