Method and apparatus for DNA purification

• US 20070197780A1
• Filed: 08/09/2006
• Published: 08/23/2007
• Est. Priority Date: 08/09/2005
• Status: Abandoned Application

• Current Assignee: Samsung Electronics Co. Ltd. (Samsung Group)
• Original Assignee: Samsung Electronics Co. Ltd. (Samsung Group)
• Inventors: Park, Jong, Peak, Sang, Yoo, Chang
• Application Number:
  US11/501,790
• Publication Number:
  US 20070197780A1
• Time in Patent Office: Days
• US Class Current: 536/25.4
• CPC Class Codes: C12N 15/1006 by means of a solid support carrier, e.g. particles, polymers

Abstract

A method and apparatus for DNA purification are provided which use a silicone structure having a Sio₂ layer formed on its surface. In the method, DNA is effectively purified from a fluid sample by maintaining the pH of the silicone structure'"'"'s surface to be lower than the pKa of silanol to make the surface of the silicone structure charged with hydroxyl groups which results in the binding of DNA present in the fluid sample, removing the residual fluid sample which fails to bind to the surface of the silicone structure, and altering the pH of the silicone structure'"'"'s surface to be higher than the pKa of silanol to separate the bound DNA from the surface of the silicone structure.

Claims

1. A method for DNA purification, which comprises:

contacting a silicone structure having a SiO₂ layer formed on a surface thereof with a fluid sample containing DNA, wherein the fluid sample has a pH lower than a pKa of silanol;

removing the fluid sample from the silicone structure; and

treating the silicone structure with a buffer having a higher pH than the pKa of silanol.

2. The method according to claim 1, which further comprises

pre-treating the surface of the silicone structure with a pH condition lower than the pKa of silanol.

3. The method according to claim 1, wherein the pH of the fluid sample ranges from 3 to 6.5.

4. The method according to claim 1, wherein the pH of the buffer ranges from 8 to 10.

5. The method according to claim 4, wherein the buffer is selected from the group consisting of phosphate, borate and carbonate.

6. The method according to claim 1, wherein the surface of the silicone structure is fabricated in a pillar type.

7. An apparatus for DNA purifications, which comprises:

a silicone structure having a SiO₂ layer formed on a surface of the silicone structure,

wherein the silicone structure comprises a definite space, an inlet for introducing a fluid into the definite space, and an outlet for discharging the fluid from the definite space;

a sample storage compartment for storing a fluid sample comprising DNA; and

a buffer storage compartment for storing a buffer having a higher pH than a pKa of silanol .

8. The apparatus according to claim 7, wherein an inner surface of the definite space of the silicone structure is fabricated in a pillar type.

9. The apparatus according to claim 7, which further comprises

a pre-treatment buffer storage compartment for storing a buffer to pre-treat the silicon structure.

10. The apparatus according to claim 7, which further comprises

an eluate storage compartment for storing an eluate which is discharged from the silicone structure through the outlet.

11. The apparatus according to claim 10, wherein the eluate storage compartment is connected to a DNA amplification part.

12. A lab-on-a-chip comprising the apparatus for DNA purification of claim 7.