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Drug delivery system based on dissolution parameters and method for changing drug saturation concentration

机译:基于溶出度参数的药物输送系统及改变药物饱和浓度的方法

摘要

The method of adjusting the saturation concentration of a drug in a transdermal composition for application to the dermis, which comprises mixing polymers having differing solubility parameters, so as to modulate the delivery of the drug. This results in the ability to achieve a predetermined permeation rate of the drug into and through the dermis. In one embodiment, a dermal composition of the present invention comprises a drug, an acrylate polymer, and a polysiloxane. The dermal compositions can be produced by a variety of methods known in the preparation of drug-containing adhesive preparations, including the mixing of the polymers, drug, and additional ingredients in solution, followed by removal of the processing solvents. The method and composition of this invention permit selectable loading of the drug into the dermal formulation and adjustment of the delivery rate of the drug from the composition through the dermis, while maintaining acceptable shear, tack, and peel adhesive properties.
机译:调节用于透皮组合物的药物在皮肤中的饱和浓度的方法,该方法包括混合具有不同溶解度参数的聚合物,以调节药物的递送。这导致能够实现药物进入和穿过真皮的预定渗透率。在一个实施方案中,本发明的皮肤组合物包含药物,丙烯酸酯聚合物和聚硅氧烷。可以通过在制备含药物的粘合剂制剂中已知的多种方法来生产皮肤组合物,包括在溶液中混合聚合物,药物和其他成分,然后除去加工溶剂。本发明的方法和组合物允许选择性地将药物加载到皮肤制剂中,并调节药物从组合物中穿过真皮的递送速率,同时保持可接受的剪切,粘性和剥离粘合性。

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