IP Library Granted Patent US 7,307,103
Granted Patent B2
US 7,307,103 · App. 10/641,687 · Granted Dec 11, 2007

Sodium dodecyl sulfate compositions for inactivating prions

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 7,307,103
App. No.
10/641,687
Granted
Dec 11, 2007
Kind
B2
Abstract

An antiseptic composition useful in destroying the infectivity of infectious proteins such as prions is disclosed. The antiseptic composition is preferably maintained at either a low pH of 4.0 or less or a high pH of 10.0 or more either of which allows for an environment under which the active component (which is preferably sodium dodecyl sulfate) destroys infectivity. The composition may be added to blood, blood products, collagen, tissues and organs prior to transplantation. The composition also may be added to livestock feed to denature any prions in the livestock. Methods of denaturing infectious proteins are also disclosed which method can use but do not require higher temperatures and long period of exposure.

Claims (17)

1. A method of rendering infectious prions non-infectious, comprising the steps of:

contacting infectious prions with a formulation comprising about 1% or more sodium dodecyl sulfate; and

maintaining the formulation at a pH in a range of from about 2.5 to about 4.5 and at a temperature in a range of from about 15° C. to about 140° C. so as to render the infectious prions completely non-infectious in two hours or less.

2. The method of claim 1 , wherein the acid is chosen from peracetic acid and acetic acid.

3. The method of claim 1 , wherein the formulation further comprises a solvent chosen from water, ethanol and methanol.

4. The method of claim 1 , wherein the infectious prion are present in livestock feed.

5. The method of claim 1 wherein the temperature is in a range of about 40° C. or less.

6. The method of claim 1 , wherein the prions are rendered completely non-infectious in one hour or less.

7. The method of claim 1 , wherein the pH is maintained by an acid present in about 1% to 20% by weight based on total weight of the formulation.

8. The method of claim 1 , wherein the sodium dodecyl sulfate is present in about 1% to 20% by weight based on total weight of the formulation.

9. The method of claim 1 , wherein the pH is maintained at about 3.4%.

10. The method as claimed in claim 1 , wherein the prions are rendered completely non-infectious in about 5 minutes or less at about 37° C.

11. The method as claimed in claim 1 , wherein the formulation is maintained at a pH of about 3.6 and the prions are rendered completely non-infectious in about 15 minutes at a temperature of about 15° C.

12. A method of rendering infectious prions non-infectious, comprising the steps of:

contacting infectious prions xvith a formulation comprising about 1% or more of a salt of an alkyl sulfate; and

maintaining the formulation at a pH in a range of from about 2.5 to about 4.5 and at a temperature in a range of from about 15° C. to about 140° C. so as to render the infectious prions completely non-infectious in two hours or less.

13. The method of claim 12 , wherein the salt of alkyl sulfate is a salt of a cation chosen from sodium, calcium and magnesium.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 24, 2016
From: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
To: NIH-DEITR
Reel/Frame 039528/0634 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 14, 2003
From: PRUSINER, STANLEY B.; SUPATTAPONE, SURACHAI
To: REGENTS OF THE UNIVERSITY OF CALIFORNIA, THE
Reel/Frame 014404/0006 →
Continuity (11)
Continuation 1005622200 · Jan 22, 2002
Continuation In Part 0990417800 · Jul 11, 2001
Continuation In Part 0969928400 · Oct 26, 2000
Continuation In Part 0949481400 · Jan 31, 2000
Continuation In Part 0944745600 · Nov 22, 1999
Continuation In Part 0932290300 · Jun 1, 1999
Continuation In Part 0923537200 · Jan 20, 1999
Continuation In Part 0915105700 · Sep 10, 1998
Continuation In Part 0902695700 · Feb 20, 1998
Continuation In Part 0880453600 · Feb 21, 1997
Related Publication 20040052833A1 · Mar 18, 2004