Size-controlled synthesis of dendrimer-stabilized silver nanoparticles for X-ray computed tomography imaging applications

Literature Information

Publication Date 2010-09-22
DOI 10.1039/C0PY00218F
Impact Factor 5.582
Authors

Han Wang, Rui Guo, Xueyan Cao, Jinglong Zhao, Yu Luo, Mingwu Shen, Guixiang Zhang


View Original

Abstract

We report a facile size-controlled synthesis of dendrimer-stabilized silver nanoparticles (Ag DSNPs) for X-ray computed tomography (CT) imaging applications. Amine-terminated generation 5 poly(amidoamine) dendrimers were used as templates to complex Ag(I) ions for subsequent reductive formation of dendrimer-entrapped Ag nanoparticles. Following a one-step acetylation reaction to transform dendrimer terminal amine to acetyl groups, Ag DSNPs can be formed. The formed Ag DSNPs were characterized using 1H NMR, UV-Vis spectrometry, transmission electron microscopy, and ζ-potential measurements. We show that through the variation of the dendrimer/Ag salt molar ratio, the size of Ag DSNPs can be controlled at the range of 8.8–23.2 nm. The formed Ag DSNPs are stable not only in water, PBS buffer, and fetal bovine serum, but also at different pH conditions (pH 5–8) and temperatures (20–50 °C). X-Ray absorption coefficient measurements show that the attenuation of Ag DSNPs is size-dependent, and the Ag DSNPs with a diameter of 16.1 nm display an X-ray attenuation intensity close to that of a clinically used iodine-based contrast agent (Omnipaque) at the same molar concentration of the active element (Ag versus iodine). This suggests that Ag DSNPs with an appropriate size have a great potential to be used as a CT imaging contrast agent, although the atomic number of Ag is lower than that of iodine. Furthermore, CT scanning showed prolonged enhancement at the point of mice injected subcutaneously with Ag DSNPs, rendering them as a promising contrast agent in CT imaging applications.

Related Literature

The role of the dihedral angle and excited cation states in ionization and dissociation of mono-halogenated biphenyls; a combined experimental and theoretical coupled cluster study

Michael Barclay, Ragnar Bjornsson, Maicol Cipriani, Andreas Terfort, D. Howard Fairbrother, Oddur Ingólfsson

2019-02-01 Paper

DOI: 10.1039/C8CP07785A

An ab initio study of sensing applications of MoB2 monolayer: a potential gas sensor

Amreen Bano, Jyoti Krishna, Devendra K. Pandey, N. K. Gaur

2019-01-29 Paper

DOI: 10.1039/C8CP07038E

Molecular and dissociative O2 adsorption on the Cu2O(111) surface

Xiaohu Yu, Caibin Zhao, Tianlei Zhang, Zhong Liu

2018-05-23 Paper

DOI: 10.1039/C8CP03035A

Fluctuation correlations as major determinants of structure- and dynamics-driven allosteric effects

Miao Yu, Yixin Chen, Zi-Le Wang

2019-02-09 Paper

DOI: 10.1039/C8CP07859A

The role of solvation models on the computed absorption and emission spectra: the case of fireflies oxyluciferin

Cristina García-Iriepa, Madjid Zemmouche, Isabelle Navizet

2019-02-04 Paper

DOI: 10.1039/C8CP07352J

UPS and UV spectroscopies combined to position the energy levels of TiO2 anatase and rutile nanopowders

Clément Maheu, Luis Cardenas, Eric Puzenat, Pavel Afanasiev, Christophe Geantet

2018-09-17 Paper

DOI: 10.1039/C8CP04614J

Oxygen-functionalized TlTe buckled honeycomb from first-principles study

Qing Lu, Yi-Ming Wen, Zhao-Yi Zeng, Xiang-Rong Chen, Qi-Feng Chen

2019-02-12 Paper

DOI: 10.1039/C8CP07246A

Bismuth oxysulfide film electrodes with giant incident photon-to-current conversion efficiency: the dynamics of properties with deposition time

Evgeny A. Bondarenko, Eugene A. Streltsov, Alexander V. Mazanik, Anatoly I. Kulak, Vytautas Grivickas, Patrik Ščajev, Ekaterina V. Skorb

2018-06-22 Paper

DOI: 10.1039/C8CP03225D

You might also like

Compound Q&A

Is 6-(3-Fluorophenyl)picolinic acid (CAS: 887982-40-3) safe?

6-(3-Fluorophenyl)picolinic acid is generally considered safe for laboratory use...

887982-40-36-(3-Fluorophenyl)pi...
Compound Q&A

What industries use (3R)-3-Pyrrolidinol (CAS: 2799-21-5)?

(3R)-3-Pyrrolidinol is used in the pharmaceutical industry as a precursor for dr...

2799-21-5(3R)-3-Pyrrolidinol
Compound Q&A

What precautions should be taken when handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-8)?

When handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-...

59779-75-8(4R,5R)-4,5-Diethoxy...
Compound Q&A

How is 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone (CAS: 90734-71-7) typically synthesized?

1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone is often synthesized via a mult...

90734-71-71-(6-Chloroimidazo[1...
Compound Q&A

What is the market or research trend for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1)?

The market for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1) remains steady,...

39180-83-1N-Ethyl-3,4-dimethyl...
Compound Q&A

What is Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate (CAS: 1019008-21-9)?

Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate is a chemical compound wit...

1019008-21-9Tert-butyl 3-(pyrrol...
Compound Q&A

What regulatory guidelines apply to 1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1)?

1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1) falls under the classi...

1228956-93-11-Bromo-3-chloro-2,4...
Compound Q&A

Is 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07-4) safe?

The safety of 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07...

1368622-07-48-Bromo-2-methyl-3,4...
Compound Q&A

Is Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate (CAS: 22785-43-9) safe?

Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate is generally safe when handled wi...

22785-43-9Benzyl [(3S)-2,6-dio...
Compound Q&A

How should 1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine (CAS: 928657-21-0) be stored?

1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine s...

928657-21-01-{[4-(4,4,5,5-Tetra...

Source Journal

Polymer Chemistry

Polymer Chemistry
CiteScore: 8.6
Self-citation Rate: 7.3%
Articles per Year: 457

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.