Marine carbohydrates offer valuable new resources for drug development
· News-MedicalThe ocean contains diverse carbohydrates that could serve as valuable resources for drug development. Algae, marine animals and microorganisms produce polysaccharides and related molecules with structures that are uncommon on land, including distinctive sulfate patterns, sugar linkages and branched architectures. These features can support antiviral, anticoagulant, immunomodulatory and antitumor activity, while also providing useful properties for drug delivery, wound healing and tissue engineering.
A review in Glycoscience & Therapy brought together findings on the sources, structures and biological activities of these marine carbohydrates and examined how some have progressed into medicines. Marine carbohydrates are often studied in terms of individual biological activities, but their clinical development requires a broader understanding of how structure, production, quality control, and mechanisms of action are connected. By examining approved drugs alongside clinical-stage candidates, the review provides a clearer picture of the progress achieved and the challenges that remain.
The authors of the review followed a clinical timeline that begins with cytarabine, a marine-inspired leukemia drug approved in the United States in 1969, and included later carbohydrate-based products derived from alginate, carrageenan and other marine materials. They also surveyed the candidates currently being evaluated in clinical trials for viral infections, cancer, metabolic disorders, tissue repair, cystic fibrosis and neurological disease.
Further, the review focused on what is required to turn a complex natural carbohydrate into a reproducible medicine. Molecular weight, sulfation pattern and monosaccharide composition can all affect activity, but they may also vary with species, season, extraction and processing.
Source:
Journal reference:
Pan, L., et al. (2026). Development of marine organisms derived carbohydrate-based drugs: From bioactivity to clinical translation. Glycoscience & Therapy. DOI: 10.1016/j.glycos.2026.100047. https://www.sciencedirect.com/science/article/pii/S3050608526000236?via%3Dihub