Evidence map›Paper›PMID 24370837›Full record

ArticleInvestigative ophthalmology & visual science2014

Biocompatible reverse thermal gel sustains the release of intravitreal bevacizumab in vivo.

Britta M Rauck, Thomas R Friberg, Carlos A Medina Mendez, Daewon Park, Veeral Shah, Richard A Bilonick, Yadong Wang

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 83 citations in OpenAlex.

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  8. Hyaluronic Acid-PEG-Based Diels-AlderBiomacromolecules · 2022
    Article
  9. PCL-PEG copolymer based injectable thermosensitive hydrogels.Journal of controlled release : official journal of the Controlled Release Society · 2022
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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

7 authors at 1 institution in 1 country.

Britta M RauckDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
Thomas R Friberg
Carlos A Medina Mendez
Daewon Park
Veeral Shah
Richard A Bilonick
Yadong Wang
University of Pittsburgh · US

Funding

Training in Biomechanics in Regenerative MedicineT32EB003392 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WOO, SAVIO L-Y. · 2005 to 2020
$4.0M
NIBIB NIH HHS 2T32EB003392-07NIBIB NIH HHS T32 EB003392
6 · The paper itself

Abstract

purposeWe assessed the in vivo release profile of bevacizumab from and biocompatibility of poly(ethylene glycol)-poly-(serinol hexamethylene urethane), or ESHU, a thermoresponsive hydrogel administered intravitreally for drug delivery.

methodsThe technical feasibility of injection was assessed quantitatively via mechanical testing. For in vivo studies, New Zealand White rabbit eyes were injected intravitreally with 0.05 mL of either: ESHU dissolved in 25 mg/mL bevacizumab, ESHU dissolved in PBS, or 25 mg/mL bevacizumab. Clinical examination included IOP measurements and examination with indirect ophthalmoscopy for signs of inflammation. Additionally, eyes were examined histologically following euthanasia. To quantify bevacizumab release, aqueous humor samples were obtained via anterior chamber paracentesis and ELISA was used to determine the concentration of drug weekly. In vitro cytotoxicity testing also was performed using bovine corneal endothelial cells.

resultsThe ESHU was injected easily through a 31-gauge needle, was well tolerated in vivo, and caused minimal cell death in vitro when compared to other common materials, such as silicone oil. The long-term presence of the gel did not affect IOP, and there was no evidence of inflammation histologically or through indirect observation. The ESHU sustained the release of bevacizumab for over 9 weeks and maintained a drug concentration that averaged 4.7 times higher than eyes receiving bolus bevacizumab injections.

conclusionsTo our knowledge, this is the first report demonstrating sustained bevacizumab release in vivo from an intravitreally injected hydrogel formulation, suggesting that this delivery system may be a promising candidate for ocular drug delivery.

Indexed as

Angiogenesis InhibitorsAnimalsAntibodies, Monoclonal, HumanizedAqueous HumorBevacizumabCattleChoroidal NeovascularizationDelayed-Action PreparationsDisease Models, AnimalDrug Delivery SystemsEnzyme-Linked Immunosorbent AssayFeasibility StudiesHydrogel, Polyethylene Glycol DimethacrylateIntravitreal InjectionsOphthalmoscopyRabbitsAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedBevacizumabDelayed-Action PreparationsHydrogel, Polyethylene Glycol DimethacrylateVascular Endothelial Growth Factor Abiocompatibilityinjectable gelocular drug deliverysustained releasethermally responsive hydrogel

Identifiers

PMID24370837
PMCPMC3901415
OpenAlexW2054525867

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.