초록 ▼

Fluid introduction is facilitated through the use of a port which extends entirely through a microfluidic substrate. Capillary forces can be used to retain the fluid within the port, and a series of samples or other fluids may be introduced through a single port by sequentially blowing the fluid out

Fluid introduction is facilitated through the use of a port which extends entirely through a microfluidic substrate. Capillary forces can be used to retain the fluid within the port, and a series of samples or other fluids may be introduced through a single port by sequentially blowing the fluid out through the substrate and replacing the removed fluid with an alternate fluid, or by displacing the fluid in part with additional fluid. In another aspect, microfluidic substrates have channels which varying in cross-sectional dimension so that capillary action spreads a fluid only within a limited portion of the channel network. In yet another aspect, the introduction ports may include a multiplicity of very small channels leading from the port to a fluid channel, so as to filter out particles or other contaminants which might otherwise block the channel at the junction between the channel and the introduction port.

대표청구항 ▼

1. A microfluidic device comprising: a substrate having a plurality of first microfluidic channels and at least one second microfluidic channel, said plurality of first channels being in fluid communication with the at least one second channel through a respective capillary limit region, the seco

1. A microfluidic device comprising: a substrate having a plurality of first microfluidic channels and at least one second microfluidic channel, said plurality of first channels being in fluid communication with the at least one second channel through a respective capillary limit region, the second channel including a first end and a second end, wherein the limit regions are disposed at an end of each respective first channel and intersect the second channel between its first and second ends; and the second channel having a cross-sectional dimension adjacent the limit regions which is larger than a cross-sectional dimension of each of the respective limit regions to inhibit wicking of fluid from the limit regions into the second channel, the first channels and the limit regions containing a polymer solution suitable for electrophoretic sample manipulation and the second channel containing a buffer fluid suitable for electroosmotic sample manipulation. 2. A microfluidic device as claimed in claim 1, wherein a minimum cross-sectional dimension of each of the limit regions is sufficiently smaller than a minimum cross-sectional dimension of the second channel such that differential capillary forces prevent fluid from wicking from the first channels through the limit regions and into the second channel when no fluid is present in the second channel. 3. A microfluidic device as claimed in claim 1, wherein the at least one second channel has at least one cross-sectional dimension of between about 0.5 and 100 microns. 4. A microfluidic device as claimed in claim 1, wherein the at least one second channel and the plurality of first channels each are about 70 microns wide and about 10 microns deep. 5. A microfluidic device as claimed in claim 1, wherein the limit regions each have a depth of about 2 microns.