Integrated system for processing microfluidic samples, and method of using same
US-2015328638-A1 · Nov 19, 2015 · US
US10364456B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10364456-B2 |
| Application number | US-201414506471-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2014 |
| Priority date | May 3, 2004 |
| Publication date | Jul 30, 2019 |
| Grant date | Jul 30, 2019 |
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Methods and systems for processing polynucleotides (e.g., DNA) are disclosed. A processing region includes one or more surfaces (e.g., particle surfaces) modified with ligands that retain polynucleotides under a first set of conditions (e.g., temperature and pH) and release the polynucleotides under a second set of conditions (e.g., higher temperature and/or more basic pH). The processing region can be used to, for example, concentrate polynucleotides of a sample and/or separate inhibitors of amplification reactions from the polynucleotides. Microfluidic devices with a processing region are disclosed.
Opening claim text (preview).
What is claimed is: 1. A method for processing polynucleotide-containing sample, the method comprising: retaining polynucleotides from a sample on a plurality of binding particles in a process chamber under a first set of conditions, wherein the retaining step comprises binding the polynucleotides to the surfaces of the plurality of binding particles comprising a poly-cationic substance, wherein the sample has a volume from 0.5 microliters to 3 milliliters; wherein the first set of conditions includes a first pH of about 8.5 or less and a first temperature, wherein the first temperature is about 50° C.; releasing the polynucleotide from the plurality of binding particles under a second set of conditions; and wherein the second set of conditions includes increasing the pH to a second pH by addition of a hydroxide solution and increasing the temperature to a second temperature, wherein the second temperature is between about 80° C. and about 100° C. 2. The method of claim 1 , wherein the second pH is about 11.3 or greater. 3. The method of claim 1 , wherein the poly-cationic substance is covalently bound to the surfaces of the binding particles. 4. The method of claim 1 , wherein the binding particles comprise one or more carboxylic groups to provide an attachment point for the poly-cationic substance. 5. The method of claim 1 , wherein the second temperature is between about 90° C. and about 100° C. 6. The method of claim 1 , wherein the heating step comprises heating the plurality of binding particles in the presence of a liquid, wherein the second temperature is insufficient to boil the liquid. 7. The method of claim 1 , further comprising maintaining the second temperature for between about 1 and 10 minutes. 8. The method of claim 1 , wherein the second temperature is maintained for between about 1 and 7 minutes. 9. The method of claim 1 , wherein the sample is heated for about 15 minutes or less while contacting the binding particles with the basic solution thereby releasing the polynucleotides. 10. The method of claim 1 , wherein the poly-cationic substance includes polyethyleneimine (PEI). 11. The method of claim 1 , wherein the poly-cationic substance has a molecular weight between 600-800 DA. 12. The method of claim 1 , wherein the ratio of the volume of original sample moved through the processing region to the volume of liquid into which the polynucleotides are released is at least about 10. 13. The method of claim 1 , wherein the particles occupy about 75 percent or less of the total volume of the process chamber. 14. A method for processing polynucleotide-containing samples, the method comprising: retaining one or more polynucleotides from a sample on a plurality of binding particles under a first set of conditions, wherein a surface of one or more binding particles is modified with a poly-cationic material, wherein the sample has a volume from 0.5 microliters to 3 milliliters; wherein the first set of conditions includes a first pH of 8.5 or less and a first temperature of about 50° C.; releasing the polynucleotide from the plurality of binding particles under a second set of conditions; and wherein the second set of conditions includes increasing the pH by at least three units by addition of a hydroxide solution and increasing the temperature by at least about 40° C. to a second temperature of at least about 90° C. 15. The method of claim 14 , wherein the pH of the second set of conditions is about 11.3 or greater. 16. The method of claim 14 , wherein the poly-cationic material includes polyethyleneimine (PEI). 17. The method of claim 14 , wherein the ratio of the volume of original sample moved through the processing region to the volume of liquid into which the polynucleotides are released is at least about 10. 18. A method for processing a polynucleotide-containing sample, the method comprising: contacting the sample with a plurality of binding particles, the binding particles retaining one or more polynucleotides thereon at a first pH and a first temperature, wherein the sample has a volume from 0.5 microliters to 3 milliliters, wherein the first temperature is about 50° C., wherein a surface of one or more binding particles is modified with a poly-cationic polyimide or polyethyleneimine (PEI); and contacting the binding particles with a basic hydroxide solution at a second pH and a second temperature, the second temperature greater than the first temperature, thereby releasing the polynucleotides from the plurality of binding particle, wherein the second temperature is between about 80° C. and about 100° C. 19. The method of claim 18 , wherein the first pH is about 8.5 or less. 20. The method of claim 18 , wherein the second pH is about 11.3 or greater.
operated by temperature variations · CPC title
using phase transition or influencing viscosity · CPC title
Polymerase chain reaction [PCR] · CPC title
by means of a solid support carrier, e.g. particles, polymers · CPC title
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