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Propylene glycol alginate sodium sulfate (PSS) is the first oral heparinoid marine drug, derived from brown algal alginic acid and marketed in 1986. Its core pharmacology, including anticoagulation, lipid-lowering, microcirculation improvement, and neuroprotection, makes it an affordable oral option for chronic ischemic cardiovascular and cerebrovascular diseases. Pharmacological studies have also revealed anti-inflammatory, anti-fibrotic, anti-metastatic, and FGF/FGFR-activating effects. Notably, these activities can be independently modulated by molecular weight and M/G ratio, enabling activity-specific structural optimization, guiding the development of safer derivatives. This review summarizes PSS’s R&D, mechanisms, clinical applications, and safety, aiming to inform precision medication strategies and inspire similar drug development.
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Xia et al. (2026) studied this question.
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