Evidence map›Paper›PMID 33854749›Full record

ArticleJournal of tissue engineering

Effective decellularisation of human saphenous veins for biocompatible arterial tissue engineering applications: Bench optimisation and feasibility in vivo testing.

Nadiah S Sulaiman, Andrew R Bond, Vito D Bruno, John Joseph, Jason L Johnson, M-Saadeh Suleiman, Sarah J George, Raimondo Ascione

Open access · goldAbstract read
In one paragraph

Article in Journal of tissue engineering. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. NovoMemHistology and histopathology · 2026
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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 3 institutions in 3 countries.

Nadiah S SulaimanBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.ORCID https://orcid.org/0000-0002-3965-1850
Andrew R BondBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.
Vito D BrunoBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.
John JosephCentre for Nanosciences and Molecular Medicine, Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham, Kochi, India.
Jason L JohnsonBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.
M-Saadeh SuleimanBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.
Sarah J GeorgeBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.
Raimondo AscioneBristol Heart Insitute and Translational Biomedical Research Centre, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol Royal Infirmary, Bristol, UK.ORCID https://orcid.org/0000-0001-8045-5619
Bristol Royal Infirmary · GBAmrita Institute of Medical Sciences and Research Centre · INUniversity Kebangsaan Malaysia Medical Centre · MY

Funding

British Heart Foundation FS/18/1/33234British Heart Foundation PG/16/104/32652Medical Research Council MR/L012723/1Medical Research Council MR/T018208/1National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/N003268/1
6 · The paper itself

Abstract

Human saphenous vein (hSV) and synthetic grafts are commonly used conduits in vascular grafting, despite high failure rates. Decellularising hSVs (D-hSVs) to produce vascular scaffolds might be an effective alternative. We assessed the effectiveness of a detergent-based method using 0% to 1% sodium dodecyl sulphate (SDS) to decellularise hSV. Decellularisation effectiveness was measured in vitro by nuclear counting, DNA content, residual cell viability, extracellular matrix integrity and mechanical strength. Cytotoxicity was assessed on human and porcine cells. The most effective SDS concentration was used to prepare D-hSV grafts that underwent preliminary in vivo testing using a porcine carotid artery replacement model. Effective decellularisation was achieved with 0.01% SDS, and D-hSVs were biocompatible after seeding. In vivo xeno-transplantation confirmed excellent mechanical strength and biocompatibility with recruitment of host cells without mechanical failure, and a 50% patency rate at 4-weeks. We have developed a simple biocompatible methodology to effectively decellularise hSVs. This could enhance vascular tissue engineering toward future clinical applications.

Indexed as

bioengineeringDecellularisationtissue engineeringvascular graft

Identifiers

PMID33854749
PMCPMC8010838
OpenAlexW3121475685

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.