The Extracting Methods of the Seeds of Yew(Taxus cuspidata Sieb) by Solvent Extraction and Its Efficacy

주목(朱木)씨앗 추출물의 제조방법 및 효능효과

  • Zhoh, Choon-Koo (Dept. of Chemical & Environmental Eng. Soonsil Univ.) ;
  • Kim, In-Young (Skin Care Cosmetic of Skin Science Institute, Enprani Co. LTD)
  • 조춘구 (숭실대학교 환경.화학공학과) ;
  • 김인영 (엔프라니(주) 피부과학연구소)
  • Published : 2002.12.30

Abstract

Yew (Taxus cuspidata Sibe) selected cultivation as drug, food and decorative plant in Gyong-gi province in Korea. To extract the water soluble active ingredients, as a extracting method, there was extracted with 20g of dried seeds with each 20g of butylene glycol(BG) and propylene glycol(PG), and 40 mL of water mixing 72 hours at $40{\pm}5^{\circ}C$, and then they were filtrated by 400 mesh. Appearance of extract of seeds was pale brown, $pH=4.5{\pm}0.5$, $gravity=1.013{\pm}0.05$, a reflective $index=1.373{\pm}0.05$, and yield=75%. Also, to extract the high purity oil from seeds, it minutely pulverized the dried seeds and added the hexane, mixing 2 hours at $20{\pm}57^{\circ}C$. And then, this filtrated it with 400-mesh. It got the purified oil through evaporating them at $55^{\circ}C$ during under vacuum. As the results, appearance was slightly brown, gravity=0.922 acid value=0.12, saponification value=192, and it should be obtained the $40{\pm}5%$ of yield. As the efficacy evalution of cosmetic field, the antioxidative activities by NBT method were stronger 86.0% from extract of talus seeds than 52.0% from green tea extract and 35.0% from skullcap extract as well as the antioxidative activities by DPPH method were stronger 93.7% from extract of seed than 60.3% from extract of green tea and 27.1% from extract of skullcap. These are more effective than other plant extracts. The collagen synthesis rate on the activating fibroblast for Taxus cuspidata Sibe extract showed 35.43%. As the activity of the skin elasticity, PPE(porcine pancreatic elastase)-inhibitory activities of talus extract was 50.8%. Anti-inflammatory activity was more effective to be taken 41.1% of taxus seed oil than 24.2% of steady glycyrrhetinate (SG) as a control.

Keywords

References

  1. 이창복(1973) 식물분류학, Ill. 향문사, 서울
  2. 김태정(1994) 한국의 산야초, 704-709. 국일미디어 , 서울
  3. 육창수(1987) 한국자원 식물도감, 13-15. 진명출판사, 서울
  4. 백태홍(1990), 천연물학회. 104. 수서원, 서울
  5. 한만우, 홍남두, 유재국(1998)
  6. V. Maurice, D. Jean, V. Fastre and R. J. Mondher (2002) Taxanes in Taxus baccata pollen. Planta Medica. 68: 36-40 https://doi.org/10.1055/s-2002-19865
  7. K. Junichi and S. Hideyuki (2002) Bioactive taxoids from the Japanese yew Taxus cuspidata. Medicinal Research Reviews. 22: 305-328 https://doi.org/10.1002/med.10005
  8. N. Erdemoglu, B. Sener and S. Ide (2001) Structural features of two taxoids from Taxus baccata L. growing in Turkey. J. Motecutar Structure. 559: 227-233 https://doi.org/10.1016/S0022-2860(00)00722-5
  9. R. M. Cusido, J. Palazon, A. N. Osorio, A. Mallol, M. Bonfill, C. Morales and M. T. Pinol (1999) Production of taxol and baccatin III by a selected Taxus baccata callus line and its derived cell suspension culture. Plant Science. 146: 101-107 https://doi.org/10.1016/S0168-9452(99)00093-X
  10. N. Erdemoglu and B. Sener (2000) Taxoids from the Heartwood of Taxus baccata L. Growing in Turkey. Natural Product Sciences. 6: 96-101
  11. C. R. Wilson, J. M. Sauer and S. B. Hooser (2001) Taxines: a review of the mechanism and toxicity of yew (Taxus spp.) alkaloids. Toxicon. 39: 175-185 https://doi.org/10.1016/S0041-0101(00)00146-X
  12. J. K. Prasain, P. Stefanowicz, T. Kiyota, F. Habeichi and Y. Konishi (2001) Taxines from the neddles of Taxus walli-chiana. Phytochem. 58: 1167-1170 https://doi.org/10.1016/S0031-9422(01)00305-3
  13. Q. Yue, Q. C. Fang and X. Liang (1996) A Taxane-11,12-oxide from Taxus yunnanensis. Phytochem. 43: 639-642 https://doi.org/10.1016/0031-9422(96)00299-3
  14. V. S. Parmar, A. Jha, K. S. Bisth, P. Taneja, S. K. Singh, A. Kumar, Poonam, R. Jain and C. E. Olsen (1999) Constituents of yew trees. Phytochem. 50: 1267-1304 https://doi.org/10.1016/S0031-9422(98)00702-X
  15. M. E. Wall and M. C. Wani (1996) Camptothecin and taxol : from discovery to clinic. J. of Ethnopharmacology 51: 239-254 https://doi.org/10.1016/0378-8741(95)01367-9
  16. 김인영, 이주동, 이계종, 정성원(2001) 대한민국공개특허, 출원번호10-2001-041646
  17. 김인영, 이계종, 정성원, 이주동, 유희창, 조춘구(2002) 화장품 산업에서 주목추출물의 효능에 관한 연구. 대한화장품학회지, 28: 80-98
  18. 김인영, 이주동, 김혁 , 김보라, 유희창(2001) 대한민국공개특허, 출원번호10-2001-041647
  19. Y. Sakihama, M. F. Cohen, S. C. Grace and H. Yamasaki (2002) Plant phenolic antioxidant and prooxidant activities: phenolics-induced oxidative damage mediated by metals in plants. Toxicology, 177: 67-80 https://doi.org/10.1016/S0300-483X(02)00196-8
  20. S. O. Awe and A. S. 0. Adeagbo (2002) Analysis of tertbutyl hydroperoxide induced constrictions of perfused vascular beds in vitro. Life Sciences, 71: 1255-1266 https://doi.org/10.1016/S0024-3205(02)01845-3
  21. H. Rubin (2002) Promise and problems in relating cellular senescence in vitro to aging in vivo. Archives of Gerontology and Geriatrics. 34: 275-286 https://doi.org/10.1016/S0167-4943(01)00221-7
  22. L. Sartor, E. Pezzato, I. Dell'Aica, R. Caniato, S. Biggin and S. Garbisa (2002) Inhibition of matrix-proteases by polyphenols: chemical insights for and-inflammatory and antiinvasion drug design, Biochemical Pharmacology. 64: 229-237 https://doi.org/10.1016/S0006-2952(02)01069-9
  23. P. Andreas, Z. Meixia, T. Katalin, K. Hildegard, F. Ute, M. Zoltan, S. Jozsef, H. Katalin, B. Kay et al. (2002) Anti-inflammatory effects of a cyclosporine receptor-binding compound, D-43787, The Joumal of Pharmacology and Experimental Therapeutics. 301: 738-746 https://doi.org/10.1124/jpet.301.2.738