Evidence map›Paper›PMID 27072720›Full record

ArticleTissue engineering. Part A2016

Cellularized Bilayer Pullulan-Gelatin Hydrogel for Skin Regeneration.

Mathew N Nicholas, Marc G Jeschke, Saeid Amini-Nik

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.4field-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

22 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Electrospinning Live Cells Using Gelatin and Pullulan.Bioengineering (Basel, Switzerland) · 2020
    Article
  13. Article
  14. Promotion of dermal regeneration using pullulan/gelatin porous skin substitute.Journal of tissue engineering and regenerative medicine · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. The Role of Serotonin during Skin Healing in Post-Thermal Injury.International journal of molecular sciences · 2018
    Article
  19. Biomaterials for Skin Substitutes.Advanced healthcare materials · 2018
    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

3 authors at 1 institution in 1 country.

Mathew N NicholasDepartment of Surgery, Sunnybrook Research Institute, Ross Tilley Burn Centre, University of Toronto , Toronto, Ontario, Canada .
Marc G JeschkeDepartment of Surgery, Sunnybrook Research Institute, Ross Tilley Burn Centre, University of Toronto , Toronto, Ontario, Canada .
Saeid Amini-NikDepartment of Surgery, Sunnybrook Research Institute, Ross Tilley Burn Centre, University of Toronto , Toronto, Ontario, Canada .
Sunnybrook Health Science Centre · CA

Funding

Hepatic ER stress contributes to morbidity and mortality after burn injury.R01GM087285 · NIGMS · SUNNYBROOK & WOMEN'S COLL HLTH SCIS CTR · PI BOEHNING, DARREN F, JESCHKE, MARC GERHARD · 2010 to 2018
$1.9M
NIGMS NIH HHS R01 GM087285
6 · The paper itself

Abstract

Skin substitutes significantly reduce the morbidity and mortality of patients with burn injuries and chronic wounds. However, current skin substitutes have disadvantages related to high costs and inadequate skin regeneration due to highly inflammatory wounds. Thus, new skin substitutes are needed. By combining two polymers, pullulan, an inexpensive polysaccharide with antioxidant properties, and gelatin, a derivative of collagen with high water absorbency, we created a novel inexpensive hydrogel-named PG-1 for "pullulan-gelatin first generation hydrogel"-suitable for skin substitutes. After incorporating human fibroblasts and keratinocytes onto PG-1 using centrifugation over 5 days, we created a cellularized bilayer skin substitute. Cellularized PG-1 was compared to acellular PG-1 and no hydrogel (control) in vivo in a mouse excisional skin biopsy model using newly developed dome inserts to house the skin substitutes and prevent mouse skin contraction during wound healing. PG-1 had an average pore size of 61.69 μm with an ideal elastic modulus, swelling behavior, and biodegradability for use as a hydrogel for skin substitutes. Excellent skin cell viability, proliferation, differentiation, and morphology were visualized through live/dead assays, 5-bromo-2'-deoxyuridine proliferation assays, and confocal microscopy. Trichrome and immunohistochemical staining of excisional wounds treated with the cellularized skin substitute revealed thicker newly formed skin with a higher proportion of actively proliferating cells and incorporation of human cells compared to acellular PG-1 or control. Excisional wounds treated with acellular or cellularized hydrogels showed significantly less macrophage infiltration and increased angiogenesis 14 days post skin biopsy compared to control. These results show that PG-1 has ideal mechanical characteristics and allows ideal cellular characteristics. In vivo evidence suggests that cellularized PG-1 promotes skin regeneration and may help promote wound healing in highly inflammatory wounds, such as burns and chronic wounds.

Indexed as

GelatinGlucansHydrogelsSkinSkin, ArtificialAnimalsFibroblastsHeterograftsHumansKeratinocytesMaleMiceMice, NudeRegenerationWound HealingGelatinGlucansHydrogelspullulan

Identifiers

PMID27072720
PMCPMC4876533
OpenAlexW2351503164

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.