4.7 Article

A specific Tween-80-Rhodamine S-MWNTs phosphorescent reagent for the detection of trace calcitonin

Journal

ANALYTICA CHIMICA ACTA
Volume 744, Issue -, Pages 60-67

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2012.07.017

Keywords

Calcitonin; Tween-80-Rhodamine S-multi-walled carbon nanotubes phosphorescent reagent; Solid substrate room temperature phosphorescence immunoassay; Prediction of human diseases

Funding

  1. Fujian Province Natural Science Foundation [2010J01053]
  2. Fujian Province Education Committee [JK2010035, JA10203, JA10277, JA11311]
  3. Fujian provincial bureau of quality and technical supervision [FJQI2011006]
  4. Scientific Research Program of Zhangzhou Institute of Technology Foundation [ZZY1101, ZZY1106, ZZY1014]

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The present study proposed a simple sensitive and specific immunoassay for the quantification of calcitonin (CT) in human serum with water-soluble multi-walled carbon nanotubes (MWNTs). The-COOH group of MWNTs could react with the -NH- group of rhodamine S (Rhod.S) molecules to form Rhod.S-MWNTs, which could emit room temperature phosphorescence (RTP) on acetate cellulose membrane (ACM) and react with Tween-80 to form micellar compound. Tween-80-Rhod.S-MWNTs (TRM), as a phosphorescent labelling reagent, could dramatically enhance the RTP signal of the system. The developed TRM phosphorescent reagent was used to label anti-calcitonin antibody (Ab(CT)) to form the TRM-Ab(CT) labelling product, which could take high specific immunoreaction with CT, and the Delta I-p (= I-p2 -I-p1, I-p2 and I-p1 were the phosphorescence intensity of the test solution and the blank sample, respectively) of the system was linear to the content of CT. Hence, a new solid substrate room temperature phosphorescence immunoassay (SSRTPIA) was established for the determination of CT in human serum. This sensitive (limit of quantification (LOQ) was 8.0 x 10(-14) g mL(-1)), accurate, selective and precise method has been applied to determine CT in human serum and predict primary osteoporosis and fractures, with the results in good agreement with those obtained by chemiluminescence immunoassay (CLIA). Simultaneously, the structure of MWNTs was characterized with scanning electron microscopy (SEM) and infrared spectroscopy (IR), and the reaction mechanisms of both labelling Ab(CT) with TRM and SSRTPIA for the determination of trace CT were discussed. (C) 2012 Elsevier B.V. All rights reserved.

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