替莫唑胺
纳米载体
生物制药
背景(考古学)
医学
胶质母细胞瘤
药理学
脑瘤
达卡巴嗪
药品
癌症研究
肿瘤科
化疗
内科学
生物
病理
生物技术
古生物学
作者
Leonardo Delello Di Filippo,Juliana H. Azambuja,Jessyca Aparecida Paes Dutra,Marcela Tavares Luiz,Jonatas Lobato Duarte,Luiza Ribeiro Nicoleti,Sara Teresinha Olalla Saad,Marlus Chorilli
标识
DOI:10.1016/j.ejpb.2021.08.011
摘要
Glioblastoma multiforme (GBM) is the most common primary brain cancer. GBM has aggressive development, and the pharmacological treatment remains a challenge due to GBM anatomical characteristics’ (the blood–brain barrier and tumor microenvironment) and the increasing resistance to marketed drugs, such as temozolomide (TMZ), the first-line drug for GBM treatment. Due to physical–chemical properties such as short half-life time and the increasing resistance shown by GBM cells, high doses and repeated administrations are necessary, leading to significant adverse events. This review will discuss the main molecular mechanisms of TMZ resistance and the use of functionalized nanocarriers as an efficient and safe strategy for TMZ delivery. GBM-targeting nanocarriers are an important tool for the treatment of GBM, demonstrating to improve the biopharmaceutical properties of TMZ and repurpose its use in anti-GBM therapy. Technical aspects of nanocarriers will be discussed, and biological models highlighting the advantages and effects of functionalization strategies in TMZ anti-GBM activity. Finally, conclusions regarding the main findings will be made in the context of new perspectives for the treatment of GBM using TMZ as a chemotherapy agent, improving the sensibility and biological anti-tumor effect of TMZ through functionalization strategies.
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