Chen Hongqi, Guan Yingying, Wang Shaozhen, Ji Yuan, Gong Mengqi, Wang Lun
Anhui Key Laboratory of Chemo-Biosensing, Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University , Wuhu 241000, People's Republic of China.
Langmuir. 2014 Nov 4;30(43):13085-91. doi: 10.1021/la502753e. Epub 2014 Oct 22.
A homogeneous immunoassay for the sensitive and selective determination of trace amounts of α-fetoprotein (AFP, a cancer marker) by detection in the near-infrared (NIR) region based on luminescence energy transfer (LET) from NaYF4:Yb,Tm/NaGdF4 core-shell upconverting nanoparticles to gold nanorods (GNRs) is presented. The carboxyl-functionalized NaYF4:Yb,Tm/NaGdF4 core-shell upconverting nanoparticles (UCNPs) were excited by a 980 nm continuous wavelength laser, and its emission peak appeared at a near-infrared wavelength (∼804 nm). The carboxyl-functionalized upconverting nanoparticles were conjugated with the anti-AFP (Ab1) and acted as donor. GNRs with a high absorption band around 790 nm, which was overlapped the UCNPs emission, were synthesized and acted as the acceptor. The donor (negatively charged) interacted with the acceptor (positively charged) via electrostatic interactions to bring them into close proximity. LET could occur, producing a quenching phenomenon. When the AFP antigens were added into the system, the binding affinity between AFP and Ab1 was stronger than the electrostatic interactions, which released the energy acceptors from the energy donors, interrupting luminescence energy transfer, and therefore, the luminescence was recovered. On the basis of the restored luminescence, a turn-on optical immunosening system was developed. Under the optimal conditions, the linear range of detection was from 0.18 to 11.44 ng/mL for AFP (R = 0.99), with a detection limit as low as 0.16 ng/mL. The proposed method has also been used to monitor AFP in human serum samples. Therefore, further study based on the NaYF4:Yb,Tm/NaGdF4 core-shell nanoparticles-GNRs construction may open the way for a new class of NIR-LET biosensors with wide applications.
本文提出了一种基于从NaYF4:Yb,Tm/NaGdF4核壳上转换纳米颗粒到金纳米棒(GNRs)的发光能量转移(LET),在近红外(NIR)区域进行检测,用于灵敏且选择性地测定痕量α-甲胎蛋白(AFP,一种癌症标志物)的均相免疫分析方法。羧基功能化的NaYF4:Yb,Tm/NaGdF4核壳上转换纳米颗粒(UCNPs)由980 nm连续波长激光激发,其发射峰出现在近红外波长(~804 nm)处。羧基功能化的上转换纳米颗粒与抗AFP(Ab1)偶联并作为供体。合成了在790 nm左右具有高吸收带且与UCNPs发射重叠的GNRs并作为受体。供体(带负电荷)通过静电相互作用与受体(带正电荷)相互作用,使它们紧密靠近。可以发生LET,产生猝灭现象。当将AFP抗原加入到体系中时,AFP与Ab1之间的结合亲和力强于静电相互作用,从而使能量受体从能量供体中释放出来,中断发光能量转移,因此,发光得以恢复。基于恢复的发光,开发了一种开启式光学免疫传感系统。在最佳条件下,AFP的检测线性范围为0.18至11.44 ng/mL(R = 0.99),检测限低至0.16 ng/mL。所提出的方法还用于监测人血清样品中的AFP。因此,基于NaYF4:Yb,Tm/NaGdF4核壳纳米颗粒-GNRs构建的进一步研究可能为一类具有广泛应用的新型近红外LET生物传感器开辟道路。