4.3 Article

Targeted imaging of esophageal adenocarcinoma with a near-infrared fluorescent peptide

Journal

BMC GASTROENTEROLOGY
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12876-021-01840-3

Keywords

Esophageal carcinoma; Peptide; Near infrared; Probe

Funding

  1. National Natural Science Foundation of China [82003152, 81370585, 81570482]
  2. Discipline Promotion Project of Xijing Hosptial [XJZT19MJ24]

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In this study, the SNF-Cy5.5 probe was synthesized and characterized for its high efficiency and purity. In vitro and in vivo tests confirmed the high affinity, specificity, and tumor-targeting efficacy of SNF-Cy5.5, making it a promising optical probe for imaging of esophageal adenocarcinoma. The in vivo experiment demonstrated excellent tumor-to-background contrast at 2 hours post-injection.
Background Targeted optical imaging offers a noninvasive and accurate method for the early detection of gastrointestinal tumors, especially for flat appearances. In our previous study, a sequence of SNFYMPL (SNF) was identified as a specific peptide to bind to esophageal carcinoma using phage-display technology. This study aimed to evaluate the tumor-targeting efficacy of Cy5.5-conjugated SNF probe for imaging of esophageal carcinoma in vitro and in vivo. Methods The SNF-Cy5.5 probe was synthesized and then identified using High Performance Liquid Chromatography (HPLC) and mass spectrometry (MS). Confocal fluorescence imaging and Flow cytometry analysis were performed to evaluate the binding specificity and the receptor binding affinity of SNF-Cy5.5 to OE33. In vivo imaging was performed to evaluate the targeting ability of SNF-Cy5.5 to esophageal carcinoma. Results The confocal imaging and flow cytometry analysis showed that SNF-Cy5.5 bound specifically to the plasma membrane of OE33 cells with a high affinity. In vivo, for non-block group, SNF-Cy5.5 probe exhibited rapid OE33 tumor targeting during 24 h p.i. and excellent tumor-to-background contrast at 2 h p.i. For the block group, SNF-Cy5.5 was not observed in the mice after 4 h p.i. Ex vivo imaging also revealed that a higher fluorescent signal intensity value of the tumors was clearly observed in the non-block group than that in the block group (2.6 +/- 0.32 x 10(9) vs. 0.8 +/- 0.08 x 10(9), p < 0.05). Conclusions SNF-Cy5.5 was synthesized and characterized with a high efficiency and purity. The higher affinity, specificity, and tumor targeting efficacy of SNF-Cy5.5 were confirmed by in vitro and in vivo tests. SNF-Cy5.5 is a promising optical probe for the imaging of esophageal adenocarcinoma.

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