Evidence map›Paper›PMID 32091189›Full record

ArticleACS applied materials & interfaces2020

Nanoengineered Osteoinductive Bioink for 3D Bioprinting Bone Tissue.

David Chimene, Logan Miller, Lauren M Cross, Manish K Jaiswal, Irtisha Singh, Akhilesh K Gaharwar

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

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  5. NIR Phosphorescent Oxygen Sensors in Natural Hydrogel Matrices.bioRxiv : the preprint server for biology · 2025
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  15. Biomedical Approach of Nanotechnology and Biological Risks: A Mini-Review.International journal of molecular sciences · 2023
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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

6 authors.

David ChimeneDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Logan MillerDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Lauren M CrossDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Manish K JaiswalDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Irtisha SinghDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M Health Science Center, Bryan, Texas 77807, United States.ORCID http://orcid.org/0000-0002-9460-3587
Akhilesh K GaharwarDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.ORCID http://orcid.org/0000-0002-0284-0201

Funding

Mineralomics: Designing mineral based therapeutics to control and direct cell functionDP2EB026265 · NIBIB · TEXAS ENGINEERING EXPERIMENT STATION · PI GAHARWAR, AKHILESH K. · 2017 to 2021
$2.4M
Nanoengineered bone repair scaffolds generated from stem cells and their secreted products for improved spinal fusionR21AR072292 · NIAMS · TEXAS A&M UNIVERSITY · PI GREGORY, CARL A. · 2019 to 2020
$349k
NIAMS NIH HHS R21 AR072292NIBIB NIH HHS DP2 EB026265
6 · The paper itself

Abstract

Bioprinting is an emerging additive manufacturing approach to the fabrication of patient-specific, implantable three-dimensional (3D) constructs for regenerative medicine. However, developing cell-compatible bioinks with high printability, structural stability, biodegradability, and bioactive characteristics is still a primary challenge for translating 3D bioprinting technology to preclinical and clinal models. To overcome this challenge, we developed a nanoengineered ionic covalent entanglement (NICE) bioink formulation for 3D bone bioprinting. The NICE bioinks allow precise control over printability, mechanical properties, and degradation characteristics, enabling custom 3D fabrication of mechanically resilient, cellularized structures. We demonstrate cell-induced remodeling of 3D bioprinted scaffolds over 60 days, demonstrating deposition of nascent extracellular matrix proteins. Interestingly, the bioprinted constructs induce endochondral differentiation of encapsulated human mesenchymal stem cells (hMSCs) in the absence of osteoinducing agent. Using next-generation transcriptome sequencing (RNA-seq) technology, we establish the role of nanosilicates, a bioactive component of NICE bioink, to stimulate endochondral differentiation at the transcriptome level. Overall, the osteoinductive bioink has the ability to induce formation of osteo-related mineralized extracellular matrix by encapsulated hMSCs in growth factor-free conditions. Furthermore, we demonstrate the ability of NICE bioink to fabricate patient-specific, implantable 3D scaffolds for repair of craniomaxillofacial bone defects. We envision development of this NICE bioink technology toward a realistic clinical process for 3D bioprinting patient-specific bone tissue for regenerative medicine.

Indexed as

Tissue EngineeringBiological Specimen BanksBioprintingBone and BonesExtracellular MatrixHumansPrinting, Three-DimensionalRegenerative MedicineTissue Scaffoldsbone bioprintinghydrogelsionic-covalent reinforcementnanomaterialsosteoinductive bioinks

Identifiers

PMID32091189
PMCPMC12833824

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Registered trials

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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.