摘要
We present a novel method to analyze clenbuterol based on a competitive microfluidic immunoassay scheme with a micro-ELISA system, and obtain a limit of detection that is less than 0.1 ng ml with a quantitative working range of 0.1 ng ml to 27.0 ng ml . The approach was envisaged to be a promising method for efficient onsite clenbuterol control with good sensitivity and portability. This journal is