Medeiros Arthur Sérgio Avelino de, Torres-Rêgo Manoela, Lacerda Ariane Ferreira, Rocha Hugo Alexandre Oliveira, Egito Eryvaldo Sócrates Tabosa do, Cornélio Alianda Maira, Tambourgi Denise V, Fernandes-Pedrosa Matheus de Freitas, da Silva-Júnior Arnóbio Antônio
Laboratory of Pharmaceutical Technology and Biotechnology, Department of Pharmacy, Federal University of Rio Grande do Norte-UFRN, Natal 59010-180, Brazil.
Graduate Program of Chemistry, Chemistry Institute, Federal University of Rio Grande do Norte, Avenue Senador Salgado Filho, 3000, Lagoa Nova, Natal 59072-970, Brazil.
Pharmaceutics. 2020 Sep 29;12(10):927. doi: 10.3390/pharmaceutics12100927.
This study assesses the efficacy of different nanoemulsion formulations as new and innovative adjuvants for improving the in vivo immunization against the scorpion venom. Nanoemulsions were designed testing key-variables such as surfactants, co-solvents, and the influence of the temperature, which would be able to induce the phase transition from a liquid crystal to a stable nanoemulsion, assessed for four months. Additionally, cationic-covered nanoemulsion with hyper-branched poly(ethyleneimine) was prepared and its performance was compared to the non-cationic ones. The physicochemical properties of the selected nanoemulsions and the interactions among their involved formulation compounds were carefully monitored. The cytotoxicity studies in murine macrophages (RAW 264.7) and red blood cells were used to compare different formulations. Moreover, the performance of the nanoemulsion systems as biocompatible adjuvants was evaluated using mice immunization protocol. The FTIR shifts and the zeta potential changes (from -18.3 ± 1.0 to + 8.4 ± 1.4) corroborated with the expected supramolecular anchoring of venom proteins on the surface of the nanoemulsion droplets. Cell culture assays demonstrated the non-toxicity of the formulations at concentrations less than 1.0 mg/mL, which were able to inhibit the hemolytic effect of the scorpion venom. The cationic-covered nanoemulsion has shown superior adjuvant activity, revealing the highest IgG titer in the immunized animals compared to both the non-cationic counterpart and the traditional aluminum adjuvant. In this approach, we demonstrate the incredible potential application of nanoemulsions as adjuvants, using a nanotechnology platform for antigen delivery system on immune cells. Additionally, the functionalization with hyper-branched poly(ethyleneimine) enhances this recognition and improves its action in immunization.
本研究评估了不同纳米乳剂配方作为新型创新佐剂在改善针对蝎毒的体内免疫方面的功效。设计纳米乳剂时测试了关键变量,如表面活性剂、助溶剂以及温度的影响,温度能够诱导从液晶到稳定纳米乳剂的相变,该过程持续评估了四个月。此外,制备了用超支化聚(乙烯亚胺)覆盖的阳离子纳米乳剂,并将其性能与非阳离子纳米乳剂进行了比较。仔细监测了所选纳米乳剂的物理化学性质及其配方成分之间的相互作用。在小鼠巨噬细胞(RAW 264.7)和红细胞中进行细胞毒性研究以比较不同配方。此外,使用小鼠免疫方案评估了纳米乳剂系统作为生物相容性佐剂的性能。傅里叶变换红外光谱(FTIR)的变化和zeta电位的变化(从-18.3±1.0到+8.4±1.4)证实了毒液蛋白在纳米乳剂液滴表面的预期超分子锚定。细胞培养试验表明,浓度低于1.0 mg/mL的配方无毒,且能够抑制蝎毒的溶血作用。阳离子覆盖的纳米乳剂显示出优异的佐剂活性,与非阳离子对应物和传统铝佐剂相比,在免疫动物中显示出最高的IgG滴度。在本研究中,我们展示了纳米乳剂作为佐剂的巨大潜在应用,利用纳米技术平台构建免疫细胞上的抗原递送系统。此外,用超支化聚(乙烯亚胺)进行功能化增强了这种识别并改善了其在免疫中的作用。