Evidence map›Paper›PMID 28762141›Full record

ArticleJournal of materials science. Materials in medicine2017

Anti-fibronectin aptamers improve the colonization of chitosan films modified with D-(+) Raffinose by murine osteoblastic cells.

L Parisi, C Galli, A Bianchera, P Lagonegro, L Elviri, A Smerieri, S Lumetti, E Manfredi, R Bettini, G M Macaluso

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In one paragraph

Article in Journal of materials science. Materials in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 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

10 authors at 2 institutions in 1 country.

L ParisiDip. Medicina e Chirurgia, University of Parma, Via Gramsci 14, 43126, Parma, Italy.
C GalliDip. Medicina e Chirurgia, University of Parma, Via Gramsci 14, 43126, Parma, Italy.
A BiancheraDip. Farmacia, University of Parma, Via Università 7, 43126, Parma, Italy.
P LagonegroIMEM-CNR National Research Council, Via Università 7, 43126, Parma, Italy.
L ElviriDip. Farmacia, University of Parma, Via Università 7, 43126, Parma, Italy.
A SmerieriCentro Universitario di Odontoiatria, University of Parma, Via Gramsci 14, 43126, Parma, Italy.
S LumettiDip. Medicina e Chirurgia, University of Parma, Via Gramsci 14, 43126, Parma, Italy.
E ManfrediDip. Medicina e Chirurgia, University of Parma, Via Gramsci 14, 43126, Parma, Italy. edoardo.manfredi@unipr.it.
R BettiniDip. Farmacia, University of Parma, Via Università 7, 43126, Parma, Italy.
G M MacalusoDip. Medicina e Chirurgia, University of Parma, Via Gramsci 14, 43126, Parma, Italy.
University of Parma · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to investigate how the enrichment of chitosan films with anti-fibronectin aptamers could enhance scaffold colonization by osteoblasts, by improving their adhesion and accelerating their proliferation. Chitosan discs were enriched with excess of anti-fibronectin aptamer. Aptamer adsorption on chitosan was monitored by measuring aptamer concentration in the supernatant by spectrophotometry, as well as its release, while functionalization was confirmed by labelling aptamers with a DNA intercalating dye. Chitosan samples were then characterized morphologically with atomic force microscopy and physically with contact angle measurement. Chitosan enrichment with fibronectin was then investigated by immunofluorescence and Bradford assay. 2% chitosan discs were then enriched with increasing doses of aptamers and used as culture substrates for MC3T3-E1 cells. Cell growth was monitored by optical microscopy, while cell viability and metabolic activity were assessed by chemiluminescence and by Resazurin Sodium Salt assay. Cell morphology was investigated by cytofluorescence and by scanning electron microscopy. Chitosan films efficiently bound and retained aptamers. Aptamers did not affect the amount of adsorbed fibronectin, but affected osteoblasts behavior. Cell growth was proportional to the amount of aptamer used for the functionalization, as well as aptamers influenced cell morphology and their adhesion to the substrate. Our results demonstrate that the enrichment of chitosan films with aptamers could selectively improve osteoblasts behavior. Furthermore, our results support further investigation of this type of functionalization as a suitable modification to ameliorate the biocompatibility of biomaterial for hard tissue engineering applications.

Indexed as

Membranes, Artificial3T3 CellsAnimalsAptamers, NucleotideChitosanMiceOsteoblastsRaffinoseTissue ScaffoldsAptamers, NucleotideChitosanMembranes, ArtificialRaffinose

Identifiers

PMID28762141
OpenAlexW2741500903

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.