Microbiota restoration therapy (MRT), compositions and methods of manufacture
Microbiota restoration therapy compositions and methods for manufacturing, processing, and/or delivering microbiota restoration therapy compositions are disclosed. An example method for manufacturing a microbiota restoration therapy composition may include collecting a human fecal sample and adding a diluent to the human fecal sample to form a diluted sample. The diluent may include a cryoprotectant. The method may also include mixing the diluted sample with a mixing apparatus and filtering the diluted sample. Filtering may form a filtrate. The method may also include transferring the filtrate to a sample bag and sealing the sample bag.
1. A microbiota restoration therapy composition, comprising:
a suspension for administration to a patient via an enema, the suspension consisting of:
a liquid cryoprotectant, the cryoprotectant comprising polyethylene glycol in saline at a concentration of 30-90 g/L;
a fecal-derived bacteria population suspended in the liquid cryoprotectant, the fecal-derived bacteria population being derived from a filtered, fresh stool sample from a human donor; and
wherein a serial dilution of 10 −5 of the suspension has a colony forming unit (CFU) count of about 30 to about 300 CFU at when cultured on a Bacteroides Bile Esculin Agar (BBE) culture plate.
2. The microbiota restoration therapy composition of claim 1 , wherein the serial dilution has about 30 to about 300 CFU when cultured on a Center for Disease Control (CDC) culture plate.
3. The microbiota restoration therapy composition of claim 1 , wherein the microbiota restoration therapy composition includes bacteria from at least two orders and at least seven different families and has a Shannon Diversity Index of 0.4-2.5 when calculated at the family level, wherein in the range of 40-60% of the bacteria is from the order Bacteroidales, in the range of 30-40% of the bacteria is from the order Clostridiales, and in the range of 36-48% of the bacteria is from the family Bacteroidaceae.
4. The microbiota restoration therapy composition of claim 1 , wherein the fresh stool sample includes 45-75 grams of feces.
5. The microbiota restoration therapy composition of claim 1 , wherein the microbiota restoration therapy composition includes bacteria from at least seven different families.
6. The microbiota restoration therapy composition of claim 1 , wherein the microbiota restoration therapy composition has a Shannon Diversity Index of 0.4-2.5 when calculated at the family level.
7. A composition for treating a digestive disorder, comprising:
an enema bag;
a microbiota restoration composition disposed within the enema bag, the microbiota restoration composition being designed to be administered to a patient via an enema;
wherein the microbiota restoration composition comprises a suspension that includes a filtered, diluted, fresh human fecal sample; and
wherein the fresh human fecal sample is suspended in a solution comprising polyethylene glycol in saline at a concentration of 30-90 g/L; and
wherein a serial dilution of 10 −5 of the suspension has a colony forming unit (CFU) count of about 30 to about 300 CFU when cultured on a Bacteroides Bile Esculin Agar (BBE) culture plate.
8. The composition of claim 7 , wherein the fresh human fecal sample includes 45-75 grams of feces.
9. The composition of claim 7 , wherein the composition includes bacteria from at least seven different families.
10. The composition of claim 7 , wherein the composition has a Shannon Diversity Index of 0.4-2.5 when calculated at the family level.
11. A microbiota restoration composition designed for administration to a patient via an enema, the microbiota restoration therapy composition comprising:
a medicament comprising a suspension capable of being stored in either a liquid state or a frozen state, the medicament being formed by the process of:
collecting a fresh stool sample from a human donor;
adding a diluent to the fresh stool sample, the diluent including 30-90 g/L of polyethylene glycol in saline;
mixing the fresh stool sample and the diluent to form a mixed composition;
filtering the mixed composition and collecting the filtrate;
pre-cooling the filtrate and then freezing the filtrate in the enema bag; and
wherein a serial dilution of 10 −5 of the suspension has a colony forming unit (CFU) count of about 30 to about 300 CFU when cultured on a Bacteroides Bile Esculin Agar (BBE) culture plate.