Evidence map›Paper›PMID 27942578›Full record

ArticleACS biomaterials science & engineering2016

Three-Dimensional Printing of Bone Extracellular Matrix for Craniofacial Regeneration.

Ben P Hung, Bilal A Naved, Ethan L Nyberg, Miguel Dias, Christina A Holmes, Jennifer H Elisseeff, Amir H Dorafshar, Warren L Grayson

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
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

59 citing papers in PubMed.

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  7. Utilization of 3D printing technology in hepatopancreatobiliary surgery.Journal of Zhejiang University. Science. B · 2024
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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.

Ben P HungDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States; Translational Tissue Engineering Center, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States.
Bilal A NavedFischell Department of Biomedical Engineering, University of Maryland, College Park, Maryland 21231, United States.
Ethan L NybergDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States; Translational Tissue Engineering Center, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States.
Miguel DiasDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States; Translational Tissue Engineering Center, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States.
Christina A HolmesDepartment of Neurosurgery, The Johns Hopkins Hospital, Baltimore 21231, Maryland, United States.
Jennifer H ElisseeffDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States; Translational Tissue Engineering Center, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States.
Amir H DorafsharDepartment of Plastic Surgery, The Johns Hopkins Hospital, Baltimore 21231, Maryland, United States.
Warren L GraysonDepartment of Biomedical Engineering, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States; Translational Tissue Engineering Center, The Johns Hopkins University School of Medicine, Baltimore 21231, Maryland, United States.

Funding

Three-dimensional printing of native bone matrixF31DE024922 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI HUNG, BEN PEN JUI · 2014 to 2015
$79k
NIDCR NIH HHS F31 DE024922
6 · The paper itself

Abstract

Tissue-engineered approaches to regenerate bone in the craniomaxillofacial region utilize biomaterial scaffolds to provide structural and biological cues to stem cells to stimulate osteogenic differentiation. Bioactive scaffolds are typically comprised of natural components but often lack the manufacturability of synthetic materials. To circumvent this trade-off, we 3D printed materials comprised of decellularized bone (DCB) matrix particles combined with polycaprolactone (PCL) to create novel hybrid DCB:PCL scaffolds for bone regeneration. Hybrid scaffolds were readily printable at compositions of up to 70% bone by mass and displayed robust mechanical properties. Assessments of surface features revealed both collagenous and mineral components of bone were present. Qualitative and quantitative assessments showed increased surface roughness relative to that of pure PCL scaffolds. These findings correlated with enhanced cell adhesion on hybrid surfaces relative to that on pure surfaces. Human adipose-derived stem cells (hASCs) cultured in DCB:PCL scaffolds without soluble osteogenic cues exhibited significant upregulation of osteogenic genes in hybrid scaffolds relative to pure PCL scaffolds. In the presence of soluble phosphate, hybrid scaffolds resulted in increased calcification. The hASC-seeded scaffolds were implanted into critical-sized murine calvarial defects and yielded greater bone regeneration in DCB:PCL scaffolds compared to that in PCL-only at 1 and 3 months post-transplantation. Taken together, these results demonstrate that 3D printed DCB:PCL scaffolds might be effective for stimulating bone regeneration.

Indexed as

3D-printingbiomaterialsbone regenerationdecellularized bonetissue engineering

Identifiers

PMID27942578
PMCPMC5142751

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.