Compositions for fecal floral transplantation and methods for making and using them and devices for delivering them
In alternative embodiments, the invention provides compositions, e.g., formulations, used for gastric, gastrointestinal and/or colonic treatments or lavage, e.g., orthostatic lavage, e.g., for inducing the purgation (e.g., cleansing) of a gastrointestinal (GI) tract, including a colon; and methods for making and using them. In alternative embodiments, compositions and methods of the invention are used for the stabilization, amelioration, treatment and/or prevention of constipation, for the treatment of abdominal pain, particularly non-specific abdominal pain, and diarrhea, including diarrhea caused by a drug side effect, a psychological condition, a disease or a condition such as Crohn's Disease, a poison, a toxin or an infection, e.g., a toxin-mediated traveler's diarrhea, or C. difficile or the pseudo-membranous colitis associated with this infection. In alternative embodiments, the invention provides pharmaceuticals and products (articles) of manufacture for delivering these compositions and formulations to an individual, e.g., a human or an animal. The invention also provides devices for delivering a fecal material to a patient.
1. A pharmaceutical composition formulated as an acid-resistant capsule, wherein the pharmaceutical composition comprises a mixture of (a) a non-selected fecal microbiota of a stool, or portion of a stool, of a human donor and (b) a cultured bacterial strain.
2. The pharmaceutical composition of claim 1 , wherein the cultured bacterial strain comprise a member of the phylum Firmicutes.
3. The pharmaceutical composition of claim 1 , wherein the cultured bacterial strain comprises a member of the genus Bacteroides.
4. The pharmaceutical composition of claim 1 , wherein the non-selected fecal microbiota is derived from a healthy human donor.
5. The pharmaceutical composition of claim 4 , wherein the non-selected fecal microbiota is mixed with fiber from the stool or portion of the stool.
6. The pharmaceutical composition of claim 4 , wherein the non-selected fecal microbiota comprises an entire microbiota of the stool or portion of the stool.
7. The pharmaceutical composition of claim 1 , wherein the cultured bacterial strain is derived from a healthy human donor.
8. The pharmaceutical composition of claim 1 , wherein the composition comprises multiple cultured bacterial strains.
9. The pharmaceutical composition of claim 1 , wherein the cultured bacterial strain comprises anaerobic bacteria.
10. The pharmaceutical composition of claim 1 , for use in treating autism in a subject in need thereof.
11. The pharmaceutical composition of claim 1 , wherein the composition further comprises an antioxidant.
12. The pharmaceutical composition of claim 1 , wherein at least one of the non-selected fecal microbiota and the cultured bacterial strain is lyophilized.
13. The pharmaceutical composition of claim 1 , wherein the non-selected fecal microbiota and the cultured bacterial strain are from different sources.
14. A method for manufacturing a pharmaceutical composition, the method comprising
mixing a cultured bacterial strain with a non-selected fecal microbiota of a stool, or portion of a stool; and formulating the resulting mixture as an acid-resistant capsule,
thereby producing the pharmaceutical composition from the mixture.
15. The method of claim 14 , further comprising culturing the cultured bacterial strain prior to the mixing.
16. The method of claim 14 , wherein the cultured bacterial strain is lyophilized.
17. The method of claim 14 , wherein the human donor is a healthy human donor.
18. The method of claim 14 , further comprising mixing a stabilizing agent with the cultured bacterial strain and the non-selected fecal microbiota.
19. The method of claim 14 , further comprising providing the pharmaceutical composition to a subject in need thereof having autism.
20. The method of claim 14 , wherein the non-selected fecal microbiota and the cultured bacterial strain are from different sources.