Evidence map›Paper›PMID 23928357›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2013

A depot-forming glucagon-like peptide-1 fusion protein reduces blood glucose for five days with a single injection.

M Amiram, K M Luginbuhl, X Li, M N Feinglos, A Chilkoti

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
6.3field-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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
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  8. Article
  9. Intratumoral delivery of brachytherapy and immunotherapy by a thermally triggered polypeptide depot.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  10. Tuning protein half-life in mouse using sequence-defined biopolymers functionalized with lipids.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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.

M AmiramDepartment of Biomedical Engineering, Duke University, Durham 27708, USA.
K M LuginbuhlDepartment of Biomedical Engineering, Duke University, Durham 27708, USA.
X LiDepartment of Biomedical Engineering, Duke University, Durham 27708, USA.
M N FeinglosDivision of Endocrinology, Metabolism, and Nutrition, Duke University Medical Center, Durham 27710, USA.
A ChilkotiDepartment of Biomedical Engineering, Duke University, Durham 27708, USA. Electronic address: chilkoti@duke.edu.
Duke University · US

Funding

Protease Operated Depot for Delivery of GLP-1R01DK091789 · NIDDK · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2012 to 2015
$1.3M
NIDDK NIH HHS R01 DK091789NIDDK NIH HHS R01DK091789
6 · The paper itself

Abstract

Peptide drugs are an exciting class of pharmaceuticals for the treatment of a variety of diseases; however, their short half-life dictates multiple and frequent injections causing undesirable side effects. Herein, we describe a novel peptide delivery system that seeks to combine the attractive features of prolonged circulation time with a prolonged release formulation. This system consists of glucagon-like peptide-1, a type-2 diabetes drug fused to a thermally responsive, elastin-like-polypeptide (ELP) that undergoes a soluble-insoluble phase transition between room temperature and body temperature, thereby forming an injectable depot. We synthesized a set of GLP-1-ELP fusions and verified their proteolytic stability and potency in vitro. Significantly, a single injection of depot forming GLP-1-ELP fusions reduced blood glucose levels in mice for up to 5 days, 120 times longer than an injection of the native peptide. These findings demonstrate the unique advantages of using ELPs to release peptide-ELP fusions from a depot combined with enhanced systemic circulation to create a tunable peptide delivery system.

Indexed as

Amino Acid SequenceAnimalsBlood GlucoseDelayed-Action PreparationsElastinGlucagon-Like Peptide 1Hypoglycemic AgentsInjectionsMaleMiceMice, Inbred C57BLMolecular Sequence DataPhase TransitionRecombinant Fusion ProteinsBlood GlucoseDelayed-Action PreparationsElastinGlucagon-Like Peptide 1Hypoglycemic AgentsRecombinant Fusion ProteinsDrug deliveryElastin-like polypeptideGlucagon-like peptide-1PeptideSubcutaneous depot

Identifiers

PMID23928357
PMCPMC3834218
OpenAlexW2029875542

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.