Evidence map›Paper›PMID 25553115›Full record

ArticleTheranostics2015

Nanogels from metal-chelating crosslinkers as versatile platforms applied to copper-64 PET imaging of tumors and metastases.

Jacques Lux, Alexander G White, Minnie Chan, Carolyn J Anderson, Adah Almutairi

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
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

14 citing papers in PubMed, 47 citations in OpenAlex.

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  12. Nanogels: An overview of properties, biomedical applications and obstacles to clinical translation.Journal of controlled release : official journal of the Controlled Release Society · 2016
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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

5 authors at 1 institution in 1 country.

Jacques Lux1. Skaggs School of Pharmacy and Pharmaceutical Sciences, and the Laboratory of Bioresponsive Materials, University of California, San Diego. 9500 Gilman Dr. 0600, La Jolla, CA 92093-0600, United States.
Alexander G White2. University of Pittsburgh Departments of Radiology, Pharmacology & Chemical Biology and Bioengineering. Molecular Imaging Laboratory, 100 Technology Drive, Pittsburgh, PA 15219, United States.
Minnie Chan1. Skaggs School of Pharmacy and Pharmaceutical Sciences, and the Laboratory of Bioresponsive Materials, University of California, San Diego. 9500 Gilman Dr. 0600, La Jolla, CA 92093-0600, United States.
Carolyn J Anderson2. University of Pittsburgh Departments of Radiology, Pharmacology & Chemical Biology and Bioengineering. Molecular Imaging Laboratory, 100 Technology Drive, Pittsburgh, PA 15219, United States.
Adah Almutairi1. Skaggs School of Pharmacy and Pharmaceutical Sciences, and the Laboratory of Bioresponsive Materials, University of California, San Diego. 9500 Gilman Dr. 0600, La Jolla, CA 92093-0600, United States. ; 3. KACST-UCSD Center for Excellence in Nanomedicine and Engineering.
University of Montana · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Chemically amplified response strategies for medical sciences; concepts borrowedDP2OD006499 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ALMUTAIRI, ADAH · 2009 to 2009
$2.3M
NCI NIH HHS P30 CA047904NCI NIH HHS P30CA047904NIH HHS DP 2OD006499
6 · The paper itself

Abstract

Metals are essential in medicine for both therapy and diagnosis. We recently created the first metal-chelating nanogel imaging agent, which employed versatile, reproducible chemistry that maximizes chelation stability. Here we demonstrate that our metal chelating crosslinked nanogel technology is a powerful platform by incorporating (64)Cu to obtain PET radiotracers. Polyacrylamide-based nanogels were crosslinked with three different polydentate ligands (DTPA, DOTA, NOTA). NOTA-based nanogels stably retained (64)Cu in mouse serum and accumulated in tumors in vivo as detected by PET/CT imaging. Measurement of radioactivity in major organs ex vivo confirmed this pattern, revealing a high accumulation (12.3% ID/g and 16.6% ID/g) in tumors at 24 and 48 h following administration, with lower accumulation in the liver (8.5% ID/g at 24 h) and spleen (5.5% ID/g). Nanogels accumulated even more efficiently in metastases (29.9% and 30.4% ID/g at 24 and 48 h). These metal-chelating nanogels hold great promise for future application as bimodal PET/MRI agents; chelation of β-emitting radionuclides could enable radiation therapy.

Indexed as

Copper RadioisotopesPolyethylene GlycolsPolyethyleneimineAnimalsDrug StabilityHumansMiceNanogelsNeoplasm MetastasisNeoplasmsPositron-Emission TomographyCopper RadioisotopesNanogelspolyethylene glycol polyethyleneimine nanogelPolyethylene GlycolsPolyethyleneiminecopper 64metal-chelating crosslinkersmetastases.NanogelsNOTAPETpreclinical imaging

Identifiers

PMID25553115
PMCPMC4279191
OpenAlexW2128549595

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.