首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >The release behavior of brilliant blue from calcium-alginate gel beads coated by chitosan: the preparation method effect.
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The release behavior of brilliant blue from calcium-alginate gel beads coated by chitosan: the preparation method effect.

机译:壳聚糖包被的海藻酸钙凝胶珠的亮蓝色释放行为:制备方法的效果。

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摘要

The aim of this study is to reveal how the release behavior of a model drug (brilliant blue, BB) from chitosan coating calcium-alginate gel beads (CCAGB) was influenced by the preparation methods. The CCAGB were prepared by dropping alginate solution into CaCl(2)/chitosan solution (method 1(a)), or into chitosan solution then gelled by CaCl(2) (method 1(b)), or into CaCl(2) solution then coated by chitosan (method 2). Scanning electron microscopy was used for morphology observation, and elemental analysis was applied to determine the chitosan content bound on calcium-alginate gel beads (CAGB). Compared to CAGB, the dried CCAGB had poorer shape and rougher surface morphology especially in methods 1(a) and (b); moreover, CCAGB was found to be more instable in 0.9% NaCl and serious burst of beads occurred when high concentration of alginate (3.0 and 5.0% w/v) was used. The influence on BB release from the beads by chitosan coating was not only related to the chitosan density on bead surface, but also preparation method and other factors. Under un-dried bead state in method 1(a), the increase of chitosan content prolonged BB release in 0.9% (w/v) NaCl; while in method 2, the increase of chitosan concentration over 0.1% (w/v) (3.0% (w/v) alginate concentration was used) resulted in more serious burst of beads and hence facilitated BB release. Furthermore, in both methods 1(a) and 2, the increase of alginate from 1.5 to 3.0 or 5.0% (w/v) usually resulted in the significant burst of beads and accelerated BB release when 0.3 or 0.5% (w/v) chitosan was used for coating. Drying process greatly influenced BB release profile due to the destroying of alginate-chitosan film. The acceleration of BB release from CCAGB by drying process was more significant in the case of method 1 than of method 2.
机译:这项研究的目的是揭示制备方法如何影响壳聚糖包被的海藻酸钙凝胶珠(CCAGB)对模型药物(亮蓝,BB)的释放行为。通过将藻酸盐溶液滴入CaCl(2)/壳聚糖溶液(方法1(a))或壳聚糖溶液中,然后通过CaCl(2)(方法1(b))凝胶化,或放入CaCl(2)溶液中来制备CCAGB然后用壳聚糖包被(方法2)。扫描电子显微镜用于形态观察,并应用元素分析确定结合在藻酸钙凝胶珠(CAGB)上的壳聚糖含量。与CAGB相比,干燥的CCAGB具有较差的形状和较粗糙的表面形态,尤其是在方法1(a)和(b)中;此外,当使用高浓度藻酸盐(3.0和5.0%w / v)时,发现在0.9%NaCl中CCAGB更加不稳定,并且珠子严重破裂。壳聚糖涂层对珠子中BB释放的影响不仅与珠子表面的壳聚糖密度有关,而且与制备方法和其他因素有关。在方法1(a)中未干燥的珠粒状态下,壳聚糖含量的增加延长了0.9%(w / v)NaCl中BB的释放;而在方法2中,壳聚糖浓度的增加超过0.1%(w / v)(使用藻酸盐浓度为3.0%(w / v))导致珠子更严重地破裂,从而促进了BB的释放。此外,在方法1(a)和2中,藻酸盐从1.5%增加到3.0%或5.0%(w / v)时,通常会导致珠粒大量破裂,当0.3%或0.5%(w / v)时BB释放加快。壳聚糖用于包衣。由于藻酸盐-壳聚糖膜的破坏,干燥过程极大地影响了BB的释放曲线。在方法1的情况下,通过干燥过程加速BB从CCAGB释放的速度比方法2更为明显。

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