Evidence map›Paper›PMID 39204445›Full record

ArticlePharmaceutics2024

A Method for the Colorimetric Quantification of Sodium Lauryl Sulphate in Tablets: A Proof of Concept.

Artūrs Paulausks, Austris Mazurs, Valentyn Mohylyuk

Abstract read
In one paragraph

Article in Pharmaceutics, 2024. 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.

Artūrs PaulausksLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, LV-1007 Riga, Latvia.ORCID 0000-0002-7446-1294
Austris MazursLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, LV-1007 Riga, Latvia.ORCID 0009-0007-4064-8521
Valentyn MohylyukLeading Research Group, Faculty of Pharmacy, Rīga Stradiņš University, LV-1007 Riga, Latvia.ORCID 0000-0002-8771-3470

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The deformulation stage of original drug products, which includes the quantification of critical excipients, is crucial for the successful development of generic drug products of solid dosage form. Sodium lauryl sulphate (SLS) belongs to the group of critical excipients due to its influence on the bioavailability of drugs, such as metformin. The purpose of this work is to carry out a feasibility study in order to develop a simple, economical, and robust analytical method for the quantification of SLS in metformin-containing tablets after their dissolution in water. Firstly, SLS is extracted with chloroform in acidic conditions, followed by the addition of methylene blue (MB) in order to form a SLS-MB ion pair, which is then measured photometrically at a wavelength of 651 nm. Additionally, interference from matrix components (excipients and APIs) was assessed, and it was found that metformin also forms a blue complex; therefore, this specific extraction method was developed. Other matrix components did not interfere with SLS determination. This method shows a well-estimated precision of 3.3% and accuracy of 5%, a calibration linearity of R

Indexed as

deformulationmatrix effectsquantificationsodium lauryl sulphatespectrometric determinationtablet dissolution

Identifiers

PMID39204445
PMCPMC11360801

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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.