Methods for treatment or prevention of damage resulting from radiation, trauma or shock
Described herein are methods of treating a subject that has been or will be exposed to radiation, trauma or shock, the method comprising identifying a subject that has been or will be exposed to radiation, and treating the subject with a compound that treats, reduces the severity or delays the onset of sepsis or reduces the likelihood of mortality in a subject upon administration of a therapeutically effective amount the compound to the subject.
1. A method of treating gastrointestinal (GI) damage in a human subject identified as having been exposed to radiation—wherein the gastrointestinal tract (GI) damage is related to the exposure to radiation, the method comprising orally administering 1 to 50 mg/kg of a compound to the subject,
wherein the compound is a compound of Formula (I):
wherein:
n is an integer between 20 and 6000; and
each R 1 is independently selected for each occurrence from hydrogen, acetyl,
wherein at least 25% of R 1 substituents are H, at least 1% of R 1 substituents are acetyl, and at least 2% of R 1 substituents are
wherein the method decreases loss of crypts and epithelium in the GI tract relative to a subject not administered with the compound, thereby treating the subject.
2. The method of claim 1 , wherein the method reduces the rate of mortality related to sepsis relative to a subject not administered with the compound.
3. The method of claim 2 , wherein the sepsis is caused by leaky gut.
4. The method of claim 1 , wherein the subject is at risk of developing sepsis as a result of exposure to radiation.
5. The method of claim 1 , wherein the method results in a decrease in the likelihood of developing leaky gut in the subject.
6. The method of claim 1 , wherein the method reduces inflammation in the subject from the radiation.
7. The method of claim 1 , wherein the method mitigates the inflammatory response in the GI tract.
8. The method of claim 1 , wherein the method protects epithelial cells from bacterial invasion.
9. The method of claim 1 , wherein the method reduces mortality after exposure of the GI tract of a subject to ionizing radiation relative to a subject not administered with the compound.
10. The method of claim 1 , wherein the radiation is from a dirty bomb, accidental nuclear incident or therapeutic radiation not related to the treatment of cancer.
11. The method of claim 1 , wherein the source of radiation is targeted to therapeutic treatment requiring destruction of the immune system.
12. The method of claim 1 , wherein the subject has or is at risk of hypotension as a physical manifestation of radiation.
13. The method of claim 1 , wherein the subject has suffered reperfusion injury.
14. The method of claim 1 , wherein the subject has or is at risk of having reduced nutrient absorption, pain, nausea, diarrhea, and/or weight loss resulting from radiation.
15. The method of claim 1 , wherein the method reduces local inflammation.
16. The method of claim 1 , wherein the method reduces systemic inflammation.
17. The method of claim 1 , wherein the method reduces pain and suffering in the subject.
18. The method of claim 1 , wherein the compound is administered at regular intervals.
19. The method of claim 1 , wherein the subject is treated for up to 3 weeks.
20. The method of claim 1 , wherein the subject is treated within 1 hour, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 10 hours, 12 hours, 16 hours, 20 hours, 24 hours, 2 days, 3 days, 4 days, 5 days, 6 days, 1 week, or 2 weeks after exposure to radiation, trauma, shock, or infection.
21. The method of claim 1 , wherein the derivatized chitosan is functionalized at between 18% and 30%.
22. The method of claim 1 , wherein the molecular weight of the derivatized chitosan is from 50 to 150 kDa.
23. The method of claim 1 , wherein the polydispersity index of the derivatized chitosan is from 1.0 to 2.5.
24. The method of claim 1 , wherein the compound is provided in a dosage to provide up to 50 mg/kg.
25. The method of claim 1 , wherein the compound is administered from about 1 to about 3 times per day.
26. The method of claim 1 , wherein subject is treated for up to 3 weeks, 2 weeks, 1 week, 6 days, 5 days, 4 days, 3 days, 2 days, or 1 day.
27. The method of claim 1 , wherein the compound is administered 1, 2, or 3 or more times every 1, 2, 3, 4, 5, or 6 days.
28. The method of claim 1 , wherein the compound is administered from about 1 to about 5 times per day.