Targeted Artemisinin Support for Immune, Gut, Liver, and Cellular Health*
What It Does
Artemisinin provides targeted support for immune system balance, gastrointestinal health, liver detoxification, and cellular oxidative stress regulation.* Sourced from Artemisia annua, this purified form allows for consistent, concentrated delivery of the plant’s most studied and biologically active compound.*
How It Works
• Artemisinin (from Artemisia annua): Supports immune modulation by influencing cytokine pathways, including NF-κB and MAPK signaling, and promoting mucosal integrity in the gut.*[2]
• Bitter Tonic Action: As a bitter compound, artemisinin may help prime digestion and modulate the gut microbiota, supporting gastrointestinal balance and healthy digestive processes.*[3,4]
• Oxidative Stress Regulation: Shown to assist in modulating redox balance and cellular antioxidant defenses, supporting healthy cellular metabolism.*[4]
• Liver Function Support: May enhance detoxification enzyme activity and regulate oxidative and metabolic pathways essential for liver efficiency and overall hepatic resilience.*[5,1]
• Pure and Concentrated: Each capsule provides a purified source of artemisinin without the variability of whole-plant extracts, where active content is typically just 0.3–0.5%.*[1]
Who It’s For
Ideal for individuals seeking focused support for immune regulation, gastrointestinal health, detoxification, and oxidative balance, especially those working with healthcare practitioners familiar with advanced botanical interventions.*
Special Features
For over 30 years, ARG has delivered purified artemisinin to healthcare practitioners. This formula ensures high quality, consistent potency, and professional-grade purity, distinguishing it from typical plant extracts.*
References
1. Golenser J, et al. Int J Parasitol. 2006;36(14):1427–1441.
2. Wang KS, et al. Immunopharmacol Immunotoxicol. 2017;39(1):28–36.
3. Lee JH, et al. Hortic Environ Biotechnol. 2015;56:697–703.
4. Addissouky TA. Discov Chem. 2025;2:10. doi:10.1007/s44371-025-00084-4
5. Xiong Y, Huang J. Chin Med. 2021;16:80. doi:10.1186/s13020-021-00489-0
