Evidence map›Paper›PMID 31249333›Full record

ArticleScientific reports2019

Efficient Grafting of Cyclodextrin to Alginate and Performance of the Hydrogel for Release of Model Drug.

Line Aa Omtvedt, Marianne Ø Dalheim, Thorbjørn T Nielsen, Kim L Larsen, Berit L Strand, Finn L Aachmann

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
1.7field-weighted citation impact, top 16% 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, 43 citations in OpenAlex.

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  12. Alginate and alginate composites for biomedical applications.Asian journal of pharmaceutical sciences · 2021
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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 2 countries.

Line Aa OmtvedtNorwegian Biopolymer Laboratory (NOBIPOL), Department of Biotechnology and Food Science, NTNU - Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
Marianne Ø DalheimNorwegian Biopolymer Laboratory (NOBIPOL), Department of Biotechnology and Food Science, NTNU - Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
Thorbjørn T NielsenDepartment of Chemistry and Bioscience, Aalborg University (AAU), 9220, Aalborg, Denmark.
Kim L LarsenDepartment of Chemistry and Bioscience, Aalborg University (AAU), 9220, Aalborg, Denmark.
Berit L StrandNorwegian Biopolymer Laboratory (NOBIPOL), Department of Biotechnology and Food Science, NTNU - Norwegian University of Science and Technology, N-7491, Trondheim, Norway.
Finn L AachmannNorwegian Biopolymer Laboratory (NOBIPOL), Department of Biotechnology and Food Science, NTNU - Norwegian University of Science and Technology, N-7491, Trondheim, Norway. finn.l.aachmann@ntnu.no.ORCID http://orcid.org/0000-0003-1613-4663
Norwegian University of Science and Technology · NOAalborg University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Controlling the rate of release of molecules from a hydrogel is of high interest for various drug delivery systems and medical devices. A strategy to alter the release profiles of soluble and poorly soluble active ingredients from hydrogels can be to combine the hydrogel forming ability of alginate with the inclusion forming ability of cyclodextrins (CyD). Here, β-CyD was grafted to alginate in a three-step synthesis using periodate oxidation, reductive amination and copper(I)-catalyzed azide-alkyne cycloaddition. A grafting degree of 4.7% mol β-CyD/mol sugar residues was obtained. The grafting degree was controlled by varying the reaction parameters where the amount of linker used in reductive amination was especially influential. Ca-alginate gel beads grafted with β-CyD showed increased uptake of the model molecule methyl orange. Release experiments showed that the grafted material had a prolonged release of methyl orange and an increased total amount of released methyl orange. These results show that the β-CyD grafted alginate is still able to form a hydrogel while the grafted cyclodextrins retain their ability to form inclusion complex with methyl orange. Further testing should be done with this system to investigate capability for drug delivery applications.

Indexed as

Drug LiberationAlginatesAzo CompoundsClick ChemistryCyclodextrinsDrug CarriersHydrogelsMolecular WeightSolubilityAlginatesAzo CompoundsCyclodextrinsDrug CarriersHydrogelsmethyl orange

Identifiers

PMID31249333
PMCPMC6597533
OpenAlexW2955547045

What OpenQuestion holds

Textmetadata
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.