Methods and articles for delivering viable cells into solid tissue
Abstract
Embodiments provide swallowable devices, preparations and methods for delivering viable cells (VC) into the GI tract including GI wall tissue or other tissue site. Particular embodiments provide a swallowable device such as a capsule for delivering VC into an intestinal wall or other site. The VC can be contained within a tissue-penetrating shell disposed in the capsule that protects the VC as they pass through the GI tract until they are inserted into GI tract tissue or other location. The shell desirably has shape, size and material consistency to be contained in a swallowable capsule, delivered from the capsule into solid tissue by the application of force on the shell and biodegrade within the solid tissue to release the VC into the tissue. Within the shell or other structure the VC can be maintained in a viability-sustaining gel that preserves the viability of the VC for selected time periods.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A method for producing a therapeutic effect in a patient, the method comprising:
swallowing an enclosure containing a tissue penetrating article which contains a mass of viable cells in a viability-sustaining gel, wherein the article passes through the gastrointestinal tract with the cells remaining viable; releasing the article from the enclosure in response to a condition in the gastrointestinal tract; and propelling the article to penetrate into gastro-intestinal tissue and releasing the cells or substances produced by the cells to produce the therapeutic effect in the patient.
3 . The method of claim 2 , wherein the therapeutic effect is glucose regulation.
4 . The method of claim 2 , wherein the therapeutic effect is a production of insulin within the patient's body.
5 . The method of claim 2 , wherein the therapeutic effect is a production of an incretin within the patient's body.
6 . The method of claim 2 , wherein the therapeutic effect is a production of gastrin within the patient's body.
7 . The method of claim 2 , wherein the therapeutic effect is an effect on the patient's immune system.
8 . The method of claim 2 , wherein the therapeutic effect is reseeding of a mucosa of the patient's small intestine, large intestine or stomach.
9 . The method of claim 2 , wherein the gastro-intestinal tissue is stomach wall tissue, intestinal wall tissue, small intestine wall tissue or peritoneal wall tissue.
10 . The method of claim 2 , wherein the condition is a pH or a pH in the small intestine.
11 . The method of claim 2 , wherein propelling the article comprises applying a propulsive force by expansion of an expandable member.
12 . The method of claim 11 , wherein the expandable member is expanded by a chemical reaction triggered in response to a pH in the small intestine or other location in the intestinal tract.
13 . The method of claim 2 , wherein the cells are in a suspended reanimatable state prior to being ingested by the patient.
14 . The method of claim 13 , wherein the cells are reanimated after ingestion of the enclosure by conditions in the intestinal tissue including at least one of temperature, blood supply or oxygen supply.
15 . The method of claim 13 , wherein the cells are frozen prior to being swallowed by the patient.
16 . The method of claim 2 , wherein the viability-sustaining gel is at least partially saturated with one of oxygen, nitrogen or other inert gas to preserve the viability of the cells.
17 . The method of claim 2 , wherein the viable cells are therapeutic cells, entero-endocrine cells, gastric enteroendocrine cells, or intestinal enteroendocrine cells.
18 . The method of claim 17 , wherein the viable cells are selected from a group consisting of pancreatic B-cells, L-cells, K-cells, G-cells, I-cells, immune cells, stem cells, mesenchymal stem cells, and hematopoietic stem cells.
19 . The method of claim 2 , wherein once delivered into intestinal tissue, the cells produce a therapeutic compound released within the body.
20 . The method of claim 19 , wherein the therapeutic compound comprises a glucose regulating compound, insulin, an incretin, or gastrin.
21 . The method of claim 19 , wherein at least a portion of the cells remain in the article while producing the therapeutic compound.Cited by (0)
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