Publication: Quantitative analysis and toxicity determination of artifacts originated in a Thai traditional medicine Prasaplai
2
Issued Date
2010-05-01
Resource Type
ISSN
17445116
13880209
13880209
Other identifier(s)
2-s2.0-77951785389
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Pharmaceutical Biology. Vol.48, No.5 (2010), 584-588
Suggested Citation
Prasan Tangyuenyongwatana, Wandee Gritsanapan Quantitative analysis and toxicity determination of artifacts originated in a Thai traditional medicine Prasaplai. Pharmaceutical Biology. Vol.48, No.5 (2010), 584-588. doi:10.3109/13880200903214223 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/28718
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Quantitative analysis and toxicity determination of artifacts originated in a Thai traditional medicine Prasaplai
Author(s)
Other Contributor(s)
Abstract
Prasaplai is a Thai traditional medicine for relieving dysmenorrhea and adjusting the menstrual cycle. Three fatty acid esters, (E)-4-(3,4- dimethoxyphenyl)but-3-en-1-yl linoleate (1), (E)-4-(3,4-dimethoxyphenyl)but-3- en-1-yl oleate (2) and (E)-4-(3,4-dimethoxyphenyl)but-3-en-1-yl palmitate (3) are formed during storage from the reaction of chemical components in two herbs, i.e., fatty acids in Nigella sativa (L.) (Ranunculaceae) and (E)-4-(3,4-dimethoxyphenyl)but-3-en-1-ol (compound D) in Zingiber cassumunar (Roxb.) (Zingiberaceae). The formations of these artifacts were monitored for 1 year and their amounts were analyzed by HPLC at certain periods of time. The results showed that artifact formation was saturated after 73 days of storage. The amount of each artifact in the saturation period ranged from 3.93±0.06 to 4.30±0.18% w/w for compound 1, 1.69±0.08 to 1.9±0.13% w/w for compound 2 and 0.09±0.003 to 0.1±0.005% w/w for compound 3. Cytotoxicity of the artifacts was evaluated using NCI-H187, KB, and BC cancer cell lines and found that the IC50 of all artifacts in all tests were higher than 20 μg/mL. For acute toxicity in mice, the LD50 of each artifact was more than 300mg/kg. © 2010 Informa UK Ltd.
