Publication | Closed Access
Liquid Crystal Emulsions as the Basis of Biological Sensors for the Optical Detection of Bacteria and Viruses
283
Citations
33
References
2009
Year
EngineeringMicrobial PathogensPathogen DetectionOptical DetectionAnalytical MicrosystemsBacteriophageMicrobial VirusBacterial PathogensMonodisperse Liquid CrystalBiosensing SystemsBioanalysisAnalytical ChemistryMicrofluidicsBiophysicsFoodborne PathogensProkaryotic VirusBiophotonicsOptical SensorsLipid‐enveloped VirusesLab-on-a-chipLipid MoleculeBiological SensorsMicrobiologyLiquid Crystal EmulsionsMedicineOptical Sensor
Abstract A versatile sensing method based on monodisperse liquid crystal (LC) emulsion droplets detects and distinguishes between different types of bacteria (Gram +ve and −ve) and viruses (enveloped and non‐enveloped). LCs of 4‐cyano‐4'‐pentylbiphenyl transition from a bipolar to radial configuration when in contact with Gram −ve bacteria ( E. coli ) and lipid‐enveloped viruses ( A/NWS/Tokyo/67 ). This transition is consistent with the transfer of lipid from the organisms to the interfaces of the micrometer‐sized LC droplets. In contrast, a transition to the radial configuration is not observed in the presence of Gram +ve bacteria ( Bacillus subtilis and Micrococcus luteus ) and non‐enveloped viruses ( M13 helper phage ). The LC droplets can detect small numbers of E. coli bacteria (1–5) and low concentrations (10 4 pfu mL −1 ) of A/NWS/Tokyo/67 virus. Monodisperse LC emulsions incubated with phosholipid liposomes (similar to the E. coli cell wall lipid) reveal that the orientational change is triggered at an area per lipid molecule of ∼46 Å 2 on an LC droplet (∼1.6 × 10 8 lipid molecules per droplet). This approach represents a novel means to sense and differentiate between types of bacteria and viruses based on their cell‐wall/envelope structure, paving the way for the development of a new class of LC microdroplet‐based biological sensors.
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