Synthesis and Characterization of Mannosylated Formulations to Deliver a Minicircle DNA Vaccine

DNA vaccines still represent an emergent area of research, giving rise to continuous progress towards several biomedicine demands. The formulation of delivery systems to specifically target mannose receptors, which are overexpressed on antigen presenting cells (APCs), is considered a suitable strate...

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Main Authors: Ana Sofia Serra (Author), Dalinda Eusébio (Author), Ana Raquel Neves (Author), Tânia Albuquerque (Author), Himanshu Bhatt (Author), Swati Biswas (Author), Diana Costa (Author), Ângela Sousa (Author)
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Published: MDPI AG, 2021-05-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ana Sofia Serra  |e author 
700 1 0 |a Dalinda Eusébio  |e author 
700 1 0 |a Ana Raquel Neves  |e author 
700 1 0 |a Tânia Albuquerque  |e author 
700 1 0 |a Himanshu Bhatt  |e author 
700 1 0 |a Swati Biswas  |e author 
700 1 0 |a Diana Costa  |e author 
700 1 0 |a Ângela Sousa  |e author 
245 0 0 |a Synthesis and Characterization of Mannosylated Formulations to Deliver a Minicircle DNA Vaccine 
260 |b MDPI AG,   |c 2021-05-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics13050673 
500 |a 1999-4923 
520 |a DNA vaccines still represent an emergent area of research, giving rise to continuous progress towards several biomedicine demands. The formulation of delivery systems to specifically target mannose receptors, which are overexpressed on antigen presenting cells (APCs), is considered a suitable strategy to improve the DNA vaccine immunogenicity. The present study developed binary and ternary carriers, based on polyethylenimine (PEI), octa-arginine peptide (R8), and mannose ligands, to specifically deliver a minicircle DNA (mcDNA) vaccine to APCs. Systems were prepared at various nitrogen to phosphate group (N/P) ratios and characterized in terms of their morphology, size, surface charge, and complexation capacity. In vitro studies were conducted to assess the biocompatibility, cell internalization ability, and gene expression of formulated carriers. The high charge density and condensing capacity of both PEI and R8 enhance the interaction with the mcDNA, leading to the formation of smaller particles. The addition of PEI polymer to the R8-mannose/mcDNA binary system reduces the size and increases the zeta potential and system stability. Confocal microscopy studies confirmed intracellular localization of targeting systems, resulting in sustained mcDNA uptake. Furthermore, the efficiency of in vitro transfection can be influenced by the presence of R8-mannose, with great implications for gene expression. R8-mannose/PEI/mcDNA ternary systems can be considered valuable tools to instigate further research, aiming for advances in the DNA vaccine field. 
546 |a EN 
690 |a HPV infection 
690 |a mannose ligands 
690 |a minicircle DNA vaccine 
690 |a polyethyleneimine 
690 |a R8 peptide 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 13, Iss 5, p 673 (2021) 
787 0 |n https://www.mdpi.com/1999-4923/13/5/673 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/b6ff402c86b64a3285cb37d1fe2dbeb6  |z Connect to this object online.