脂质体
傅里叶变换红外光谱
扫描电子显微镜
材料科学
毒品携带者
药物输送
药品
抗癌药
核化学
色谱法
活力测定
体外
纳米技术
化学
药理学
化学工程
医学
生物化学
工程类
复合材料
作者
Wei Zong,Ying Hu,Yingchun Su,Nan Luo,Xunan Zhang,Qingchuan Li,Xiaojun Han
标识
DOI:10.3109/02652048.2016.1156176
摘要
Stimuli-responsive drug carriers are considered to play important roles in chemotherapy. We fabricated pH-sensitive polydopamine-protected liposomes (liposome@PDA) drug delivery systems, which were characterised with microscope, scanning electron microscope (SEM), UV-vis spectrometer and Fourier transform infrared (FTIR) technieques. The typical chemotherapeutic agent, 5-fluorouracil (5-FU), was loaded into liposome@PDA capsules. The maximum release percentages of 5-FU are 3.2%, 29.5%, 52.7%, 76.7% in the solution with pH 7.42, 6.87, 4.11 and 3.16, respectively. The in vitro cell cytotoxity experiments were carried out using 5-FU-loaded capsules at pH 6.87 solution, which simulate the true pH around cancerous cells. At 1.5 μM concentration, the free 5-FU, 5-FU-loaded liposome capsules and 5-FU-loaded capsules showed the cell viability of 50.56%, 22.66% and 21.63%, respectively. It confirms that drug-loaded capsules performed better than free drug. The results demonstrate the great potential of liposome@PDA capsules as carriers in biomedical applications.
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