Macrophage cell membrane infused biomimetic liposomes for glioblastoma targeted therapy

被引:14
|
作者
Mendanha, D.
Castro, J. Vieira de
Casanova, M. R.
Gimondi, S.
Ferreira, H.
Neves, N. M. [1 ]
机构
[1] Univ Minho, Res Inst Biomat, Headquarters European Inst Excellence Tissue Engn, Res Grp, Zona Ind Gandra, P-4805017 Guimaraes, Portugal
关键词
Biomimetic liposomes; Cell membrane; Glioblastoma; Macrophages; DRUG-DELIVERY; NANOPARTICLES; NANOCARRIERS; TEMOZOLOMIDE;
D O I
10.1016/j.nano.2023.102663
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma (GBM) is a highly aggressive malignant brain tumor currently without an effective treatment. Inspired by the recent advances in cell membrane biomimetic nanocarriers and by the key role of macrophages in GBM pathology, we developed macrophage membrane liposomes (MML) for GBM targeting. For the first time, it was assessed the role of macrophage polarization states in the effectiveness of these drug delivery systems. Interestingly, we observed that MML derived from M2 macrophages (M2 MML) presents higher uptake and increased delivery of the anticarcinogenic drug doxorubicin compared to M1 macrophage-derived nanocarriers (M1 MML) and control liposomes (CL). Moreover, the lowest uptake by macrophages of MML reveals promising immune escaping properties. Notably, M2 macrophages unveiled a higher expression of integrin CD49d, a crucial protein involved in the bilateral communication of macrophages with tumor cells. Therefore, our findings suggest the potential of using M2 macrophage membranes to develop novel nanocarriers targeting GBM.(c) 2023 Published by Elsevier Inc.
引用
收藏
页数:12
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