Integrated analytical approach to micro- and macroalgae: tailored extraction strategies for sustainable biorefineries

This study evaluates the solvent-dependent extraction of Arthrospira platensis and Ascophyllum nodosum to guide sustainable marine biorefinery design. SOXTHERM rapid extractions were performed with n-hexane, ethanol−water (1:1, v/v), and water under controlled severity (3 h,n = 2). Ethanol−water consistently delivered the highest yields for A. platensis (25% DW ± 2.2) and A. nodosum (26% DW ± 2.2), with differences confirmed by a permutation test (p < 0.05). Hexane selectively enriched lipophilic fractions, whereas water favored polar constituents. For A. platensis, ethanol−water exceeded hexane (Δ20.3% DW ± 2.5) and water (Δ15.0% DW ± 1.2). For A. nodosum, differences were smaller versus water (Δ3.5% DW ± 3.6) but pronounced versus hexane (Δ23.5% DW ± 1.5). A. platensis extracts were protein-rich and contained long-chain polyunsaturated fatty acids, while A. nodosum extracts exhibited a high mineral content and structural carbohydrates. Ultra-high-resolution FT-ICR-MS revealed thousands of molecular features, including putative lipid-like and nitrogenous species; all structural assignments remain putative without MS/MS confirmation. Notably, biopterin analogues were detected in A. platensis water extracts, and polyphenolic signatures dominated A. nodosum ethanol−water extracts. Operationally, ethanol−water is recommended for scouting wide compositional space, while processing micro- and macroalgae requires desalting and antifoam strategies to mitigate foaming during polar extractions.

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Publication Details

Journal
University of Limerick Institutional Repository (University of Limerick)
Published
2026-01-14
DOI
https://doi.org/10.34961/19187
Primary Topic
Seaweed-derived Bioactive Compounds
Type
article
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article

Integrated analytical approach to micro- and macroalgae: tailored extraction strategies for sustainable biorefineries

Roland Haseneder, Anna Trubetskaya, Jan Zuber, Yvonne Joseph et al.
University of Limerick Institutional Repository (University of Limerick)
Seaweed-derived Bioactive Compounds
article

Integrated analytical approach to micro- and macroalgae: tailored extraction strategies for sustainable biorefineries

Roland Haseneder, Anna Trubetskaya, Jan Zuber, Yvonne Joseph, Carla Vogt, Stefan R. Kaschabek, Volker Herdegen, Italo Pisano, Luis Leimbrock
article en

Abstract

This study evaluates the solvent-dependent extraction of Arthrospira platensis and Ascophyllum nodosum to guide sustainable marine biorefinery design. SOXTHERM rapid extractions were performed with n-hexane, ethanol−water (1:1, v/v), and water under controlled severity (3 h,n = 2). Ethanol−water consistently delivered the highest yields for A. platensis (25% DW ± 2.2) and A. nodosum (26% DW ± 2.2), with differences confirmed by a permutation test (p < 0.05). Hexane selectively enriched lipophilic fractions, whereas water favored polar constituents. For A. platensis, ethanol−water exceeded hexane (Δ20.3% DW ± 2.5) and water (Δ15.0% DW ± 1.2). For A. nodosum, differences were smaller versus water (Δ3.5% DW ± 3.6) but pronounced versus hexane (Δ23.5% DW ± 1.5). A. platensis extracts were protein-rich and contained long-chain polyunsaturated fatty acids, while A. nodosum extracts exhibited a high mineral content and structural carbohydrates. Ultra-high-resolution FT-ICR-MS revealed thousands of molecular features, including putative lipid-like and nitrogenous species; all structural assignments remain putative without MS/MS confirmation. Notably, biopterin analogues were detected in A. platensis water extracts, and polyphenolic signatures dominated A. nodosum ethanol−water extracts. Operationally, ethanol−water is recommended for scouting wide compositional space, while processing micro- and macroalgae requires desalting and antifoam strategies to mitigate foaming during polar extractions.

University of Limerick Institutional Repository (University of Limerick)
Openalex Percentile: Top 87%
Seaweed-derived Bioactive Compounds
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