Tetrahydrocurcumin
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Specification
Test Items |
Standard |
Tetrahydrocurcumin (CAS: 36062-04-1) |
98% by HPLC |
Loss on drying |
≤0.5% |
Residue on ignition |
≤0.1% |

Metabolic Advantage

Multi-Target Action

High Safety
1.Molecular Target Network
2.Pharmacokinetics
Absorption
80% oral bioavailability (low glucuronidation).
Distribution
High in liver and brain (brain/plasma ratio=1.8:1).
Metabolism
Hepatic CYP2D6-mediated methylation (active metabolites).
Excretion
Primarily biliary (90% clearance in 72h).
Clinical Applications
Indications & Protocols
Condition |
Regimen |
Evidence |
Osteoarthritis |
200 mg/day ×12 weeks |
↓35% WOMAC score* |
Melasma |
2% cream bid ×8 weeks |
↓50% MASI score |
Mild Cognitive Impairment |
100 mg bid (Phase II) |
↑2 MMSE points |
*Multicenter RCT (n=300)
Special Populations
Hepatic Impairment: Reduce dose 50% (Child-Pugh B).
Elderly: No dose adjustment (monitor blood pressure).
Dosage and Administration
Formulations
Softgel Capsules: 100 mg/capsule (MCT oil carrier).
Topicals: 1–3% serums/creams.
Injection: 20 mg/mL (dilute in saline).
Dosing Guidelines
Use |
Dose |
Duration |
Anti-Inflammatory |
200–400 mg/day |
8–12 weeks |
Skin Brightening |
Topical bid |
≥8 weeks |
Neuroprotection |
100–200 mg/day |
Long-term |
Safety Evaluation
Adverse Reactions
System |
Incidence |
Manifestations |
Gastrointestinal |
2% |
Mild diarrhea |
Dermatologic |
0.5% |
Contact dermatitis |
Hepatic |
<0.1% |
Reversible ALT↑ |
Contraindications & Interactions
Absolute CI:
Curcuminoid allergy.
Complete biliary obstruction.
Cautions:CYP2D6 substrates (e.g., metoprolol): May ↑30% plasma concentration.
Research Progress Green max
Novel Formulations
Nanostructured Lipid Carriers: ↑15× transdermal absorption.
Sustained-Release Microspheres: Single injection maintains efficacy for 7 days.
New Indications
Diabetic Nephropathy: Inhibits TGF-β1/Smad3 (↓40% fibrosis in animals).
Parkinson’s Disease: Protects dopaminergic neurons (↑35% TH+ cells in MPTP models).
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