Antisense oligonucleotides and their technical suitability to nebulization

雾化器 寡核苷酸 核酸 气溶胶化 粘度 锁核酸 气溶胶 磷酸二酯键 化学 生物医学工程 纳米技术 吸入 材料科学 色谱法 生物化学 DNA 有机化学 麻醉 复合材料 医学 核糖核酸 基因
作者
Leonardo L. Seidl,Regina Moog,Kirsten A. Graeser
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:661: 124390-124390 被引量:1
标识
DOI:10.1016/j.ijpharm.2024.124390
摘要

In vivo studies investigating the inhalative efficacy of biotherapeutics, such as nucleic acids, usually do not perform an aerosolization step, rather the solution is directly administered into the lungs e.g. intratracheally. In addition, there is currently very little information on the behavior of nucleic acid solutions when subjected to the physical stress of the nebulization process. In this study, the aim was to assess the technical suitability of Locked Nucleic Acids (LNAs), as a model antisense oligonucleotide, towards nebulization using two commercially available nebulizers. A jet nebulizer (Pari LC Plus) and a vibrating mesh nebulizer (Aerogen Solo) were employed and solutions of five different LNAs investigated in terms of their physical and chemical stability to nebulization and the quality of the generated aerosols. The aerosol properties of the Aerogen Solo were mainly influenced by the viscosity of the solutions with the output rate and the droplet size decreasing with increasing viscosity. The Pari LC Plus was less susceptible to viscosity and overall the droplet size was smaller. The LNAs tolerated both nebulization processes and the integrity of the molecules was shown. Chemical stability of the molecules from the Aerogen Solo was confirmed, whereas aerosol generation with the Pari LC Plus jet nebulizer led to a slight increase of phosphodiester groups in a fully phosphorothiolated backbone of the LNAs. Overall, it could be shown that nebulization of different LNAs is possible and inhalation can therefore be considered a potential route of administration.
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