Evidence map›Paper›PMID 40643184›Full record

ArticleJournal of clinical laboratory analysis2025

Ultra-Sensitive Quantification of Indoxyl Sulfate and 3-Carboxy-4-Methyl-5-Propyl-2-Furanpropanoic Acid in Plasma Using Ultra-Performance Liquid Chromatography Coupled to Quadrupole Time-of-Flight Mass Spectrometry.

Jun Negami, Yosuke Suzuki, Haruki Sato, Daiki Toyama, Ayako Oda, Ryota Tanaka, Hiroyuki Ono, Tadasuke Ando, Toshitaka Shin, Hiroki Itoh and 1 more

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 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

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

11 authors.

Jun NegamiDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Yosuke SuzukiDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7092-4618
Haruki SatoDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Daiki ToyamaDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Ayako OdaDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Ryota TanakaDepartment of Clinical Pharmacy, Oita University Hospital, Yufu, Oita, Japan.ORCID https://orcid.org/0000-0002-8452-7971
Hiroyuki OnoDepartment of Clinical Pharmacy, Oita University Hospital, Yufu, Oita, Japan.
Tadasuke AndoDepartment of Urology, Oita University Faculty of Medicine, Yufu, Oita, Japan.
Toshitaka ShinDepartment of Urology, Oita University Faculty of Medicine, Yufu, Oita, Japan.
Hiroki ItohDepartment of Clinical Pharmacy, Oita University Hospital, Yufu, Oita, Japan.
Keiko OhnoDepartment of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUremic toxins such as indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) are accumulated in patients with chronic kidney disease (CKD). Recent studies have shown that the accumulation of indoxyl sulfate and CMPF alters the activity of organic anion transporting polypeptide (OATP) 1B and cytochrome P450 (CYP) 3A, respectively. We established and validated a novel ultra-sensitive method for simultaneous quantification of indoxyl sulfate and CMPF using ultra-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS).

methodIn this method, plasma samples were prepared by solid phase extraction, then analyzed by UPLC-QTOF/MS to measure concentrations of analytes. Using only 5 μL of human plasma per assay, the calibration range was 0.05-200 μg/mL and the lower limit of quantification was 0.05 μg/mL for both indoxyl sulfate and CMPF.

resultsThis assay met the acceptance criteria of the U.S. Food and Drug Administration bioanalytical method validation guidance. The clinical applicability of this assay was evaluated by measuring plasma concentrations in healthy volunteers and CKD patients. All measured concentrations were within the calibration range.

conclusionOur novel assay may contribute to the estimation of variation of OATP1B and CYP3A activities in patients, including those with CKD.

Indexed as

FuransIndicanMass SpectrometryPropionatesChromatography, High Pressure LiquidHumansLimit of DetectionRenal Insufficiency, ChronicReproducibility of Results3-carboxy-4-methyl-5-propyl-2-furanpropanoic acidFuransIndicanPropionates3‐carboxy‐4‐methyl‐5‐propyl‐2‐furanpropanoic acidchronic kidney diseaseindoxyl sulfateplasmaquadrupole time‐of‐flight mass spectrometryuremic toxin

Identifiers

PMID40643184
PMCPMC12378369

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.