Evidence map›Paper›PMID 32872512›Full record

ArticleNanomaterials (Basel, Switzerland)2020

Fluorescent Imprinted Nanoparticles for the Effective Monitoring of Irinotecan in Human Plasma.

Martina Tommasini, Elena Pellizzoni, Valentina Iacuzzi, Elena Marangon, Paola Posocco, Cristina Forzato, Paolo Bertoncin, Giuseppe Toffoli, Marina Resmini, Federico Berti

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

10 authors at 3 institutions in 2 countries.

Martina TommasiniDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
Elena PellizzoniDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
Valentina IacuzziPhD School in Nanotechnology, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
Elena MarangonCRO-National Cancer Institute, SOC - Experimental and Clinical Pharmacology, Via Gallini 2, 33081 Aviano (PN), Italy.
Paola PosoccoDepartment of Engineering and Architecture, University of Trieste, Via Valerio 6/1, 34127 Trieste, Italy.
Cristina ForzatoDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
Paolo BertoncinDepartment of Life Sciences, University of Trieste, Via Giorgieri 5, 34127 Trieste, Italy.
Giuseppe ToffoliCRO-National Cancer Institute, SOC - Experimental and Clinical Pharmacology, Via Gallini 2, 33081 Aviano (PN), Italy.
Marina ResminiSchool of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London E14NS, UK.
Federico BertiDepartment of Chemical and Pharmaceutical Sciences, University of Trieste, Via Giorgieri 1, 34127 Trieste, Italy.
University of Trieste · ITCentro di Riferimento Oncologico · ITQueen Mary University of London · GB

Funding

Associazione Italiana per la Ricerca sul Cancro 12214
6 · The paper itself

Abstract

Fluorescent, imprinted nanosized polymers for the detection of irinotecan have been synthesised using a napthalimide polymerisable derivative (2-allyl-6-[2-(aminoethyl)-amino] napthalimide) as functional monomer. The imprinted polymers contain ethylene glycol dimethacrylate (EGDMA) as a cross-linker and were prepared by high dilution radical polymerisation in dimethylsulphoxide (DMSO). The material was able to rebind irinotecan up to 18 nmol/mg with good specificity. Fluorescence emission at 525 nm (excitation at 448 nm) was quenched by increasing concentrations of irinotecan via a static mechanism and also in analytically useful environments as mixtures of human plasma and organic solvents. This allowed the direct detection of irinotecan (in the 10 nM-30 µM range) in human plasma treated with acetonitrile; the limit of detection (LOD) was 9.4 nM, with within-run variability of 10% and day-to-day variability of 13%.

Indexed as

fluorescencehuman plasmaimprinted nanogelsirinotecantherapeutic drug monitoring

Identifiers

PMID32872512
PMCPMC7558923
OpenAlexW3081695693

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.