Drug intelligence / Profile preview

phosphatidylserine + curcumin

Development stage
Preclinical
Lead developer
Pharmin USA
Modality
Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Oral
01

Overview

Phosphatidylserine + curcumin (also known as PSL-Cur or PSLs-Cur) is an investigational liposomal combination formulation developed by Pharmin USA. It consists of phosphatidylserine liposomes encapsulating curcumin, a natural polyphenol extracted from turmeric (*Curcuma longa*). This formulation is designed to enhance the oral bioavailability of curcumin, which typically suffers from poor gastrointestinal absorption. Preclinical studies in rat models of glucocorticoid-induced osteoporosis have demonstrated that the combination significantly improves bone serum markers, mechanical strength, osteoprotegerin (OPG) gene expression, and cortical/trabecular bone mass, showing superior efficacy compared to alendronate. Its mechanism of action involves the inhibition of inflammatory mediators such as COX-1, COX-2, TNF, and lipoxygenase, alongside the modulation of bone remodeling pathways.

Other names
phosphatidylserine liposome-curcuminphosphatidylserine liposomes containing curcuminPSL-CurPSLs-Cur
02

Targets

PTGS2 (Prostaglandin-Endoperoxide Synthase 2)TNFA (Tumor necrosis factor alpha (soluble))ALOX5 (Arachidonate 5-lipoxygenase)PGHS-1 (Prostaglandin G/H Synthase 1)

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