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靈芝子實體之均相成膜及其性質探討

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本研究的主要目的在於:利用靈芝子實體殘渣在均相的狀態下製備薄 膜,適用於傷口修復及軟組織的吸收性修復。另一方面並進一步對靈 芝子實體殘渣作結構鑑別。首先以靈芝子實體萃取過有效成份後的殘 渣為材料,先將殘渣以粉碎機研成碎屑,接著以不同條件的 NaOH 為 變因進行鹼處理,鹼處理過後的殘渣以清水沖洗至中性,繼之以不同 條件的 NaClO3 為變因進行脫色,以清水沖洗至中性,且 AgNO3 檢 測無 Cl- 離子殘留。歷經鹼處理及脫色手續的殘渣,將其以冷凍乾燥 乾燥三日,之後取出乾燥過的樣品,取不同條件下的樣品,以 8% 的 濃度置於二元溶劑系 6% LiCl/DMAc 中溶解三日,完成後依序成膜,

再以 Ethanol/Acetone/Water 各 120 、 15 、 60 秒迅速浸泡後撈起,

以清水放流 24 小時並平鋪在 Teflon 紙上,待其風乾,即可得到初步 的靈芝膜。靈芝膜以 DMA 測強度並進行細胞毒性測試,初步評估可 行; NMR 、 IR 、 GC/MASS 測得靈芝子實體主結構的幾丁質以 C-3 與其它 b-1,4-Glucan 鍵結; X-ray 及 DSC 測樣品處理前後結晶狀態的 相異點。並將之前溶解的靈芝溶液以黏度計測分子量,最後綜合數據 找出最合適的成膜條件,大量製造後並計劃與生體相關的實驗。

靈芝子實體之均相成膜及其性質探討

(2)

Ganoderma membrane in homogeneous conditions for wound healing and absortive rep aring of soft tissues was investigated as well as the structure of Ganoderma residues was indentified in present study. Ganoderma residues after removing the triterpenes and pol ysaccharide were used for the treatment with several concentrations of NaOH, then the t reated residues were water-washed to neutral pH. The NaOH treated residues were blea ched with various concentrations of NaClO3 before another water-washed to remove pi gment. Washing was lasted until the AgNO3 indicated negative reaction in the leach. Af ter that, bleached Ganoderma residues were lyophilized for 3 days and 8% of the dried s amples were dissolved in , a binary solvent, 6% LiCl/DMAc system for 3 days. The diss olved systems were put subsequently in ethanol for 120 seconds, then in acetone for 15 seconds, and finally in water for 60 seconds. The membranes were water-washed for 24 hours and then casted on Teflon papers to allow on drying in room temperature to produ ce a transparent membrane. Chemical structrure of GANOCHITIN was analysed by N MR, IR, GC/MASS to identify the Chitin structure with a cross-linked b-glucan at C-3 p osition. The strength measured by DMA indicated that GANOCHITIN has a stronger te nsile. MTT assay of GANOCHITIN showed no cytotoxicity to cell line. Analysis DSC and X-ray indicated that degree of crystallinity increased slightly after dissoling and cas ting. The viscosity of the dissolving samples was measured to compare molecular weigh t with another by viscosity meter. The result of the present study could be useful for the optimation for large scale production of GANOCHITIN and further test in vivo.

Preparation of Ganoderma residue under homogeneous conditions and its properties

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