Direct and Continuous Monitoring of Multicomponent Antibiotic Gentamicin in Blood at Single-Molecule Resolution
Changjian Zhao, Yu Wang, Chen Chen, Yibo Zhu, Zhuang Miao, Xingyu Mou, Weidan Yuan, Zhihao Zhang, Kaiju Li, Mutian Chen, Weibo Liang, Ming Zhang, Wenqian Miao, Yuhan Dong, Dong Deng, Jianping Wu, Bowen Ke, Rui Bao, Jia Geng
Abstract
Point-of-care monitoring of small molecules in biofluids is crucial for clinical diagnosis and treatment. However, the inherent low degree of recognition of small molecules and the complex composition of biofluids present significant obstacles for current detection technologies. Although nanopore sensing excels in the analysis of small molecules, the direct detection of small molecules in complex biofluids remains a challenge. In this study, we present a method for sensing the small molecule drug gentamicin in whole blood based on the mechanosensitive channel of small conductance in Pseudomonas aeruginosa ( Pa MscS) nanopore. Pa MscS can directly detect gentamicin and distinguish its main components with only a monomethyl difference. The ’molecular sieve’ structure of Pa MscS enables the direct measurement of gentamicin in human whole blood within 10 min. Furthermore, a continuous monitoring device constructed based on Pa MscS achieved continuous monitoring of gentamicin in live rats for approximately 2.5 h without blood consumption, while the drug components can be analyzed in situ. This approach enables rapid and convenient drug monitoring with single-molecule level resolution, which can significantly lower the threshold for drug concentration monitoring and promote more efficient drug use. Moreover, this work also lays the foundation for the future development of continuous monitoring technology with single-molecule level resolution in the living body.