Evidence map›Paper›PMID 28989813›Full record

ArticleNature biomedical engineering2016

A brush-polymer conjugate of exendin-4 reduces blood glucose for up to five days and eliminates poly(ethylene glycol) antigenicity.

Yizhi Qi, Antonina Simakova, Nancy J Ganson, Xinghai Li, Kelli M Luginbuhl, Imran Özer, Wenge Liu, Michael S Hershfield, Krzysztof Matyjaszewski, Ashutosh Chilkoti

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
12.2field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Article
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  5. Article
  6. All-PEG-Like Block Copolymers Self-Assemble into Stealth Nanocarriers for Drug Delivery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Polymeric Nanomaterials for Atherosclerosis Diagnosis and Treatment.Polymer science & technology (Washington, D.C.) · 2025
    Review
  11. Article
  12. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Yizhi QiDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Antonina SimakovaDepartment of Chemistry, Carnegie Mellon University, Pittsburgh, PA, USA.
Nancy J GansonDepartment of Medicine, Division of Rheumatology, Duke University Medical Center, Durham, NC, USA.
Xinghai LiDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Kelli M LuginbuhlDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Imran ÖzerDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Wenge LiuDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Michael S HershfieldDepartment of Medicine, Division of Rheumatology, Duke University Medical Center, Durham, NC, USA.
Krzysztof MatyjaszewskiDepartment of Chemistry, Carnegie Mellon University, Pittsburgh, PA, USA.
Ashutosh ChilkotiDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Duke University · USCarnegie Mellon University · USDuke Medical Center · US

Funding

Site-Specific Growth of Stealth Polymer from Peptide TherapeuticsR01DK092665 · NIDDK · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2011 to 2014
$1.3M
NIDDK NIH HHS R01 DK092665
6 · The paper itself

Abstract

The delivery of therapeutic peptides and proteins is often challenged by a short half-life, and thus the need for frequent injections that limit efficacy, reduce patient compliance and increase treatment cost. Here, we demonstrate that a single subcutaneous injection of site-specific (C-terminal) conjugates of exendin-4 (exendin) - a therapeutic peptide that is clinically used to treat type 2 diabetes - and poly[oligo(ethylene glycol) methyl ether methacrylate] (POEGMA) with precisely controlled molecular weights lowered blood glucose for up to 120 h in fed mice. Most notably, we show that an exendin-C-POEGMA conjugate with an average of 9 side-chain ethylene glycol (EG) repeats exhibits significantly lower reactivity towards patient-derived anti-poly(ethylene glycol) (PEG) antibodies than two FDA-approved PEGylated drugs, and that reducing the side-chain length to 3 EG repeats completely eliminates PEG antigenicity without compromising

Identifiers

PMID28989813
PMCPMC5627778
OpenAlexW2557421336

What OpenQuestion holds

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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.