National Institute of Infectious Diseases and Vaccinology , National Health Research Institutes , 35053 Miaoli , Taiwan.
Graduate Institute of Biomedical Sciences , China Medical University , 40402 Taichung , Taiwan.
ACS Appl Mater Interfaces. 2018 Apr 18;10(15):12553-12561. doi: 10.1021/acsami.8b03044. Epub 2018 Apr 9.
To accomplish an innovative vaccine design, there are two key challenges: developing formulations that avoid cold chain shipment and finding a delivery vehicle that is absorbable in vivo. Here, we explored the design and performance of a colloidal vesicle that enabled us to consider both challenges. We used polymeric bioresorbable amphiphiles as surface-active agents for stabilizing oily/aqueous interfaces and formed a colloidal vehicle named polysorbasome (PSS, polymeric absorbable vesicle), without using conventional emulsifiers such as sorbitan esters or their ethoxylates. Homogenizing the oil/water compartments forms a colloid containing an aqueous solution in its core and provides an oily barrier that isolates the encapsulated material from external materials. In this form, the PSS serves as a depot for sustained delivery of vaccine antigens. Following vaccination, the antigen-specific antibodies and the cell-mediated immunity can be manipulated after the antigen being formulated with PSS particles. Then, the degradability intrinsic to the polymeric bioresorbable amphiphiles complies with the destruction and further absorbance of the vehicles in vivo. The structural features of these versatile vesicles based on bioresorbable amphiphilic engineering may provide new insights into vaccine delivery.
为了实现创新的疫苗设计,存在两个关键挑战:开发避免冷链运输的配方和寻找可在体内吸收的输送载体。在这里,我们探索了胶体囊泡的设计和性能,使我们能够同时考虑这两个挑战。我们使用聚合生物可吸收两亲物作为稳定油/水界面的表面活性剂,并形成一种胶体载体,称为多聚体囊泡(PSS,聚合可吸收囊泡),而不使用传统的乳化剂,如山梨坦酯或其乙氧基化物。均匀化油/水隔室形成含有核心水溶液的胶体,并提供油性屏障,将封装材料与外部材料隔离开来。在这种形式下,PSS 作为疫苗抗原持续递送的储库。接种疫苗后,可以在用 PSS 颗粒配制抗原后,对抗原特异性抗体和细胞介导的免疫进行操作。然后,聚合生物可吸收两亲物固有的降解性符合载体在体内的破坏和进一步吸收。基于生物可吸收两亲物工程的这些多功能囊泡的结构特征可能为疫苗输送提供新的见解。