Abstract:
Apparatus and a method for determining a quench-indicating parameter of a test sample utilizing a liquid scintillation counter are disclosed. The number of counts in a spectrum resulting from subtraction of a spectrum generated without an external source of radiation from a spectrum generated with an external source of radiation is utilized. The total number of counts is cumulatively summed from a higher energy level to a lower energy level and a curve representing this sum is generated. A portion of this curve is fitted with a function such as a straight line and the intersection of that function with the zero count axis is the intersection energy level which is an indication of the measure of quench of the test sample.
Abstract:
A method of concentrating and measuring the amount of cells in a sample is described. A-sample containing the plurality of cells is passed upwardly or laterally through a series of membrane filters and concentrated on the filter. The filter membrane containing the concentrated cell is then sequentially treated with lysing agent to release the adenosine triphosphate from the organism and a luminescent reagent to react with the released adenosine triphosphate. A luminescent response is thereby produced directly on the filter membrane and this luminescent response is measured with a luminometer. Not only does this method provide an accurate way of detecting very minute quantities of cells but it provides a relatively quick and easy method of concentrating and measuring cells in large volumes of biological or industrial samples which contain low levels of organisms. This method can also be used to identify and measure sources of adenosine triphosphate. Another aspect of the disclosed method is the utilization of a series of filters, each of which traps and concentrates cells of different size. For example, a sample containing a plurality of cell types can be passed through a series of filter membranes, with different pore size each of which allows passage of all but one unicellular organism, resulting in a concentration of different cells on different filter membranes. The filter membranes can then be processed and measured on the luminometer as described above.
Abstract:
A method and apparatus for preventing or limiting damage to capillaries used to dispense microdrops measures the voltage produced by a piezoelectric transducer when the capillary contacts a solid surface or the phase shift occurring when the piezoelectric transducer is operated at its resonant frequency. After distinguishing the voltage created from such contact from the voltage produced from unrelated random sources, corrective action is taken, in one aspect by stopping the relative movement of the capillary and the surface being contacted. The method and apparatus may also be employed to determine the position of a solid or liquid surface.
Abstract:
A system for dispensing precise quantities of a transfer liquid (24) is described. The system comprises an enclosed space (214, 234, 235) containing a fluid column, the fluid column including the transfer liquid (24) and a system liquid (20). The enclosed space has an outlet (36) and the column is arranged with the transfer liquid (24) being adjacent to the outlet (63) and the system liquid (20) being distant to the outlet (63). Means (218) are provided for supplying the system liquid (20) into the fluid column (24, 20); and means are present for providing the transfer liquid (24) into the enclosed space (214, 234, 236). The system further includes means (212) for dispensing a quantity of the transfer liquid (24) as at least one droplet out of the outlet (63) without introducing any fluid into the enclosed space (214, 234, 236) during dispensing, means (244) for sensing pressure change in the enclosed space resulting from the volume of the transfer liquid being dispensed and means (224) for converting the pressure change to a volume of the transfer liquid (24) dispensed by the dispensing means (212), wherein ejection of individual drops of the transfer liquid (24) can be detected by the means for sensing pressure change (244).
Abstract:
A microvolume liquid handling system includes a microdispenser employing a piezoelectric transducer attached to a glass capillary, a positive displacement pump for priming and aspirating transfer liquid into the microdispenser, controlling the pressure of the liquid system, and washing the microdispenser between liquid transfers, and a pressure sensor to measure the liquid system pressure and produce a corresponding electrical signal. The pressure signal is used to verify and quantify the microvolume of transfer liquid dispensed and is used to perform automated calibration and diagnostics on the microdispenser. In another embodiment of the microvolume liquid handling system, a system reservoir is connected with tubing to a pressure control system for controlling the liquid system pressure in the system reservoir. The system reservoir is coupled to one or more microdispensers through a distribution tube having a branched section for each microdispenser. In this embodiment, each microdispenser is coupled to its own flow sensor and to enable a system controller to respectively measure and control the flow of liquid in the each microdispenser. Dispensing of a single sub-nanoliter drop can be detected in real time. As the result of dispensing the liquid in sub-nanoliter droplets, the dispensed volume can be precisely controlled. The dispenser automatically detects the liquid surface of the transfer liquid, automatically aspirate, analyze desired volume of the transfer liquid, dispense the transfer liquid without contacting the destination vessel or its contents, and automatically wash off the transfer liquid from dispensing system after each transfer. This system is capable of automatically sensing liquid surfaces, aspirating liquid to be transferred, and then dispensing small quantities of liquid with high accuracy, speed and precision. The system is pulsated at high frequency to prevent or eliminate clogging. Immiscible liquid between the transfer liquid and the system liquid reduces the required amount of transfer liquid needed for dispensing.
Abstract:
A universal microplate analyzer capable of carrying out measurements on samples contained in the wells of microplates (42) by fluorescence, absorbance, luminescence employs at least two light sources (32a, 32b) and optical fiber channels (34a-c) for directing excitation light to the sample wells. Flexibility of operation is provided by arrays of mirrors (22a-c), apertures (44, 56, 58), and polarizers (48) which can be positioned as required for the analysis to be carried out.
Abstract:
A system for imaging radiation emitted by assay couples into a photoelectric detector, the system including a fibre optic bundle (100) for conveying light to the detector, wherein a microlens (118), preferably a drum lens, is located at the impact end of the fibre optic bundle to match the field of view of the bundle to a potential area of interest in a sample.