Omer Walaa E, Abdelbar Mostafa F, El-Kemary Nesma M, Fukata Naoki, El-Kemary Maged A
Institute of Nanoscience and Nanotechnology, Kafrelsheikh University 33516 Kafr Elsheikh Egypt
International Center for Materials Nanoarchitectonics, National Institute for Materials Science Tsukuba Ibaraki 305-0044 Japan.
RSC Adv. 2021 Sep 20;11(49):31047-31057. doi: 10.1039/d1ra05121k. eCollection 2021 Sep 14.
Fluorometric quantification of biological molecules is a key feature used in many biosensing studies. Fluorescence resonance energy transfer (FRET) using highly fluorescent quantum dots offers highly sensitive detection of the in-proximity wide variety of analyst molecules. In this contribution, we report the use of carbon quantum dots (CDs) for the ultrasensitive optical biosensing of cancer antigen 125 (CA-125) in the early malignant stage. This approach is based on monitoring the quenching of CDs luminescence at 535 nm by CA-125 after excitation at 425 nm and pH 10. The calibration of this method was performed in the concentration range of CA-125 from 0.01 to 129 U ml ( = 0.99) with a detection limit of 0.66 U ml, which matches remarkably with the standard chemiluminometric method in control and real patient samples. The sensing mechanism for cancer antigen 125 assessment was discussed on the basis of fluorescence quenching of CDs and time-resolved photoluminescence spectroscopy. The current method is easy, sensitive, cost-effective and provides a wide range of validity, which helps in overcoming the limitations of high cost and time consumption exhibited by many other traditional clinical assays for CA-125 quantification.
生物分子的荧光定量分析是许多生物传感研究中使用的关键特性。利用高荧光量子点的荧光共振能量转移(FRET)可对多种邻近的分析物分子进行高灵敏度检测。在本论文中,我们报道了使用碳量子点(CDs)对早期恶性阶段的癌抗原125(CA - 125)进行超灵敏光学生物传感。该方法基于在425 nm激发且pH值为10的条件下,监测CA - 125对CDs在535 nm处发光的猝灭。此方法在CA - 125浓度范围为0.01至129 U/ml(R² = 0.99)内进行校准,检测限为0.66 U/ml,在对照样本和实际患者样本中与标准化学发光法的结果显著匹配。基于CDs的荧光猝灭和时间分辨光致发光光谱对癌抗原125评估的传感机制进行了讨论。当前方法简便、灵敏、具有成本效益且具有广泛的有效性,有助于克服许多其他传统临床CA - 125定量检测方法所表现出的高成本和耗时的局限性。