Modality switching between therapy and imaging based on the excitation wavelength dependence of dual-function agents in folic acid-conjugated graphene oxides

被引:2
作者
Jun, Seung Won [1 ]
Kwon, Junyoung [1 ]
Chun, Soo Kyung [1 ]
Lee, Hyun Ah [2 ]
Lee, Jaebeom [1 ]
Hwang, Dae Youn [2 ]
Dong, Chen-Yuan [3 ]
Kim, Chang-Seok [1 ]
机构
[1] Pusan Natl Univ, Dept Cognomechatron Engn, Busan 46241, South Korea
[2] Pusan Natl Univ, Dept Biomat Sci, Miryang 50463, South Korea
[3] Natl Taiwan Univ, Dept Phys, Taipei 10617, Taiwan
基金
新加坡国家研究基金会;
关键词
TARGETED DRUG-DELIVERY; PHOTOTHERMAL THERAPY; ANTICANCER DRUGS; FOLATE RECEPTOR; GOLD NANORODS; CELL THERAPY; NANOPARTICLES; NANOMATERIALS; MICROSCOPY; CANCER;
D O I
10.1364/BOE.9.000705
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Owing to its near infrared (NIR) absorption, graphene oxide (GO) is promising for both photothermal (PT) therapy and multiphoton (MP) imaging. Novel therapy/imaging modality switching is proposed here based on the selected excitation wavelength of femtosecond (FS) laser. GO-based destruction of cancer cells is demonstrated when the laser power of 800-nm-wavelength FS laser is increased above 7 mW. However, GO-based imaging is mainly monitored without damaging the sample when using 1200-nm wavelength FS laser in the same laser power range. Folic acid (FA) conjugated graphene oxide (FA-GO) was synthesized for selective cancer cell targeting. Dual-function FA-GO-based cancer cell targeting agents were experimentally optimized to enable therapy/imaging modality switching. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
引用
收藏
页码:705 / 717
页数:13
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