Literature DB >> 18570391

Minimal chemical modification of reductive end of dextran to produce an amphiphilic polysaccharide able to incorporate onto lipid nanocapsules.

Antoine Richard1, Alexandre Barras, Amena Ben Younes, Nicole Monfilliette-Dupont, Patricia Melnyk.   

Abstract

In order to graft an amphiphilic polysaccharide to lipid nanocapsules, we present here a new method of dextran lipidation. The lipidation strategy is based on the formation of an oxime linkage between the amphiphilic hydroxylamine C16E20ONH2 and the reductive end of a 40 kDa dextran. This chemoselective reaction allows us to control the lipidation site and the number of lipid introduced on the dextran molecule. This new amphiphilic dextran was used to coat the surface of lipid nanocapsules. The coating efficiency was followed by dynamic light scattering and the presence of the polysaccharide was confirmed by (1)H NMR and observed by electronic microscopy.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18570391     DOI: 10.1021/bc700444t

Source DB:  PubMed          Journal:  Bioconjug Chem        ISSN: 1043-1802            Impact factor:   4.774


  2 in total

1.  Synthesis of Hydrophilic Aminooxy Linkers and Multivalent Cores for Chemoselective Aldehyde/Ketone Conjugation.

Authors:  Katherine D McReynolds; Dustin Dimas; Hoang Le
Journal:  Tetrahedron Lett       Date:  2014-04-02       Impact factor: 2.415

2.  Chemoselective ligation in the functionalization of polysaccharide-based particles.

Authors:  Tristan T Beaudette; Joel A Cohen; Eric M Bachelder; Kyle E Broaders; Jessica L Cohen; Edgar G Engleman; Jean M J Fréchet
Journal:  J Am Chem Soc       Date:  2009-08-05       Impact factor: 15.419

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.