Bozkir Asuman, Hayta Gokhan
Department of Pharmaceutical Technology, Faculty of Pharmacy, Ankara University, Ankara, Turkey.
J Drug Target. 2004 Apr;12(3):157-64. doi: 10.1080/10611860410001688018.
In this study, investigations have been carried out to prepare adjuvant active delivery systems; multiple water-in-oil-in-water (w/o/w) emulsion formulations, containing influenza virus surface antigen Hemagglutinin (HA). A modified two-stage emulsification method has been used to prepare multiple emulsions. After improving multiple (w/o/w) emulsion formulations; F1: purified antigen solution (PAS)/soybean oil, HCO-40 and span 80/pluronic F-68, F2: PAS and HPbetaCD/soybean oil, HCO-40 and span 80/pluronic F-68, F3: PAS/squalane, HCO-40 and span 80/pluronic F-68, formulations were selected for the stability study that continued for a 3 month duration. To evaluate the stability of these formulations, microscopic observation, osmolarities of the internal and external aqueous phases, pH, globule size and viscosity were determined. SDS-PAGE (silver staining) was used to evaluate HA and the micro-bicinchoninic acid (mBCA) assay was used to determine the in vitro release of antigen from formulations. Immune responses of formulations were investigated in Wistar Albino rats and compared with the immune response raised against the conventional vaccine. These responses were detected with Hemagglutination Inhibition (HAI) assay. The results of this study demonstrated that HA was well entrapped in the multiple (w/o/w) emulsion formulations. Molecular weight and antigenicity of the entrapped HA were not affected by the emulsification procedure. These results suggest that multiple emulsion formulations entrapping influenza antigen may have potential for immunization studies as one of the vaccine delivery system with adjuvant properties.
在本研究中,已开展了相关调查以制备佐剂活性递送系统;即含有流感病毒表面抗原血凝素(HA)的多重水包油包水(w/o/w)乳液制剂。采用了一种改良的两步乳化法来制备多重乳液。在改进多重(w/o/w)乳液制剂后;F1:纯化抗原溶液(PAS)/大豆油、HCO - 40和司盘80/普朗尼克F - 68,F2:PAS和HPβCD/大豆油、HCO - 40和司盘80/普朗尼克F - 68,F3:PAS/角鲨烷、HCO - 40和司盘80/普朗尼克F - 68,选择这些制剂进行为期3个月的稳定性研究。为评估这些制剂的稳定性,测定了微观观察、内外部水相的渗透压、pH、液滴大小和粘度。采用SDS - PAGE(银染)评估HA,采用微量BCA法测定制剂中抗原的体外释放。在Wistar白化大鼠中研究了制剂的免疫反应,并与针对传统疫苗产生的免疫反应进行比较。通过血凝抑制(HAI)试验检测这些反应。本研究结果表明,HA被良好地包裹在多重(w/o/w)乳液制剂中。包裹的HA的分子量和抗原性不受乳化过程的影响。这些结果表明,包裹流感抗原的多重乳液制剂作为具有佐剂特性的疫苗递送系统之一,可能具有用于免疫研究的潜力。