Evidence map›Paper›PMID 20117157›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2010

Injectable intratumoral depot of thermally responsive polypeptide-radionuclide conjugates delays tumor progression in a mouse model.

Wenge Liu, J Andrew MacKay, Matthew R Dreher, Mingnan Chen, Jonathan R McDaniel, Andrew J Simnick, Daniel J Callahan, Michael R Zalutsky, Ashutosh Chilkoti

Abstract readEvaluation Study
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.2field-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

42 citing papers in PubMed, 97 citations in OpenAlex.

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  18. Injectable polypeptide micelles that form radiation crosslinked hydrogels in situ for intratumoral radiotherapy.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

9 authors at 3 institutions in 1 country.

Wenge LiuDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
J Andrew MacKay
Matthew R Dreher
Mingnan Chen
Jonathan R McDaniel
Andrew J Simnick
Daniel J Callahan
Michael R Zalutsky
Ashutosh Chilkoti
Duke University · USNational Institutes of Health Clinical Center · USUniversity of Southern California · US

Funding

Thermally Targeted Drug Delivery by Elastin BiopolymersR01EB000188 · NIBIB · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2002 to 2015
$3.9M
Local Radionuclide Delivery to Solid Tumors by Injectible BiopolymerR01CA138784 · NCI · DUKE UNIVERSITY · PI LIU, WENGE · 2009 to 2014
$1.6M
pH sensitive elastin-like-peptides for tumor targetingF32CA123889 · NCI · DUKE UNIVERSITY · PI MACKAY, JOHN ANDREW · 2006 to 2007
$95k
Image Guided Focused Ultrasound For Drug Delivery and Tissue AblationZIACL040012 · CLC · CLINICAL CENTER · PI WOOD, BRADFORD · 2009 to 2024
$0k
Interventional OncologyZIACL040015 · CLC · CLINICAL CENTER · PI WOOD, BRADFORD · 2009 to 2025
$0k
NCI NIH HHS 5F32-CA-123889NCI NIH HHS F32 CA123889NCI NIH HHS R01 CA138784NIBIB NIH HHS R01 EB000188
6 · The paper itself

Abstract

This study evaluated a biodegradable drug delivery system for local cancer radiotherapy consisting of a thermally sensitive elastin-like polypeptide (ELP) conjugated to a therapeutic radionuclide. Two ELPs (49 kDa) were synthesized using genetic engineering to test the hypothesis that injectable biopolymeric depots can retain radionuclides locally and reduce the growth of tumors. A thermally sensitive polypeptide, ELP(1), was designed to spontaneously undergo a soluble-insoluble phase transition (forming viscous microparticles) between room temperature and body temperature upon intratumoral injection, while ELP(2) was designed to remain soluble upon injection and to serve as a negative control for the effect of aggregate assembly. After intratumoral administration of radionuclide conjugates of ELPs into implanted tumor xenografts in nude mice, their retention within the tumor, spatio-temporal distribution, and therapeutic effect were quantified. The residence time of the radionuclide-ELP(1) in the tumor was significantly longer than the thermally insensitive ELP(2) conjugate. In addition, the thermal transition of ELP(1) significantly protected the conjugated radionuclide from dehalogenation, whereas the conjugated radionuclide on ELP(2) was quickly eliminated from the tumor and cleaved from the biopolymer. These attributes of the thermally sensitive ELP(1) depot improved the antitumor efficacy of iodine-131 compared to the soluble ELP(2) control. This novel injectable and biodegradable depot has the potential to control advanced-stage cancers by reducing the bulk of inoperable tumors, enabling surgical removal of de-bulked tumors, and preserving healthy tissues.

Indexed as

AnimalsAntigensBiopolymersDosage FormsDrug Delivery SystemsElastinFemaleHot TemperatureInjectionsMiceMice, NudeNeoplasmsNeoplastic ProcessesPeptidesRadioisotopesAntigensBiopolymersDosage FormsElastinPeptidesRadioisotopes

Identifiers

PMID20117157
PMCPMC2862899
OpenAlexW1972219660

What OpenQuestion holds

Textmetadata
LicenceTDM
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.