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Modified Microparticles of Calcium Alginate Gel for Controlled Release of Anesthetics

机译:海藻酸钙凝胶的改性微粒用于麻醉剂的控制释放

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The aim of this work is the development of controlled delivery system immobilized by local anesthetics on the basis of modified microparticles of calcium alginate gels. The kazkain, rikhlokain, lidokain and novokain were used as local anesthetics. Modified microparticles were obtained by syringed dropwise a solution of ansthetics in sodium alginate into solution of polymers such as chitosan in calcium chloride. The obtained modified alginate microparticles were contained immobilized anesthetics in core of particles and a surface layer of polymer. Effects of polymer concentration and exposure duration on the thickness of polymer coating were determined. The release of anesthetics from the modified alginate gel particles into a physiological solution with different thickness of coating were studied. All the release data show the typical pattern for a matrix controlled mechanism. The cumulative amount of drug released from alginate gels was linearly related to the square root of the time and the release rate decreased this time. The process is controlled by the diffusion of anesthetics through the polymeric coating. The data shown a possibility of the regulation of the rate of anesthetics release from the modified alginate particles by way of alternation of thickness of the polymer coating. The anesthetic effect of the alginate microparticles containing drugs was tested on rats by method "tail flick" according two criteria: full analgesia - the absence of reaction on pain and sufficient analgesia - exceeding of pain threshold sensibility two and more times. Medical-biological tests show that the duration of anesthetic activity for the drug-containing alginate beads increases at 5-8 times in comparison of free drugs.
机译:这项工作的目的是在藻酸钙凝胶改性微粒的基础上,开发由局麻药固定的可控递送系统。卡兹卡因,利什卡因,利多卡因和新卡因被用作局部麻醉剂。通过将麻醉剂在海藻酸钠中的溶液逐滴注射到聚合物如壳聚糖在氯化钙中的溶液中,获得改性的微粒。所获得的改性藻酸盐微粒在颗粒的核和聚合物的表面层中包含固定的麻醉剂。确定了聚合物浓度和暴露时间对聚合物涂层厚度的影响。研究了麻醉剂从改性藻酸盐凝胶颗粒释放到具有不同涂层厚度的生理溶液中的情况。所有发布数据均显示了矩阵控制机制的典型模式。从藻酸盐凝胶释放的药物的累积量与时间的平方根线性相关,并且这次的释放速率降低。该过程通过麻醉剂在聚合物涂层中的扩散来控制。数据显示了通过改变聚合物涂层的厚度来调节从改性藻酸盐颗粒释放麻醉剂的速率的可能性。通过“尾巴甩动”方法根据两个标准在大鼠上测试了含有药物的藻酸盐微粒的麻醉效果:完全镇痛-对疼痛没有反应,并且镇痛充分-超过疼痛阈值敏感性两次以上。医学生物学测试表明,与游离药物相比,含药物藻酸盐微珠的麻醉活性持续时间增加了5到8倍。

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