Optimization of an analytical methodology to determine microplastic contamination in different seaweed groups (Phaeophyceae, Rhodophyta and Chlorophyta).

Seaweed are primary producers and potential vectors of microplastics (MPs) contamination, yet robust extraction methods that digest complex algal matrices while preserving polymer integrity remain limited. A sequential enzymatic-oxidative digestion was optimized for three seaweeds (Fucus vesiculosus, Chondrus crispus and Ulva lactuca). The optimized process involved the initial addition of cellulase (1% w/v, 24 h, 50 °C) followed by H₂O₂ (30% v/v, 48-72 h, 65 °C). Across nine 0.5 g dry-weight sub-replicates (3 per seaweed), 30 MPs were found (6.7 MPs/g⁻¹). The integrity of polymers was assessed for 12 MPs polymers, with acceptable performance being defined as ≥ 90% recovery and spectroscopic (through FTIR analysis) identifiability. Eight polymers met this threshold (90-101%). Four polymers were adversely affected with the long 72 H₂O₂ incubation, namely: cellulose-acetate (53% recovery), polyamide (61%), acrylic (3%) and rayon (2%). Although polymers remained identifiable, sequential digestion produced mass loss and visible changes (e.g. polyamide opacity, cellulose-acetate brittleness), which may increase fragmentation and miss-identification. Therefore, the protocol is suitable for most common MPs, but not for rayon and acrylic, and should be applied cautiously where cellulose-acetate or polyamide are expected.

• Publication year

  2026

• Venue

  MethodsX

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine, Environmental Science

• Identifiers
  DOI 10.1016/j.mex.2026.103816PMID 41743046PMCID PMC12930080
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

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