Evidence map›Paper›PMID 30011859›Full record

ArticleMolecules (Basel, Switzerland)2018

A Combined Approach of NMR and Mass Spectrometry Techniques Applied to the α-Cyclodextrin/Moringin Complex for a Novel Bioactive Formulation

David Mathiron, Renato Iori, Serge Pilard, Thangavelu Soundara Rajan, David Landy, Emanuela Mazzon, Patrick Rollin, Florence Djedaïni-Pilard

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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

20 citing papers in PubMed.

  1. International journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Aqueous extracts ofBiofilm · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Moringin, A Stable Isothiocyanate fromMolecules (Basel, Switzerland) · 2020
    Article
  18. Article
  19. Article
  20. 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

8 authors.

David MathironPlateforme Analytique, Institut de Chimie de Picardie FR 3085 CNRS, Université de Picardie Jules Verne, 33 rue St Leu, 80039 Amiens, France. david.mathiron@u-picardie.fr.
Renato IoriConsiglio per la Ricerca in Agricoltura e L'analisi Dell'economia Agraria, Centro di Ricerca Agricoltura e Ambiente (CREA-AA), Via di Corticella 133, 40128 Bologna, Italy. renato.iori48@gmail.com.ORCID 0000-0002-2493-6941
Serge PilardPlateforme Analytique, Institut de Chimie de Picardie FR 3085 CNRS, Université de Picardie Jules Verne, 33 rue St Leu, 80039 Amiens, France. serge.pilard@u-picardie.fr.
Thangavelu Soundara RajanIstituti di Ricovero e Cura a Carattere Scientifico, IRCCS Centro Neurolesi "Bonino-Pulejo", Via Provinciale Palermo, Contrada Casazza, 98124 Messina, Italy. tsrajanpillai@gmail.com.ORCID 0000-0001-8728-6176
David LandyUnité de Chimie Environnementale et Interactions sur le Vivant (UCEIV, EA 4492), ULCO, F-59140 Dunkerque, France. david.landy@univ-littoral.fr.
Emanuela MazzonIstituti di Ricovero e Cura a Carattere Scientifico, IRCCS Centro Neurolesi "Bonino-Pulejo", Via Provinciale Palermo, Contrada Casazza, 98124 Messina, Italy. emazzon.irccs@gmail.com.ORCID 0000-0002-5073-717X
Patrick RollinInstitut de Chimie Organique et Analytique (ICOA), Université d'Orléans et CNRS, UMR 7311, BP 6759, F-45067 Orléans, France. patrick.rollin@univ-orleans.fr.
Florence Djedaïni-PilardLaboratoire de Glycochimie, des Antimicrobiens et des Agroressources UMR 7378, Université de Picardie Jules Verne, 33 rue St Leu, 80039 Amiens, France. florence.pilard@u-picardie.fr.ORCID 0000-0002-2841-0023

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Moringin, obtained via enzymatic conversion of the glucosinolate precursor glucomoringin, is an uncommon member of the isothiocyanate class, and has been proven to possess a broad range of biological activities such as antitumor activity, protection against neurodegenerative disorders and bactericidal effects. Since moringin is weakly soluble in water and unstable in aqueous medium, cyclodextrins (CDs) were considered for the development of a new moringin formulation, with a view to improving its solubility and stability in aqueous solution for use as an anti-inflammatory. A combined structural study using proton nuclear magnetic resonance (¹H-NMR), diffusion-ordered spectroscopy (DOSY) and ion mobility mass spectrometry (IM-MS) is reported, highlighting the formation of a 1:1 α-CD/moringin inclusion complex. The association constant

Indexed as

alpha-CyclodextrinsAnimalsIsothiocyanatesMagnetic Resonance SpectroscopyMass SpectrometryMiceRAW 264.7 Cellsalpha-CyclodextrinsIsothiocyanatesmoringinanti-inflammatorycyclodextrinisothiocyanatemass spectrometry (MS)Moringa oleiferamoringinnuclear magnetic resonance (NMR)

Identifiers

PMID30011859
PMCPMC6099948

What OpenQuestion holds

Textmetadata
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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.