Evidence map›Paper›PMID 22200610›Full record

ArticleActa biomaterialia2012

bFGF-containing electrospun gelatin scaffolds with controlled nano-architectural features for directed angiogenesis.

Ramon B Montero, Ximena Vial, Dat Tat Nguyen, Sepehr Farhand, Mark Reardon, Si M Pham, Gavriil Tsechpenakis, Fotios M Andreopoulos

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2012. 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
3.7field-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

36 citing papers in PubMed, 108 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Ramon B MonteroDepartment of Biomedical Engineering, University of Miami, Coral Gables, FL, USA.
Ximena Vial
Dat Tat Nguyen
Sepehr Farhand
Mark Reardon
Si M Pham
Gavriil Tsechpenakis
Fotios M Andreopoulos
University of Miami · USIndiana University – Purdue University Indianapolis · US

Funding

Rational design of cytokine releasing angiogenic constructsR21EB012136 · NIBIB · UNIVERSITY OF MIAMI CORAL GABLES · PI ANDREOPOULOS, FOTIOS MATTHAIOS · 2010 to 2011
$398k
NIBIB NIH HHS R21 EB012136NIBIB NIH HHS R21-EB012136-01
6 · The paper itself

Abstract

Current therapeutic angiogenesis strategies are focused on the development of biologically responsive scaffolds that can deliver multiple angiogenic cytokines and/or cells in ischemic regions. Herein, we report on a novel electrospinning approach to fabricate cytokine-containing nanofibrous scaffolds with tunable architecture to promote angiogenesis. Fiber diameter and uniformity were controlled by varying the concentration of the polymeric (i.e. gelatin) solution, the feed rate, needle to collector distance, and electric field potential between the collector plate and injection needle. Scaffold fiber orientation (random vs. aligned) was achieved by alternating the polarity of two parallel electrodes placed on the collector plate thus dictating fiber deposition patterns. Basic fibroblast growth factor (bFGF) was physically immobilized within the gelatin scaffolds at variable concentrations and human umbilical vein endothelial cells (HUVEC) were seeded on the top of the scaffolds. Cell proliferation and migration was assessed as a function of growth factor loading and scaffold architecture. HUVECs successfully adhered onto gelatin B scaffolds and cell proliferation was directly proportional to the loading concentrations of the growth factor (0-100 bFGF ng/mL). Fiber orientation had a pronounced effect on cell morphology and orientation. Cells were spread along the fibers of the electrospun scaffolds with the aligned orientation and developed a spindle-like morphology parallel to the scaffold's fibers. In contrast, cells seeded onto the scaffolds with random fiber orientation, did not demonstrate any directionality and appeared to have a rounder shape. Capillary formation (i.e. sprouts length and number of sprouts per bead), assessed in a 3-D in vitro angiogenesis assay, was a function of bFGF loading concentration (0 ng, 50 ng and 100 ng per scaffold) for both types of electrospun scaffolds (i.e. with aligned or random fiber orientation).

Indexed as

Tissue ScaffoldsCapillariesCells, CulturedDelayed-Action PreparationsElectrochemistryEndothelial CellsEquipment DesignFibroblast Growth Factor 2GelatinHumansMaterials TestingNanostructuresNeovascularization, PhysiologicRotationDelayed-Action PreparationsFibroblast Growth Factor 2Gelatin

Identifiers

PMID22200610
PMCPMC3432918
OpenAlexW1990962898

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.