Method and system for sample preparation
A disposable cartridge for preparing a nucleic acid sample including a stationary cartridge body and a cylindrical rotor rotationally mounted to the cartridge body. The cartridge body includes: (i) a cylindrical surface defining a fixed port and (ii) a syringe barrel defining a bore in fluid communication with the fixed port. When the disposable cartridge is disposed in combination with an assay system, syringe barrel is configured to receive a moveable plunger, i.e., to stroke the plunger into and out of the barrel. The rotor is seated within a cavity of the cartridge body such that a mating surface thereof slideably engages a cylindrical surface of the cavity. The rotor comprises a plurality of chambers fluidly connecting to a plurality of ports along the mating surface at different radial positions such that at least one of the chambers is fluidly connected to one of the ports by a connecting channel. Rotation of the rotor aligns one of the rotor ports with the fixed port such that fluid may be moved into and out of the chambers in response to axial displacement of the moveable plunger.
1. A system for preparing a nucleic acid sample comprising disposable cartridge and an actuation device operative to sequentially perform various assay tests, the disposable cartridge comprising:
a cartridge body having a cylindrical surface defining a fixed port and a syringe barrel defining a bore in fluid communication with the fixed port, the syringe barrel configured to receive a moveable plunger; and
a rotor having a mating surface slideably engaging the cylindrical surface of the cartridge body and rotatably mounting thereto, the rotor comprising:
a plurality of chambers fluidly connecting to a plurality of ports along the mating surface at different radial positions, at least one of the chambers fluidly connecting to one of the ports by a connecting channel;
wherein rotation of the rotor aligns one of the rotor ports with the fixed port such that fluid may be moved into and out of the chambers in response to axial displacement of the moveable plunger,
the actuation device comprising:
a cartridge drive for rotating the rotor; and
a plunger drive for connecting to and axially displacing the moveable plunger.
2. The system as recited in claim 1 , wherein the actuation device further comprises an identifying marker from the group of: a barcode label and a Radio Frequency IDentification (RFID) tag.
3. The system as recited in claim 1 , wherein the actuation device connects to a computer network to assay a biological sample.
4. The system as recited in claim 1 , wherein the actuation device further comprises a global positioning system.
5. The system as recited in claim 1 , wherein the actuation device further comprises a first heater and a second heater, the first heater being controlled independently relative to the second heater.
6. The system as recited in claim 5 wherein the first heater and the second heater are fixedly mounted proximate the rotor and wherein the rotor rotates as a function of the heaters upon actuation of the cartridge drive.
7. The system as recited in claim 1 , wherein the actuation device comprises a magnet fixedly mounted proximate the rotor and offset from a center thereof such that the rotor rotates as a function of the strength of the magnetic field upon actuation of the cartridge drive.
8. The system as recited in claim 1 , wherein the cartridge body includes an input port, and output port, reaction chamber disposed between the input and output ports and a signal processor disposed within the reaction chamber to detect the presence of a nucleic acid sequence.
9. The system as recited in claim 1 , wherein the actuation device is portable.
10. The system as recited in claim 1 , wherein the actuation device further comprises a sensor mount configured to receive a biological probe chip to detect the presence of a target analyte.
11. The system as recited in claim 10 , wherein the actuation device further comprises a microprocessor receiving input command signals from the chip to determine whether the target analyte is present.
12. The system as recited in claim 1 , wherein the actuation device further comprises a device producing ultrasonic vibrations to activate reactions in one or more of the plurality of chambers.