Department of Neurosurgery, the First Hospital of Jilin University, 1 Xinmin Street, Changchun, 130061, P. R. China.
Jilin Collaborative Innovation Center for Antibody Engineering, Jilin Medical University, 5 Jilin Street, Jilin, 132000, P. R. China.
Macromol Rapid Commun. 2024 Nov;45(21):e2400662. doi: 10.1002/marc.202400662. Epub 2024 Sep 12.
Glioblastoma is one of the most aggressive and treatment-resistant forms of primary brain cancer, posing significant challenges in effective therapy. This study aimed to enhance the effectiveness of glioblastoma therapy by developing a unique nanomedicine composed of Pluronic F127-complexed PEGylated poly(glutamic acid)-cisplatin (PLG-PEG/PF127-CDDP). PLG-PEG/PF127-CDDP demonstrated an optimal size of 133.97 ± 12.60 nm, facilitating efficient cell uptake by GL261 glioma cells. In vitro studies showed significant cytotoxicity against glioma cells with a half-maximal (50%) inhibitory concentration (IC50) of 12.61 µg mL at 48 h and a 72.53% ± 1.89% reduction in cell invasion. Furthermore, PLG-PEG/PF127-CDDP prolonged the circulation half-life of cisplatin to 9.75 h in vivo, leading to a more than 50% reduction in tumor size on day 16 post-treatment initiation in a murine model of glioma. The treatment significantly elevated lactate levels in GL261 cells, indicating enhanced metabolic disruption. Therefore, PLG-PEG/PF127-CDDP offers a promising approach for glioblastoma therapy due to its effects on improving drug delivery efficiency, therapeutic outcomes, and safety while minimizing systemic side effects. This work underscores the potential of polymer-based nanomedicines in overcoming the challenges of treating brain tumors, paving the way for future clinical applications.
胶质母细胞瘤是最具侵袭性和耐药性的原发性脑癌之一,对有效治疗构成重大挑战。本研究旨在通过开发由泊洛沙姆 F127 复合聚乙二醇化聚(谷氨酸)-顺铂(PLG-PEG/PF127-CDDP)组成的独特纳米医学来提高胶质母细胞瘤治疗的效果。PLG-PEG/PF127-CDDP 的最佳粒径为 133.97 ± 12.60nm,有利于 GL261 神经胶质瘤细胞的有效摄取。体外研究表明,对神经胶质瘤细胞具有显著的细胞毒性,在 48 小时时半最大(50%)抑制浓度(IC50)为 12.61μg mL,细胞侵袭减少 72.53%±1.89%。此外,PLG-PEG/PF127-CDDP 在体内将顺铂的循环半衰期延长至 9.75 小时,导致在荷瘤小鼠模型中治疗开始后第 16 天肿瘤体积减少 50%以上。该治疗方法显著提高了 GL261 细胞中的乳酸水平,表明代谢破坏增强。因此,PLG-PEG/PF127-CDDP 为胶质母细胞瘤治疗提供了一种很有前途的方法,因为它可以提高药物递送效率、治疗效果和安全性,同时最大限度地减少全身副作用。这项工作突出了聚合物基纳米医学在克服治疗脑肿瘤挑战方面的潜力,为未来的临床应用铺平了道路。