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Detection of serum CC16 by a rapid and ultrasensitive magnetic chemiluminescence immunoassay for lung disease diagnosis.
Duan, Kaili; Xiang, Yu; Deng, Yilong; Chen, Junman; Liu, Ping.
Afiliación
  • Duan K; Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), 12550 College of Laboratory Medicine, Chongqing Medical University , Chongqing, China.
  • Xiang Y; Department of Laboratory Medicine, 12550 The First Affiliated Hospital of Chongqing Medical University , Chongqing, China.
  • Deng Y; Bioscience (Tianjin) Diagnostic Technology Co., Ltd, Tianjin, China.
  • Chen J; Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), 12550 College of Laboratory Medicine, Chongqing Medical University , Chongqing, China.
  • Liu P; Key Laboratory of Clinical Laboratory Diagnostics (Ministry of Education), 12550 College of Laboratory Medicine, Chongqing Medical University , Chongqing, China.
Clin Chem Lab Med ; 2024 Jul 30.
Article en En | MEDLINE | ID: mdl-39072498
ABSTRACT

OBJECTIVES:

It has been reported that serum Clara cell secreted protein 16 (CC16) is a potential biomarker for lung injury diseases, but currently, there is no other method that is faster, more accurate, or more sensitive being applied in clinical practice apart from ELISA. The current study was designed to established a magnetic nanoparticles chemiluminescence immunoassay (MNPs-CLIA) for highly sensitive automated detection of serum Clara cell secretory protein 16 (CC16), and validated its diagnostic performance for lung disease.

METHODS:

The study included the expression of CC16 recombinant protein, the preparation and screening of its monoclonal antibody (MAb), as well as the construction, optimization and analytical evaluation of the MNPs-CLIA method. The clinical application value of this method was investigated by detecting CC16 level in 296 serum samples.

RESULTS:

The linear range of the MNPs-CLIA assay system was 0.2-50 ng/mL, and the limit of detection was 0.037 ng/mL. Performance parameters such as specificity, recovery rate, and precision can meet the industry standards of in vitro diagnostic reagents. The established method reveals consistent results with ELISA (R2=0.9962) currently used clinically, and it also exhibits satisfactory diagnostic efficacy of silicosis, chronic obstructive pulmonary disease (COPD), and pulmonary sarcoidosis, with areas under the curve (AUC) of 0.9748, 0.8428 and 0.9128, respectively.

CONCLUSIONS:

Our established MNPs-CLIA method has the advantages of automation, high throughput, rapidity, and simplicity, and can be promoted for widely popularized in clinical applications. MNPs-CLIA detection of serum CC16 has efficient diagnostic potentiality for predicting and diagnosing lung diseases.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Chem Lab Med Asunto de la revista: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Clin Chem Lab Med Asunto de la revista: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2024 Tipo del documento: Article País de afiliación: China