Evidence map›Paper›PMID 34926414›Full record

ArticleFrontiers in bioengineering and biotechnology2021

3D Bioprinting of Pectin-Cellulose Nanofibers Multicomponent Bioinks.

Matteo Pitton, Andrea Fiorati, Silvia Buscemi, Lucio Melone, Silvia Farè, Nicola Contessi Negrini

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 41 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 2 institutions in 1 country.

Matteo PittonDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
Andrea FioratiDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
Silvia BuscemiDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
Lucio MeloneDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
Silvia FarèDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
Nicola Contessi NegriniDepartment of Chemistry, Materials, and Chemical Engineering "G. Natta", Politecnico di Milano, Milan, Italy.
National Interuniversity Consortium of Materials Science and Technology · ITPolitecnico di Milano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pectin has found extensive interest in biomedical applications, including wound dressing, drug delivery, and cancer targeting. However, the low viscosity of pectin solutions hinders their applications in 3D bioprinting. Here, we developed multicomponent bioinks prepared by combining pectin with TEMPO-oxidized cellulose nanofibers (TOCNFs) to optimize the inks' printability while ensuring stability of the printed hydrogels and simultaneously print viable cell-laden inks. First, we screened several combinations of pectin (1%, 1.5%, 2%, and 2.5% w/v) and TOCNFs (0%, 0.5%, 1%, and 1.5% w/v) by testing their rheological properties and printability. Addition of TOCNFs allowed increasing the inks' viscosity while maintaining shear thinning rheological response, and it allowed us to identify the optimal pectin concentration (2.5% w/v). We then selected the optimal TOCNFs concentration (1% w/v) by evaluating the viability of cells embedded in the ink and eventually optimized the writing speed to be used to print accurate 3D grid structures. Bioinks were prepared by embedding L929 fibroblast cells in the ink printed by optimized printing parameters. The printed scaffolds were stable in a physiological-like environment and characterized by an elastic modulus of E = 1.8 ± 0.2 kPa. Cells loaded in the ink and printed were viable (cell viability >80%) and their metabolic activity increased in time during the

Indexed as

3D printingbioprintingcellulose nanofiberhydrogelmulticomponent bioinkpectin

Identifiers

PMID34926414
PMCPMC8678092
OpenAlexW4200410411

What OpenQuestion holds

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LicenceCC BY
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.