Suppr超能文献

具有增强载药能力和缓释能力的丙烯酸/环糊精水凝胶。

Acrylic/cyclodextrin hydrogels with enhanced drug loading and sustained release capability.

作者信息

Siemoneit Ulf, Schmitt Christoph, Alvarez-Lorenzo Carmen, Luzardo Asteria, Otero-Espinar Francisco, Concheiro Angel, Blanco-Méndez José

机构信息

Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15782-Santiago de Compostela, Spain.

出版信息

Int J Pharm. 2006 Apr 7;312(1-2):66-74. doi: 10.1016/j.ijpharm.2005.12.046. Epub 2006 Feb 7.

Abstract

The influence of the proportion of acrylamidomethyl-gamma-cyclodextrin (gamma-CD-NMA) on loading and release of the hydrophobic triamcinolone acetonide (TA) and the hydrophilic propranolol (PR) by acrylic acid hydrogels was evaluated. gamma-CD-NMA was synthesized by condensation of gamma-cyclodextrin (gamma-CD) with N-(hydroxymethyl) acrylamide. Hydrogels were prepared with gamma-CD-NMA and sodium acrylate (3 M or 4 M), using N,N'-methylen(bisacrylamide) (BIS) as cross-linker, by free radical polymerization into glass moulds of 2 mm wide and were cut as discs (10 mm diameter). gamma-CD-NMA did not modify the pH-dependent swelling of the hydrogels, but significantly increased the swelling degree in the 40:60 ethanol:water, medium in which TA can be dissolved. Hydrogels prepared with gamma-CD-NMA above 5% (w/w of total monomers) showed a remarkably higher capacity to load TA, e.g., 33 mg/g dry hydrogel versus 0.6 mg/g dry hydrogel without gamma-CD-NMA. This is explained by the formation of 1:1 inclusion complexes of TA with gamma-CD mers that overcomes the lack of interactions with the acrylic groups of the network. The release of TA in water, 0.1 N HCl, or pH 6.8 phosphate buffer was sustained for at least 24 h, whatever the pH and the composition of the medium used. In contrast, loading of PR from the water solutions was greater for hydrogels prepared with 3 M acrylate than with 4 M acrylate, irrespective to their content in gamma-CD-NMA, and in less than 2 h ca. 80% PR was released. The lower affinity of PR for the gamma-CD cavities, compared to the strong intensity of the electrostatic interactions with the acrylic acid groups, explains why the incorporation of gamma-CD-NMA did not increased the loading and control release capacity of the hydrogels of this hydrophilic drug. In summary, the copolymerisation of CD with acrylic monomers can provide highly hydrophilic pH-sensitive networks which load large amounts of hydrophobic drugs and release them in a sustained way.

摘要

评估了丙烯酰胺甲基 -γ-环糊精(γ-CD-NMA)的比例对丙烯酸水凝胶负载和释放疏水性曲安奈德(TA)和亲水性普萘洛尔(PR)的影响。γ-CD-NMA 通过γ-环糊精(γ-CD)与 N-(羟甲基)丙烯酰胺缩合合成。使用 N,N'-亚甲基双丙烯酰胺(BIS)作为交联剂,将γ-CD-NMA 和丙烯酸钠(3 M 或 4 M)通过自由基聚合制备水凝胶,使其进入 2 mm 宽的玻璃模具中,并切成圆盘(直径 10 mm)。γ-CD-NMA 并未改变水凝胶的 pH 依赖性溶胀,但显著增加了在 40:60 乙醇:水介质中的溶胀度,在该介质中 TA 可溶解。用高于 5%(占总单体重量)的γ-CD-NMA 制备的水凝胶显示出显著更高的负载 TA 的能力,例如,33 mg/g 干水凝胶,而不含γ-CD-NMA 的干水凝胶为 0.6 mg/g。这是由于 TA 与γ-CD 单体形成了 1:1 的包合物,克服了与网络丙烯酸基团缺乏相互作用的问题。无论使用的介质的 pH 和组成如何,TA 在水、0.1 N HCl 或 pH 6.8 的磷酸盐缓冲液中的释放持续至少 24 小时。相比之下,无论γ-CD-NMA 的含量如何,用 3 M 丙烯酸盐制备的水凝胶从水溶液中负载 PR 的量都比用 4 M 丙烯酸盐制备的水凝胶大,并且在不到 2 小时内约 80%的 PR 被释放。与与丙烯酸基团的强静电相互作用强度相比,PR 对γ-CD 腔的亲和力较低,这解释了为什么γ-CD-NMA 的加入并未增加这种亲水性药物水凝胶的负载和控释能力。总之,CD 与丙烯酸单体的共聚可以提供高度负载大量疏水性药物并持续释放它们的亲水性网络。

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