Evidence map›Paper›PMID 21300184›Full record

ArticleActa biomaterialia2011

Matrix metalloproteinase-sensitive thermogelling polymer for bioresponsive local drug delivery.

Vivek Kumar Garripelli, Jin-Ki Kim, Sejin Son, Won Jong Kim, Michael A Repka, Seongbong Jo

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. MMP-responsiveRSC advances · 2019
    Article
  8. Article
  9. Article
  10. Enzyme-responsive polymer hydrogels for therapeutic delivery.Experimental biology and medicine (Maywood, N.J.) · 2016
    Review
  11. Article
  12. Review
  13. 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

6 authors at 3 institutions in 2 countries.

Vivek Kumar GarripelliDepartment of Pharmaceutics, School of Pharmacy, The University of Mississippi, University, 38677, USA.
Jin-Ki Kim
Sejin Son
Won Jong Kim
Michael A Repka
Seongbong Jo
University of Mississippi · USPohang University of Science and Technology · KRUniversity of North Carolina at Chapel Hill · US

Funding

SOURCING, ACQUISITION AND DATABASE COREP20RR021929 · NCRR · UNIVERSITY OF MISSISSIPPI · PI EL-ALFY, ABIR T · 2006 to 2010
$11.1M
RENOVATION OF FOURTH FLOOR OF FASER HALLC06RR014503 · NCRR · UNIVERSITY OF MISSISSIPPI · PI WELLS, BARBARA G · 1999 to 1999
–
NCRR NIH HHS C06 RR014503NCRR NIH HHS C06 RR-14503-01NCRR NIH HHS P20 RR021929
6 · The paper itself

Abstract

Development of a successful bioresponsive drug delivery system requires exquisite engineering of the materials so that they are able to respond to signals stemming from the physiological environment. In this study we propose a new Pluronic(®) based thermogelling system containing matrix metalloproteinase-2 (MMP2) responsive peptide sequences. A novel thermosensitive multiblock co-polymer comprising an MMP2-labile octapeptide (Gly-Pro-Val-Gly-Leu-Ile-Gly-Lys) was synthesized from a Pluronic(®) triblock co-polymer. The polymer was designed to form a thermogel at body temperature and degrade in the presence of MMP overexpressed in a tumor. The synthesized polymer was a multiblock co-polymer with ∼2.5 U of Pluronic(®). The multiblock co-polymer solutions exhibited reverse thermal gelation around body temperature. The gelation temperatures of the multiblock co-polymer solutions were lower than those of the corresponding Pluronic(®) monomer at a particular concentration. The cytotoxicity of the synthesized polymer was lower compared with the monomer. The solubility of the hydrophobic anticancer drug paclitaxel was enhanced in the polymer solutions by micelle formation. The synthesized polymer was preferentially degraded in the presence of MMP. Paclitaxel release was dependent on the enzyme concentration. These findings suggest that the synthesized polymer has potential as a controlled drug delivery system due to its unique phase transition and bioresponsive behavior.

Indexed as

Drug Delivery SystemsTemperatureBiocompatible MaterialsCalorimetry, Differential ScanningCell Line, TumorCell SurvivalChromatography, GelCircular DichroismGelsHumansMagnetic Resonance SpectroscopyMatrix MetalloproteinasesMicellesMolecular WeightPaclitaxelPhase TransitionBiocompatible MaterialsGelsMatrix MetalloproteinasesMicellesPaclitaxelPoloxamerPolymers

Identifiers

PMID21300184
PMCPMC3082466
OpenAlexW2043132471

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.