Evidence map›Paper›PMID 39511040›Full record

ArticleAnalytical sciences : the international journal of the Japan Society for Analytical Chemistry2025

Resonance-enhanced multiphoton ionization time-of-flight mass spectrometry for direct analysis of liposome-encapsulated compounds.

Keishi Yamashita, Kento Sakakibara, Yuta Kouyama, Hitomi Sugiyama, Tomohiro Ueyama, Koji Nishijima, Tomohiro Uchimura

Abstract read
In one paragraph

Article in Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 2025. 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

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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

7 authors.

Keishi YamashitaDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan.
Kento SakakibaraDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan.
Yuta KouyamaDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan.
Hitomi SugiyamaDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan.
Tomohiro UeyamaDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan.
Koji NishijimaGeneral Center for Perinatal, Maternal and Neonatal Medicine, Niigata University Medical and Dental Hospital, 1-754, Asahimachi-dori, Chuo-ku, Niigata, 951-8520, Japan.
Tomohiro UchimuraDepartment of Materials Science and Engineering, Graduate School of Engineering, University of Fukui, 3-9-1 Bunkyo, Fukui, 910-8507, Japan. uchimura@u-fukui.ac.jp.ORCID http://orcid.org/0000-0003-4816-6328

Funding

JSPS KAKENHI 23H03040
6 · The paper itself

Abstract

The direct measurement of compounds encapsulated into liposomes without pretreatment allows verification of both the encapsulation efficiency and the release rate of liposomes in their original state. In the present study, the direct analysis of liposomes was conducted via resonance-enhanced multiphoton ionization time-of-flight mass spectrometry (REMPI-TOFMS). When analyte species (2-phenoxyethanol) encapsulated in liposomes were measured online, spike signals appeared in a time profile of the peak area for 2-phenoxyethanol, which suggested a dispersion of the compound in this sample. In addition, the spikes disappeared when the liposomes collapsed following the addition of a Triton X-100 aqueous solution. These results strongly suggest that the appearance of spikes arises from the compound encapsulated into the dispersed liposomes. REMPI-TOFMS has an inherent characteristic of superior selectivity, which suggests that this process would be useful for achieving a precise evaluation of the release properties of target compounds even in a liposome sample containing a large variety of components.

Indexed as

LiposomesMass SpectrometryPhotonsTime FactorsLiposomesLiposomeREMPI–TOFMS

Identifiers

PMID39511040
PMCPMC11750879

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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.