Background : The 1,2-unsaturated PAs, reported to be widely present in medicinal plants belonging to Asteraceae, Boraginaceae, and Fabaceae, cause hepatotoxicity and genotoxicity in humans and animals. Hence, there is a need for an analytical method that allows these dangerous plant toxins to be determined. In this study, we developed a method that can be used for the rapid and accurate determination of nine toxic PAs in medicinal plants using ultra-pressure liquid chromatography–electrospray ionization–quadrupole–time-of-flight mass spectrometry (UPLC-ESI-Q-TOF). Methods and Results : The compounds were eluted onto a C18 column with 0.1% formic acid and acetonitrile, and separated with good resolution within 11 min. all analytes was characterized by its precursor ions generated by ESI-Q-TOF and fragment ions produced by collision-induced dissociation (CID), which were used as a reliable database. The proposed analytical method was verified with reference to the ICH guidelines. The proposed UPLC-ESI-Q-TOF method was applied to four medicinal plants, and lycopsamin, echimidine, senkirkine and senecionine were detected by matching with reference standard, and additional six PAs were tentatively identified though chemical profiling. In addition, the QuEchERS method was the most efficient in comparison with methods like hot water and methanol in extraction efficiency of pyrrolizidine alkaloids. Conclusion : The our proposed method can determine PAs rapidly and accurately in medicinal plants and will be utilize as an important data for other researchers who need analytical information of PAs.

Background : Turmeric (Curcuma longa L.) and black pepper (Piper nigrum L.) have traditionally been used as Asian medicinal and culinary herb. Curcumin, a major compound of turmeric, has been known to have antitumor activity. However, curcumin is bioavailable because it is rapidly metabolized and released from the body. Therefore, the addition of adjuvants such as piperine, a potent inhibitor of drug metabolism, is one of the ways to increase the bioavailability of curcumin. Methods and Results : The yields of turmeric and black pepper ethanolic extracts (TM and BP) are 18.2 and 8.2% (w/w), respectively. The EC50 values of A549 and NCI-H292 cells exposed to TM were 77.8 ㎍/㎖ and 92.0 ㎍/㎖, respectively. No significant cytotoxicity was observed up to the 400 ㎍/㎖ in the A549 and NCI-H292 exposed to BP. Based on the central composite design, the co-treatment of TM and BP enhanced the cytotoxicity of A549 and NCI-H292 cells. The optimal combination concentration (optimal EC50 value) of TM and BP calculated by the response surface methodology assay were 48.5 and 241.7 ㎍/㎖. The conbination index assay confirmed that the cytotoxic effect at optimal combinatino concentration was due to the synergistic effect. Conclusion : We hypothesized that co-treatment of TM and BP enhanced cytotoxicity more than single treatment of TM against lung cancer cells, and cell death at this time may synergetic cytotoxicity effects associated with curcumin metabolism.

Background : The effects of heat treatments on the phycochemical charateristics and antioxidant activities of ginkgo nuts were investigated by roasting at various temperatures (150, 180, and 210℃) for 60 min. Methods and Results : For each roasting temperatures, pH, total acidity, chromaticity, total cyanide content, reducing power, total polyphenol content, 2,2’-diphenyl-1-picrylhydrazyl (DPPH) and 2,2’-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging activities were compared and analyzed. As the roasting temperature and time increased, the pH and total cyanide content decreased from 7.32 to 6.31 and from 697 to 282 ㎍/㎎, respectively, while total acidity increased from 0.40 to 0.84%. There was an 11 or more color difference (ΔE) between the non-heated ginkgo nut and heated ginkgo nuts, indicating a remarkable color difference. The antioxidant activities, including reducing power, total polyphenol content, and DPPH and ABTS radical scavenging activities increased rapidly at 210℃ according to increasing in roasting temperature and time. Conclusion : These results suggest that the ginkgo nut with heat treatment could be used in food materials and medicines for decreasing cyanide content as well as for increasing antioxidant compound content.

Background : F. fomentarius extracts have been recently reported to process immune-stimulatory and anti-inflammatory effects. In this study, we evaluated the anti-mutagenic effect of F. fomentarius ethanol extracts and the effective chemical components from the extract were analyzed by LC-Q-TOF. Methods and Results : F. fomentarius was extracted with 70% ethanol yielding a crude extract 6.8%. The crude extract was fractionated sequentially to diethyl ether, chloroform, dichloromethane, butanol and water with a yield of 43.9%, 2.958%, 6.8%, 21.6% and 25.5.%, respectively. The anti-mutagenic effect of F. fomentarius extract and its fractions was tested in Ames test by two type of Salmonella typhimurium (TA98 and TA100). Among the five fractions, diethyl ether has shown the highest and significant anti-mutagenic effect (98.3%, at 3,000 ㎍/plate concentration). Moreover, we investigated the chemical constituents of the extract using UPLC-Q-TOF. A total of 10 compounds such as flavonoids (velutin, 3, 4′,5-Trihydroxy-3′,7-dimethoxyflavanone) and fatty acids (γ-linoleic acid, stearic acid) and deterpenoid (kirenol) were tentatively identified with an accurate mass within 10 ppm mass error. Also, flavonoids and fatty acids were detected with higher rate than other compounds based on obtained chromatograms. Conclusion : We demonstrated that F. fomentarius extract and fractions have anti-mutagenic activity through Ames test. Furthermore, we will carry out isolation of each components from its fraction and use them to conduct additional anti-mutagenic test.