Devices and methods for detection and quantification of immunological proteins, pathogenic and microbial agents and cells
The present invention provides microfluidic pScreen™ devices for quantifying the concentration of DNA fragments in a liquid sample by using magnetic-responsive silica micro-beads and nonmagnetic-responsive silica micro-beads. The devices of the present invention allow for rapid, simple and inexpensive quantification of DNA fragment concentration in a sample. The devices do not require complex instrumentation and can be performed in less than three minutes. Moreover, they are compatible with complex samples including, without limitation, unpurified PCR amplification products, and thus can be expected to seamlessly integrate into various common molecular biology techniques and workflows.
1. A microfluid device for quantifying the concentration of DNA fragments, comprising:
a sample inlet defined by an opening for accepting a liquid sample;
a sealing layer positioned atop the microfluidic device;
a reaction chamber in continuous fluid connection with the sample inlet;
a micro-channel splitter in continuous fluid connection with the reaction chamber, said micro-channel bifurcating to form a calibration micro-channel and a test micro-channel;
a control graduated column in continuous fluid connection with the calibrated micro-channel;
a test graduated column in continuous fluid connection with the test-micro channel;
a venting hole located at the end of each of the graduated columns that is placed through the sealing layer; and
a magnetic field gradient adjacent to the test micro-channel.
2. The microfluid device of claim 1 , wherein the liquid sample containing a mixture of magnetic-responsive silica micro-beads, nonmagnetic-responsive silica micro-beads, a chaotropic buffer, and an aliquot of a DNA fragment sample is placed on the inlet of the microfluidic device.
3. The microfluid device of claim 2 , wherein the concentration of nonmagnetic-responsive silica micro-beads ranges from between 10 μg/μl and 60 μg/μ in the liquid sample.
4. The microfluid device of claim 2 , wherein the concentration of magnetic-responsive silica micro-beads ranges from between 1.0 μg/μl and 3.0 μg/μL in the liquid sample.
5. The microfluid device of claim 1 , wherein the presence of DNA fragments triggers the formation of large magnetic-responsive clusters, said magnetic-responsive clusters aggregating in proximity of the magnetic field gradient to produce a localized restriction, said restriction retarding flow of the liquid sample in the test graduated column.
6. The microfluid device of claim 1 , wherein the control graduated column and the test graduated column are connected to one another via a joining channel, and a venting hole located at the end of the control column is placed through the sealing layer to stop the flow in the test channel when the liquid flowing in the control column fills to a desired volume.