透過您的圖書館登入
IP:18.189.3.137
  • 學位論文

熱敏感式甲殼素水凝膠應用在肝癌治療之研究

Study of thermosensitive chitosan-based hydrogel for the hepatoma therapy

指導教授 : 謝栢滄
若您是本文的作者,可授權文章由華藝線上圖書館中協助推廣。

摘要


本研究旨在利用甲殼素為基材製成熱敏感型水凝膠應用於肝癌之療效評估。甲殼素/甘油磷酸鹽(C/GP)水凝膠具備生物相容性及生物降解性且天然無毒性的優點,以水凝膠為載體與高能量貝他射線的錸-188及化療藥物Doxorubicin合併作為治療肝腫瘤藥物。本研究已完成C/GP/188Re-Tin colloid/Dox體外釋放,由實驗證實C/GP水凝膠系統可以有效地將藥物188Re-Tin colloid合併Dox 滯留進而達到延緩釋放長達48小時。然而,在C/GP/188Re-Tin colloid之動物體內生物分佈情形及初步的療效評估,由核醫造影研究中顯示C/GP/188Re-Tin colloid於直接腫瘤注射後至48小時仍無明顯擴散至其他器官。在療效評估方面,透過治療後大鼠肝腫瘤大小測量及肝臟病理切片實驗結果證實C/GP/188Re-Tin colloid能夠有效抑制腫瘤細胞生長而提高治療效果。

關鍵字

肝癌 水凝膠 錸-188 甲殼素

並列摘要


This study used chitosan as base for making thermosensitive and in situ formed hydrogel assessing the efficacy of treatment of liver cancer. Chitosan /β-glycerophosphate (C / GP) hydrogel is a biocompatible and biodegradable of a non-toxic and natural advantages, it can combined with rhenium -188 which include higher energy beta emission and doxorubicin (C/GP/188Re-Tin colloid/Dox)for the treatment of liver cancer. This study has been completed C/GP/188Re-Tin colloid / Dox in vitro release, confirmed by the experimental C / GP hydrogel system can be effectively combined 188Re-Tin colloid and Dox to achieve slow release of remaining live up to 48 hours. However, in C/GP/188Re-Tin colloid of animal bio-distribution and preliminary efficacy assessment by the nuclear medicine studies, also showed C/GP/188Re-Tin colloid directly to 48 hours after injection of tumor is still no significant proliferation. In the efficacy evaluation, tumor size, measured by liver biopsy and liver pathology results confirmed C/GP/188Re-Tin colloid could inhibit tumor cell growth and to improve treatment.

並列關鍵字

Liver cancer Hydrogel 188Re-Tin colloid Chitosan

參考文獻


1. Sundram, F., Radionuclide therapy of hepatocellular carcinoma. 2006.
2. Livraghi, T., et al., Sustained complete response and complications rates after radiofrequency ablation of very early hepatocellular carcinoma in cirrhosis: Is resection still the treatment of choice? Hepatology, 2008. 47(1): p. 82-89.
3. Szyszko, T., et al., Therapy options for treatment of hepatic malignancy. European Journal of Nuclear Medicine and Molecular Imaging, 2008. 35(10): p. 1824-1826.
4. Han, H.D., et al., A chitosan hydrogel-based cancer drug delivery system exhibits synergistic antitumor effects by combining with a vaccinia viral vaccine. International Journal of Pharmaceutics, 2008. 350(1-2): p. 27-34.
5. Bhattarai, N., J. Gunn, and M. Zhang, Chitosan-based hydrogels for controlled, localized drug delivery. Advanced Drug Delivery Reviews, 2010. 62(1): p. 83-99.

延伸閱讀