Toxicity evaluation of standardized and nanoliposomal extracts of Labisia pumila whole plant (Blume, Myrsinaceae) in Sprague Dawley rats
Purpose: To investigate the toxicity of Labisia pumila standardized extract (LPE) and its liposomal extract (LLP). Methods: For acute toxicity study, LPE or LLP was orally administered (2000 mg/kg) in single doses to Sprague Dawley rats and the routine activity of the rats was continuously monitored...
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| Main Authors: | , , , , , , , |
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| Format: | Indexed Article |
| Language: | English |
| Published: |
2018
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| Online Access: | http://discol.umk.edu.my/id/eprint/7330/1/Toxicity%20evaluation%20of%20standardized%20and%20nanoliposomal%20extracts%20of%20Labisia%20pumila%20whole%20plant%20%28Blume%2C%20Myrsinaceae%29%20in%20Sprague%20Dawley%20rats.pdf http://discol.umk.edu.my/id/eprint/7330/ https://www.ajol.info/index.php/tjpr/article/view/178173 |
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| Summary: | Purpose: To investigate the toxicity of Labisia pumila standardized extract (LPE) and its liposomal
extract (LLP).
Methods: For acute toxicity study, LPE or LLP was orally administered (2000 mg/kg) in single doses to
Sprague Dawley rats and the routine activity of the rats was continuously monitored for a total of 14
days. After 14 days of treatment, all rats were sacrificed and their vital organs were excised, weighed
and macroscopically examined, while for a repeated dose toxicity study, the rats were orally
administered with LPE or LLP at the selected doses (250, 500 and 1000 mg/kg) for a period of 28 days.
The animals were sacrificed (anaesthetized by sodium pentobarbitone and blood was collected by
cardiac puncture), followed by examination of their body organs and blood serum.
Results: LPE and LLP at 2000 mg/kg did not produce mortality or significant changes in the general
behaviour, body weight and organ gross appearance of the rats. In repeated dose toxicity study no
significant changes in, growth, organ weights, haematological parameters, biochemical values and
histological features of vital organs of the treated groups, compared to the control group.
Conclusion: The no-adverse-effect-level for LPE and LLP is (1000 mg/kg/day) when administered
orally for 28 days. |
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