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Mannosylated liposomes with built-in peptidoglycan based immunomodulators for subunit vaccines formulations (CROSBI ID 638464)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | domaća recenzija

Štimac, Adela ; Frkanec, Ruža ; Frkanec, Leo Mannosylated liposomes with built-in peptidoglycan based immunomodulators for subunit vaccines formulations // Book of Abstract of the Congress of the Croatian Society of Biochemistry and Molecular Biology on the Occasion of the 40th Anniversary / Katalinić, Maja ; Kovarik, Zrinka (ur.). Zagreb, 2016. str. 105-105

Podaci o odgovornosti

Štimac, Adela ; Frkanec, Ruža ; Frkanec, Leo

engleski

Mannosylated liposomes with built-in peptidoglycan based immunomodulators for subunit vaccines formulations

This study is focused on the preparation of mannosylated liposomes with built-in small molecule immunopotentiators for targeted, receptors mediated, delivery of antigens and adjuvants. The liposomes are recognized as attractive drug delivery carriers characterized by the absence of toxicity and low intrinsic immunogenicity. Mannose receptors (MR) have very important role in a large variety of cellular recognition processes, particularly those with immune function. MR present on the cell surface of different immunocompetent cells such as macrophages and dendritic cells, are considered to be pattern-recognition receptors. Therefore, they could be responsible for the receptor mediated uptake of mannosylated antigens, biologically active molecules containing mannose or mannose targeted drug delivery systems.1, 2 In the continuation of our studies, our interest is in finding a potent targeted delivery vehicle for drugs, especially for subunit vaccines.3 Mannosylated liposome preparations with incorporated model antigen, ovalbumin (OVA), and immunomodulators, PGM and Ad2TP2, were prepared and characterized. The influence of mannosylated liposomal formulations of antigen and immunomodulators on the specific immune reaction in mice was tested. The liposomes were mannosylated in two ways, by covalent attachment of p-aminophenyl-α-D-mannopyranoside to the preformed liposomes and by incorporation of synthetic di- and tetramannosyl- lipoconjugates into the lipid bilayer of liposomes. The coupling efficiency of p-aminophenyl-α-D-mannopyranoside to the preformed liposomes and entrapment efficiency of OVA and immunomodulators into mannosylated liposomes were measured spectrophotometrically and by using HPLC. Evaluation of adjuvant activity of mannosylated liposomes with built-in immunomodulators in vivo, has shown their significant immunomodulatory effect. 1. C. Kelly, C. Jefferies, S.-A. Cryan, Journal of Drug Delivery 2011 (2011), Article ID 727241. 2. J. M. Irache, H. H. Salman, C. Gamazo, S. Espuelas, Expert. Opin. Drug. Deliv. 5 (2008) 703-724. 3. A. Štimac, S. Šegota, M. Dutour Sikirić, R. Ribić, L. Frkanec, V. Svetličić, S. Tomić, B. Vranešić, R. Frkanec, Biochim. Biophys. Acta 1818 (2012) 2252-2259

liposomes ; targeted delivery ; immunomodulator ; mannose receptor

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Podaci o prilogu

105-105.

2016.

objavljeno

Podaci o matičnoj publikaciji

Book of Abstract of the Congress of the Croatian Society of Biochemistry and Molecular Biology on the Occasion of the 40th Anniversary

Katalinić, Maja ; Kovarik, Zrinka

Zagreb:

1847-7836

Podaci o skupu

Congress of the Croatian Society of Biochemistry and Molecular Biology on the Occasion of the 40th Anniversary

poster

01.06.2016-04.06.2016

Split, Hrvatska

Povezanost rada

Kemija, Temeljne medicinske znanosti