Evidence map›Paper›PMID 40399588›Full record

ArticleInternational journal of cosmetic science2025

Indirubin as a red hair Colourant from Indigofera tinctoria L.

Skrollan Klaas, Volkmar Vill, Fabian Straske

Abstract read
In one paragraph

Article in International journal of cosmetic science, 2025. 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

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

1 citing paper in PubMed.

  1. Indirubin as a red hair Colourant from Indigofera tinctoria L.International journal of cosmetic science · 2025
    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

3 authors.

Skrollan KlaasHenkel AG & Co. KGaA, Hamburg, Germany.ORCID https://orcid.org/0009-0004-4951-7665
Volkmar VillDepartment of Chemistry, University of Hamburg, Hamburg, Germany.ORCID https://orcid.org/0000-0001-6527-9426
Fabian StraskeHenkel AG & Co. KGaA, Hamburg, Germany.ORCID https://orcid.org/0000-0003-4673-9647

Funding

Hamburgische Investitions- und Förderbank (IFB)
6 · The paper itself

Abstract

objectiveDetailed understanding of the indigo and indirubin synthesis pathway to control their formation and the corresponding colour result on hair should be obtained. Managing the formation of the dye molecules indigo and indirubin the characteristic colour shift which takes place within the days after application of Indigofera tinctoria L.-based hair colouration should be eliminated. Thus, intense, more reliable and stable colour results on hair from the natural resource I. tinctoria L. are achieved offering benefits to the consumer resulting in higher acceptance of plant-based colouration products.

methodsVarious colourations with I. tinctoria L. crushed leaves powder and cysteine, isatin or ascorbic acid on yak hair strands were carried out at room temperature or 37°C. Colour assessment was conducted with L*-, a*-, and b*-values/coordinates of three-dimensional CIE-Lab-colour. Coloured hair strands were pulverized with a ball mill to extract dyeing compounds from hair fibres with either a mixture of ultrapure water and acetonitrile or dimethyl sulfoxide at 80°C. Afterwards, the supernatant was collected, and dyeing compounds were quantified via high-performance liquid chromatography.

resultsIt was proven that delayed development of indirubin in addition to the directly formed indigo molecule leads to the observed colour shift on hair fibres when dyeing them with I. tinctoria L. Further, a previously unseen, immediate formation of a stable red colour result was achieved by introducing isatin and cysteine or ascorbic acid to the dyeing procedure. By extraction and subsequent analysis of the dye molecules from the coloured hair fibres, it was confirmed that the addition of isatin and a reducing agent to indigo dyeing prevents the formation of the indigo molecule and favours the formation of indirubin.

conclusionBased on the findings, including the instant formation of indirubin instead of the indigo molecule in the presence of isatin and cysteine or ascorbic acid causing an immediate stable red colour result after the application of I. tinctoria L. on hair, a revised indigo and indirubin synthesis pathway for I. tinctoria L. application including the effect of said additives to the colour outcome is presented.

Indexed as

Hair ColorHair DyesIndigoferaIndolesChromatography, High Pressure LiquidHumansHair DyesindirubinIndolesbiosynthesis pathwaychemical analysiscolour cosmeticshair treatmentindigospectroscopy

Identifiers

PMID40399588
PMCPMC12489879

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.