본 연구에서는 해삼속의 폴리페놀과 플라보노이드의 생리활성물질을 추출하기 위한 용매분획의 수율을 확인하고자 연구를 시도하였다. 이미 보고된 사례에서 50%에탄올 추출 용매분획은 해삼 항산화 물질의 높은 수율 결과로 확인되었다. 해삼의 항산화물질 추출량을 결정짓는 것은 추출에 적용된 추출용 매분획의 결과로 확인되었다. 또한 ‘추출용매에 따라 해삼생리활성 항산화물질 추출함량이 크게 차이가 있다.’는 선행연구를 통해 용매분획추출에 관한 필요성의 결과를 얻었다. 50%에탄올 추출 용매분획의 해삼추 출물에 포함된 페놀물질의 높은 항산화성분 추출 결과가 증명되었다. 추출용매분획 연구사례에서 수율이 가장 저조한 아세트산에틸 용매분획은 다른 용매분획에 비해 높은 페놀함량을 수확하여 항산화효과가 확인되었다. 이에, 추출 용매분획물의 적용에 따른 수율변화를 통해 항산화추출물의 높은 수율에 미치는 영향을 확인 하였다. 따라서 본 연구를 통해 50%에탄올 용매의 최적화된 해삼생리활성물질 추출 용매분획으로 검증되었다.

Background : Gastrodia elata Blume (G. elata) is important medicinal resource in korea. Gastrodin and 4-hydroxybenzyl alcohol (4-HBA) are major active compounds of G. elata, and ρ-cresol is major cause of off-odor like pig slurry from G. elata. The off-odor can decrease the quality of fresh G. elata as well as its products. Therefore, this study was performed to investigate the influence of extraction temperature on bio-active and odorous compounds of G. elata extract. Methods and Results : G. elata was extracted with distilled water at 0, 30, 60, and 90℃ for 20, 40, 60, and 120 min. Gastrodin and 4-HBA contents were analyzed by using a HPLC-UVD, and ρ-cresol content was analyzed by using a SPME-GC-MS. Gastrodin content increased as increasing extraction temperature and time, and showed the highest value in extract at 90℃. 4-HBA content showed the highest value at 60℃, and increased as increasing extraction time. Total content of gastrodin and 4-HBA was higher in extract from G. elata at 60℃ for 120 min than other extracts. ρ-Cresol content was varied according to extraction temperature, and was lower in extract at 30 and 60℃ than 0 and 90℃. Conclusion : These results indicated that the extraction temperature can affect the bio-active components and off-odor of G. elata extract, and 60℃ is appropriate to improve the qualities including bio-active component and off-odor of G. elata extract and its products.

This study has been conducted to establish the optimal extraction process and HPLC analysis method for thedetermination of marker compounds as a part of the materials standardization for the development of health functionalfood materials from Astragali radix. Five extraction conditions including the shaking extraction at room temperature andthe reflux extraction at 85℃ with 30%, 50% and 95% ethanol were evaluated. Reflux extraction with 50% ethanol showedthe highest extraction yield as 27.27±2.27%, while the extraction under reflux with 95% ethanol showed significantly thelowest yield of 10.55±0.24%. The quantitative determination methods of calycosin-7-O-β-D-glucoside and calycosin asmarker compounds of Astragali radix extracts were optimized by HPLC analysis using a Thermo Hypersil column(4.6×250㎜, 5㎛) with the gradient elution of water and acetonitrile as the mobile phase at the flow rate of 0.8mL min-¹and a detection wavelength of 230㎚. The HPLC/UV method was applied successfully to the quantification of two markercompounds in Astragali radix extracts after validation of the method with the linearity, accuracy and precision. The con-tents of calycosin-7-O-β-D-glucoside and calycosin in 50% ethanol extracts by reflux extraction were significantly higher as1,700.3±30.4 and 443.6±8.4㎍ g-1, respectively, comparing with those in other extracts. The results indicate that thereflux extraction with 50% ethanol at 85℃ is optimal for the extraction of Astragali radix, and the established HPLCmethod are very useful for the evaluation of marker compounds in Astragali radix extracts to develop the health functionalmaterial from Astragali radix.