Evidence map›Paper›PMID 29891757›Full record

ArticleNutrients2018

A Novel Biomimetic Tool for Assessing Vitamin K Status Based on Molecularly Imprinted Polymers.

Kasper Eersels, Hanne Diliën, Joseph W Lowdon, Erik Steen Redeker, Renato Rogosic, Benjamin Heidt, Marloes Peeters, Peter Cornelis, Petra Lux, Chris P Reutelingsperger and 3 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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

13 authors at 3 institutions in 3 countries.

Kasper EerselsMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. kasper.eersels@maastrichtuniversity.nl.ORCID 0000-0002-0214-1320
Hanne DiliënMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. hanne.dilien@maastrichtuniversity.nl.
Joseph W LowdonMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. joe.lowdon@maastrichtuniversity.nl.
Erik Steen RedekerMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. erik.steenredeker@maastrichtuniversity.nl.ORCID 0000-0002-5658-5066
Renato RogosicMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. renato.rogosic@maastrichtuniversity.nl.
Benjamin HeidtMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. benjamin.heidt@maastrichtuniversity.nl.ORCID 0000-0003-1629-3146
Marloes PeetersDivision of Chemistry and Environmental Science, School of Science and the Environment, Faculty of Science and Engineering, Manchester Metropolitan University, Chester Street, Manchester M1 5GD, UK. m.peeters@mmu.ac.uk.ORCID 0000-0002-0429-8073
Peter CornelisSoft-Matter Physics and Biophysics Section, Department of Physics and Astronomy, KU Leuven, Celestijnenlaan 200 D, B-3001 Leuven, Belgium. peter.cornelis@kuleuven.be.ORCID 0000-0002-7218-0851
Petra LuxDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Universiteitssingel 50, 6200 MD Maastricht, The Netherlands. p.lux@maastrichtuniversity.nl.
Chris P ReutelingspergerDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Universiteitssingel 50, 6200 MD Maastricht, The Netherlands. c.reutelingsperger@maastrichtuniversity.nl.
Leon J SchurgersDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Universiteitssingel 50, 6200 MD Maastricht, The Netherlands. l.schurgers@maastrichtuniversity.nl.ORCID 0000-0001-7867-6957
Thomas J CleijMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. thomas.cleij@maastrichtuniversity.nl.ORCID 0000-0003-0172-9330
Bart van GrinsvenMaastricht Science Programme, Faculty of Science and Engineering, Maastricht University P.O. Box 616, 6200 MD Maastricht, The Netherlands. bart.vangrinsven@maastrichtuniversity.nl.ORCID 0000-0002-6939-0866
Maastricht University · NLKU Leuven · BEManchester Metropolitan University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitamin K was originally discovered as a cofactor required to activate clotting factors and has recently been shown to play a key role in the regulation of soft tissue calcification. This property of vitamin K has led to an increased interest in novel methods for accurate vitamin K detection. Molecularly Imprinted Polymers (MIPs) could offer a solution, as they have been used as synthetic receptors in a large variety of biomimetic sensors for the detection of similar molecules over the past few decades, because of their robust nature and remarkable selectivity. In this article, the authors introduce a novel imprinting approach to create a MIP that is able to selectively rebind vitamin K₁. As the native structure of the vitamin does not allow for imprinting, an alternative imprinting strategy was developed, using the synthetic compound menadione (vitamin K₃) as a template. Target rebinding was analyzed by means of UV-visible (UV-VIS) spectroscopy and two custom-made thermal readout techniques. This analysis reveals that the MIP-based sensor reacts to an increasing concentration of both menadione and vitamin K₁. The Limit of Detection (LoD) for both compounds was established at 700 nM for the Heat Transfer Method (HTM), while the optimized readout approach, Thermal Wave Transport Analysis (TWTA), displayed an increased sensitivity with a LoD of 200 nM. The sensor seems to react to a lesser extent to Vitamin E, the analogue under study. To further demonstrate its potential application in biochemical research, the sensor was used to measure the absorption of vitamin K in blood serum after taking vitamin K supplements. By employing a gradual enrichment strategy, the sensor was able to detect the difference between baseline and peak absorption samples and was able to quantify the vitamin K concentration in good agreement with a validation experiment using High-Performance Liquid Chromatography (HPLC). In this way, the authors provide a first proof of principle for a low-cost, straightforward, and label-free vitamin K sensor.

Indexed as

Biomimetic MaterialsBiosensing TechniquesBinding SitesBiomarkersChromatography, High Pressure LiquidHumansLimit of DetectionMaterials TestingMolecular ImprintingPolymersProof of Concept StudyProtein BindingProtein ConformationReproducibility of ResultsSpectrophotometry, UltravioletStructure-Activity RelationshipBiomarkersPolymersVitamin K 1Vitamin K 3HPLC validationsynthetic receptorsthermal biosensorvitamin K

Identifiers

PMID29891757
PMCPMC6024727
OpenAlexW2805164883

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.