One‐Step, Room‐Temperature Synthesis of Glutathione‐Capped Iron‐Oxide Nanoparticles and their Application in In Vivo T1‐Weighted Magnetic Resonance Imaging. Issue 19 (9th July 2014)
- Record Type:
- Journal Article
- Title:
- One‐Step, Room‐Temperature Synthesis of Glutathione‐Capped Iron‐Oxide Nanoparticles and their Application in In Vivo T1‐Weighted Magnetic Resonance Imaging. Issue 19 (9th July 2014)
- Main Title:
- One‐Step, Room‐Temperature Synthesis of Glutathione‐Capped Iron‐Oxide Nanoparticles and their Application in In Vivo T1‐Weighted Magnetic Resonance Imaging
- Authors:
- Liu, Chien‐Liang
Peng, Yung‐Kang
Chou, Shang‐Wei
Tseng, Wei‐Hsuan
Tseng, Yu‐Jui
Chen, Hsieh‐Chih
Hsiao, Jong‐Kai
Chou, Pi‐Tai - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The room‐temperature, aqueous‐phase synthesis of iron‐oxide nanoparticles (IO NPs) with glutathione (GSH) is reported. The simple, one‐step reduction involves GSH as a capping agent and tetrakis(hydroxymethyl)phosphonium chloride (THPC) as the reducing agent; GSH is an anti‐oxidant that is abundant in the human body while THPC is commonly used in the synthesis of noble‐metal clusters. Due to their low magnetization and good water‐dispersibility, the resulting GSH‐IO NPs, which are 3.72 ± 0.12 nm in diameter, exhibit a low <italic>r</italic><sub>2</sub> relaxivity (8.28 m<sc>m</sc><sup>−1</sup>s<sup>−1</sup>) and <italic>r</italic><sub>2</sub>/<italic>r</italic><sub>1</sub> ratio (2.28)—both of which are critical for <italic>T</italic><sub>1</sub> contrast agents. This, together with the excellent biocompatibility, makes these NPs an ideal candidate to be a <italic>T</italic><sub>1</sub> contrast agent. Its capability in cellular imaging is illustrated by the high signal intensity in the <italic>T</italic><sub>1</sub>‐weighted magnetic resonance imaging (MRI) of treated HeLa cells. Surprisingly, the GSH‐IO NPs escape ingestion by the hepatic reticuloendothelial system, enabling strong vascular enhancement at the internal carotid artery and superior sagittal sinus, where detection of the thrombus is critical for diagnosing a stroke. Moreover, serial<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The room‐temperature, aqueous‐phase synthesis of iron‐oxide nanoparticles (IO NPs) with glutathione (GSH) is reported. The simple, one‐step reduction involves GSH as a capping agent and tetrakis(hydroxymethyl)phosphonium chloride (THPC) as the reducing agent; GSH is an anti‐oxidant that is abundant in the human body while THPC is commonly used in the synthesis of noble‐metal clusters. Due to their low magnetization and good water‐dispersibility, the resulting GSH‐IO NPs, which are 3.72 ± 0.12 nm in diameter, exhibit a low <italic>r</italic><sub>2</sub> relaxivity (8.28 m<sc>m</sc><sup>−1</sup>s<sup>−1</sup>) and <italic>r</italic><sub>2</sub>/<italic>r</italic><sub>1</sub> ratio (2.28)—both of which are critical for <italic>T</italic><sub>1</sub> contrast agents. This, together with the excellent biocompatibility, makes these NPs an ideal candidate to be a <italic>T</italic><sub>1</sub> contrast agent. Its capability in cellular imaging is illustrated by the high signal intensity in the <italic>T</italic><sub>1</sub>‐weighted magnetic resonance imaging (MRI) of treated HeLa cells. Surprisingly, the GSH‐IO NPs escape ingestion by the hepatic reticuloendothelial system, enabling strong vascular enhancement at the internal carotid artery and superior sagittal sinus, where detection of the thrombus is critical for diagnosing a stroke. Moreover, serial <italic>T</italic><sub>1</sub>‐ and <italic>T</italic><sub>2</sub>‐weighted time‐dependent MR images are resolved for a rat's kidneys, unveiling detailed cortical‐medullary anatomy and renal physiological functions. The newly developed GSH‐IO NPs thus open a new dimension in efforts towards high‐performance, long‐circulating MRI contrast agents that have biotargeting potential.</p> </abstract> … (more)
- Is Part Of:
- Small. Volume 10:Issue 19(2014:Oct.)
- Journal:
- Small
- Issue:
- Volume 10:Issue 19(2014:Oct.)
- Issue Display:
- Volume 10, Issue 19 (2014)
- Year:
- 2014
- Volume:
- 10
- Issue:
- 19
- Issue Sort Value:
- 2014-0010-0019-0000
- Page Start:
- 3962
- Page End:
- 3969
- Publication Date:
- 2014-07-09
- Subjects:
- Nanotechnology -- Periodicals
Nanoparticles -- Periodicals
Microtechnology -- Periodicals
620.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1613-6829 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/smll.201303868 ↗
- Languages:
- English
- ISSNs:
- 1613-6810
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8309.952000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4348.xml