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Last Updated: March 28, 2024

Claims for Patent: 10,415,014


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Summary for Patent: 10,415,014
Title:Method for the ex vivo cultivation of oral mucosal epithelial progenitor cells and oral mucosal epithelial cells
Abstract: A method for the ex vivo cultivation of oral mucosal epithelial progenitor cells and oral mucosal epithelial cells includes: subjecting an oral mucosal tissue to an enzymatic digestion treatment with collagenase, so as to obtain cell aggregates which include oral mucosal epithelial progenitor cells and oral mucosal epithelial cells; cultivating the cell aggregates with an amniotic membrane in a serum-free platelet lysate-containing medium in the absence of feeder cells, so that the cell aggregates are adhered onto the amniotic membrane; and subsequently cultivating the cell aggregates adhered on the amniotic membrane in a serum-free proliferation-facilitating medium in the absence of feeder cells.
Inventor(s): Ma; Hui-Kang (Taoyuan, TW), Ma; Shih-Chieh (Taoyuan, TW)
Assignee: Chang Gung Memorial Hospital, Linkou (Taoyuan, TW)
Application Number:15/454,876
Patent Claims:1. A method for the ex vivo cultivation of oral mucosal epithelial progenitor cells and oral mucosal epithelial cells, comprising: subjecting an oral mucosal tissue to an enzymatic digestion treatment with collagenase, so as to obtain cell aggregates which include oral mucosal epithelial progenitor cells and oral mucosal epithelial cells; cultivating the cell aggregates with an amniotic membrane in a serum-free platelet lysate-containing medium in the absence of feeder cells, so that the cell aggregates are adhered onto the amniotic membrane; and cultivating the cell aggregates adhered on the amniotic membrane in a serum-free proliferation facilitating medium that is different from the serum-free platelet lysate-containing medium and is free of platelet lysate in the absence of feeder cells, so that the oral mucosal epithelial progenitor cells and the oral mucosal epithelial cells in the cell aggregates proliferate.

2. The method according to claim 1, wherein the enzymatic digestion treatment is conducted under shaking at a speed ranging from 800 rpm to 1600 rpm.

3. The method according to claim 1, wherein the enzymatic digestion treatment is conducted under shaking at 1,200 rpm.

4. The method according to claim 1, wherein the enzymatic digestion treatment is conducted in a serum-free supplemented hormonal epithelial medium in the absence of feeder cells.

5. The method according to claim 1, wherein the amniotic membrane is a denuded amniotic membrane.

6. The method according to claim 1, wherein the serum-free platelet lysate-containing medium comprises PLTMax.RTM. platelet lysate.

7. The method according to claim 6, wherein the serum-free platelet lysate-containing medium further comprises an epithelial cell growth medium.

8. The method according to claim 7, wherein the epithelial cell growth medium is a supplemented hormonal epithelial medium.

9. The method according to claim 8, wherein the supplemented hormonal epithelial medium comprises a basal medium, a growth factor, and insulin.

10. The method according to claim 9, wherein the basal medium is selected from the group consisting of Dulbecco's Modified Eagle's Medium (DMEM), Minimal Essential Medium, Basal Medium Eagle, DMEM/F-12 (Nutrient Mixture F-12), DMEM/F-10 (Nutrient Mixture F-10), .alpha.-Minimal essential Medium, Glasgow's Minimal Essential Medium, KnockOut DMEM, and combinations thereof.

11. The method according to claim 9, wherein the growth factor is selected from the group consisting of a recombinant human epidermal growth factor, keratinocyte growth factor, hepatocyte growth factor, and combinations thereof.

12. The method according to claim 1, wherein the serum-free proliferation facilitating medium is selected from the group consisting of EpiLife.RTM. medium, Keratinocyte-serum free medium (SFM), Stemline.RTM. Keratinocyte Medium II, DermaLife.RTM. K Serum-Free Keratinocyte Culture Medium, and combinations thereof.

13. The method according to claim 12, wherein the serum-free proliferation facilitating medium is EpiLife.RTM. medium.

14. The method according to claim 13, wherein the serum-free proliferation facilitating medium further comprises a supplement.

15. The method according to claim 14, wherein the supplement is selected from the group consisting of Supplement S7, BPE-free Keratinocyte Medium Supplement, and a combination thereof.

16. The method according to claim 1, wherein the serum-free proliferation facilitating medium suppresses the proliferation of mesenchymal cells and fibroblasts that are present in the cell aggregates.

17. The method according to claim 1, wherein the serum-free platelet lysate-containing medium and serum-free proliferation facilitating medium are animal-derived component-free media.

18. A method for the ex vivo cultivation of oral mucosal epithelial progenitor cells and oral mucosal epithelial cells, comprising: subjecting an oral mucosal tissue to an enzymatic digestion treatment with collagenase, so as to obtain cell aggregates which include oral mucosal epithelial progenitor cells and oral mucosal epithelial cells; cultivating the cell aggregates with an amniotic membrane in a serum-free platelet lysate-containing medium that includes PLTMax.RTM. platelet lysate in the absence of feeder cells, so that the cell aggregates are adhered onto the amniotic membrane; and cultivating the cell aggregates adhered on the amniotic membrane in a serum-free EpiLife.RTM. medium in the absence of feeder cells, so that the oral mucosal epithelial progenitor cells and the oral mucosal epithelial cells in the cell aggregates proliferate, and the proliferation of mesenchymal cells and fibroblasts that are present in the cell aggregates is suppressed.

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