Evidence map›Paper›PMID 29396921›Full record

ArticleJournal of biomedical materials research. Part A2018

A thermoresponsive, citrate-based macromolecule for bone regenerative engineering.

Simona Morochnik, Yunxiao Zhu, Chongwen Duan, Michelle Cai, Russell R Reid, Tong-Chuan He, Jason Koh, Igal Szleifer, Guillermo A Ameer

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

9 authors.

Simona MorochnikBiomedical Engineering Department and Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois, USA.
Yunxiao ZhuBiomedical Engineering Department, Northwestern University, Evanston, Illinois, USA.
Chongwen DuanBiomedical Engineering Department, Northwestern University, Evanston, Illinois, USA.
Michelle CaiBiomedical Engineering Department, Northwestern University, Evanston, Illinois, USA.
Russell R ReidDepartment of Surgery, Plastic and Reconstructive Surgery, The University of Chicago Medical Center, Chicago, Illinois, 60637, USA.
Tong-Chuan HeDepartment of Orthopaedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center, Chicago, Illinois, 60637, USA.
Jason KohNorthShore Orthopaedic Institute, NorthShore University HealthSystem, 2650 Ridge Avenue Suite 2505, Evanston, Illinois, 60201, USA.
Igal SzleiferBiomedical Engineering Department and Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois, USA.
Guillermo A AmeerBiomedical Engineering Department and Chemistry of Life Processes Institute, Northwestern University, Evanston, Illinois, USA.

Funding

Chemistry of Life Processes Predoctoral Training ProgramT32GM105538 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2013 to 2022
$2.7M
NIGMS NIH HHS T32 GM105538
6 · The paper itself

Abstract

There is a need in orthopaedic and craniomaxillofacial surgeries for materials that are easy to handle and apply to a surgical site, can fill and fully conform to the bone defect, and can promote the formation of new bone tissue. Thermoresponsive polymers that undergo liquid to gel transition at physiological temperature can potentially be used to meet these handling and shape-conforming requirements. However, there are no reports on their capacity to induce in vivo bone formation. The objective of this research was to investigate whether the functionalization of the thermoresponsive, antioxidant macromolecule poly(poly-ethyleneglycol citrate-co-N-isopropylacrylamide) (PPCN), with strontium, phosphate, and/or the cyclic RGD peptide would render it a hydrogel with osteoinductive properties. We show that all formulations of functionalized PPCN retain thermoresponsive properties and can induce osteodifferentiation of human mesenchymal stem cells without the need for exogenous osteogenic supplements. PPCN-Sr was the most osteoinductive formulation in vitro and produced robust localized mineralization and osteogenesis in subcutaneous and intramuscular tissue in a mouse model. Strontium was not detected in any of the major organs. Our results support the use of functionalized PPCN as a valuable tool for the recruitment, survival, and differentiation of cells critical to the development of new bone and the induction of bone formation in vivo. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 1743-1752, 2018.

Indexed as

OsteogenesisAdipose TissueAntioxidantsBiocompatible MaterialsBone RegenerationCell AdhesionCell LineCell ProliferationCells, CulturedCitric AcidFibroblastsHumansMesenchymal Stem CellsPeptides, CyclicPhosphatesStem CellsAntioxidantsBiocompatible MaterialsCitric Acidcyclic arginine-glycine-aspartic acid peptidePeptides, CyclicPhosphatesStrontiumbioengineeringbone µCTfracture healingmatrix mineralizationstem cells

Identifiers

PMID29396921
PMCPMC5951299

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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.