Table 7.
Fucoidan Source | Aim of Study | Type of Study | Outcome | Reference |
---|---|---|---|---|
Radiolabelled fucoidan source unspecified | Safety | Human clinical | Safe to use. Maximum activity in liver. Activity reduced to <5% after 24 h. | [6] |
Undaria pinnatifida
Fucus evanescens Saccharina cichorioides Costaria costata Fucus vesiculosus Eisenia bicyclis |
Thrombolytic activity of fucoidan | In vivo mouse thrombosis model, iv | Fucoidans inhibit the tPA-PAI1 complex, indicating activation of plasma tissue-type plasminogen activator is a mechanism of fucoidan-mediated thrombolysis in a mouse thrombosis model | [89] |
Unspecified | Thrombolytic therapy based on fucoidan nanoparticles with rtPA | In vivo mouse model with induced clotting, iv | Successful thrombolysis | [88] |
Laminaria japonica | Anti-thrombotic | In vivo mouse model. Oral delivery |
Lower MW fucoidan was most effective | [28] |
Fucus vesiculosus and 18 gradually depolymerised fractions | Degraded fucoidan fractions | In vitro | Anti-inflammatory activity, however only negligible anticoagulant activity and FXII-activating potency | [91] |
Fucus vesiculosus
Macrocystis pyrifera Undaria pinnatifida |
Intravenous fucoidan administration prior to SPIONs | In vivo mouse model In vitro |
Increased residence time of circulating SPIONs for imaging by blocking their uptake by reticuloendothelial uptake | [90] |