Xiaobo Yang, Yuze Sun, Huan Jin, Hailin Zhou, Yunqiao Yang, Yanan Su, Jinan Wang, Zhiwei Zhao, Wenyao Yu, Moli Wu, Qian Wang, Conghongting Liu, Wen Sun, Changyuan Wang, Chong Wang, Li Lv, Mingzhan Li, Jing Ning, Brant E Isakson, Yinan Wang, Xiaohong Shu
The clinical translation of Pterostilbene, a neuroactive stilbene with broad therapeutic potential, is hampered by its poor aqueous solubility and insufficient brain accumulation. To address these limitations, we developed a folate receptor-targeted polymeric micelle system (F-Pt/M) using poly (ethylene glycol)-block-poly (ε-caprolactone) copolymers. The optimized F-Pt/M exhibited a small hydrodynamic diameter (∼133 nm), high drug loading, and increased the apparent solubility of pterostilbene by 25-fold. In folate receptor-expressing U251 and RG-2 glioma cells, F-Pt/M significantly enhanced cellular uptake via folate-mediated endocytosis and showed superior cytotoxicity compared to non-targeted micelles. In an orthotopic RG-2 glioma model, intravenous administration of F-Pt/M improved brain accumulation and prolonged median survival by 76.5% relative to free drug. Mechanistically, the enhanced anti-glioma efficacy was associated with induction of apoptosis and inhibition of the STAT3 signaling pathway. These findings establish folate-targeted micelles as a robust and versatile nanoplatform for delivering poorly soluble bioactive compounds to the brain, with pterostilbene representing a promising candidate for further neuro-oncological development.