Hyaluronate Functionalized Multi-Wall Carbon Nanotubes Filled with Carboplatin as a Novel Drug Nanocarrier against Murine Lung Cancer Cells

被引:22
作者
Salas-Trevino, Daniel [1 ]
Saucedo-Cardenas, Odila [1 ,2 ]
de Jesus Loera-Arias, Maria [1 ]
Rodriguez-Rocha, Humberto [1 ]
Garcia-Garcia, Aracely [1 ]
Montes-de-Oca-Luna, Roberto [1 ]
Pina-Mendoza, Edgar, I [1 ]
Contreras-Torres, Flavio F. [3 ]
Garcia-Rivas, Gerardo [4 ]
Soto-Dominguez, Adolfo [1 ]
机构
[1] Univ Autonoma Nuevo Leon, Fac Med, Dept Histol, Monterrey 64460, Mexico
[2] Ctr Invest Biomed Noreste CIBIN IMSS, Dept Genet Mol, Monterrey 64720, Mexico
[3] Tecnol Monterrey, Escuela Ingn & Ciencias, Monterrey 64849, Mexico
[4] Tecnol Monterrey, Escuela Med, Monterrey 64849, Mexico
关键词
multi-wall carbon nanotubes; nanomedicine; tumor cells; hyaluronate; carboplatin; IN-VIVO; TARGETED DELIVERY; TOXICITY; RELEASE; INHIBITION; CISPLATIN; THERAPY; PRODRUG; VITRO;
D O I
10.3390/nano9111572
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon nanotubes (CNTs) have emerged in recent years as a potential option for drug delivery, due to their high functionalization capacity. Biocompatibility and selectivity using tissue-specific biomolecules can optimize the specificity, pharmacokinetics and stability of the drug. In this study, we design, develop and characterize a drug nanovector (oxCNTs-HA-CPT) conjugating oxidated multi-wall carbon nanotubes (oxCNTs) with hyaluronate (HA) and carboplatin (CPT) as a treatment in a lung cancer model in vitro. Subsequently, we exposed TC-1 and NIH/3T3 cell lines to the nanovectors and measured cell uptake, cell viability, and oxidative stress induction. The characterization of oxCNTs-HA-CPT reveals that on their surface, they have HA. On the other hand, oxCNTs-HA-CPT were endocytosed in greater proportion by tumor cells than by fibroblasts, and likewise, the cytotoxic effect was significantly higher in tumor cells. These results show the therapeutic potential that nanovectors possess; however, future studies should be carried out to determine the death pathways involved, as well as their effect on in vivo models.
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页数:11
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