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Comprehensive multiscale characterization, in vivo antioxidant activity, and subacute toxicity assessment of pearl
Shaik Abdullah Nawabjan1, G S Muthu Iswarya1, Xinyue Yu1
1School of Biological Sciences, The University of Hong Kong, Pok Fu Lam Road, Hong Kong Special Administrative Region of China.
Journal of Ethnopharmacology
|August 1, 2026
Summary
Pearl powder exhibits significant antioxidant effects and a good safety profile in mice, suggesting its potential as a natural treatment for oxidative stress. Further clinical research is recommended to confirm these findings.
Area of Science:
- Biochemistry
- Pharmacology
- Materials Science
Background:
- Pearl powder, utilized in Traditional Chinese Medicine for centuries, is recognized for its detoxifying, regenerative, and anti-aging properties.
- This study focuses on pearl powder derived from Hong Kong pearl oysters (Pinctada imbricata).
Purpose of the Study:
- To conduct a comprehensive physicochemical characterization of pearl powder.
- To evaluate the in vivo antioxidant activity and subacute oral toxicity of pearl powder in C57BL/6J mice.
Main Methods:
- Physicochemical characterization involved Raman spectroscopy, HR-TEM, AFM, BET, and XPS.
- In vivo antioxidant activity was assessed using FRAP, TEAC, ORAC, and MDA assays in mice orally administered pearl powder.
- Subacute oral toxicity was evaluated over 28 days following OECD Guideline 407.
Main Results:
- Pearl powder demonstrated dose-dependent antioxidant activity, evidenced by increased FRAP, TEAC, and ORAC values and reduced MDA levels in liver, kidney, and spleen.
- The toxicity study revealed no mortality or adverse effects, establishing a No Observed Adverse Effect Level (NOAEL) of 500 mg/kg body weight.
- Minor biochemical variations observed lacked pathological significance.
Conclusions:
- Pearl powder possesses potent antioxidant properties and a favorable safety profile.
- These findings support the potential development of pearl powder as a natural therapeutic agent for conditions associated with oxidative stress.
- Clinical studies are necessary to validate these preclinical results.

