Evidence map›Paper›PMID 41996039›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2026

Limited Sampling Strategies to Estimate the Exposition of Different Lipid Nanocaspules.

Jean-Luc Cissé, Samuel Legeay, Vincent Lebreton

Abstract read
PubMed Publisher
In one paragraph

Article in European journal of drug metabolism and pharmacokinetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Jean-Luc CisséUniv Angers, MINT Inserm U1066, CNRS 6021, IRIS1-IBS-CHU, SFR ICAT, 4 Rue Larrey, 49000, Angers, France.
Samuel LegeayUniv Angers, MINT Inserm U1066, CNRS 6021, IRIS1-IBS-CHU, SFR ICAT, 4 Rue Larrey, 49000, Angers, France.
Vincent LebretonUniv Angers, MINT Inserm U1066, CNRS 6021, IRIS1-IBS-CHU, SFR ICAT, 4 Rue Larrey, 49000, Angers, France. vincent.lebreton@univ-angers.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe use of nanoparticles in the field of drug delivery and the optimization of pharmacokinetic profiles in vivo is a growing area of research. The aim of this study is to determine the key sampling times and the factors that exert a significant influence on the development of a pharmacokinetic model that can reliably predict the area under the curve (AUC) of lipid nanocapsules in rats using a limited sampling strategy (LSS).

methodsThis study was conducted in rats following intravenous injection of lipid nanocapsules (LNCs). Förster resonance energy transfer (FRET)-based quantification was used to monitor pharmacokinetics across ten initial time points. A limited sampling strategy (LSS) model was developed using principal component multiple linear regression, combined with recursive feature elimination and leave-one-out crossvalidation (RFECV-LOOCV).

resultsThe final model is based on three sampling time points (180, 360, and 600 min) and demonstrates strong predictive performance (R

conclusionsThis approach reduces the number of blood samples by 70% while maintaining high accuracy. The main limitations concern its generalizability to other formulations or species, which would require additional validation.

Indexed as

LipidsModels, BiologicalNanocapsulesAnimalsArea Under CurveFluorescence Resonance Energy TransferInjections, IntravenousMaleNanoparticlesRatsLipidsNanocapsules

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.