In this communication, a laminated, flexible, microfluidic-integrated, all CNT based liquid-gated transistor and biosensor are reported that comprises single walled CNTs for both the semiconducting channel as well as the contact electrodes. The proposed architecture eliminates the need for lithography, electrode definition processes, and also circumvents substrate surface compatibility issues. Real-time detection of 1 pM poly-L-lysine in a liquid-gated transistor comprising only two materials, single walled CNTs and polydimethoxysilane substrate with microfluidic channel, is demonstrated.
The successful discovery and subsequent development of small molecule inhibitors of drug targets relies on the establishment of robust, cost-effective, quantitative, and physiologically relevant in vitro assays that can support prolonged screening and optimization campaigns. The current study illustrates the process of developing and validating an enzymatic assay for the discovery of small molecule inhibitors using alkaline phosphatase from bovine intestine as model target. The assay development workflow includes an initial phase of optimization of assay materials, reagents, and conditions, continues with a process of miniaturization and automation, and concludes with validation by quantitative measurement of assay performance and signal variability. The assay is further evaluated for dose–response and mechanism-of-action studies required to support structure–activity-relationship studies. Emphasis is placed on the most critical aspects of assay optimization and other relevant considerations, including the technology, assay materials, buffer constituents, reaction conditions, liquid handling equipment, analytical instrumentation, and quantitative assessments. Examples of bottlenecks encountered during assay development and strategies to address them are provided.
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