Delivery of Tempol from Polyurethane Nanocapsules to Address Oxidative Stress Post-Injury.

IF 3.9 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS Bioconjugate Chemistry Pub Date : 2025-02-19 Epub Date: 2025-02-08 DOI:10.1021/acs.bioconjchem.4c00360
Temitope Ale, Tolulope Ale, Kimberly J Baker, Kameel M Zuniga, Jack Hutcheson, Erin Lavik
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Abstract

Traumatic brain injuries (TBIs) result in significant morbidity and mortality due to the cascade of secondary injuries involving oxidative stress and neuroinflammation. The development of effective therapeutic strategies to mitigate these effects is critical. This study explores the fabrication and characterization of polyurethane nanocapsules for the sustained delivery of Tempol, a potent antioxidant. The nanocapsules were designed to extend the release of Tempol over a 30-day period, addressing the prolonged oxidative stress observed post-TBI. Tempol-loaded polyurethane nanocapsules were synthesized using interfacial polymerization and nanoemulsion techniques. Two generations of nanocapsules were produced, differing in Tempol loading and PEGylation levels. The first generation, with lower Tempol loading, exhibited an average size of 159.8 ± 12.61 nm and a Z-average diameter of 771.9 ± 87.95 nm. The second generation, with higher Tempol loading, showed an average size of 141.4 ± 6.13 nm and a Z-average diameter of 560.7 ± 171.1 nm. The zeta potentials were -18.9 ± 5.02 mV and -11.9 ± 3.54 mV for the first and second generations, respectively. Both generations demonstrated the presence of urethane linkages, confirmed by Fourier Transform Infrared Spectroscopy (FTIR). Loading studies revealed Tempol concentrations of 61.94 ± 3.04 μg/mg for the first generation and 77.61 ± 3.04 μg/mg for the second generation nanocapsules. Release profiles indicated an initial burst followed by a sustained, nearly linear release over 30 days. The higher PEGylation in the second generation nanocapsules is advantageous for intravenous administration, potentially enhancing their therapeutic efficacy in TBI treatment. This study demonstrates the feasibility of using polyurethane nanocapsules for the prolonged delivery of Tempol, offering a promising approach to manage oxidative stress and improve outcomes in TBI patients. Future work will include testing these nanocapsules in vivo to determine their potential at modulating recovery from TBI.

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聚氨酯纳米胶囊递送Tempol以解决损伤后的氧化应激。
创伤性脑损伤(tbi)由于涉及氧化应激和神经炎症的继发性损伤级联导致显著的发病率和死亡率。开发有效的治疗策略来减轻这些影响是至关重要的。本研究探讨了聚氨酯纳米胶囊的制备和表征,用于持续递送Tempol,一种有效的抗氧化剂。纳米胶囊旨在延长Tempol在30天内的释放,解决tbi后观察到的延长氧化应激。采用界面聚合和纳米乳液技术合成了负载tempol的聚氨酯纳米胶囊。生产了两代纳米胶囊,不同的Tempol负载和聚乙二醇化水平。第一代Tempol负载较低,平均尺寸为159.8±12.61 nm, z -平均直径为771.9±87.95 nm。第二代Tempol负载较高,平均尺寸为141.4±6.13 nm, z -平均直径为560.7±171.1 nm。1代和2代的zeta电位分别为-18.9±5.02 mV和-11.9±3.54 mV。通过傅里叶变换红外光谱(FTIR)证实,两代化合物都证明了氨基甲酸乙酯键的存在。第一代纳米胶囊的Tempol浓度为61.94±3.04 μg/mg,第二代纳米胶囊的Tempol浓度为77.61±3.04 μg/mg。释放概况表明,最初的爆发,随后持续,近线性释放超过30天。第二代纳米胶囊中较高的聚乙二醇化有利于静脉给药,可能增强其在TBI治疗中的治疗效果。这项研究证明了使用聚氨酯纳米胶囊延长Tempol递送的可行性,为管理氧化应激和改善TBI患者的预后提供了一种有前途的方法。未来的工作将包括在体内测试这些纳米胶囊,以确定它们在调节TBI恢复方面的潜力。
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
Bioconjugate Chemistry
Bioconjugate Chemistry 生物-化学综合
CiteScore
9.00
自引率
2.10%
发文量
236
审稿时长
1.4 months
期刊介绍: Bioconjugate Chemistry invites original contributions on all research at the interface between man-made and biological materials. The mission of the journal is to communicate to advances in fields including therapeutic delivery, imaging, bionanotechnology, and synthetic biology. Bioconjugate Chemistry is intended to provide a forum for presentation of research relevant to all aspects of bioconjugates, including the preparation, properties and applications of biomolecular conjugates.
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