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Design of High-Relaxivity Polyelectrolyte Nanocapsules Based on Citrate Complexes of Gadolinium(III) of Unusual Composition

Through nuclear magnetic relaxation and pH-metry, the details of the complexation of gadolinium(III) ions with citric acid (H L) in water and aqueous solutions of cationic polyelectrolytes are established. It is shown that the presence of poly(ethylene imine) (PEI) in solution affects magnetic relax...

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Bibliographic Details
Published in:International journal of molecular sciences 2021-10, Vol.22 (21), p.11590
Main Authors: Burilova, Evgenia, Solodov, Alexander, Shayimova, Julia, Zhuravleva, Julia, Shurtakova, Darya, Evtjugin, Vladimir, Zhiltsova, Elena, Zakharova, Lucia, Kashapov, Ruslan, Amirov, Rustem
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Language:English
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Summary:Through nuclear magnetic relaxation and pH-metry, the details of the complexation of gadolinium(III) ions with citric acid (H L) in water and aqueous solutions of cationic polyelectrolytes are established. It is shown that the presence of poly(ethylene imine) (PEI) in solution affects magnetic relaxation behavior of gadolinium(III) complexes with citric acid (Cit) to a greater extent than polydiallyldimethylammonium chloride (PDDC). A large increase in relaxivity (up to 50 mM s ) in the broad pH range (4-8) is revealed for the gadolinium(III)-citric acid-PEI system, which is particularly strong in the case of PEI with the molecular weight of 25 and 60 kDa. In weakly acidic medium (pH 3-7), the presence of PEI results in the formation of two tris-ligand associates [Gd(H L) ] and [Gd(H L) (HL)] , which do not exist in aqueous medium. In weakly alkaline medium (pH 7-10), formation of ternary complexes Gd(III)-Cit-PEI with the Gd(III)-to-Cit ratio of 1:2 is evidenced. Using transmission electron microscopy (TEM) and dynamic light scattering techniques (DLS), the formation of the particles with the size of 50-100 nm possessing narrow molecular-mass distribution (PDI 0.08) is determined in the solution containing associate of PEI with tris-ligand complex [Gd(H L) (HL)] .
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms222111590