Nose-to-Brain Delivery of Biomimetic Nanoparticles for Glioblastoma Targeted Therapy

被引:0
|
作者
Ferreira, Natalia Noronha [1 ]
Leite, Celisnolia Morais [1 ]
Moreno, Natalia Sanchez [1 ]
Miranda, Renata Rank [1 ]
Lins, Paula Maria Pincela [2 ]
Rodero, Camila Fernanda [1 ]
de Oliveira Junior, Edilson [3 ]
Lima, Eliana Martins [3 ]
Reis, Rui M. [4 ,5 ]
Zucolotto, Valtencir [1 ]
机构
[1] Univ Sao Paulo, Phys Inst Sao Carlos, Nanomed & Nanotoxicol Grp, BR-13560970 Sao Carlos, SP, Brazil
[2] Hasselt Univ, Biomed Res Inst BIOMED, Fac Med & Life Sci, B-3590 Diepenbeek, Belgium
[3] Univ Fed Goias UFG, Fac Farm, Lab Nanotecnol Farmaceut & Sistemas Liberacao Far, FarmaTec, 5a Ave C Rua 240 S-N,Praca Univ, BR-74605170 Goiania, Go, Brazil
[4] Barretos Canc Hosp, Mol Oncol Res Ctr, BR-14784400 Barretos, SP, Brazil
[5] Univ Minho, Life & Hlth Sci Res Inst ICVS, Sch Med, Campus Gualtar, P-4710057 Braga, Portugal
基金
巴西圣保罗研究基金会;
关键词
biomimetic delivery systems; Temozolomide; nanotechnology; PLGA-based nanoparticles; glioblastomatreatment; homotypic recognition; nose-to-braindelivery; LOADED PLGA NANOPARTICLES; DRUG-RELEASE; IN-VIVO; DISSOLUTION PROFILES; TEMOZOLOMIDE; MEMBRANE; NANOCARRIERS; PACLITAXEL; STRATEGIES; SYSTEMS;
D O I
10.1021/acsami.4c16837
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Glioblastoma (GBM) is an extremely aggressive form of brain cancer that remains challenging to treat, especially owing to the lack of effective targeting and drug delivery concerns. Due to its anatomical advantages, the nose-to-brain strategy is an interesting route for drug delivery. Nanoengineering has provided technological tools and innovative strategies to overcome biotechnological limitations, which is promising for improving the effectiveness of conventional therapies. Herein, we designed a biomimetic multifunctional nanostructure produced by polymeric poly(d,l-lactic-co-glycolic) acid (PLGA) core loaded with Temozolomide (TMZ) coated with cell membrane isolated from glioma cancer cells. The developed nanostructures (NP-MB) were fully characterized, and their biological performance was investigated extensively. The results indicate that NP-MB could control TMZ release and promote TMZ permeation in the ex vivo nasal porcine mucosa. The higher cytotoxicity of NP-MB in different glioma cell lines, particularly against U251 cells, reinforces their potential for homotypic targeting. The chicken chorioallantoic membrane assay revealed a tumor size reduction and antiangiogenic activity. In vivo biodistribution studies showed that NP-MB effectively reaches the brain following nasal administration. These findings suggest that NP-MB holds promise as a biomimetic nanoplatform for effective targeting and homotypic recognition in GBM therapy with high potential for clinical translation.
引用
收藏
页码:484 / 499
页数:16
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