Evidence map›Paper›PMID 25297314›Full record

ArticleJournal of the Royal Society, Interface2014

Structural changes and biological responsiveness of an injectable and mouldable monetite bone graft generated by a facile synthetic method.

G Cama, B Gharibi, J C Knowles, S Romeed, L DiSilvio, S Deb

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 23 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

G CamaBiomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK.
B GharibiBiomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK.
J C KnowlesDivision of Biomaterials and Tissue Engineering, UCL Eastman Dental Institute, 256 Gray's Inn Road, London WC1X 8LD, UK Department of Nanobiomedical Science and BK21 Plus NBM Global Research Centre for Regenerative Medicine, Dankook University, Cheonan 330-714, Republic of Korea.
S RomeedBiomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK.
L DiSilvioBiomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK.
S DebBiomaterials, Biomimetics and Biophotonics, King's College London Dental Institute, Floor 17, Tower Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK sanjukta.deb@kcl.ac.uk.
Guy's Hospital · GBKing's College London · GBDankook University · KR

Funding

Wellcome Trust
6 · The paper itself

Abstract

Brushite (dicalcium phosphate dihydrate) and monetite (dicalcium phosphate anhydrous) are of considerable interest in bone augmentation owing to their metastable nature in physiological fluids. The anhydrous form of brushite, namely monetite, has a finer microstructure with higher surface area, strength and bioresorbability, which does not transform to the poorly resorbable hydroxyapatite, thus making it a viable alternative for use as a scaffold for engineering of bone tissue. We recently reported the formation of monetite cements by a simple processing route without the need of hydrothermal treatment by using a high concentration of sodium chloride in the reaction mix of β-tricalcium phosphate and monocalcium phosphate monohydrate. In this paper, we report the biological responsiveness of monetite formed by this method. The in vitro behaviour of monetite after interaction and ageing both in an acellular and cellular environment showed that the crystalline phase of monetite was retained over three weeks as evidenced from X-ray diffraction measurements. The crystal size and morphology also remained unaltered after ageing in different media. Human osteoblast cells seeded on monetite showed the ability of the cells to proliferate and express genes associated with osteoblast maturation and mineralization. Furthermore, the results showed that monetite could stimulate osteoblasts to undergo osteogenesis and accelerate osteoblast maturation earlier than cells cultured on hydroxyapatite scaffolds of similar porosity. Osteoblasts cultured on monetite cement also showed higher expression of osteocalcin, which is an indicator of the maturation stages of osteoblastogenesis and is associated with matrix mineralization and bone forming activity of osteoblasts. Thus, this new method of fabricating porous monetite can be safely used for generating three-dimensional bone graft constructs.

Indexed as

Bone SubstitutesMaterials TestingCalcium PhosphatesCells, CulturedCellular SenescenceHumansOsteoblastsBone Substitutescalcium phosphate, dibasic, anhydrouscalcium phosphate, dibasic, dihydrateCalcium Phosphatesbone defectsbone substitutemonetite

Identifiers

PMID25297314
PMCPMC4223900
OpenAlexW2034152627

What OpenQuestion holds

Textmetadata
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.