A sialic acid-targeted near-infrared theranostic for signal activation based intraoperative tumor ablation.

نویسندگان

  • Xuanjun Wu
  • Mingzhu Yu
  • Bijuan Lin
  • Hongjie Xing
  • Jiahuai Han
  • Shoufa Han
چکیده

Agents enabling tumor staging are valuable for cancer surgery. Herein, a targetable sialic acid-armed near-infrared profluorophore (SA-pNIR) is reported for fluorescence guided tumor detection. SA-pNIR consists of a sialic acid entity effective for in vivo tumor targeting and a profluorophore which undergoes lysosomal acidity-triggered fluorogenic isomerization. SA-pNIR displays a number of advantageous biomedical properties in mice, e.g. high tumor-to-normal tissue signal contrast, long-term retention in tumors and low systemic toxicity. In addition, SA-pNIR effectively converts NIR light into cytotoxic heat in cells, suggesting tumor-activatable photothermal therapy. With high performance tumor illumination and lysosome-activatable photothermal properties, SA-pNIR is a promising agent for detection and photothermal ablation of surgically exposed tumors.

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منابع مشابه

A sialic acid-targeted near-infrared theranostic for signal activation based intraoperative tumor ablation† †Electronic supplementary information (ESI) available: All experimental procedures; synthesis and characterization of SA-pNIR and Glu-pNIR; time course studies on cellular uptake of SA-pNIR; metabolic incorporation of SA-pNIR into cellular proteins; and whole body images of mice with overdosed SA-pNIR and Glu-pNIR. See DOI: 10.1039/c4sc02248c Click here for additional data file.

Department of Chemical Biology, College of Key Laboratory for Chemical Biology of Fuji Spectrochemical Analysis & Instrumentation Xiamen University, Xiamen, 361005, Ch +86-0592-2181728 State Key Laboratory of Cellular Stress Bio School of Life Sciences, Xiamen University, X † Electronic supplementary informatio procedures; synthesis and characterizat course studies on cellular uptake of SA-pNIR...

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عنوان ژورنال:
  • Chemical science

دوره 6 1  شماره 

صفحات  -

تاریخ انتشار 2015