Evidence map›Paper›PMID 24853463›Full record

ArticleInternational journal of pharmaceutics2014

pH-Responsive poly(itaconic acid-co-N-vinylpyrrolidone) hydrogels with reduced ionic strength loading solutions offer improved oral delivery potential for high isoelectric point-exhibiting therapeutic proteins.

Michael C Koetting, Nicholas A Peppas

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Oral Drug Delivery Technologies-A Decade of Developments.The Journal of pharmacology and experimental therapeutics · 2019
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. pH-Sensitive stimulus-responsive nanocarriers for targeted delivery of therapeutic agents.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
  13. Article
  14. Review
  15. Article
  16. Micro/nanofabricated platforms for oral drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  17. Stimulus-responsive hydrogels: Theory, modern advances, and applications.Materials science & engineering. R, Reports : a review journal · 2015
    Article
  18. Long-term delivery of protein therapeutics.Expert opinion on drug delivery · 2015
    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

2 authors.

Michael C KoettingMcKetta Department of Chemical Engineering, The University of Texas at Austin, C0400, Austin, TX 78712, United States. Electronic address: mkoetting@utexas.edu.
Nicholas A PeppasMcKetta Department of Chemical Engineering, The University of Texas at Austin, C0400, Austin, TX 78712, United States; Department of Biomedical Engineering, The University of Texas at Austin, C0800, Austin, TX 78712, United States; College of Pharmacy, The University of Texas at Austin, C0400, Austin, TX 78712, United States. Electronic address: peppas@che.utexas.edu.

Funding

pH Sensitive Complex Hydrogels for Protein Drug ReleaseR01EB000246 · NIBIB · UNIVERSITY OF TEXAS AUSTIN · PI LOWMAN, ANTHONY M, PEPPAS, NICHOLAS A · 2002 to 2014
$3.8M
NIBIB NIH HHS R01 EB000246NIBIB NIH HHS R01-EB000246-19
6 · The paper itself

Abstract

pH-Responsive hydrogels comprised of itaconic acid copolymerized with N-vinylpyrrolidone (P(IA-co-NVP)) were synthesized and tested as carriers for the oral delivery of high isoelectric point (pI) exhibiting therapeutic proteins. Swelling studies show that P(IA-co-NVP) hydrogels exhibit significantly greater and faster pH-responsive swelling than previously studied methacrylic acid-based hydrogels, achieving up to 68% greater equilibrium swelling and 10.4 times greater swelling in time-limited experiments. Using salmon calcitonin as a model high pI protein therapeutic, we show that P(IA-co-NVP) hydrogels exhibit significantly greater delivery potential than methacrylic acid-based hydrogels. Additionally, we show that utilizing a lower ionic strength solution during drug loading significantly improves drug delivery potential for high pI therapeutics. By using a 1.5mM PBS buffer rather than the standard 150 mM PBS buffer during loading, up to 83 times as much calcitonin can be delivered in neutral conditions, with up to a 9.6-fold improvement in percent release. Using P(IA-co-NVP) hydrogel microparticles and a low ionic strength loading solution, up to 48 μg calcitonin/mg hydrogel can be delivered in small intestinal conditions. Based on expected absorption in the small intestine, this is sufficient delivery potential for achieving therapeutic dosage via a single, regularly-sized pill taken daily.

Indexed as

Administration, OralCaco-2 CellsCalcitoninCell SurvivalDrug CarriersDrug LiberationHumansHydrogelsHydrogen-Ion ConcentrationIsoelectric PointOsmolar ConcentrationPolymersPyrrolidinonesSolutionsCalcitoninDrug CarriersHydrogelspoly(itaconic acid-co-N-vinylpyrrolidone)PolymersPyrrolidinonessalmon calcitoninSolutionsIonic strengthIsoelectric pointItaconic acidOral drug deliverypH-Responsive hydrogelsProtein therapeutics

Identifiers

PMID24853463
PMCPMC4096305

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Registered trials

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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.