Cheeveewattanagul Nopchulee, Guajardo Yévenes Cristian F, Bamrungsap Suwussa, Japrung Deanpen, Chalermwatanachai Thanit, Siriwan Chonpiti, Warachit Oranut, Somasundrum Mithran, Surareungchai Werasak, Rijiravanich Patsamon
Pilot Plant and Development Training Institute, Nanoscience and Nanotechnology Research Cluster, King Mongkut's University of Technology Thonburi (KMUTT), Bang Khun Thian Campus, Bangkok, 10150, Thailand.
National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency (NSTDA), Thailand Science Park, Pathumthani, 12120, Thailand.
Anal Chim Acta. 2021 Apr 15;1154:338302. doi: 10.1016/j.aca.2021.338302. Epub 2021 Feb 16.
We report a new highly selective detection platform for human albumin (HA) in urine based on aptamer-functionalised magnetic particles. Magnetic separation and re-dispersion was utilised to expose the HA-bound particles to a methylene blue solution. A second magnetic collection step was then used to allow the methylene blue supernatant to be reduced at an unmodified screen-printed electrode. Since methylene blue adsorbs to HA, the reduction current fell in proportion to HA concentration. There was no interference from compounds such as dopamine, epinephrine, vanillylmandelic acid, normetanephrine, metanephrine and creatinine in artificial urine at the concentrations at which they would be expected to appear. A calibration equation was derived to allow for the effect of pH on the response. This enabled measurement to be made directly in clinical urine samples of varying pH. After optimisation of experimental parameters, the total assay time was 40 min and the limit of detection was between 0.93 and 1.16 μg mL, depending on the pH used. HA could be detected up to 400 μg mL, covering the range from normoalbuminuria to macroalbuminuria. Analysis of urine samples of patients, with diabatic nephropathy, type I & II diabetes mellitus and chronic kidney disease, from a local hospital showed good agreement with the standard urinary human albumin detection method.
我们报道了一种基于适配体功能化磁性颗粒的新型高选择性尿液中人白蛋白(HA)检测平台。利用磁分离和再分散将结合了HA的颗粒暴露于亚甲基蓝溶液中。然后进行第二次磁收集步骤,以使亚甲基蓝上清液在未修饰的丝网印刷电极上被还原。由于亚甲基蓝吸附到HA上,还原电流与HA浓度成比例下降。在人工尿液中预期会出现的多巴胺、肾上腺素、香草扁桃酸、去甲变肾上腺素、变肾上腺素和肌酐等化合物,在相应浓度下不会产生干扰。推导了一个校准方程以考虑pH对响应的影响。这使得能够直接在不同pH值的临床尿液样本中进行测量。优化实验参数后,总检测时间为40分钟,检测限在0.93至1.16μg/mL之间,具体取决于所使用的pH值。HA的检测上限可达400μg/mL,涵盖了从正常白蛋白尿到大量白蛋白尿的范围。对当地医院患有糖尿病肾病、I型和II型糖尿病以及慢性肾病患者的尿液样本进行分析,结果与标准尿人白蛋白检测方法吻合良好。