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Dual anticancer drug/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging

机译:双重抗癌药物/超顺磁性氧化铁负载PLGA基纳米颗粒用于癌症治疗和磁共振成像

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摘要

We developed dual paclitaxel (PTX)/superparamagnetic iron oxide (SPIO)-loaded PLGA-based nanoparticles for a theranostic purpose. Nanoparticles presented a spherical morphology and a size of 240 nm. The PTX and iron loading were 1.84 ± 0.4 and 10.4 ± 1.93 mg/100 mg respectively. Relaxometry studies and phantom MRI demonstrated their efficacy as T2 contrast agent. Significant cellular uptake by CT26 cells of nanoparticles was shown by Prussian blue staining and fluorescent microscopy. While SPIO did not show any toxicity in CT-26 cells, PTX-loaded nanoparticles had a cytotoxic activity. PTX-loaded nanoparticle (5 mg/kg) with or without co-encapulated SPIO induced in vivo a regrowth delay of CT26 tumors. Together these multifunctional nanoparticles may be considered as future nanomedicine for simultaneous molecular imaging, drug delivery and real-time monitoring of therapeutic response.
机译:我们开发了双重紫杉醇(PTX)/超顺磁性氧化铁(SPIO)负载的PLGA基纳米颗粒,用于治疗治疗目的。纳米粒子呈现球形形态,尺寸为240 nm。 PTX和铁负荷分别为1.84±0.4和10.4±1.93 mg / 100 mg。松弛测量研究和体模MRI证明了它们作为T2造影剂的功效。普鲁士蓝染色和荧光显微镜显示纳米颗粒CT26细胞对细胞的显着摄取。尽管SPIO在CT-26细胞中未显示任何毒性,但装载PTX的纳米颗粒具有细胞毒性活性。有或没有共同包封的SPIO的PTX负载纳米颗粒(5 mg / kg)在体内诱导CT26肿瘤的再生延迟。这些多功能纳米粒子可以一起被认为是未来的纳米药物,用于同时进行分子成像,药物递送和实时监测治疗反应。

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