Issue 20, 2016

A targeted agent with intercalation structure for cancer near-infrared imaging and photothermal therapy

Abstract

A new targeted photothermal agent used in cancer photothermal therapy (PTT) is synthesized by co-intercalation of indocyanine green (ICG) and targeting folic acid (FA) into the interlamellar gallery of layered double hydroxide (LDH). The resulting composite material (ICG–FA/LDH) possesses an interlayer distance of 2.503 nm, and a uniform particle size with an equivalent hydrodynamic diameter of 127 nm. ICG presents a monomeric state in the LDH gallery, owing to the supermolecular interactions between the LDH host and ICG guest, which results in a largely-enhanced photothermal conversion efficiency. In vitro tests performed with KB cells demonstrate a highly enhanced cellar uptake and excellent imaging ability for the ICG–FA/LDH. The photothermal conversion studies show that an ultra-low dosage of ICG–FA/LDH (equivalent ICG 10 μg mL−1) under weak near-infrared (NIR) irradiation (8 min; 1.1 W cm−2) achieves a significant temperature increase from 19.8 °C to 51.0 °C. Therefore, a satisfactory in vitro PTT effectiveness of the ICG–FA/LDH composite is obtained, and it exhibits cellular damage as high as 87.4% with an ultra-low dosage of ICG (8 μg mL−1) and weak NIR irradiation (1.1 W cm−2, 12 min). In addition, the photothermal agent ICG–FA/LDH displays good targeting capability, biocompatibility and low cytotoxicity. It is expected that the unique ICG–FA/LDH with integrated fluorescence imaging and photothermal therapy can be potentially used in the cell labeling and PTT area.

Graphical abstract: A targeted agent with intercalation structure for cancer near-infrared imaging and photothermal therapy

Supplementary files

Article information

Article type
Paper
Submitted
10 Nov 2015
Accepted
15 Jan 2016
First published
04 Feb 2016

RSC Adv., 2016,6, 16608-16614

Author version available

A targeted agent with intercalation structure for cancer near-infrared imaging and photothermal therapy

C. Li, R. Liang, R. Tian, S. Guan, D. Yan, J. Luo, M. Wei, D. G. Evans and X. Duan, RSC Adv., 2016, 6, 16608 DOI: 10.1039/C5RA23686J

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