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Facile Formation of Gold-Nanoparticle-Loaded γ-Polyglutamic Acid Nanogels for Tumor Computed Tomography Imaging.
- Source :
-
Bioconjugate chemistry [Bioconjug Chem] 2017 Nov 15; Vol. 28 (11), pp. 2692-2697. Date of Electronic Publication: 2017 Nov 03. - Publication Year :
- 2017
-
Abstract
- The formation of gold nanoparticle (Au NP)-loaded γ-polyglutamic acid (γ-PGA) nanogels (NGs) for computed tomography (CT) imaging of tumors is reported. γ-PGA with carboxyl groups activated by 1-ethyl-3-[3-(dimethylamino)propyl] carbodiimide hydrochloride is first emulsified to form NGs and then in situ chemically cross-linked with polyethylenimine (PEI)-entrapped Au NPs with partial polyethylene glycol (PEG) modification ([(Au <superscript>0</superscript> ) <subscript>200</subscript> -PEI·NH <subscript>2</subscript> -mPEG]). The formed γ-PGA-[(Au <superscript>0</superscript> ) <subscript>200</subscript> -PEI·NH <subscript>2</subscript> -mPEG] NGs with a size of 108.6 ± 19.1 nm display an X-ray attenuation property better than commercial iodinated small-molecular-contrast agents and can be uptaken by cancer cells more significantly than γ-PGA-stabilized single Au NPs at the same Au concentrations. These properties render the formed NGs with an ability to be used as an effective contrast agent for the CT imaging of cancer cells in vitro and a tumor model in vivo. The developed hybrid NGs may be promising for the CT imaging or theranostics of different biosystems.
- Subjects :
- Animals
Gold pharmacokinetics
HeLa Cells
Humans
Male
Mice, Inbred BALB C
Mice, Nude
Nanogels
Nanoparticles analysis
Polyethylene Glycols chemistry
Polyethylene Glycols pharmacokinetics
Polyethyleneimine chemistry
Polyethyleneimine pharmacokinetics
Polyglutamic Acid chemistry
Polyglutamic Acid pharmacokinetics
Gold chemistry
Nanoparticles chemistry
Neoplasms diagnostic imaging
Polyglutamic Acid analogs & derivatives
Tomography, X-Ray Computed methods
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4812
- Volume :
- 28
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Bioconjugate chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29083866
- Full Text :
- https://doi.org/10.1021/acs.bioconjchem.7b00571