Evidence map›Paper›PMID 19883608›Full record

ArticleBiophysical journal2009

A simple and highly sensitive method for magnetic nanoparticle quantitation using 1H-NMR spectroscopy.

Jonathan Gunn, Rajan K Paranji, Miqin Zhang

Abstract read
In one paragraph

Article in Biophysical journal, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jonathan GunnDepartment of Materials Science and Engineering, University of Washington, Seattle, Washington, USA.
Rajan K Paranji
Miqin Zhang

Funding

Multifuctional Nanovector For Diagnosis And Treatment Of Pediatric Brain CancerR01EB006043 · NIBIB · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2007 to 2010
$1.6M
Nanovectors For Brain Tumor Diagnosis And TreatmentR01CA134213 · NCI · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2007 to 2011
$1.5M
Nanotechnology Platform for Pediatric Brain Cancer Imaging and TherapyR01CA119408 · NCI · UNIVERSITY OF WASHINGTON · PI ZHANG, MIQIN · 2005 to 2009
$1.4M
Training in Engineered BiomaterialsT32GM065098 · NIGMS · UNIVERSITY OF WASHINGTON · PI RATNER, BUDDY D · 2003 to 2007
$930k
NCI NIH HHS R01 CA119408NCI NIH HHS R01CA119408NCI NIH HHS R01 CA134213NCI NIH HHS R01CA134213NIBIB NIH HHS R01 EB006043NIBIB NIH HHS R01EB006043NIGMS NIH HHS T32 GM065098NIGMS NIH HHS T32GM065098
6 · The paper itself

Abstract

Iron oxide superparamagnetic nanoparticles (SPIONs) have drawn significant attention because of their potential impact on medical diagnosis and therapy. However, the difficulty of achieving reliable and standardized quantification of these nanoparticles has limited the uniform study of nanoparticle systems. Current measurement techniques have limited sensitivity, and are sophisticated and subject to individual instrumental settings. Here, a characterization method using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy is presented that can quantify SPIONs regardless of surface modification. In addition to routine quantification of SPIONs during nanoparticle development, the method can also be used with in vitro nanoparticle assays and potentially with tissue samples for biodistribution studies. Specifically, measurement of water relaxivity shifts (R(1) or R(2)) of dissolved SPION samples is correlated with nanoparticle concentration. Unmodified and dextran- and poly(ethylene glycol)-coated SPIONs gave linear correlations between SPION concentration and R(1) and R(2) relaxivities over five orders of magnitude, to below 10 ppb iron. Quantification of SPION concentration was also demonstrated in the presence of RAW 264.7 macrophage cells. A linear correlation between the SPION concentration and relaxivities was observed to <10 ng Fe/mL. This method is a rapid and inexpensive approach for quantitation of SPIONs and exhibits a number of advantages over many of the current methods for quantitative SPION analysis.

Indexed as

AnimalsBiophysicsCarbocyaninesDextransDose-Response Relationship, DrugFerric CompoundsMacrophagesMagnetic Resonance SpectroscopyMagneticsMetal NanoparticlesMiceNanotechnologyPolyethylene GlycolsSpectrometry, FluorescenceCarbocyaninesCY5.5 cyanine dyeDextransFerric Compoundsferric oxidePolyethylene Glycols

Identifiers

PMID19883608
PMCPMC2770602

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.