Article Overview
Abstract
Curcumin, a polyphenolic compound derived from turmeric, has garnered interest for its full-size therapeutic ability, along with anti-inflammatory, antioxidant, and anticancer properties. However, its clinical efficacy is often compromised by troubles related to poor bioavailability, fast metabolism, and instability. Recent improvements in formulation era have brought about progressive shipping structures designed to decorate curcumin's pharmacological profile. This evaluate explores novel formulations inclusive of nanoparticle-primarily based structures, liposomes, self-emulsifying drug shipping structures (SEDDS), and cyclodextrin complexes. We talk their mechanisms, blessings, and effect on curcumin’s bioavailability, stability, and therapeutic effectiveness. By comparing latest research, this assessment goals to provide a comprehensive assessment of ways these improvements can overcome traditional limitations and improve curcumin-based totally treatments.
Keywords: Curcumin, Bioavailability, Nanoparticle-Based Systems, Liposomes, Self-Emulsifying Drug Delivery Systems (SEDDS), Cyclodextrin Complexes, Pharmacological Efficacy.
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