通过闪速纳米沉淀法,可以轻松制造出 pH 值响应型乙缩醛葡聚糖纳米颗粒,用于在细胞内释放有效载荷。

0 MATERIALS SCIENCE, MULTIDISCIPLINARY
Krystal A Hughes, Bishal Misra, Maryam Maghareh, Parinya Samart, Ethan Nguyen, Salik Hussain, Werner J Geldenhuys, Sharan Bobbala
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引用次数: 0

摘要

乙缩醛葡聚糖(Ac-Dex)纳米粒子因其敏锐的 pH 值响应性和高度的生物降解性而备受关注。Ac-Dex 纳米粒子通常通过单乳液或双乳液方法配制,使用聚乙烯醇作为稳定剂。乳液法需要使用有毒的有机溶剂,如二氯甲烷或氯仿,并且需要多步处理才能形成稳定的 Ac-Dex 纳米粒子。在此,我们介绍一种简单的闪速纳米沉淀(FNP)方法,它利用密闭的喷射混合器和无毒溶剂乙醇来快速形成 Ac-Dex 纳米粒子。使用非离子 PEG 化表面活性剂、D-α-生育酚聚乙二醇琥珀酸酯(TPGS)或 Pluronic(F-127)稳定 Ac-Dex 纳米粒子。使用 FNP 形成的 Ac-Dex 纳米粒子具有高度单分散性,可稳定封装多种有效载荷,包括疏水性、亲水性和大分子。冻干后,Ac-Dex TPGS 纳米粒子至少能稳定保存一年,有效载荷保留率超过 80%。Ac-Dex 纳米粒子对细胞无毒,并能在细胞内将有效载荷释放到细胞质中。体内研究表明,静脉注射 Ac-Dex TPGS 纳米粒子后,其生物分布主要集中在肝、肺和脾脏。综上所述,FNP 技术可轻松制造和装载 Ac-Dex 纳米粒子,并将有效载荷精确释放到细胞内环境中,从而实现多种治疗应用。 pH 响应型乙醛葡聚糖可使用 TPGS 或 F-127 等非离子表面活性剂进行配制,以便在细胞内释放有效载荷。通过简单、可扩展的闪速纳米沉淀技术,利用密闭的撞击喷射混合器,可以制造出高度单分散和稳定的纳米颗粒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Flash nanoprecipitation allows easy fabrication of pH-responsive acetalated dextran nanoparticles for intracellular release of payloads.

Flash nanoprecipitation allows easy fabrication of pH-responsive acetalated dextran nanoparticles for intracellular release of payloads.

Acetalated dextran (Ac-Dex) nanoparticles are currently of immense interest due to their sharp pH-responsive nature and high biodegradability. Ac-Dex nanoparticles are often formulated through single- or double-emulsion methods utilizing polyvinyl alcohol as the stabilizer. The emulsion methods utilize toxic organic solvents such as dichloromethane or chloroform and require multi-step processing to form stable Ac-Dex nanoparticles. Here, we introduce a simple flash nanoprecipitation (FNP) approach that utilizes a confined impinging jet mixer and a non-toxic solvent, ethanol, to form Ac-Dex nanoparticles rapidly. Ac-Dex nanoparticles were stabilized using nonionic PEGylated surfactants, D-α-Tocopherol polyethylene glycol succinate (TPGS), or Pluronic (F-127). Ac-Dex nanoparticles formed using FNP were highly monodisperse and stably encapsulated a wide range of payloads, including hydrophobic, hydrophilic, and macromolecules. When lyophilized, Ac-Dex TPGS nanoparticles remained stable for at least one year with greater than 80% payload retention. Ac-Dex nanoparticles were non-toxic to cells and achieved intracellular release of payloads into the cytoplasm. In vivo studies demonstrated a predominant biodistribution of Ac-Dex TPGS nanoparticles in the liver, lungs, and spleen after intravenous administration. Taken together, the FNP technique allows easy fabrication and loading of Ac-Dex nanoparticles that can precisely release payloads into intracellular environments for diverse therapeutic applications. pH-responsive Acetalateddextran can be formulated using nonionic surfactants, such as TPGS or F-127, for intracellular release of payloads. Highly monodisperse and stable nanoparticles can be created through the simple, scalable flash nanoprecipitation technique, which utilizes a confined impingement jet mixer.

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