Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/26108
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18034/20233 (89%)
造访人次 : 23695409      在线人数 : 519
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/26108


    標題: 牛樟芝醱酵中草藥萃取物及其轉化代謝物之抗老化活性探討
    Studies on the antiaging activities of bio-transformed metabolites of Antrodia cinnamomea fermented with medicinal herbal extracts
    作者: 許嘉茹
    貢獻者: 化妝品科技研究所
    呂尚謙
    關鍵字: 生物轉化
    抗老化
    醱酵
    中草藥
    牛樟芝
    fermentation
    medicinal herbal extracts
    Antrodia cinnamomea
    日期: 2012
    上傳時間: 2012-11-28 15:30:38 (UTC+8)
    摘要: 牛樟芝(Antrodia cinnamomea)為台灣本土特有種的藥用真菌,根據研究指出其子實體或菌絲體具有保護肝臟、抗氧化、抗發炎及抑制腫瘤等功效。故本研究藉牛樟芝菌絲體液態深層培養來醱酵5種中草藥,乃是利用牛樟芝菌絲體的酵素系統對中草藥的成份進行生物轉化作用(bio-transformation);另外,進一步分析牛樟芝醱酵各種中草藥後產生的轉化代謝物(bio-transformed metabolites)對於皮膚抗老化之活性。研究結果顯示,處理濃度為5.0%時,只有牛樟芝丹參醱酵液具細胞毒性,其餘醱酵液之細胞存活率皆在80.0%以上;而當處理濃度提高至10.0%時,則牛樟芝桑白皮及女貞子之醱酵液具有較低的細胞毒性,其餘醱酵液之細胞存活率甚低。另一方面,在酵素活性抑制分析試驗中,以最終濃度5.0%的牛樟芝丹參、女貞子及牡丹皮之醱酵液為較具抑制MMP-2及MMP-9的作用,當濃度提高至10.0%時抑制效果越趨顯著。再從5種中草藥醱酵液中挑選出丹參、女貞子及牡丹皮進行膠原蛋白保護之含量分析,發現添加了中草藥的醱酵液可達到延緩膠原蛋白破壞之效果,值得注意的是牛樟芝丹參醱酵液保護膠原蛋白被降解的能力為最強。因此,綜合上述實驗結果,我們認為利用牛樟芝醱酵中草藥萃取物之生物轉化代謝物的確具有可探討性,並可應用於抗老化化粧品原料之開發。
    Antrodia cinnamomea is an endemic fungus grown in Taiwan. Recent studies demonstrated that the fruiting body or mycelia of A. cinnamomea have several bioactivities, including liver protection, anti-oxidation, anti-inflammation and anti-tumor. In this study, A. cinnamomea mycelial submerged culture is applied to perform the fermentation with 5 medicinal herbal extracts. The enzymes presented in mycelial submerged culture of A. cinnamomea will be employed to carry out bio-transformation of medicinal herbal extracts. Additionally, the objective of this project is planned to investigate the antiaging activities of bio-transformed metabolites isolated from A. cinnamomea submerged culture which co-fermented with those medicinal herbal extracts. The experimental results showed that when 3T3 cell were treated with the concentration of 5.0%, cytotoxicity was found only from the A. cinnamomea submerged fermentative Salvia miltiorrhiza product; as well as, the cell survival rates of other fermented A. cinnamomea medicinal herbal extracts are above 80.0%. When treated with the concentration which increased to 10.0%, the products from A. cinnamomea submerged fermentation with Morus alba, and Ligustrum lucidum showed low cytotoxicities; however, survival rates of the others was relatively low. On the other hand, the analyses by gelatin based zymography showed that the products from A. cinnamomea submerged fermentative Salvia miltiorrhiza, Ligustrum lucidum, and Paeonia suffruticosa, exhibited the abilities of inhibition toward MMP-2 and MMP-9 with the concentration of 5%; moreover, inhibitive capacities were remarkably increased when the concentration elevated 10.0%. As a result, we selected the Salvia miltiorrhiza, Ligustrum lucidum, and Paeonia suffruticosa fermentative products from 5 kinds of medicine herbal fermentative products proceeded to collagen protection assay. We found that collagen degradation was delayed by supplementation of medicinal herbal extracts fermentative products. It is worth noticing that A. cinnamomea submerged fermentative Salvia miltiorrhiza product showed the strongest ability to promote collagen accumulation. In conclusion, we suggest that future researches can confer with bio-transformation of medicinal herbal extracts by A. cinnamomea, and these bio-transformed products can be developed as effective antiaging agents used in skincare cosmetics.
    關聯: 校內校外均不公開,學年度:100,112頁
    显示于类别:[化妝品應用與管理系(所)] 博碩士論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML1588检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈