首页> 外国专利> SOLID LIPID NANOPARTICLES FOR DRUG DELIVERY, A PROCESS FOR THE PREPARATRION THEREOF, AND AN INJECTION COMPRISING THE SAME

SOLID LIPID NANOPARTICLES FOR DRUG DELIVERY, A PROCESS FOR THE PREPARATRION THEREOF, AND AN INJECTION COMPRISING THE SAME

机译:用于药物递送的固体脂质纳米颗粒,其制备方法以及包括该脂质体的注射剂

摘要

A solid lipid nanoparticle for drug delivery, which has a form containing a nano lipid nuclear is provided to have high stability of formulation and apply to hydrophilic drug, hydrophobic drug, and protein drug. A solid lipid nanoparticle for drug delivery has a nano lipid nuclear comprising a mixed lipid matrix of cacao butter and drug in a shell which is formed with poloxamer. The poloxamer is poloxamer 407, 124, 188, 235, 237, 238, 338 or their combination. The nano particle comprises 5-30 weight part of cacao butter based on the 100 weight of poloxamer and has 100-300 nm of average diameter. The solid lipid nanoparticle is used in a form of anticancer drug, or therapeutic agent for osteoporosis.
机译:提供具有包含纳米脂质核的形式的用于药物递送的固体脂质纳米颗粒,以具有高的制剂稳定性,并适用于亲水性药物,疏水性药物和蛋白质药物。用于药物递送的固体脂质纳米颗粒具有纳米脂质核,该纳米脂质核在由泊洛沙姆形成的壳中包含可可脂和药物的混合脂质基质。泊洛沙姆是泊洛沙姆407、124、188、235、237、238、338或它们的组合。纳米颗粒基于100重量的泊洛沙姆包含5-30重量份的可可脂,并且具有100-300nm的平均直径。固体脂质纳米颗粒以抗癌药或骨质疏松症治疗剂的形式使用。

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