In recent decades, drug research has increasingly shifted toward herbal molecules instead of synthetic ones, due to their low toxicity and better compliance. Among these phytosterols, plantderived sterol compounds have garnered significant attention for their therapeutic and nutritional benefits. Specifically, β-Sitosterol (BSS) has been extensively studied because of its cholesterollowering, anti-inflammatory, and anticancer properties. However, its limited water solubility and modest absorption in the gastrointestinal tract, along with first-pass metabolism (FPM), greatly reduce its oral bioavailability, thus restricting its clinical usefulness. To address these challenges, advances in emerging drug delivery systems (NDDS)-such as nanoparticles, liposomes, micelles, and nanostructured lipid carriers-and formulation techniques like solid dispersions, hydrotropy, self-emulsifying drug delivery systems, and complexation methods, have proven effective in enhancing BSS solubility, stability, and systemic bioavailability. Innovative technologies like 3D printing-based dosage forms also offer promise for personalized and controlled drug release. The unique aspect of this review is its comprehensive approach, integrating traditional and novel strategies to improve BSS bioavailability and assessing their regulatory relevance through the Biopharmaceutics Classification System (BCS) framework. This paper not only summarizes the latest advances in NDDS for BSS but also highlights translational challenges, future prospects, and targeted delivery options, bridging the gap between laboratory research and clinical application.
Sharma et al. (Fri,) studied this question.