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METHOD FOR THE PREPARATION OF BIOCOMPATIBLE POLYMERIC NANOPARTICLES FOR DRUG DELIVERY AND NANOPARTICLES PREPARED THEREBY

机译:制备生物相容性高分子纳米颗粒的方法及其制备的纳米颗粒

摘要

Disclosed are biocompatible polymeric nanoparticles for drug delivery and a method for preparing the same. They can be prepared by mixing a tri-block copolymer, PEG, and a drug at a predetermined temperature to give a homogeneous polymeric mixture; solidifying the homogeneous polymeric mixture at room temperature; and dissolving the solidified polymeric mixture in an aqueous solution. Based on a polymer melting process, the method makes it easy to produce poloxamer nanoparticles at low cost. The nanoparticles show desired particle sizes suitable for use in drug delivery and a uniform particle size distribution. Consisting of a bilayer structure, the nanoparticles can contain sparingly soluble drugs. Also, the nanoparticles contain no organic solvents and are thus safe to the body because they are free of organic solvent residuals. Further, after being administered into the body, the nanoparticles with a high content of sparingly soluble drug entrapped therein can safely deliver the drug to target sites and stably release the drug at a controlled rate.
机译:公开了用于药物递送的生物相容性聚合物纳米颗粒及其制备方法。它们可以通过在预定温度下将三嵌段共聚物,PEG和药物混合以得到均匀的聚合物混合物来制备。在室温下固化均匀的聚合物混合物;将固化的聚合物混合物溶解在水溶液中。基于聚合物熔融过程,该方法使得容易以低成本生产泊洛沙姆纳米颗粒。纳米颗粒显示出适合用于药物递送的所需粒度和均匀的粒度分布。由双层结构组成,纳米颗粒可以包含微溶药物。而且,纳米颗粒不含有机溶剂,因此对人体安全,因为它们不含有机溶剂残留物。此外,在被施用到体内之后,其中包埋有高含量的微溶药物的纳米颗粒可以安全地将药物递送至靶位并且以受控的速率稳定地释放药物。

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