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脂质体纳米材料:胶质瘤治疗领域的后起之秀
Authors Gan Y, Yu Y, Xu H , Piao H
Received 24 March 2024
Accepted for publication 22 June 2024
Published 5 July 2024 Volume 2024:19 Pages 6757—6776
DOI https://doi.org/10.2147/IJN.S470478
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Jie Huang
Yu Gan,1,2 Yingying Yu,1 Huizhe Xu,2 Haozhe Piao1
1Department of Neurosurgery, Cancer Hospital of China Medical University, Cancer Hospital of Dalian University of Technology, Liaoning Cancer Hospital & Institute, Shenyang, Liaoning Province, People’s Republic of China; 2Central Laboratory, Cancer Hospital of China Medical University, Cancer Hospital of Dalian University of Technology, Liaoning Cancer Hospital & Institute, Shenyang, Liaoning Province, People’s Republic of China
Correspondence: Huizhe Xu; Haozhe Piao, Email xuhuizhe@cancerhosp-ln-cmu.com; pzpy@163.com
Abstract: Glioma is a primary malignant tumor in the central nervous system. In recent years, the treatment of glioma has developed rapidly, but the overall survival of glioma patients has not significantly improved. Due to the presence of the blood–brain barrier and intracranial tumor barrier, many drugs with good effects to cure glioma in vitro cannot be accurately transported to the corresponding lesions. In order to enable anti-tumor drugs to overcome the barriers and target glioma, nanodrug delivery systems have emerged recently. It is gratifying that liposomes, as a multifunctional nanodrug delivery carrier, which can be compatible with hydrophilic and hydrophobic drugs, easily functionalized by various targeted ligands, biodegradable, and hypoimmunogenic in vivo, has become a quality choice to solve the intractable problem of glioma medication. Therefore, we focused on the liposome nanodrug delivery system, and summarized its current research progress in glioma. Hopefully, this review may provide new ideas for the research and development of liposome-based nanomaterials for the clinical treatment of glioma.
Keywords: glioma, blood‒brain barrier, nanomaterials, liposome, nanoparticle drug delivery system