Use Of Medulliadrenal Chromaffin Cells Or Peptide Functional Cells
AssigneeYilong Xue
InventorsYilong Xue, Guanghua Liu
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Abstract
The present invention relates to new use of medulliadrenal chromaffin cells or opioid-peptidergic cells, in particular to their use for treating and/or relieving withdrawal syndrome resulting from drug addiction or drug abuse.
Claims9
Use of medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering in the manufacture of a product for treating and/or relieving withdrawl syndrome resulting from drug addiction or abuse.
A method for treating and/or relieving withdrawl syndrome resulting from drug addiction or abuse, comprising administering by injection to a drug addict or abuser medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering.
A product for treating or relieving withdrawl syndrome, comprising medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering, in particular APA microencapsulated medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering.
A medicine of microencapsulated bovine medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering for treating or relieving withdraw syndrome, characterized in that said medicine is prepared by the following steps:
- (1) mixing the bovine medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering with a sodium alginate solution of 10-20 g/L to form a suspension, said suspension containing 0.1-1010 cells per liter;
- (2) dispersing the suspension of step (1) into a calcium chloride or calcium lactate solution of 80-120 mmol/L in the form of droplets of 150-1000 μm in diameter using a spraying device, the two liquids being in such a proportion that the resulting mixture contains 0.1-1×108 cells per liter, leaving to stand for 5-20 minutes, discarding the supernatant after complete precipitation, to obtain the calcium alginate bead precipitates comprising bovine medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering;
- (3) adding the precipitates from step (2) into a polylysine solution of 0.3-0.7 g/L in such a proportion that the resulting mixture contains 0.2-2×108 cells per liter, mixing thoroughly, leaving to stand for 5-20 minutes, discarding the supernatant after complete precipitation, to obtain the precipitates;
- (4) adding the precipitates from step (3) into a sodium alginate solution of 1.0-2.0 g/L in such a proportion that the resulting mixture contains 0.2-2×108 cells per liter, mixing thoroughly, leaving to stand for 3-15 minutes, discarding the supernatant after complete precipitation, to obtain the precipitates;
- (5) adding the precipitates from step (4) into a sodium citrate solution of 40-70 mmol/L in such a proportion that the resulting mixture contains 0.2-2×108 cells per liter, mixing thoroughly, leaving to stand for 5-20 minutes, discarding the supernatant after complete precipitation, to obtain the precipitates of microencapsulated bovine medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering;
- (6) washing the precipitates from step (5) by adding them into a sodium chloride solution of 9 g/L, finally transferring the precipitates into a cell culture, culturing and storing as a medicine of microencapsulated bovine medulliadrenal chromaffin cells or opioid-peptidergic cells obtained e.g. by genetic engineering for treating or relieving withdrawl syndrome.
Dependencies are inferred from the claim text.