In Vitro Resistance-Predicting Studies and In Vitro Resistance-Related Parameters-A Hit-to-Lead Perspective

Despite the urgent need for new antibiotics, very few innovative antibiotics have recently entered clinics or clinical trials. To provide a constant supply of new drug candidates optimized in terms of their potential to select for resistance in natural settings, in vitro resistance-predicting studie...

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Main Authors: Joanna Krajewska (Author), Stefan Tyski (Author), Agnieszka E. Laudy (Author)
Format: Book
Published: MDPI AG, 2024-08-01T00:00:00Z.
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100 1 0 |a Joanna Krajewska  |e author 
700 1 0 |a Stefan Tyski  |e author 
700 1 0 |a Agnieszka E. Laudy  |e author 
245 0 0 |a In Vitro Resistance-Predicting Studies and In Vitro Resistance-Related Parameters-A Hit-to-Lead Perspective 
260 |b MDPI AG,   |c 2024-08-01T00:00:00Z. 
500 |a 10.3390/ph17081068 
500 |a 1424-8247 
520 |a Despite the urgent need for new antibiotics, very few innovative antibiotics have recently entered clinics or clinical trials. To provide a constant supply of new drug candidates optimized in terms of their potential to select for resistance in natural settings, in vitro resistance-predicting studies need to be improved and scaled up. In this review, the following in vitro parameters are presented: frequency of spontaneous mutant selection (FSMS), mutant prevention concentration (MPC), dominant mutant prevention concentration (MPC-D), inferior-mutant prevention concentration (MPC-F), and minimal selective concentration (MSC). The utility of various adaptive laboratory evolution (ALE) approaches (serial transfer, continuous culture, and evolution in spatiotemporal microenvironments) for comparing hits in terms of the level and time required for multistep resistance to emerge is discussed. We also consider how the hit-to-lead stage can benefit from high-throughput ALE setups based on robotic workstations, do-it-yourself (DIY) continuous cultivation systems, microbial evolution and growth arena (MEGA) plates, soft agar gradient evolution (SAGE) plates, microfluidic chips, or microdroplet technology. Finally, approaches for evaluating the fitness of in vitro-generated resistant mutants are presented. This review aims to draw attention to newly emerged ideas on how to improve the in vitro forecasting of the potential of compounds to select for resistance in natural settings. 
546 |a EN 
690 |a antimicrobial agents 
690 |a antimicrobial resistance 
690 |a resistance-related parameters 
690 |a mutant selection 
690 |a MPC 
690 |a hit-to-lead stage 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 17, Iss 8, p 1068 (2024) 
787 0 |n https://www.mdpi.com/1424-8247/17/8/1068 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/f94e359f7f984c04b45c05e7b79439a1  |z Connect to this object online.