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特异性相互作用提高了嵌段共聚物胶束在水性介质中的负载能力。

Specific interactions improve the loading capacity of block copolymer micelles in aqueous media.

作者信息

Giacomelli Cristiano, Schmidt Vanessa, Borsali Redouane

机构信息

Laboratoire de Chimie des Polymères Organiques (LCPO)-ENSCPB, Université Bordeaux 1, 16 Av. Pey Berland, 33607 Pessac Cedex, France.

出版信息

Langmuir. 2007 Jun 19;23(13):6947-55. doi: 10.1021/la700337s. Epub 2007 May 25.

Abstract

Block copolymer micelles find application in many fields as nanocarriers, especially in drug delivery. We report herein that specific interactions between hydrophobic guest molecules and core-forming segments can significantly improve the loading capacity of polymeric micelles. High loading capacities (>100% weight/weight of polymer (w/wp)) were systematically observed for the encapsulation of probes containing weak carboxylic acid groups by micellar nanoparticles having poly[2-(dialkylamino)ethyl methacrylate] cores (i.e., particles whose cargo space exhibits antagonist weak base functions), as demonstrated by the incorporation of indomethacin (IND), ibuprofen (IBPF), and trans-3,5-bis(trifluoromethyl)cinnamic acid (F-CIN) into either poly(ethylene oxide)-b-poly[2-(diisopropylamino)ethyl methacrylate] (PEO-b-PDPA) or poly(glycerol monomethacrylate)-b-PDPA (PG2MA-b-PDPA) micelles. The esterification of IND yielding to a nonionizable IND ethyl ester derivative (IND-Et) caused an abrupt decrease in the micellar loading capacity down to 10-15% w/wp. Similar results were also obtained when IND was combined with nonionizable block copolymers such as PEO-b-polycaprolactone (PEO-b-PCL) and PEO-b-poly(glycidyl methacrylate) (PEO-b-PGMA). The existence of acid-base interactions between the solubilizate and the weak polybase block forming the micelle core was confirmed by 1H NMR measurements. However, the incorporation of high numbers of hydrophobic guest molecules inside polymeric micelles can provoke not only an increase in the hydrodynamic size (2RH) of the objects but also a substantial change in the morphology (transition from spheres to cylinders). The application of the Higuchi model showed that the probe release followed a diffusion-controlled mechanism, and diffusion coefficients (D) on the order of 10-18-10-17 cm2/s were determined for IND release from 1.0 mg/mL PEO113-b-PDPA50 + 100% w/wp IND. Probe release from micelles with weak polybase-based cores can also be triggered by changes in the solution pH.

摘要

嵌段共聚物胶束作为纳米载体在许多领域有应用,尤其是在药物递送方面。我们在此报告,疏水性客体分子与形成核的链段之间的特定相互作用可显著提高聚合物胶束的负载能力。通过将吲哚美辛(IND)、布洛芬(IBPF)和反式-3,5-双(三氟甲基)肉桂酸(F-CIN)掺入聚(环氧乙烷)-b-聚[2-(二异丙基氨基)乙基甲基丙烯酸酯](PEO-b-PDPA)或聚(甘油单甲基丙烯酸酯)-b-PDPA(PG2MA-b-PDPA)胶束中,系统地观察到具有聚[2-(二烷基氨基)乙基甲基丙烯酸酯]核的胶束纳米颗粒(即其载药空间表现出拮抗弱碱功能的颗粒)对含有弱羧酸基团的探针的包封具有高负载能力(>聚合物重量/重量的100%(w/wp))。IND酯化生成不可电离的IND乙酯衍生物(IND-Et)导致胶束负载能力急剧下降至10-15%w/wp。当IND与不可电离的嵌段共聚物如PEO-b-聚己内酯(PEO-b-PCL)和PEO-b-聚(甲基丙烯酸缩水甘油酯)(PEO-b-PGMA)结合时,也获得了类似的结果。通过1H NMR测量证实了增溶剂与形成胶束核的弱聚碱嵌段之间存在酸碱相互作用。然而,在聚合物胶束内掺入大量疏水性客体分子不仅会导致物体的流体动力学尺寸(2RH)增加,还会导致形态发生实质性变化(从球形转变为圆柱形)。Higuchi模型的应用表明,探针释放遵循扩散控制机制,并且测定了从1.0 mg/mL PEO113-b-PDPA50 + 100%w/wp IND中释放IND的扩散系数(D)约为10-18-10-17 cm2/s。具有弱聚碱基核的胶束中的探针释放也可由溶液pH值的变化触发。

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