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两亲性 Pluronic 嵌段共聚物的混合胶束形成:对控制和靶向药物传递的影响。

Mixed micelle formation with hydrophobic and hydrophilic Pluronic block copolymers: implications for controlled and targeted drug delivery.

机构信息

Government College of Pharmacy, Aurangabad 431005, Maharashtra, India.

出版信息

Colloids Surf B Biointerfaces. 2011 Dec 1;88(2):691-6. doi: 10.1016/j.colsurfb.2011.08.002. Epub 2011 Aug 6.

Abstract

Pluronic block copolymers offer affluent phase behavioral characteristics and are extensively investigated for drug delivery applications. Hydrophobic Pluronics produce larger aggregates whereas hydrophilic Pluronics often generate small-sized micelles in aqueous milieu. To overcome the limitations and combine the advantages of different kinds of Pluronics the mixing of such two types of Pluronics is studied here, especially for hydrophobic Pluronic L81 and relatively hydrophilic Pluronic P123. Critical micelle concentration (CMC) of the developed binary mixtures was 0.032 mg/ml as evidenced from pyrene fluorescence spectroscopy and is located in between that of the individual Pluronics. Dynamic light scattering (DLS) showed very small particle sizes (∼20 nm) and low polydispersity indices for most of the mixed micelles. Transmission electron microscopy (TEM) demonstrated spherical shape of micelles. Based upon the ratio of hydrophobic and hydrophilic Pluronics, dispersions of varied stability were obtained. With 0.1/1.0 wt.% and 0.5/3.0 wt.% of Pluronic L81/P123, stable dispersions were obtained. Stability was assessed from turbidity measurement, size analysis and clarity of dispersion on standing. Micelles were also found to be stable in bovine serum albumin (BSA) solution. Mixed micelles showed fairly high entrapment efficiency, loading capacity and sustained release profile for aceclofenac (Acl), a model hydrophobe. Presence of salt lowered Acl solubilization in micelles. Thermodynamic parameters for Acl solubilization in mixed micelles revealed high partition coefficient values and spontaneity of drug solubilization. Thus, the developed novel mixed micelles hold promise in controlled and targeted drug delivery owing to their very small size, high entrapment efficiency and stability.

摘要

两亲嵌段共聚物具有丰富的相行为特征,广泛应用于药物传递系统。疏水性 Pluronic 会产生较大的聚集物,而亲水性 Pluronic 通常在水介质中生成小尺寸的胶束。为了克服各种 Pluronic 的局限性并结合其优点,研究了两种类型 Pluronic 的混合,特别是疏水性 Pluronic L81 和相对亲水性 Pluronic P123。芘荧光光谱法证实,所开发的二元混合物的临界胶束浓度(CMC)为 0.032mg/ml,位于两种 Pluronic 单独的 CMC 之间。动态光散射(DLS)显示大多数混合胶束的粒径非常小(约 20nm)且多分散指数低。透射电子显微镜(TEM)显示了胶束的球形形状。基于疏水性和亲水性 Pluronic 的比例,获得了不同稳定性的分散体。当 Pluronic L81/P123 的比例为 0.1/1.0wt.%和 0.5/3.0wt.%时,可获得稳定的分散体。稳定性是通过浊度测量、粒径分析和分散体静置时的清晰度来评估的。胶束在牛血清白蛋白(BSA)溶液中也表现出稳定。混合胶束对模型疏水性药物醋氯芬酸(Acl)表现出相当高的包封效率、载药量和持续释放特性。盐的存在降低了 Acl 在胶束中的溶解度。混合胶束中 Acl 增溶的热力学参数表明药物增溶具有较高的分配系数值和自发性。因此,由于其非常小的粒径、高包封效率和稳定性,所开发的新型混合胶束有望在控制和靶向药物传递中得到应用。

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