Evidence map›Paper›PMID 41203780›Full record

ArticleScientific reports2025

Streamlined spectrofluorimetric assay for Pramipexole using acid red 87 quenching strategy for tablet and uniformity evaluation.

Ahmed A Abu-Hassan

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

1 author.

Ahmed A Abu-HassanDepartment of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Assiut Branch, Al-Azhar University, Assiut, 71524, Egypt. Ahmedabuhassan@azhar.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pramipexole (PPX) is prescribed for alleviating parkinson's disease symptoms like tremors and mobility issues, as well as addressing the discomfort in the legs and sudden leg movement impulses associated with restless legs syndrome. This study presents a practical, direct, non-extractive, and cost-effective analytical strategy for the quantitative determination of PPX. The method leverages fluorimetric detection, specifically monitoring the quenching effect on the emission intensity of Acid red 87, a fluorone dye. Complexation between PPX and Acid Red 87 occurs rapidly within a single reaction vessel under acidic conditions. A linear relationship was established between the observed decrease in Acid red 87 fluorescence intensity and PPX concentration, enabling the construction of a calibration curve spanning 50 to 1400 ng/mL. Critical variables influencing the PPX-dye complex system were systematically investigated and optimized. Comprehensive validation studies, conducted in accordance with International Council for Harmonisation (ICH) guidelines, confirmed the method's reliability. The validated approach was subsequently applied successfully to assay PPX in pharmaceutical tablets and to evaluate tablet content uniformity.

Indexed as

Azo CompoundsPramipexoleTabletsCalibrationHumansReproducibility of ResultsSpectrometry, FluorescenceAzo CompoundsPramipexoleTabletsAcid red 87AssayIon-pairSpectrofluorimetricTablets

Identifiers

PMID41203780
PMCPMC12594968

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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 OpenQuestion graph.