首页> 外文期刊>Journal of biomaterials and nanobiotechnology. >Release of Anticancer Drug 5-Fluorouracil from Different Ionically Crosslinked Alginate Beads
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Release of Anticancer Drug 5-Fluorouracil from Different Ionically Crosslinked Alginate Beads

机译:从不同的离子交联的藻酸盐微珠中释放抗癌药物5-氟尿嘧啶

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In this research; the release of 5-Fluorouracil (5-FU) from different ionically crosslinked alginate (Alg) beads was investigated by using Fe3+, Al3+, Zn2+, and Ca2+, ions as crosslinking agent. The prepared beads were characterized by Fourier Transform Infrared Spectroscopy (FTIR) Differential Scanning Calorimetry (DSC) and Scanning Electron Micros-copy (SEM). The drug release studies were carried out at three pH values 1.2, 6.8 and 7.4 respectively each for two hours. The effects of the preparation conditions as crosslinker type, drug/polymer (w/w) ratio, crosslinker concentration and time of exposure to crosslinker on the release of 5-FU were investigated for 6 hours at 37℃. It was observed that 5-FU release from the beads followed the order of Fe > Zn > Al > Ca-Alg and increased with increasing drug/polymer ratio. At the end of 6 hours, the highest 5-FU release was found to be 90% (w/w) for Fe-Alg beads at the drug/polymer ratio of 1/8 (w/w), crosslinker concentration of 0.05 M, exposure time of 10 minutes respectively. The swelling measurements of the beads supported the release results. Release kinetics was described by Fickian and non-Fickian approaches.
机译:在这项研究中;以Fe3 +,Al3 +,Zn2 +和Ca2 +离子为交联剂,研究了5-氟尿嘧啶(5-FU)从不同的离子交联藻酸盐(Alg)珠中的释放。通过傅立叶变换红外光谱(FTIR)差示扫描量热法(DSC)和扫描电子显微镜(SEM)对制备的珠进行表征。分别在三个pH值1.2、6.8和7.4下进行药物释放研究两个小时。在37℃下,研究了制备条件如交联剂类型,药物/聚合物(w / w)比,交联剂浓度和暴露于交联剂的时间对5-FU释放的影响。观察到从珠粒中释放出5-FU的顺序是Fe> Zn> Al> Ca-Alg,并且随着药物/聚合物比的增加而增加。在6小时结束时,发现在药物/聚合物比为1/8(w / w),交联剂浓度为0.05的情况下,Fe-Alg珠的最高5-FU释放量为90%(w / w) M,曝光时间分别为10分钟。珠粒的溶胀测量结果支持释放结果。释放动力学由Fickian和非Fickian方法描述。

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