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用于在宽温度范围内储存和处理的无水核酸纳米颗粒。

Anhydrous Nucleic Acid Nanoparticles for Storage and Handling at Broad Range of Temperatures.

机构信息

Nanoscale Science Program, Department of Chemistry, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.

Department of Physics and Optical Science, The University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.

出版信息

Small. 2022 Apr;18(13):e2104814. doi: 10.1002/smll.202104814. Epub 2022 Feb 6.

Abstract

Recent advances in nanotechnology now allow for the methodical implementation of therapeutic nucleic acids (TNAs) into modular nucleic acid nanoparticles (NANPs) with tunable physicochemical properties which can match the desired biological effects, provide uniformity, and regulate the delivery of multiple TNAs for combinatorial therapy. Despite the potential of novel NANPs, the maintenance of their structural integrity during storage and shipping remains a vital issue that impedes their broader applications. Cold chain storage is required to maintain the potency of NANPs in the liquid phase, which greatly increases transportation costs. To promote long-term storage and retention of biological activities at higher temperatures (e.g., +50 °C), a panel of representative NANPs is first exposed to three different drying mechanisms-vacuum concentration (SpeedVac), lyophilization (Lyo), and light-assisted drying (LAD)-and then rehydrated and analyzed. While SpeedVac primarily operates using heat, Lyo avoids temperature increases by taking advantage of pressure reduction and LAD involves a near-infrared laser for uniform drying in the presence of trehalose. This work compares and defines refinements crucial in formulating an optimal strategy for producing stable, fully functional NANPs and presents a forward advancement in their development for clinical applications.

摘要

纳米技术的最新进展使得有办法将治疗性核酸(TNAs)有条理地导入具有可调理化性质的模块化核酸纳米颗粒(NANPs)中,这些性质可与所需的生物学效应相匹配,提供均一性,并调节多种 TNAs 的递送来进行组合治疗。尽管新型 NANPs 具有潜力,但在储存和运输过程中保持其结构完整性仍然是一个至关重要的问题,这阻碍了它们的更广泛应用。需要冷链储存来保持液相中 NANPs 的效力,这大大增加了运输成本。为了促进在较高温度(例如+50°C)下的长期储存和保留生物活性,首先将一组有代表性的 NANPs 暴露于三种不同的干燥机制——真空浓缩(SpeedVac)、冷冻干燥(Lyo)和光辅助干燥(LAD),然后再进行水化和分析。虽然 SpeedVac 主要利用热量进行操作,但 Lyo 通过利用减压来避免温度升高,而 LAD 则涉及近红外激光,在存在海藻糖的情况下进行均匀干燥。这项工作比较并定义了在制定生产稳定、功能齐全的 NANPs 的最佳策略中至关重要的改进,并为其临床应用的发展提供了一个前进的方向。

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