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. 2022 Jan;28(1):75-83.
doi: 10.1111/srt.13093. Epub 2021 Sep 21.

Lipid distribution on ethnic hairs by Fourier transform infrared synchrotron spectroscopy

Affiliations

Lipid distribution on ethnic hairs by Fourier transform infrared synchrotron spectroscopy

Clara Barba et al. Skin Res Technol. 2022 Jan.

Abstract

Background: A synchrotron-based Fourier transform infrared micro-spectrometer (μ-FTIR) allows the spatial determination of lipids across the different layers of ethnic hairs and differentiates between the lipid order arrangement and quantity.

Materials and methods: The three ethnic fibers were delipidized, the lipid extracts were characterized, and the delipidized fibers were studied by dynamic vapor sorption experiments (DVS) and FTIR-synchrotron techniques.

Results: The average spectra from the different hair regions exhibited the most intense CH2 sym peaks on the medulla, followed by those from the cuticle and cortex for all hairs of different ethnicities. Differences in the lipid fraction of the three hair types have been observed, and they can explain some barrier properties. African virgin hair was demonstrated to have more lipids mainly in the medulla, which implies an important hydrophobicity with low hysteresis between absorption and desorption water vapor processes. In addition, these lipids are highly disordered, mainly in the cuticle, which can be related to its high water vapor diffusion. Asian and Caucasian virgin hairs presented a similar lipid order in all regions, with similar diffusion coefficients. Results indicate that the higher order of the lipid bilayer hinders water permeation kinetics in some way.

Conclusion: The differences in the presence and organization of the lipids in the different regions of the African hair can account for its differentiation with regards to moisturization and swelling from the other types of fibers.

Keywords: hair; lipids; permeability; synchrotron; μ-FTIR.

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Figures

FIGURE 1
FIGURE 1
Cross‐sections observed by optical microscopy for Caucasian hair selected to analyze by μ‐FTIR, regions were manually determined
FIGURE 2
FIGURE 2
Chemical map of second derivative obtained at 2850 cm−1 (CH2 symmetric stretching) of Caucasian virgin hair (a) and Caucasian delipidized hair (b)
FIGURE 3
FIGURE 3
Quantification of hair lipids in Caucasian (C), Asian (AS) and African (AF) using TLC/FID. Apolar Lipids (APOLAR), free fatty acids (FFA), cholesterol (CHOL) and polar lipids (POLAR)
FIGURE 4
FIGURE 4
Hysteresis curves for Caucasian (C), Asian (AS) and African (AF) virgin and lipid extracted hair fibres
FIGURE 5
FIGURE 5
(A) Lipid peak amplitude and (B) Lipid peak position (mean values ± SD) of μ‐FTIR analysis before and after lipid extraction for Caucasian (C), Asian (AS) and African (AF) hairs in the cuticle (CU), cortex (CO) and medulla (M). (*p < .05, statistics between hairs non‐extracted and lipid extracted)

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