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糖分子诱导金-甲氨蝶呤缀合物的形成:制备、组装机制及生物测定研究。

Induction of Au-methotrexate conjugates by sugar molecules: production, assembly mechanism, and bioassay studies.

机构信息

Jiangsu Key Laboratory of Biofunctional Material, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China.

Jiangsu Key Laboratory of Biofunctional Material, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing 210023, China; Shandong Bingkun Tengtai Ceramics Technology Co. Ltd., Zibo 255321, China.

出版信息

Int J Pharm. 2018 Mar 1;538(1-2):65-78. doi: 10.1016/j.ijpharm.2017.12.051. Epub 2018 Jan 16.

Abstract

Au-methotrexate (Au-MTX) conjugates induced by sugar molecules were produced by a simple, one-pot, hydrothermal growth method. Herein, the Au(III)-MTX complexes were used as the precursors to form Au-MTX conjugates. Addition of different types of sugar molecules with abundant hydroxyl groups resulted in the formation of Au-MTX conjugates featuring distinct characteristics that could be explained by the diverse capping mechanisms of sugar molecules. That is, the instant-capping mechanism of glucose favored the generation of peanut-like Au-MTX conjugates with high colloidal stability while the post-capping mechanism of dextran and sucrose resulted in the production of Au-MTX conjugates featuring excellent near-infrared (NIR) optical properties with a long-wavelength plasmon resonance near 630-760 nm. Moreover, in vitro bioassays showed that cancer cell viabilities upon incubation with free MTX, Au-MTX conjugates doped with glucose, dextran and sucrose for 48 h were 74.6%, 55.0%, 62.0%, and 63.1%, respectively. Glucose-doped Au-MTX conjugates exhibited a higher anticancer activity than those doped with dextran and sucrose, therefore potentially presenting a promising treatment platform for anticancer therapy. Based on the present study, this work may provide the first example of using biocompatible sugars as regulating agents to effectively guide the shape and assembly behavior of Au-MTX conjugates. Potentially, the synergistic strategy of drug molecules and sugar molecules may offer the possibility to create more gold-based nanocarriers with new shapes and beneficial features for advanced anticancer therapy.

摘要

通过简单的一锅水热生长方法制备了由糖分子诱导的 Au-甲氨蝶呤(Au-MTX)缀合物。在此,将 Au(III)-MTX 配合物用作形成 Au-MTX 缀合物的前体。添加具有丰富羟基的不同类型的糖分子导致形成具有不同特征的 Au-MTX 缀合物,这些特征可以通过糖分子的不同封端机制来解释。也就是说,葡萄糖的即时封端机制有利于生成具有高胶体稳定性的花生状 Au-MTX 缀合物,而葡聚糖和蔗糖的后封端机制则有利于生成具有长波长等离子体共振的优异近红外(NIR)光学特性的 Au-MTX 缀合物,波长在 630-760nm 附近。此外,体外生物测定表明,在用游离 MTX、掺杂葡萄糖、葡聚糖和蔗糖的 Au-MTX 缀合物孵育 48 小时后,癌细胞活力分别为 74.6%、55.0%、62.0%和 63.1%。与掺杂葡聚糖和蔗糖的 Au-MTX 缀合物相比,掺杂葡萄糖的 Au-MTX 缀合物表现出更高的抗癌活性,因此可能为抗癌治疗提供有前途的治疗平台。基于本研究,这项工作可能为首次使用生物相容性糖作为调节剂来有效指导 Au-MTX 缀合物的形状和组装行为提供了实例。潜在地,药物分子和糖分子的协同策略可能为具有新形状和有益特性的新型基于金的纳米载体用于先进的抗癌治疗提供了可能性。

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