Abstract

Transdisciplinary approaches involving areas such as material design, nanotechnology, chemistry, and immunology have to be utilized to rationally design efficacious vaccines carriers. Nanoparticle-based platforms can prolong the persistence of vaccine antigens, which could improve vaccine immunogenicity. Several biodegradable polymers have been studied as vaccine delivery vehicles(1); in particular, polyanhydride particles have demonstrated the ability to provide sustained release of stable protein antigens and to activate antigen presenting cells and modulate immune responses. The molecular design of these vaccine carriers needs to integrate the rational selection of polymer properties as well as the incorporation of appropriate targeting agents. High throughput automated fabrication of targeting ligands and functionalized particles is a powerful tool that will enhance the ability to study a wide range of properties and will lead to the design of reproducible vaccine delivery devices. The addition of targeting ligands capable of being recognized by specific receptors on immune cells has been shown to modulate and tailor immune responses. C-type lectin receptors (CLRs) are pattern recognition receptors (PRRs) that recognize carbohydrates present on the surface of pathogens. The stimulation of immune cells via CLRs allows for enhanced internalization of antigen and subsequent presentation for further T cell activation. Therefore, carbohydrate molecules play an important role in the study of immune responses; however, the use of these biomolecules often suffers from the lack of availability of structurally well-defined and pure carbohydrates. An automation platform based on iterative solution-phase reactions can enable rapid and controlled synthesis of these synthetically challenging molecules using significantly lower building block quantities than traditional solid-phase methods. Herein we report a protocol for the automated solution-phase synthesis of oligosaccharides such as mannose-based targeting ligands with fluorous solid-phase extraction for intermediate purification. After development of automated methods to make the carbohydrate-based targeting agent, we describe methods for their attachment on the surface of polyanhydride nanoparticles employing an automated robotic set up operated by LabVIEW as previously described. Surface functionalization with carbohydrates has shown efficacy in targeting CLRs and increasing the throughput of the fabrication method to unearth the complexities associated with a multi-parametric system will be of great value (Figure 1a).

Highlights

  • The molecular design of these vaccine carriers needs to integrate the rational selection of polymer properties as well as the incorporation of appropriate targeting agents

  • After development of automated methods to make the carbohydrate-based targeting agent, we describe methods for their attachment on the surface of polyanhydride nanoparticles employing an automated robotic set up operated by LabVIEW as previously described10

  • The synthesized compound was characterized by 1H nuclear magnetic resonance (NMR) in a VXR 400 MHz spectrometer using CDCl3 as solvent

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Summary

High-throughput Carbohydrate Synthesis

It is ensured that before the addition of the promoter, the mixture of donor and acceptor is stirred for at least 30 min. 6. Once the program is started, the robotic arm transfers the solutions of donor and acceptor into the reaction vial sequentially. The cartridges are washed with 100% methanol to obtain the desired fluorous-tagged product. The reaction can again be continued for a longer period and the programmed time required can be modified. After the completion of the reaction, the product is purified by FSPE and subjected to dissolution in anhydrous toluene followed by evaporation to remove residual water. Complete deprotection (removal of all remaining protecting groups) of the final target molecule is completed outside the automation platform as a rule because it usually involves explosive hydrogen gas and palladium. The product was passed through celite pad to get rid of palladium to get pure final product

High-throughput Nanoparticle Surface Functionalization
Representative Results
Discussion
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