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首页> 外文期刊>ACS applied materials & interfaces >Quantum-Dot-Based Theranostic Micelles Conjugated with an Anti-EGFR Nanobody for Triple-Negative Breast Cancer Therapy
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Quantum-Dot-Based Theranostic Micelles Conjugated with an Anti-EGFR Nanobody for Triple-Negative Breast Cancer Therapy

机译:基于量子点的Theranostic胶束与抗EGFR纳米体缀合,用于三阴性乳腺癌治疗

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A quantum-dot (QD)-based micelle conjugated with an anti-epidermal growth factor receptor (EGFR) nanobody (Nb) and loaded with an anticancer drug, aminoflavone (AF), has been engineered for EGFR-overexpressing cancer theranostics. The near-infrared (NIR) fluorescence of the indium phosphate core/zinc sulfide shell QDs (InP/ZnS QDs) allowed for in vivo nanoparticle biodistribution studies. The anti-EGFR nanobody 7D12 conjugation improved the cellular uptake and cytotoxicity of the QD-based micelles in EGFR-overexpressing MDA-MB-468 triple-negative breast cancer (TNBC) cells. In comparison with the AF-encapsulated nontargeted (i.e., without Nb conjugation) micelles, the AF-encapsulated Nb-conjugated (i.e., targeted) micelles accumulated in tumors at higher concentrations, leading to more effective tumor regression in an orthotopic triple-negative breast cancer xenograft mouse model. Furthermore, there was no systemic toxicity observed with-the treatments. Thus, this QD-based Nb-conjugated micelle may serve as an effective theranostic nanoplatform for EGFR-overexpressing cancers such as TNBCs.
机译:基于抗表皮生长因子受体(EGFR)纳米缺陷(NB)缀合的量子点(QD)的胶束,并用抗癌药物,氨氟戊酮(AF)加载,已经为EGFR-过度表达癌症治疗。磷酸铟/硫化锌壳QDS(INP / ZnS QDS)的近红外(NIR)荧光允许体内纳米颗粒生物分布研究。抗EGFR纳米体7d12缀合改善了EGFR过表达MDA-MB-468三重阴性乳腺癌(TNBC)细胞中的基于QD基胶束的细胞吸收和细胞毒性。与与AF-包封的Nontargeted(即,没有Nb缀合)胶束相比,在较高浓度下累积在肿瘤中积聚的AF包封的Nb缀合(即,靶向)胶束,导致在原位三负乳房中的更有效的肿瘤消退癌症异种移植鼠标模型。此外,未观察到治疗的全身毒性。因此,该基于QD的Nb缀合的胶束可以用作EGFR过表达癌等诸如TNBC的癌症的有效治疗纳米纳薄晶片。

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