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Baicalin facilitated the transfer of electrons from Fe (2+) to dissolved oxygen. Baicalin has the capacity to protect IEC-6 cells and the intercellular tight junctions from LPS-induced injury. The mechanisms may be associated with inhibiting the production of inflammatory cytokines, and up-regulating the mRNA and protein expression of ZO-1. Baicalin had no effects on the pharmacokinetics of caffeine and its metabolites in vivo, following single oral administration in rats. Anti-inflammatory properties of baicalin may be resulted from the inhibition of IL-6, IL-8, and TNF-α expression via preventing signaling NF-κB pathway in HBE16 airway epithelial cells.
| Cell Experiment | |
|---|---|
| Cell lines | OVCAR-3, A2780/CP70, IOSE-364 |
| Preparation method | Cells (5000/well) were seeded into 96-well plates and incubated for 24 h before being treated with zero to 160 μg/mL Baicalin and Baicalein (containing 10% FBS RPMI 1640) in triplicates for another 24 h. |
| Concentrations | 160 μg/mL |
| Incubation time | 24 h |
| Animal Experiment | |
|---|---|
| Animal models | |
| Formulation | |
| Dosages | |
| Administration | |
| Molecular Weight | 446.36 |
| Formula | C21H18O11 |
| CAS Number | 21967-41-9 |
| Solubility (25°C) | DMSO ≥ 90 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
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