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Development and Noninvasive Characterization of Hormone Releasing In Situ Forming Implants

机译:原位成形植入物释放激素的开发和非侵袭性

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In the human body aldosterone plays a major role in the regulation of the salt water balance and the blood pressure. To investigate the pathophysiological effects of aldosterone in a mouse model appropriate drug delivery systems, that release the drug in a constant and continuous manner, are needed. Therefore novel in situ forming implants were developed as alternative aldosterone releasing depots. The non-invasive analytical method electron spin resonance (ESR) spectroscopy was applied to characterize in situ the implant formation by direct and continuous quantification of polymer precipitation and solvent exchange rates. Therewith influences of several key formulation parameters, such as type of the solvent and the polymer have been investigated. In this context AB di- and triblock copolymers of poly(ethylene glycol) (PEG) and poly(lactide-co-glycolide) (PLGA) were firstly explored as polymeric matrices for in situ forming implants. The phase separation kinetics and therewith the aldosterone releases were highly dependent on the hydrophilic character and the molecular weight of the used polymers.
机译:在人体中,醛固酮在盐水平衡和血压调节中发挥着重要作用。为了研究醛固酮在小鼠模型适当的药物递送系统中的病理生理学作用,需要以恒定和连续的方式释放药物。因此,在原位成形植入物中的新颖被开发为替代的醛固酮释放仓库。应用非侵入性分析方法电子自旋共振(ESR)光谱通过直接和连续定量的聚合物沉淀和溶剂汇率来表征原位植入物形成。研究了几种关键配方参数的影响,例如溶剂的类型和聚合物。在这种上下文中,首先探讨聚(乙二醇)(PEG)和聚(丙交酯 - 共乙二醇酰基)(PLGA)的二嵌段和聚(丙交酯 - 共乙酰化)(PLGA)作为原位成型植入物的聚合物基质。相分离动力学和其中醛酮释放高度依赖于亲水性特征和使用过的聚合物的分子量。

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