IP Library Patent Application 11008577
Patent Application
App. No. 11/008,577

Targeting damaged lung tissue using compositions

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/008,577
Abstract

The present invention relates to methods and compositions for targeting damaged lung tissue. Compositions provided feature a targeting moiety coupled to one or more other moieties, including, for example, a cross-linkable moiety, an imaging moiety, and/or one or more other targeting moieties. The methods and compositions of the invention find use, for example, in detecting and treating a pulmonary condition such as emphysema.

Claims (39)

1 . A composition comprising a cross-linkable moiety and a targeting moiety wherein said moieties are coupled and wherein said targeting moiety targets damaged lung tissue.

2 . The composition as recited in claim 1 wherein lung tissue comprises epithelial lining fluid.

3 . The composition as recited in claim 1 wherein said composition does not comprise a polysaccharide or a carbohydrate moiety.

4 . The composition as recited in claim 1 wherein said composition does not comprise a mutant plasminogen activator-inhibitor type 1.

5 . The composition as recited in claim 1 wherein said targeting moiety targets a damage-correlated moiety.

6 . The method as recited in claim 5 wherein said damage-correlated moiety comprises a cell surface marker.

7 . The method as recited in claim 5 wherein said damage-correlated moiety comprises an ECM component.

8 . The composition as recited in claim 1 wherein said targeting moiety targets elastase.

9 . The composition as recited in claim 1 wherein said targeting moiety targets neutrophil elastase.

10 . The composition as recited in claim 1 wherein said targeting moiety comprises a protease inhibitor moiety.

11 . The composition as recited in claim 1 wherein said targeting moiety comprises an alpha-1 antitrypsin moiety.

12 . The composition as recited in claim 11 wherein said alpha-1 antitrypsin moiety is a recombinant alpha-1 antitrypsin moiety.

13 . The composition as recited in claim 1 wherein said targeting moiety comprises an elafin moiety.

14 . The composition as recited in claim 13 wherein said elafin moiety is a recombinant elafin moiety

15 . The composition as recited in claim 1 wherein said targeting moiety comprises a serpin moiety.

16 . The composition as recited in claim 15 wherein said serpin moiety is a recombinant serpin moiety

17 . The composition as recited in claim 15 wherein said serpin moiety is a secretory leukoprotease inhibitor (SLP1) moiety.

18 . The composition as recited in claim 17 wherein said secretory leukoprotease inhibitor (SLP1) moiety is a recombinant secretory leukoprotease inhibitor (SLP1) moiety.

19 . The composition as recited in claim 1 wherein said targeting moiety targets at least one matrix metalloproteinase selected from MMP-1, MMP-2, MMP-3, MMP-4, MMP-5, MMP-6, MMP-7, MMP-8, and MMP-9.

20 . The composition as recited in claim 19 wherein said composition does not comprise a hyaluronic acid or a salt thereof.

21 . The composition as recited in claim 1 wherein said targeting moiety targets desmosine and/or isodesmosine.

22 . The composition as recited in claim 1 wherein said targeting moiety targets CD8 and/or CD4.

23 . The composition as recited in claim 1 wherein said targeting moiety targets a smoke-related moiety.

24 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises a hydroxyl group.

25 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises a carboxyl group.

26 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises an ester group.

27 . The method as recited in claim 1 wherein said cross-linkable moiety comprises a cyano group.

28 . The method as recited in claim 1 wherein said cross-linkable moiety comprises a thiol group.

29 . The method as recited in claim 1 wherein said cross-linkable moiety comprises a cysteine group.

30 . The method as recited in claim 1 wherein said cross-linkable moiety comprises a carbonyl group.

31 . The method as recited in claim 1 wherein said cross-linkable moiety comprises an aldehyde group.

32 . The method as recited in claim 1 wherein said cross-linkable moiety comprises a ketone group.

33 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises a primary amine group and/or a secondary amine group.

34 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises a lysine group.

35 . The composition as recited in claim 1 wherein said cross-linkable moiety comprises a fibrinogen and/or a fibrin.

36 . The composition as recited in claim 1 wherein said composition is less than 10 microns.

37 . The composition as recited in claim 1 wherein said composition is less than 5 microns.

38 . The composition as recited in claim 1 wherein said composition is less than 1 micron.

39 . The composition as recited in claim 1 wherein said composition further comprises an imaging moiety coupled to said targeting moiety and/or to said cross-linkable moiety.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2005
From: GONG, GLEN; DIECK, RONALD
To: PNEUMRX, INC.
Reel/Frame 016385/0147 →