Hsu Shih-Hsiang, Hung Shao-Chiang, Chen Yu-Kun, Jian Zhi-Hao
.
Sensors (Basel). 2014 Dec 25;15(1):331-40. doi: 10.3390/s150100331.
Various analytes can be verified by surface plasmon resonance, thus continuous improvement of this sensing technology is crucial for better sensing selection and higher sensitivity. The SPR sensitivity on the wavelength modulation is enhanced with increasing wavelengths. The telecommunication wavelength range was then utilized to detect Mycobacterium tuberculosis (MTB) deoxyribonucleic acid (DNA) under two situations, without immobilization and with 5'-thiol end labeled IS6100 DNA probes, for SPR sensitivity comparison. The experimental data demonstrated that the SPR sensitivity increased more than 13 times with the wavelength modulation after immobilization. Since the operating wavelength accuracy of a tunable laser source can be controlled within 0.001 nm, the sensitivity and resolution on immobilized MTB DNA were determined as 1.04 nm/(μg/mL) and 0.9 ng/mL, respectively.
多种分析物可通过表面等离子体共振进行验证,因此不断改进这种传感技术对于更好的传感选择和更高的灵敏度至关重要。随着波长增加,波长调制的表面等离子体共振灵敏度会增强。然后利用电信波长范围在两种情况下检测结核分枝杆菌(MTB)脱氧核糖核酸(DNA),一种是未固定,另一种是用5'-硫醇末端标记的IS6100 DNA探针,以比较表面等离子体共振灵敏度。实验数据表明,固定后通过波长调制表面等离子体共振灵敏度提高了13倍以上。由于可调谐激光源的工作波长精度可控制在0.001 nm以内,固定的MTB DNA的灵敏度和分辨率分别确定为1.04 nm/(μg/mL)和0.9 ng/mL。