Evidence map›Paper›PMID 34718838›Full record

ArticleAnalytical and bioanalytical chemistry2022

Discriminative and quantitative analysis of norepinephrine and epinephrine by surface-enhanced Raman spectroscopy with gold nanoparticle suspensions.

Antoine Dowek, Marion Berge, Patrice Prognon, François-Xavier Legrand, Eric Larquet, Ali Tfayli, Laetitia Minh Mai Lê, Eric Caudron

Abstract read
PubMed Publisher
In one paragraph

Article in Analytical and bioanalytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
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

8 authors.

Antoine DowekService de Pharmacie, Hôpital européen Georges Pompidou, APHP.Centre Université-Paris, 20 rue Leblanc, 75015, Paris, France. antoine.dowek@universite-paris-saclay.fr.ORCID http://orcid.org/0000-0002-0834-1083
Marion BergeService de Pharmacie, Hôpital européen Georges Pompidou, APHP.Centre Université-Paris, 20 rue Leblanc, 75015, Paris, France.
Patrice PrognonService de Pharmacie, Hôpital européen Georges Pompidou, APHP.Centre Université-Paris, 20 rue Leblanc, 75015, Paris, France.
François-Xavier LegrandCNRS, Institut Galien Paris Sud, Université Paris-Saclay, 92296, Châtenay-Malabry, France.
Eric LarquetLaboratoire de Physique de la Matière Condensée (LPMC), Ecole Polytechnique, CNRS, Institut Polytechnique de Paris, 91128, Palaiseau, France.
Ali TfayliLipides, Systèmes Analytiques et Biologiques, Université Paris-Saclay, 92296, Châtenay-Malabry, France.
Laetitia Minh Mai LêService de Pharmacie, Hôpital européen Georges Pompidou, APHP.Centre Université-Paris, 20 rue Leblanc, 75015, Paris, France.
Eric CaudronService de Pharmacie, Hôpital européen Georges Pompidou, APHP.Centre Université-Paris, 20 rue Leblanc, 75015, Paris, France.

Funding

Fondation ARC pour la Recherche sur le Cancer Marion Berge
6 · The paper itself

Abstract

Surface-enhanced Raman spectroscopy (SERS) is a powerful analytical technique capable of increasing the Raman signal of an analyte using specific nanostructures. The close contact between those nanostructures, usually a suspension of nanoparticles, and the molecule of interest produces an important exaltation of the intensity of the Raman signal. Even if the exaltation leads to an improvement of Raman spectroscopy sensitivity, the complexity of the SERS signal and the numbers of parameters to be controlled allow the use of SERS for detection rather than quantification. The aim of this study was to develop a robust discriminative and quantitative analysis in accordance with pharmaceutical standards. In this present work, we develop a discriminative and quantitative analysis based on the previous optimized parameters obtained by the design of experiments fixed for norepinephrine (NOR) and extended to epinephrine (EPI) which are two neurotransmitters with very similar structures. Studying the short evolution of the Raman signal intensity over time coupled with chemometric tools allowed the identification of outliers and their removal from the data set. The discriminant analysis showed an excellent separation of EPI and NOR. The comparative analysis of the data showed the superiority of the multivariate analysis after logarithmic transformation. The quantitative analysis allowed the development of robust quantification models from several gold nanoparticle batches with limits of quantification of 32 µg/mL for NOR and below 20 µg/mL for EPI even though no Raman signal is observable for such concentrations. This study improves SERS analysis over ultrasensitive detection for discrimination and quantification using a handheld Raman spectrometer.

Indexed as

EpinephrineGoldMetal NanoparticlesNorepinephrineSpectrum Analysis, RamanEpinephrineGoldNorepinephrineDiscriminative analysisGold nanoparticlesMathematical designNeurotransmittersQuantitative analysisSurface-enhanced Raman spectroscopy

Identifiers

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.