Evidence map›Paper›PMID 26655062›Full record

ReviewJournal of controlled release : official journal of the Controlled Release Society2016

Controlled release of biologics for the treatment of type 2 diabetes.

Caslin A Gilroy, Kelli M Luginbuhl, Ashutosh Chilkoti

Abstract readReview
In one paragraph

Review in Journal of controlled release : official journal of the Controlled Release Society, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.6field-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

19 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. 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
  8. Review
  9. Article
  10. Genetically Encoded Cholesterol-Modified Polypeptides.Journal of the American Chemical Society · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Oral delivery of biologics using drug-device combinations.Current opinion in pharmacology · 2017
    Review
  18. Article
  19. Review
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 at 1 institution in 1 country.

Caslin A Gilroy *Department of Biomedical Engineering, 136 Hudson Hall, Box 90281, Duke University, Durham, NC 27708, USA.
Kelli M Luginbuhl *Department of Biomedical Engineering, 136 Hudson Hall, Box 90281, Duke University, Durham, NC 27708, USA.
Ashutosh ChilkotiDepartment of Biomedical Engineering, 136 Hudson Hall, Box 90281, Duke University, Durham, NC 27708, USA.
Duke University · US

Funding

Protease Operated Depot for Delivery of GLP-1R01DK091789 · NIDDK · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2012 to 2015
$1.3M
Site-Specific Growth of Stealth Polymer from Peptide TherapeuticsR01DK092665 · NIDDK · DUKE UNIVERSITY · PI CHILKOTI, ASHUTOSH · 2011 to 2014
$1.3M
NIDDK NIH HHS R01 DK091789NIDDK NIH HHS R01 DK092665
6 · The paper itself

Abstract

Type 2 diabetes is a rapidly growing disease that poses a significant burden to the United States healthcare system. Despite the many available treatments for the disease, close to half of diagnosed type 2 diabetes cases are not properly managed, largely due to inadequate patient adherence to prescribed treatment regimens. Methods for improving delivery - and thereby easing administration - of type 2 drugs have the potential to greatly improve patient health. This review focuses on two peptide drugs - insulin and glucagon-like peptide 1 (GLP-1) - for treatment of type 2 diabetes. Peptide drugs offer the benefits of high potency and specificity but pose a significant delivery challenge due to their inherent instability and short half-life. The development of insulin and GLP-1 analogs highlights the broad spectrum of drug delivery strategies that have been used to solve these problems. Numerous structural modifications and formulations have been introduced to optimize absorption, residence time, stability, route of delivery and frequency of administration. Continual improvements in delivery methods for insulin and GLP-1 receptor agonists are paving the way towards better patient compliance and improved disease management, and thereby enhanced patient quality of life.

Indexed as

Amino Acid SequenceAnimalsBiological ProductsBlood GlucoseDelayed-Action PreparationsDiabetes Mellitus, Type 2Drug Delivery SystemsHumansHypoglycemic AgentsInsulinTreatment OutcomeBiological ProductsBlood GlucoseDelayed-Action PreparationsHypoglycemic AgentsInsulinControlled releaseDiabetesDrug deliveryGLP-1InsulinPeptide

Identifiers

PMID26655062
PMCPMC4889564
OpenAlexW2188597575

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.