Evidence map›Paper›PMID 42199999›Full record

ArticleInternational journal of analytical chemistry2026

A Stability-Indicating RP-HPLC Method for Simultaneous Determination of Triclabendazole and Levamisole in Oral Suspension Formulation.

Abdalla Ahmed Elbashir, Khalid Malik M Hamid

Abstract read
In one paragraph

Article in International journal of analytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

2 authors.

Abdalla Ahmed ElbashirDepartment of Chemistry, College of Science, King Faisal University, P. O. Box 400, Al-Ahsa, 31982, Saudi Arabia, kfu.edu.sa.ORCID https://orcid.org/0000-0002-6769-812X
Khalid Malik M HamidDepartment of Chemistry, Faculty of Science, University of Khartoum, Khartoum, Sudan, uofk.edu.ORCID https://orcid.org/0009-0000-8948-1557

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A fast, simple, and precise stability-indicating high-performance liquid chromatographic (HPLC) method was developed for analysis of triclabendazole (TBZ) and levamisole (LEV) in oral suspension. Using a mobile phase composed of acetonitrile, methanol, and water (50:40:10, v/v/v), with the pH adjusted to 4.6 with 0.1 M phosphoric acid. The mobile phase was filtered, degassed, and pumped at a flow rate of 1.0 mL/min. Detection was performed at 245 nm. The proposed method was validated with respect to specificity, linearity, limit of detection (LOD) and limit of quantification (LOQ), interday and intraday precision, robustness, and accuracy. The retention times for TBZ and LEV were found to be about 3.116 and 1.385 min, respectively. Calibration plots were linear with correlation coefficient of 0.9999 in the concentration range of 200-800 and 150-600 μg/mL for TBZ and LEV, respectively. The method was verified to be stability indicating by separating the active ingredients from their stressed testing degradation products. The procedure proved acceptable robustness to variations in flow rate, wavelength, and column temperature. The method was conveniently used for the analysis of TBZ and LEV in oral suspension.

Indexed as

RP-HPLCstability-indicating methodtriclabendazole and levamisole

Identifiers

PMID42199999
PMCPMC13199681

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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.