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Quantitative analysis of chloramphenicol residues in shrimp muscle tissues by Chemiluminescent enzyme immunoassay

Author

Listed:
  • Xu Chuanlai

    (School of Food Science and Technology, Southern Yangtze University, Wuxi, Jiangsu Province, People's Republic ofChina)

  • Peng Cifang

    (School of Food Science and Technology, Southern Yangtze University, Wuxi, Jiangsu Province, People's Republic ofChina)

  • Hao Kai

    (School of Food Science and Technology, Southern Yangtze University, Wuxi, Jiangsu Province, People's Republic ofChina)

  • Jin Zhengyu

    (School of Food Science and Technology, Southern Yangtze University, Wuxi, Jiangsu Province, People's Republic ofChina)

  • Wang Wukang

    (School of Food Science and Technology, Southern Yangtze University, Wuxi, Jiangsu Province, People's Republic ofChina)

Abstract

A competitive indirect chemiluminescent enzyme immunoassay (ic-CLEIA) has been developed for the determination of chloramphenicol (CAP) residues in shrimp. After the optimisation of four physico-chemical parameters, i.e. incubation time, concentration of Tween-20, concentration of PBS and its pH, the method developed gave a limit of detection of 0.01 ng/ml and a detection range from 0.03 ng/ml to 23.7 ng/ml, with an ED50 of 0.47 ng/ml. The developed method has been validated on spiked shrimp samples in terms of precision (intra- and interassay coefficient variations of less than 10% and 15%, respectively), and of accuracy (mean recovery from 95% to 123%). All these parameters being better than those of the ELISA method which is widely used to detect chloramphenicol, it may be suggested that the CLEIA method can be used to detect aquatic samples instead of ELISA.

Suggested Citation

  • Xu Chuanlai & Peng Cifang & Hao Kai & Jin Zhengyu & Wang Wukang, 2005. "Quantitative analysis of chloramphenicol residues in shrimp muscle tissues by Chemiluminescent enzyme immunoassay," Czech Journal of Food Sciences, Czech Academy of Agricultural Sciences, vol. 23(6), pages 251-256.
    • Handle: RePEc:caa:jnlcjf:v:23:y:2005:i:6:id:3399-cjfs
    DOI: 10.17221/3399-CJFS
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