Evidence map›Paper›PMID 36430944›Full record

ArticleInternational journal of molecular sciences2022

Degradation of Polymer-Drug Conjugate Nanoparticles Based on Lactic and Itaconic Acid.

Mai Dang Le Vuong, Mohamed Haouas, Merve Seray Ural, Didier Desmaële, Charlotte Martineau-Corcos, Ruxandra Gref

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Itaconate and its derivatives in human health and diseases.Signal transduction and targeted therapy · 2026
    Review
  2. Revisiting applications of itaconic acid-based polymers obtained by (poly)condensation chemistry.Green chemistry : an international journal and green chemistry resource : GC · 2026
    Review
  3. Article
  4. Article
  5. 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

6 authors at 1 institution in 1 country.

Mai Dang Le VuongCNRS, Institut Lavoisier de Versailles, UVSQ, Université Paris-Saclay, 78000 Versailles, France.
Mohamed HaouasCNRS, Institut Lavoisier de Versailles, UVSQ, Université Paris-Saclay, 78000 Versailles, France.ORCID 0000-0002-2133-702X
Merve Seray UralCNRS, Institut des Sciences Moléculaires d'Orsay, Université Paris-Saclay, 91405 Orsay, France.
Didier DesmaëleCNRS, Institut Galien Paris-Saclay, Université Paris-Saclay, 91400 Orsay, France.
Charlotte Martineau-CorcosCNRS, Institut Lavoisier de Versailles, UVSQ, Université Paris-Saclay, 78000 Versailles, France.
Ruxandra GrefCNRS, Institut des Sciences Moléculaires d'Orsay, Université Paris-Saclay, 91405 Orsay, France.ORCID 0000-0002-7869-0908
Centre National de la Recherche Scientifique · FR

Funding

French National Research Agency ANR-10-INBS-04/FranceBioImagingFrench National Research Agency ANR-10-LABX-0035French National Research Agency ANR-11-EQPX-0029/MorphoscopeFrench National Research Agency ANR-11-IDEX-0003-02/ Saclay Plant SciencesFrench National Research Agency ANR-11-LBX-0039
6 · The paper itself

Abstract

Tuberculosis (TB) is still a significant threat to human health. A promising solution is engineering nanoparticulate drug carriers to deliver anti-TB molecules. Itaconic acid (ITA) potentially has anti-TB activity; however, its incorporation in nanoparticles (NP) is challenging. Here we show an approach for preparing polymer-ITA conjugate NPs and a methodology for investigating the NP degradation and ITA release mechanism. The conjugate was synthesized by the two-directional growing of polylactic acid (PLA) chains, followed by capping their extremities with ITA. The poly(lactate)-itaconate PLA-ITA was then used to formulate NPs. The degradation and drug release processes of the polymer conjugate NPs were studied qualitatively and quantitatively. The molecular structures of released species were characterized by using liquid NMR spectroscopy and mass spectrometry. We discovered a complex NP hydrolysis process forming diverse oligomers, as well as monomeric lactic acid (LA) and drug ITA. The slow degradation process led to a low release of free drugs, although raising the pH from 5.3 to 7.4 induced a slight increase in the amounts of released products. TEM images showed that bulk erosion is likely to play the primary role in the degradation of PLA-ITA NPs. The overall results and methodology can be of interest for understanding the mechanisms of NP degradation and drug release of this new polymer-drug conjugate system.

Indexed as

NanoparticlesPolymersHumansPolyestersSuccinatesitaconic acidPolyestersPolymersSuccinatesdrug deliveryitaconic acidNMR spectroscopypoly(lactic acid)polymer nanoparticles

Identifiers

PMID36430944
PMCPMC9699510
OpenAlexW4309719922

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.