Evidence map›Paper›PMID 27544807›Full record

ArticleActa biomaterialia2016

Micropore-induced capillarity enhances bone distribution in vivo in biphasic calcium phosphate scaffolds.

Laurence E Rustom, Thomas Boudou, Siyu Lou, Isabelle Pignot-Paintrand, Brett W Nemke, Yan Lu, Mark D Markel, Catherine Picart, Amy J Wagoner Johnson

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 103 citations in OpenAlex.

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  18. Calcium Phosphate-Based Biomaterials for Bone Repair.Journal of functional biomaterials · 2022
    Review
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  20. Review
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 at 5 institutions in 3 countries.

Laurence E RustomDepartment of Bioengineering, University of Illinois at Urbana-Champaign, 1270 Digital Computer Laboratory, MC-278, 1304 West Springfield Avenue, Urbana, IL 61801, USA; University Grenoble Alpes, LMGP, 38000 Grenoble, France. Electronic address: rustom2@illinois.edu.
Thomas BoudouUniversity Grenoble Alpes, LMGP, 38000 Grenoble, France; CNRS UMR 5628 (LMGP), 3 parvis Louis Néel, 38016 Grenoble, France. Electronic address: thomas.boudou@grenoble-inp.fr.
Siyu LouUniversity Grenoble Alpes, LMGP, 38000 Grenoble, France; CNRS UMR 5628 (LMGP), 3 parvis Louis Néel, 38016 Grenoble, France; School of Materials Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, 200240 Shanghai, China. Electronic address: lousiyushanghai@gmail.com.
Isabelle Pignot-PaintrandUniversity Grenoble Alpes, LMGP, 38000 Grenoble, France; CNRS UMR 5628 (LMGP), 3 parvis Louis Néel, 38016 Grenoble, France. Electronic address: isabelle.paintrand@grenoble-inp.fr.
Brett W NemkeSchool of Veterinary Medicine, University of Wisconsin - Madison, 2015 Linden Drive, Madison, WI 53706, USA. Electronic address: brett.nemke@wisc.edu.
Yan LuSchool of Veterinary Medicine, University of Wisconsin - Madison, 2015 Linden Drive, Madison, WI 53706, USA. Electronic address: yan.lu@wisc.edu.
Mark D MarkelSchool of Veterinary Medicine, University of Wisconsin - Madison, 2015 Linden Drive, Madison, WI 53706, USA. Electronic address: mark.markel@wisc.edu.
Catherine PicartUniversity Grenoble Alpes, LMGP, 38000 Grenoble, France; CNRS UMR 5628 (LMGP), 3 parvis Louis Néel, 38016 Grenoble, France. Electronic address: catherine.picart@grenoble-inp.fr.
Amy J Wagoner JohnsonDepartment of Bioengineering, University of Illinois at Urbana-Champaign, 1270 Digital Computer Laboratory, MC-278, 1304 West Springfield Avenue, Urbana, IL 61801, USA; University Grenoble Alpes, LMGP, 38000 Grenoble, France; Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, 1206 West Green Street, Urbana, IL 61801, USA. Electronic address: ajwj@illinois.edu.
University of Wisconsin–Madison · USUniversité Grenoble Alpes · FRUniversity of Illinois Urbana-Champaign · USInstitut Néel · FRLaboratoire des Matériaux et du Génie Physique · FR

Funding

European Research Council 259370
6 · The paper itself

Abstract

unlabelledThe increasing demand for bone repair solutions calls for the development of efficacious bone scaffolds. Biphasic calcium phosphate (BCP) scaffolds with both macropores and micropores (MP) have improved healing compared to those with macropores and no micropores (NMP), but the role of micropores is unclear. Here, we evaluate capillarity induced by micropores as a mechanism that can affect bone growth in vivo. Three groups of cylindrical scaffolds were implanted in pig mandibles for three weeks: MP were implanted either dry (MP-Dry), or after submersion in phosphate buffered saline, which fills pores with fluid and therefore suppresses micropore-induced capillarity (MP-Wet); NMP were implanted dry. The amount and distribution of bone in the scaffolds were quantified using micro-computed tomography. MP-Dry had a more homogeneous bone distribution than MP-Wet, although the average bone volume fraction, BVF‾, was not significantly different for these two groups (0.45±0.03 and 0.37±0.03, respectively). There was no significant difference in the radial bone distribution of NMP and MP-Wet, but the BVF‾, of NMP was significantly lower among the three groups (0.25±0.02). These results suggest that micropore-induced capillarity enhances bone regeneration by improving the homogeneity of bone distribution in BCP scaffolds. The explicit design and use of capillarity in bone scaffolds may lead to more effective treatments of large and complex bone defects. STATEMENT OF SIGNIFICANCE: The increasing demand for bone repair calls for more efficacious bone scaffolds and calcium phosphate-based materials are considered suitable for this application. Macropores (>100μm) are necessary for bone ingrowth and vascularization. However, studies have shown that microporosity (<20μm) also enhances growth, but there is no consensus on the controlling mechanisms. In previous in vitro work, we suggested that micropore-induced capillarity had the potential to enhance bone growth in vivo. This work illustrates the positive effects of capillarity on bone regeneration in vivo; it demonstrates that micropore-induced capillarity significantly enhances the bone distribution in the scaffold. The results will impact the design of scaffolds to better exploit capillarity and improve treatments for large and load-bearing bone defects.

Indexed as

Capillary ActionAnimalsBone and BonesBone RegenerationCalcium PhosphatesOrgan SizePorositySus scrofaTissue ScaffoldsX-Ray Microtomographycalcium phosphateCalcium PhosphatesBone regenerationCalcium phosphate scaffoldCapillary actionMicro-computed tomographyMicroporosity

Identifiers

PMID27544807
PMCPMC5045872
OpenAlexW2511633631

What OpenQuestion holds

Textmetadata
LicenceTDM
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.