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首页> 外文期刊>Colloid and polymer science >Preparation of poly(butylcyanoacrylate) drug carriers by nanoprecipitation using a pre-synthesized polymer and different colloidal stabilizers
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Preparation of poly(butylcyanoacrylate) drug carriers by nanoprecipitation using a pre-synthesized polymer and different colloidal stabilizers

机译:使用预合成的聚合物和不同的胶体稳定剂通过纳米沉淀法制备聚(氰基丙烯酸丁酯)药物载体

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摘要

Classically, drug-loaded poly(alkylcyanoacrylate) colloidal carriers are prepared by the drug entrapment during emulsion polymerization. However, a number of chemically sensitive drugs are unstable in the conditions of polymerization or can be irreversibly inactivated by the highly reactive monomer. Furthermore, the particle size distribution and the molecular weight of formed polymer depend strongly on the polymerization conditions. Here, we investigate the nanoprecipitation approach for the preparation of pure and drug-load poly(butylcyanoacrylate) nanoparticles. This method allows the successful entrapment of lipophilic and chemically labile drugs by avoiding the contact with highly reactive monomers. The anticancer agent chlorambucil is chosen as the model drug for the incorporation and release studies. Pure and drug-loaded nanoparticles are successfully prepared using various stabilizers (Polysorbate 80, Pluronic F68, Dextran 40). The nanoparticles coated with Polysorbate 80 are of highest interest since they could overcome the blood-brain barrier and the multidrug resistance in cancer cells. Such nanoparticles can be easily prepared by the nanoprecipitation approach reported here.
机译:经典地,载有药物的聚(氰基丙烯酸烷基酯)胶体载体是通过乳液聚合过程中的药物截留来制备的。但是,许多化学敏感性药物在聚合条件下不稳定,或者可以被高反应性单体不可逆地灭活。此外,形成的聚合物的粒度分布和分子量强烈取决于聚合条件。在这里,我们研究了制备纯净和载药量聚(氰基丙烯酸丁酯)纳米粒子的纳米沉淀方法。通过避免与高反应性单体接触,该方法可以成功地捕获亲脂性和化学不稳定药物。选择抗癌药苯丁酸氮芥作为掺入和释放研究的模型药物。使用各种稳定剂(聚山梨酯80,Pluronic F68,右旋糖酐40)成功制备了纯净且载有药物的纳米颗粒。涂覆有聚山梨酯80的纳米颗粒具有最高的吸引力,因为它们可以克服血脑屏障和癌细胞中的多药耐药性。这样的纳米颗粒可以通过本文报道的纳米沉淀方法容易地制备。

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