Abstract:
A system and process is disclosed for measuring a fluorophore in a sample, such as a sample of a biological material. The process and system is particularly well suited to measuring fluorescent lifetimes of many different biological parameters. The system includes a time-of-flight sensor that can operate at a modulation rate capable of measuring fluorescent lifetimes that are extremely short, such as lasting only a few nanoseconds. Although the system and process have broad applicability, the system and process are particularly well suited for measuring metabolic characteristics of cells, such as pH, oxygen, and temperature.
Abstract:
A system for performing optical spectroscopy measurements includes a light source for generating an input optical beam and an interferometer. The interferometer includes a beam splitter that splits the input optical beam into first and second light beams; a first light path that directs the first light beam through a sample containing an analyte to a first output port; and a second light path that directs the second light beam to the first output port. At least one of the first and second light paths adjusts a relative phase of a corresponding one of the first and second light beams, so that the first and second light beams are out of phase at the first output port, substantially canceling background light and outputting sample light corresponding to a portion of the first light signal absorbed by the sample in the sample cell. A detection system detects the output sample light.
Abstract:
A system for performing optical spectroscopy measurements includes a light source for generating an input optical beam and an interferometer. The interferometer includes a beam splitter that splits the input optical beam into first and second light beams; a first light path that directs the first light beam through a sample containing an analyte to a first output port; and a second light path that directs the second light beam to the first output port. At least one of the first and second light paths adjusts a relative phase of a corresponding one of the first and second light beams, so that the first and second light beams are out of phase at the first output port, substantially canceling background light and outputting sample light corresponding to a portion of the first light signal absorbed by the sample in the sample cell. A detection system detects the output sample light.