光觸發微脂粒系統之研發

Taipei Medical University Institutional Repository > 醫學工程學院 > 生醫材料暨組織工程研究所 > 博碩士論文 > Item 987654321/6694

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題名:	光觸發微脂粒系統之研發 Liposomal doxorubicin phototriggered release system
作者:	吳宏達 Hong-Dah Wu
貢獻者:	生物醫學材料研究所
關鍵詞:	穩定度微脂粒磷脂質光觸發釋放 Liposome phototriggered release
日期:	2004
上傳時間:	2009-09-11 17:08:39 (UTC+8)
摘要:	目前所使用的Liposomal-Doxorubicin 雖然在臨床使用上的確具有降低副作用的效果, 但是當微脂粒累積在腫瘤組織之後，由於釋放速率過慢，造成單位時間細胞內的Doxorubicin (Dox) 濃度過低，因而限制了藥效。本實驗方向為研發一種具有光觸發釋放能力的Liposomal-Doxorubucin-Hematporphyrin (LDH)，利用紅光激發包覆在微脂粒脂雙層中的光感物質Hematporphyrin (Hp)，使其產生自由基及單態氧，造成磷脂質脂肪酸鏈的過氧化作用，進而使微脂粒的穩定度降低，使包覆在微脂粒的Dox 能夠釋放出來。實驗採取傳統的薄膜水合法，並添加Cholesterol (ch)，利用此方式可以穩定地同時包覆Hp以及Dox，在不同配方的釋放速率結果發現，當配方中添加越多的Cholesterol，添加越少的L-α-Phosphatidylcholine (Egg PC)，藥物釋放的速率越慢，所製備的微脂粒在經過635 nm 的紅光觸發後的確可以提高藥物釋放的速率，以及脂雙層的通透性，由細胞毒性測試結果證實，觀察到A431 細胞在經過實驗所製備的LDH 處理兩小時之後，結果發現在LDH那組給予光照的能量越高，對於細胞的毒性也越大。 Using the Liposomal-Doxorubicin has indeed lowered the cardiac toxicity of Doxorubicin. However, release from the liposomes after accumulated in the cancerous tissue was too slow and resulted in low concentrations of doxorubicin in the target cells, and thus limits the effect of the treatment. In this study, we used the red light to activate the Hematoporphyrin encapsulated in the lipid bilayer in the Liposomal-Doxorubicin-Hematoporphyrin system. After being activated, singlet oxygen as well as free radicals were formed and resulted in peroxidation of tht lipids, de-stablized the liposomes, and subsequently released the encapsulated Doxorubicin. Liposomes were prepared by the traditional film-hydration method. Cholesterol was added to stabilize Hematoporphyrin and Doxorubicin in the liposomes. Release results showed that by increasing the cholesterol concentration or decreasing the L-α-Phosphatidylcholine (Egg PC) in the formulation, drug release was slower accordingly. After irradiated by 635 nm red light, drug release from the liposomes was faster and the bilayer permeability of the liposomes was increased. Cell toxicity tests indicated that the toxicity was higher when the dosed cultured cells were exposed to higher light irradiation.
資料類型:	thesis
顯示於類別:	[生醫材料暨組織工程研究所] 博碩士論文

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