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制备和控制亚 100nm 纯纳米药物的大小。

Preparation and size control of sub-100 nm pure nanodrugs.

机构信息

Center of Super-Diamond and Advanced Films (COSDAF) & Department of Physics and Materials Science, City University of Hong Kong , Kowloon, Hong Kong SAR, People's Republic of China.

出版信息

Nano Lett. 2015 Jan 14;15(1):313-8. doi: 10.1021/nl503598u. Epub 2014 Dec 18.

Abstract

Pure nanodrugs (PNDs), nanoparticles consisting entirely of drug molecules, have been considered as promising candidates for next-generation nanodrugs. However, the traditional preparation method via reprecipitation faces critical challenges including low production rates, relatively large particle sizes, and batch-to-batch variations. Here, for the first time, we successfully developed a novel, versatile, and controllable strategy for preparing PNDs via an anodized aluminum oxide (AAO) template-assisted method. With this approach, we prepared PNDs of an anticancer drug (VM-26) with precisely controlled sizes reaching the sub-20 nm range. This template-assisted approach has much higher feasibility for mass production comparing to the conventional reprecipitation method and is beneficial for future clinical translation. The present method is further demonstrated to be easily applicable for a wide range of hydrophobic biomolecules without the need of custom molecular modifications and can be extended for preparing all-in-one nanostructures with different functional agents.

摘要

纯纳米药物(PNDs),由完全由药物分子组成的纳米颗粒,被认为是下一代纳米药物的有前途的候选者。然而,通过再沉淀的传统制备方法面临着包括低生产速率、相对较大的粒径和批间变化在内的关键挑战。在这里,我们首次成功地开发了一种新颖的、通用的和可控的通过氧化铝模板辅助方法制备 PNDs 的策略。通过这种方法,我们制备了具有精确控制尺寸的抗癌药物(VM-26)的 PNDs,达到了亚 20nm 的范围。与传统的再沉淀方法相比,这种模板辅助方法具有更高的大规模生产可行性,有利于未来的临床转化。本方法进一步证明可广泛应用于各种疏水性生物分子,而无需进行定制分子修饰,并可扩展用于制备具有不同功能试剂的一体化纳米结构。

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