Evidence map›Paper›PMID 16325951›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2006

Novel oral insulin delivery systems based on complexation polymer hydrogels: single and multiple administration studies in type 1 and 2 diabetic rats.

Mariko Morishita, Takahiro Goto, Koji Nakamura, Anthony M Lowman, Kozo Takayama, Nicholas A Peppas

Abstract readComparative Study
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.5field-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

36 citing papers in PubMed, 188 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. PEGylated insulin loaded complexation hydrogels for protected oral delivery.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Micro and nanoscale technologies in oral drug delivery.Advanced drug delivery reviews · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Recent advances in hemophilia B therapy.Drug delivery and translational research · 2017
    Review
  15. Article
  16. Article
  17. Stimulus-responsive hydrogels: Theory, modern advances, and applications.Materials science & engineering. R, Reports : a review journal · 2015
    Article
  18. Article
  19. Review
  20. Article
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

6 authors at 3 institutions in 2 countries.

Mariko MorishitaDepartment of Pharmaceutics, Hoshi University, Ebara, Shinagawa, Tokyo, Japan. morisita@hoshi.ac.jp <morisita@hoshi.ac.jp>
Takahiro Goto
Koji Nakamura
Anthony M Lowman
Kozo Takayama
Nicholas A Peppas
Hoshi University · JPDrexel University · USThe University of Texas at Austin · US

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 EB000246-13A2NIBIB NIH HHS R01 EB000246
6 · The paper itself

Abstract

Insulin-loaded polymer microparticles (ILP) composed of crosslinked poly(methacrylic acid) and poly(ethylene glycol) are multi-functional carriers showing high insulin incorporation efficiency, a rapid insulin release in the intestine based on their pH-dependent complexation properties, enzyme-inhibiting effects and mucoadhesive characteristics. Thus, they are potential carriers for insulin delivery via an oral route. Recent studies suggest that the polymer composition and particle size of ILP strongly influenced insulin bioavailability. Therefore, the present study aimed at finding an optimal formulation and designing carriers for oral insulin delivery using in vivo experiments. Various types of ILPs were prepared and administered orally to healthy and type 1 and 2 diabetic rats. The most promising formulation was subsequently used for in vivo multiple oral administration studies using diabetic rats. The microparticles of diameters of <53 microm (SS-ILP) composed of a 1:1 molar ratio of methacrylic acid/ethylene glycol units showed the most pronounced hypoglycaemic effects following oral administration to healthy rats, achieving a 9.5% pharmacological availability compared to subcutaneous insulin injection. Their usefulness was also confirmed with both type 1 and 2 diabetic rat groups. In a multiple administration study, SS-ILP significantly suppressed the postprandial rise in blood glucose and showed continuous hypoglycaemic effects following 3 times/day oral administration to both diabetic rat groups in the presence of foods. These results indicate that the blood glucose levels of diabetic rats can be effectively controlled by oral SS-ILP administration, and thus SS-ILP would be a promising delivery carrier of insulin via the oral route.

Indexed as

Administration, OralAnimalsBlood GlucoseDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2Dose-Response Relationship, DrugDrug Administration ScheduleDrug Delivery SystemsHydrogelsInsulinMalePolymersRatsRats, WistarBlood GlucoseHydrogelsInsulinPolymers

Identifiers

PMID16325951
PMCPMC4467730
OpenAlexW1976233456

What OpenQuestion holds

Textmetadata
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.