Transferrin-Conjugated PLGA Nanoparticles for Co-Delivery of Temozolomide and Bortezomib to Glioblastoma Cells

被引:16
|
作者
Ramalho, Maria Joao [1 ,2 ]
Torres, Ines David [1 ,2 ]
Loureiro, Joana Angelica [1 ,2 ]
Lima, Jorge [3 ,4 ,5 ]
Pereira, Maria Carmo [1 ,2 ]
机构
[1] Univ Porto, Fac Engn, LEPABE Lab Proc Engn Environm Biotechnol & Energy, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[2] Univ Porto, Fac Engn, ALiCE Associate Lab Chem Engn, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[3] Univ Porto, i3S Inst Invest & Inovacao Saude, R Alfredo Allen, P-420010135 Porto, Portugal
[4] Univ Porto, Ipatimup Inst Patol & Imunol Mol, Rua Julio Amaral de Carvalho 45, P-4200135 Porto, Portugal
[5] Univ Porto, Fac Med, Alameda Prof Hernani Monteiro, P-4200319 Porto, Portugal
基金
欧盟地平线“2020”;
关键词
high-grade glioma; brain tumor; MGMT protein; drug resistance mechanisms; alkylatingagents; poly(lactic-co-glycolic acid); brain delivery; transferrin receptor; METHYLTRANSFERASE MGMT; IRON-BINDING; RELEASE; BRAIN; DOXORUBICIN; INHIBITION; INCREASES; PROMOTER;
D O I
10.1021/acsanm.3c02122
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma (GBM)represents almost half of primarybrain tumors,and its standard treatment with the alkylating agent temozolomide(TMZ) is not curative. Treatment failure is partially related to intrinsicresistance mechanisms mediated by the O6-methylguanine-DNA methyltransferase(MGMT) protein, frequently overexpressed in GBM patients. Clinicaltrials have shown that the anticancer agent bortezomib (BTZ) can increaseTMZ's therapeutic efficacy in GBM patients by downregulatingMGMT expression. However, the clinical application of this therapeuticstrategy has been stalled due to the high toxicity of the combinedtherapy. The co-delivery of TMZ and BTZ through nanoparticles (NPs)of poly(lactic-co-glycolic acid) (PLGA) is proposedin this work, aiming to explore their synergistic effect while decreasingthe drug's toxicity. The developed NPs were optimized by centralcomposite design (CCD), then further conjugated with transferrin(Tf) to enhance their GBM targeting ability by targeting the blood-brainbarrier (BBB) and the cancer cells. The obtained NPs exhibited suitableGBM cell delivery features (sizes lower than 200 nm, low polydispersity,and negative surface charge) and a controlled and sustained releasefor 20 days. The uptake and antiproliferative effect of the developedNPs were evaluated in in vitro human GBM models.The obtained results disclosed that the NPs are rapidly taken up bythe GBM cells, promoting synergistic drug effects in inhibiting tumorcell survival and proliferation. This cytotoxicity was associatedwith significant cellular morphological changes. Additionally, thebiocompatibility of unloaded NPs was evaluated in healthy brain cells,demonstrating the safety of the nanocarrier. These findings provethat co-delivery of BTZ and TMZ in Tf-conjugated PLGA NPs is a promisingapproach to treat GBM, overcoming the limitations of current therapeuticstrategies, such as drug resistance and increased side effects.
引用
收藏
页码:14191 / 14203
页数:13
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