MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, Beijing Key Laboratory of Lignocellulose Chemistry, College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, PR China.
MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, Beijing Key Laboratory of Lignocellulose Chemistry, College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, PR China.
Colloids Surf B Biointerfaces. 2018 May 1;165:191-198. doi: 10.1016/j.colsurfb.2018.01.049. Epub 2018 Jan 31.
A novel rosin-based ester tertiary amine (RETA) with three hydrophilic groups and a rigid hydrophobic group was synthesized from rosin by Diels-Alder addition, acylation and esterification reactions. RETA was characterized by infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance spectroscopy (C NMR). Results from testing surface tension, zeta potential, and transmission electron spectroscopy showed that RETA had unique pH responsiveness. RETA self-assembled into worm-like micelles, spherical micelles 130 nm in diameter and big spherical worm-like aggregates with diameter of 2 μm at pH = 5.76, 8.04 and 9.38, respectively. The critical micelle concentration (CMC) of RETA was 0.42 mmol/L, and the surface tension at CMC (γ) was 38.73 mN/m when pH was 8.04. The RETA had a potential application in delivering doxorubicin hydrochloride (DOX) due to the pH responsiveness. Self-assembly mixed systems of RETA and rosin-based phosphoric acid (DDPD) were designed to improve emulsification. The mixed systems had obvious synergistic effects and unexpected emulsification. The γ and CMC of mixtures were 41.74 mN/m and 0.20 mmol/L, the size of mixture micelles increased up to 300 nm in the optimum molar ratio of RETA/DDPD (7:3) by TEM and cryo-TEM. It was worth noting that the mixture system formed vesicles in the RETA/DDPD molar ratio of 5:5. The stability time of emulsion with RETA and DDPD as emulsifier were only 63 s and 52 s respectively, but the stability time increased to 234 s in the optimum molar ratio. In addition, the formation mechanisms of micelles at different pH and in various mixtures were discussed in detail. What's more, cytotoxicity results showed that the toxicity of RETA was lower significantly than that of lecithin, a food ingredient in egg yolk and soybean. The cell viability was more than 83% in the high concentration of RETA (4000 μg/ml).
一种新型松香基酯叔胺(RETA),具有三个亲水基团和一个刚性疏水基团,由松香通过 Diels-Alder 加成、酰化和酯化反应合成。RETA 的结构通过红外光谱(FT-IR)和质子核磁共振谱(C NMR)进行了表征。表面张力、动电位和透射电子显微镜测试结果表明,RETA 具有独特的 pH 响应性。RETA 自组装成蠕虫状胶束、直径为 130nm 的球形胶束和直径为 2μm 的大球形蠕虫状聚集体,分别在 pH=5.76、8.04 和 9.38 时。RETA 的临界胶束浓度(CMC)为 0.42mmol/L,当 pH=8.04 时,CMC 时的表面张力(γ)为 38.73mN/m。由于 pH 响应性,RETA 具有递药盐酸阿霉素(DOX)的潜力。设计了 RETA 和松香基磷酸酯(DDPD)的自组装混合体系以改善乳化。混合体系具有明显的协同作用和意外的乳化作用。在 RETA/DDPD 的最佳摩尔比(7:3)下,混合体系的γ和 CMC 分别为 41.74mN/m 和 0.20mmol/L,通过 TEM 和 cryo-TEM 观察到混合胶束的尺寸增加到 300nm。值得注意的是,在 RETA/DDPD 的摩尔比为 5:5 时,混合体系形成了囊泡。RETA 和 DDPD 作为乳化剂的乳液稳定性时间分别只有 63s 和 52s,但在最佳摩尔比下,稳定性时间增加到 234s。此外,详细讨论了不同 pH 值和不同混合物中胶束的形成机制。此外,细胞毒性结果表明,RETA 的毒性明显低于蛋黄和大豆中食品成分卵磷脂。在高浓度 RETA(4000μg/ml)下,细胞活力大于 83%。