Status Quo in the Liposome-Based Therapeutic Strategies Against Glioblastoma: "Targeting the Tumor and Tumor Microenvironment"

被引:1
|
作者
Haseeb, Mohd [1 ]
Khan, Imran [1 ,2 ]
Kartal, Zeynep [1 ]
Mahfooz, Sadaf [1 ,3 ]
Hatiboglu, Mustafa Aziz [1 ,4 ]
机构
[1] Bezmialem Vakif Univ, Beykoz Inst Life Sci & Biotechnol, Dept Mol Biol, Yalikoy St, TR-34820 Istanbul, Turkiye
[2] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Coll Med, Dept Radiat Oncol, Omaha, NE 68198 USA
[4] Bezmialem Vakif Univ, Med Sch, Dept Neurosurg, Vatan St, TR-34093 Istanbul, Turkiye
关键词
liposomes; glioblastoma; microglia; TME; temozolomide; nanoparticles; ACCELERATED BLOOD CLEARANCE; DRUG-DELIVERY; ORAL DELIVERY; INTRANASAL DELIVERY; LIPID NANOPARTICLES; POLYETHYLENE-GLYCOL; CATIONIC LIPOSOMES; GLIOMA-CELLS; BRAIN; DOXORUBICIN;
D O I
10.3390/ijms252011271
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glioblastoma is the most aggressive and fatal brain cancer, characterized by a high growth rate, invasiveness, and treatment resistance. The presence of the blood-brain barrier (BBB) and blood-brain tumor barrier (BBTB) poses a challenging task for chemotherapeutics, resulting in low efficacy, bioavailability, and increased dose-associated side effects. Despite the rigorous treatment strategies, including surgical resection, radiotherapy, and adjuvant chemotherapy with temozolomide, overall survival remains poor. The failure of current chemotherapeutics and other treatment regimens in glioblastoma necessitates the development of new drug delivery methodologies to precisely and efficiently target glioblastoma. Nanoparticle-based drug delivery systems offer a better therapeutic option in glioblastoma, considering their small size, ease of diffusion, and ability to cross the BBB. Liposomes are a specific category of nanoparticles made up of fatty acids. Furthermore, liposomes can be surface-modified to target a particular receptor and are nontoxic. This review discusses various methods of liposome modification for active/directed targeting and various liposome-based therapeutic approaches in the delivery of current chemotherapeutic drugs and nucleic acids in targeting the glioblastoma and tumor microenvironment.
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页数:37
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