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用于抗癌药物控释和多模态成像的高亲水性发光磁性介孔碳纳米球

Highly Hydrophilic Luminescent Magnetic Mesoporous Carbon Nanospheres for Controlled Release of Anticancer Drug and Multimodal Imaging.

作者信息

Mohapatra Sasmita, Rout Smruti R, Das Rahul K, Nayak Santoshi, Ghosh Sudip K

机构信息

Department of Chemistry, National Institute of Technology , Rourkela, India 769008.

Department of Biotechnology, Indian Institute of Technology , Kharagpur, India 721302.

出版信息

Langmuir. 2016 Feb 16;32(6):1611-20. doi: 10.1021/acs.langmuir.5b03898. Epub 2016 Feb 3.

Abstract

Judicious combination of fluorescence and magnetic properties along with ample drug loading capacity and control release property remains a key challenge in the design of nanotheranostic agents. This paper reports the synthesis of highly hydrophilic optically traceable mesoporous carbon nanospheres which can sustain payloads of the anticancer drug doxorubicin and T2 contrast agent such as cobalt ferrite nanoparticles. The luminescent magnetic hybrid system has been prepared on a mesoporous silica template using a resorcinol-formaldehyde precursor. The mesoporous matrix shows controlled release of the aromatic drug doxorubicin due to disruption of supramolecular π-π interaction at acidic pH. The particles show MR contrast behavior by affecting the proton relaxation with transverse relaxivity (r2) 380 mM(-1) S(-1). The multicolored emission and upconversion luminescence property of our sample are advantageous in bioimaging. In vitro cell experiments shows that the hybrid nanoparticles are endocyted by the tumor cells through passive targeting. The pH-responsive release of doxorubicin presents chemotherapeutic inhibition of cell growth through induction of apoptosis.

摘要

在纳米诊疗剂的设计中,将荧光和磁性特性与充足的药物负载能力及控释特性进行合理结合,仍然是一项关键挑战。本文报道了一种高度亲水性、具有光学可追踪性的介孔碳纳米球的合成,该纳米球能够负载抗癌药物阿霉素和T2造影剂,如钴铁氧体纳米颗粒。利用间苯二酚-甲醛前驱体,在介孔二氧化硅模板上制备了发光磁性混合体系。由于在酸性pH值下超分子π-π相互作用的破坏,介孔基质显示出芳香族药物阿霉素的控释。这些颗粒通过影响质子弛豫,横向弛豫率(r2)为380 mM(-1) S(-1),表现出磁共振造影行为。我们样品的多色发射和上转换发光特性在生物成像中具有优势。体外细胞实验表明,杂化纳米颗粒通过被动靶向被肿瘤细胞内吞。阿霉素的pH响应释放通过诱导细胞凋亡呈现出对细胞生长的化疗抑制作用。

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