Characterization of mucins, glycosaminoglycans, and bioactive compounds in Helix aspersa’s slime by spectroscopic and biochemical analysis

• SS is rich in biological macromolecules, including mucins and glycosaminoglycans. • NMR, FT-IR, and Raman confirm mucins, glycosaminoglycans, and peptides in SS. • SS inhibits the cholinesterases, tyrosinase, amylase and glucosidase enzymes. • SS is a rich source of phenolic compounds and is a powerful antioxidant. • Stabilized SS has better composition, stability and biological activities. Snail slime (SS), a secretion produced by Helix aspersa , is a complex biological matrix rich in macromolecules has gained considerable interest due to its biologically relevant components and potential applications in medicine, cosmetics, and biotechnology. This study focuses on the chemical characterization of SS, comparing stabilized commercial slime with preservatives to a non-stabilized natural, preservative-free variant. Advanced analytical techniques, such as Attenuated Total Reflection Fourier Transform Infrared Spectroscopy, Nuclear Magnetic Resonance, Solid-Phase Microextraction Gas Chromatography-Mass Spectrometry, Raman spectroscopy, and Thermal analysis were employed to identify key metabolites and bioactive compounds. Moreover, quantitative assays were performed to evaluate the antioxidant, metal chelation and enzyme inhibition activities. Analytical techniques identified mucins, glycosaminoglycans, antimicrobial peptides, and antioxidants, with variations in composition influenced by processing methods. Quantitative assays revealed that SS possesses strong antioxidant properties, significant metal chelation capacity, and inhibitory activity against cholinesterases, tyrosinase, amylase, and glucosidase. Cellular assays further demonstrated its non-toxic nature and capacity to enhance dermal fibroblast viability. Furthermore, the stabilized commercially used SS has better composition, stability and activities compared to non-stabilized SS. Additionally, this is the first direct comparison of stabilized and non-stabilized SS, using multimethod analytical approach, and correlation of chemical composition with bioactivity. These findings underscore SS’s complex composition and potential in biomedical and cosmetic applications, particularly in wound healing, antimicrobial, antioxidants, anti-aging formulations, and enzyme inhibitory therapies.

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Publication Details

Journal
Journal of Molecular Structure
Published
2025-09-01
DOI
https://doi.org/10.1016/j.molstruc.2025.143838
Citations
1
Primary Topic
Fungal Biology and Applications
Type
article
Field-Weighted Citation Impact
1.39
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article

Characterization of mucins, glycosaminoglycans, and bioactive compounds in Helix aspersa’s slime by spectroscopic and biochemical analysis

Susi Zara, Mattia Spano, Stefano Di Giacomo, Antonella Fontana et al.
1 citations
Journal of Molecular Structure
Fungal Biology and Applications
1.39
article

Characterization of mucins, glycosaminoglycans, and bioactive compounds in Helix aspersa’s slime by spectroscopic and biochemical analysis

Susi Zara, Mattia Spano, Stefano Di Giacomo, Antonella Fontana, Luisa Mannina, Stefanıa Garzoli, Pietro Di Profio, Amelia Cataldi, Pantaleone Bruni, Muhammad Rashad, Simone Carradori, Stefania Ferrari, Michele M. Ciulla, Gökhan Zengin
article en
1 citations

Abstract

• SS is rich in biological macromolecules, including mucins and glycosaminoglycans. • NMR, FT-IR, and Raman confirm mucins, glycosaminoglycans, and peptides in SS. • SS inhibits the cholinesterases, tyrosinase, amylase and glucosidase enzymes. • SS is a rich source of phenolic compounds and is a powerful antioxidant. • Stabilized SS has better composition, stability and biological activities. Snail slime (SS), a secretion produced by Helix aspersa , is a complex biological matrix rich in macromolecules has gained considerable interest due to its biologically relevant components and potential applications in medicine, cosmetics, and biotechnology. This study focuses on the chemical characterization of SS, comparing stabilized commercial slime with preservatives to a non-stabilized natural, preservative-free variant. Advanced analytical techniques, such as Attenuated Total Reflection Fourier Transform Infrared Spectroscopy, Nuclear Magnetic Resonance, Solid-Phase Microextraction Gas Chromatography-Mass Spectrometry, Raman spectroscopy, and Thermal analysis were employed to identify key metabolites and bioactive compounds. Moreover, quantitative assays were performed to evaluate the antioxidant, metal chelation and enzyme inhibition activities. Analytical techniques identified mucins, glycosaminoglycans, antimicrobial peptides, and antioxidants, with variations in composition influenced by processing methods. Quantitative assays revealed that SS possesses strong antioxidant properties, significant metal chelation capacity, and inhibitory activity against cholinesterases, tyrosinase, amylase, and glucosidase. Cellular assays further demonstrated its non-toxic nature and capacity to enhance dermal fibroblast viability. Furthermore, the stabilized commercially used SS has better composition, stability and activities compared to non-stabilized SS. Additionally, this is the first direct comparison of stabilized and non-stabilized SS, using multimethod analytical approach, and correlation of chemical composition with bioactivity. These findings underscore SS’s complex composition and potential in biomedical and cosmetic applications, particularly in wound healing, antimicrobial, antioxidants, anti-aging formulations, and enzyme inhibitory therapies.

Journal of Molecular StructureVol. 1349
Selçuk University (TR), University of Chieti-Pescara (IT), Sapienza University of Rome (IT)
Openalex Percentile: Top 17%
Fungal Biology and Applications
1.39
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