Evidence map›Paper›PMID 26365781›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2015

Enzymatically-responsive pro-angiogenic peptide-releasing poly(ethylene glycol) hydrogels promote vascularization in vivo.

Amy H Van Hove, Kathleen Burke, Erin Antonienko, Edward Brown, Danielle S W Benoit

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 69 citations in OpenAlex.

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  14. Article
  15. Biohybrid Nanosystems for Cancer Treatment: Merging the Best of Two Worlds.Advances in experimental medicine and biology · 2021
    Article
  16. Vascularization in tissue engineering: fundamentals and state-of-art.Progress in biomedical engineering (Bristol, England) · 2020
    Article
  17. Article
  18. Review
  19. Degradable poly(ethylene glycol) (PEG)-based hydrogels for spatiotemporal control of siRNA/nanoparticle delivery.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  20. Development of controlled drug delivery systems for bone fracture-targeted therapeutic delivery: A review.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2018
    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

5 authors at 1 institution in 1 country.

Amy H Van HoveDepartment of Biomedical Engineering, 207 Robert B. Goergen Hall, University of Rochester, Rochester, NY 14627, USA. Electronic address: amy.h.vanhove@rochester.edu.
Kathleen BurkeDepartment of Biomedical Engineering, 207 Robert B. Goergen Hall, University of Rochester, Rochester, NY 14627, USA. Electronic address: kathleen_Burke@URMC.Rochester.edu.
Erin AntonienkoDepartment of Biomedical Engineering, 207 Robert B. Goergen Hall, University of Rochester, Rochester, NY 14627, USA. Electronic address: eantonie@u.rochester.edu.
Edward BrownDepartment of Biomedical Engineering, 207 Robert B. Goergen Hall, University of Rochester, Rochester, NY 14627, USA; Department of Neurobiology and Anatomy, University of Rochester, 601 Elmwood Ave, Rochester, NY, 14642, USA. Electronic address: Edward_Brown@URMC.Rochester.edu.
Danielle S W BenoitDepartment of Biomedical Engineering, 207 Robert B. Goergen Hall, University of Rochester, Rochester, NY 14627, USA; Department of Biomedical Genetics, 601 Elmwood Ave, University of Rochester, Rochester, NY 14642, USA; Department of Chemical Engineering, 206 Gavett Hall, University of Rochester, Rochester, NY 14627 USA; Center for Musculoskeletal Research, 601 Elmwood Ave, University of Rochester Medical Center, Rochester, NY 14642, USA. Electronic address: benoit@bme.rochester.edu.
University of Rochester · US

Funding

The T32 Predoctoral Training Program in Immunology (PTPI)T32AI007285 · NIAID · UNIVERSITY OF ROCHESTER · PI Scott Andrew Gerber, JACQUES Robert · 1986 to 2026
$7.6M
Tissue Engineering Strategies to Revitalize Bone AllograftsR01AR064200 · NIAMS · UNIVERSITY OF ROCHESTER · PI Danielle S. Benoit · 2013 to 2026
$4.0M
Exploring the Role of Collagen Structure in Breast Cancer Metastatic ProgressionF31CA183351 · NCI · UNIVERSITY OF ROCHESTER · PI BURKE, KATHLEEN ANNE · 2014 to 2014
$23k
NCI NIH HHS F31 CA183351NIAID NIH HHS T32 AI007285NIAMS NIH HHS R01 AR064200
6 · The paper itself

Abstract

Therapeutic angiogenesis holds great potential for a myriad of tissue engineering and regenerative medicine approaches. While a number of peptides have been identified with pro-angiogenic behaviors, therapeutic efficacy is limited by poor tissue localization and persistence. Therefore, poly(ethylene glycol) hydrogels providing sustained, enzymatically-responsive peptide release were exploited for peptide delivery. Two pro-angiogenic peptide drugs, SPARC113 and SPARC118, from the Secreted Protein Acidic and Rich in Cysteine, were incorporated into hydrogels as crosslinking peptides flanked by matrix metalloproteinase (MMP) degradable substrates. In vitro testing confirmed peptide drug bioactivity requires sustained delivery. Furthermore, peptides retain bioactivity with residual MMP substrates present after hydrogel release. Incorporation into hydrogels achieved enzymatically-responsive bulk degradation, with peptide release in close agreement with hydrogel mass loss and released peptides retaining bioactivity. Interestingly, SPARC113 and SPARC118-releasing hydrogels had significantly different degradation time constants in vitro (1.16 and 8.77×10(-2) h(-1), respectively), despite identical MMP degradable substrates. However, upon subcutaneous implantation, both SPARC113 and SPARC118 hydrogels exhibited similar degradation constants of ~1.45×10(-2) h(-1), and resulted in significant ~1.65-fold increases in angiogenesis in vivo compared to controls. Thus, these hydrogels represent a promising pro-angiogenic approach for applications such as tissue engineering and ischemic tissue disorders.

Indexed as

Angiogenic ProteinsAnimalsBridged Bicyclo CompoundsCells, CulturedDelayed-Action PreparationsDrug CarriersFemaleHeptanesHuman Umbilical Vein Endothelial CellsHydrogelsMatrix Metalloproteinase 2Mice, Inbred BALB CNeovascularization, PhysiologicOligopeptidesOsteonectinPolyethylene Glycols(2.2.1)bicyclohept-2-eneAngiogenic ProteinsBridged Bicyclo CompoundsDelayed-Action PreparationsDrug CarriersHeptanesHydrogelsMatrix Metalloproteinase 2OligopeptidesOsteonectinPolyethylene GlycolsAngiogenesisControlled drug releaseEnzymeHydrogelPeptide

Identifiers

PMID26365781
PMCPMC4626208
OpenAlexW1467804957

What OpenQuestion holds

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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.