Do Linalool-Loaded Solid Lipid Nanoparticles Improve the Quality of Naval Medical Research Institute Mouse Sperm During Freezing/Thawing and Handling Processes?

IF 1.6 4区 生物学
Zahra Asadi, Faranak Aghaz, Zohreh Rahimi, Elham Arkan, Asad Vaisi-Raygani
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引用次数: 0

Abstract

Introduction: Handling, freezing, and thawing of sperm causes oxidative stress, compromising sperm quality. Nanotechnology offers platforms for the smart delivery of antioxidants during these processes. Objectives: A solid lipid nanoparticle (SLN) was used to deliver linalool, as an antioxidant supplementation to Naval Medical Research Institute mouse sperm during handling, freezing, and thawing. Methods: Linalool-loaded solid lipid nanoparticle (L-SLN) was made using the self-assembly method. After the assessment of physicochemical properties, the impact of L-SLN (10, 20, 30, and 50 µg/mL) on sperm motility, viability, sperm DNA fragmentation (SDF), nitric oxide (NO) production, and the activity of superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (CAT), was investigated after its addition to the handling, freezing, and thawing media. Results: L-SLN was successfully created with a size of 262 ± 9.5 and a zeta potential of -28.5 ± 7.12, with an extended-release over time. During handling and freezing, supplementing corresponding media with L-SLN resulted in increased sperm motility and viability, specifically at 30 µg/mL. The percentage of SDF also decreased in post-thawed sperm at 30 µg/mL. L-SLN also led to elevated post-thawed NO production at 20 µg/mL, as well as increased SOD activity at 20 and 30 µg/mL. It also enhanced CAT and GPx activity at 30 and 10 µg/mL respectively. In handling media, L-SLN at 10 µg/mL could enhance NO production, CAT, and SOD activity, and at 20 µg/mL also boosted NO production and GPx activity. Generally, there was no significant improvement in sperm parameters with the mutual concentration of L-SLN for thawing media. Conclusions: Treating sperm extender media with 20 and 30 µg/mL of L-SLN and handling media with 10 and 30 µg/mL of L-SLN could improve sperm parameters following these interventions. L-SLN is a new antioxidant for sperm handling and freezing media, which may be applicable in human reproductive efforts.

载芳樟醇固体脂质纳米颗粒在冷冻/解冻和处理过程中改善小鼠精子质量吗?
简介:处理、冷冻和解冻精子会引起氧化应激,影响精子质量。纳米技术为在这些过程中智能输送抗氧化剂提供了平台。目的:采用固体脂质纳米粒(SLN)向海军医学研究所小鼠精子输送芳樟醇作为抗氧化剂,在处理、冷冻和解冻过程中补充芳樟醇。方法:采用自组装法制备载芳樟醇固体脂质纳米粒(L-SLN)。在对理化性质进行评估后,研究了L-SLN(10、20、30和50µg/mL)在处理、冷冻和解冻培养基中添加后对精子活力、活力、精子DNA片段化(SDF)、一氧化氮(NO)生成以及超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)活性的影响。结果:成功制备了L-SLN,体积为262±9.5,ζ电位为-28.5±7.12,随时间缓释。在处理和冷冻过程中,添加相应的L-SLN培养基可以增加精子的活力和活力,特别是在30µg/mL时。解冻后精子中SDF的百分比在30µg/mL时也有所下降。当浓度为20µg/mL时,L-SLN还能提高解冻后NO的产量,并增加20和30µg/mL时的SOD活性。CAT和GPx活性分别在30和10µg/mL时增强。在处理培养基中,10µg/mL的L-SLN能提高NO生成、CAT和SOD活性,20µg/mL的L-SLN也能提高NO生成和GPx活性。一般来说,L-SLN的相互浓度对精子参数没有显著改善。结论:用20和30µg/mL的L-SLN处理精子扩展培养基,10和30µg/mL的L-SLN处理培养基,可改善精子参数。L-SLN是一种新的精子处理和冷冻介质抗氧化剂,可用于人类生殖活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biopreservation and Biobanking
Biopreservation and Biobanking Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
自引率
12.50%
发文量
114
期刊介绍: Biopreservation and Biobanking is the first journal to provide a unifying forum for the peer-reviewed communication of recent advances in the emerging and evolving field of biospecimen procurement, processing, preservation and banking, distribution, and use. The Journal publishes a range of original articles focusing on current challenges and problems in biopreservation, and advances in methods to address these issues related to the processing of macromolecules, cells, and tissues for research. In a new section dedicated to Emerging Markets and Technologies, the Journal highlights the emergence of new markets and technologies that are either adopting or disrupting the biobank framework as they imprint on society. The solutions presented here are anticipated to help drive innovation within the biobank community. Biopreservation and Biobanking also explores the ethical, legal, and societal considerations surrounding biobanking and biorepository operation. Ideas and practical solutions relevant to improved quality, efficiency, and sustainability of repositories, and relating to their management, operation and oversight are discussed as well.
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