Chitosan (2 mg/mL; 48 hours; SKMEL28 and RPMI7951 cells) treatment presents a reduced growth potential.
Chitosan (2 mg/mL; 48 hours; RPMI7951 cells) treatment shows potent pro-apoptotic effects against RPMI7951 through the mitochondrial pathway.
Chitosan (2 mg/mL; 48 hours; RPMI7951 cells) treatment induces an up regulation of pro-apoptotic molecules such as Bax and a down regulation of anti-apoptotic proteins like Bcl-2 and Bcl-XL.
Low-molecular-weight chitosan can penetrate bacterial cell walls, bind with DNA and inhibit DNA transcription and mRNA synthesis, while high-molecular-weight Chitosan can bind to the negatively charged components on the bacterial cell wall. It forms an impermeable layer around the cell, changes cell permeability and blocks transport into the cell. Chitosan also can be used in water treatment, wound-healing materials, pharmaceutical excipient or drug carrier, obesity research and as a scaffold for tissue engineering.
Cell Viability Assay
| Cell Line: |
SKMEL28 and RPMI7951 cells |
| Concentration: |
2 mg/mL |
| Incubation Time: |
48 hours |
| Result: |
Presented a reduced growth potential.
|
Apoptosis Analysis
| Cell Line: |
RPMI7951 cells |
| Concentration: |
2 mg/mL |
| Incubation Time: |
48 hours |
| Result: |
Had potent pro-apoptotic effects against RPMI7951.
|
Western Blot Analysis
| Cell Line: |
RPMI7951 cells |
| Concentration: |
2 mg/mL |
| Incubation Time: |
48 hours |
| Result: |
Induced an up regulation of pro-apoptotic molecules such as Bax and a down regulation of anti-apoptotic proteins like Bcl-2 and Bcl-XL.
|