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Preparation of ferric ion crosslinked acrylamide grafted poly (vinyl alcohol)/sodium alginate microspheres and application in controlled release of anticancer drug 5-fluorouracil

机译:铁离子交联丙烯酰胺接枝聚乙烯醇/海藻酸钠微球的制备及其在抗癌药物5-氟尿嘧啶控释中的应用

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Ionically crosslinked microspheres of acrylamide (AAm) grafted poly (vinyl alcohol) (PVA)/sodium alginate (NaAlg) were prepared by crosslinking with FeCl3 and 5-fluorouracil (5-FU), which is an anticancer drug and was successfully encapsulated into the microspheres. The graft copolymer (PVA-g-PAAm) was characterized by using Fourier transform infrared spectroscopy (FTIR) and elemental analysis. The prepared microspheres were characterized by FTIR and scanning electron microscopy (SEM). Microspheres were also characterized by particle diameter, equilibrium swelling values and release profiles. The release studies were carried out at three pH values 1.2, 6.8 and 7.4, respectively, each for 2?h. The effects of preparation conditions as PVA-g-PAAm/NaAlg ratio, drug/polymer ratio, crosslinker concentration and exposure time to FeCl3 on the release of 5-FU were investigated for 6?h at 37?°C. The highest 5-FU release was found to be as 99.57% (w/w) at the end of 6?h for PVA-g-PAAm/NaAlg ratio of 1:4 (w/w), drug/polymer ratio of 1:8 (w/w), crosslinker concentration of 0.05?M and exposure time of 10?min. The release results were also supported by the swelling measurements of the microspheres. Release kinetics was described by Fickian and non-Fickian approaches.
机译:丙烯酰胺(AAm)接枝的聚乙烯醇(PVA)/藻酸钠(NaAlg)的离子交联微球是通过与FeCl 3 和5-氟尿嘧啶(5-FU)交联制备的。抗癌药,并已成功封装到微球中。通过使用傅里叶变换红外光谱(FTIR)和元素分析对接枝共聚物(PVA-g-PAAm)进行了表征。制备的微球通过FTIR和扫描电子显微镜(SEM)表征。微球的特征还在于粒径,平衡溶胀值和释放曲线。分别在三个pH值1.2、6.8和7.4下进行释放研究,每个pH值持续2 h。研究了制备条件如PVA-g-PAAm / NaAlg比,药物/聚合物比,交联剂浓度以及FeCl 3 的暴露时间对5-FU在37℃释放6?h的影响。 ℃。当PVA-g-PAAm / NaAlg比为1:4(w / w),药物/聚合物比为1时,在6?h结束时,最高5-FU释放为99.57%(w / w)。 :8(w / w),交联剂浓度为0.05?M,暴露时间为10?min。释放结果也得到微球溶胀测量的支持。释放动力学由Fickian和非Fickian方法描述。

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