Treatment of tissue adhesion

1. A method comprising:

reducing or preventing tissue adhesion formation between organs or between organs and other tissues in a subject after a surgical procedure, wherein the surgical procedure is selected from a group consisting of gynecological reproductive surgery, abdominal surgery, spinal and laparoscopic surgery, hepatic surgery, neurosurgical procedures and orthopedic procedures, by administering an effective amount of a dry powder composition comprising fibrinogen, thrombin and trehalose, or isomers or salts thereof, to exposed or separated tissues during the surgical procedure, wherein the dry powder composition contains about 0.5 to 20% w/w fibrinogen and about 25 to 1000 IU/g thrombin.

2. The method according to claim 1 , wherein the dry powder composition comprises a mixture of first microparticles that comprise fibrinogen and second microparticles that comprise thrombin.

3. The method according to claim 1 wherein the dry powder composition contains about 0.5 to 20% w/w fibrinogen and about 100 to 500 IU/g thrombin.

4. The method according to claim 1 wherein the trehalose, isomer or salt thereof is selected from or more of hydrated crystalline trehalose, anhydrous crystalline trehalose, anhydrous amorphous trehalose, α,α-trehalose, α,β-trehalose (neo-trehalose), β,β-trehalose (iso-trehalose), or a mixture thereof.

5. The method according to claim 1 , wherein the dry powder composition comprises a mixture of first microparticles that comprise fibrinogen and second microparticles that comprise thrombin, and wherein said first microparticles contain 0.5 to 20% w/w fibrinogen and wherein said second microparticles comprise 25 to 1000 IU/g thrombin.

6. The method as claimed in claim 1 , wherein the dry powder composition further comprises 0.001 to 95% w/w of additive material, by weight of the composition.

7. The method according to claim 6 , wherein the additive material comprises a biocompatible, water-absorbent material.

8. The method according to claim 6 , wherein the additive material comprises a biocompatible, water-swellable material.

9. The method according to claim 6 , wherein the additive material comprises a biocompatible, water-insoluble material.

10. The method according to claim 6 , wherein the additive material comprises a polysaccharide.

11. The method according to claim 6 , wherein the additive material has an average particle size of from about 10 nm to 1000 um.

12. The method as claimed in claim 11 , wherein the average particle size is from about 10 to 500 um.