Biopharmaceutical modulatory effects of newly engineered bile acid-Tyloxapol nanogels for attenuation of cytotoxicity in auditory cells

IF 4.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Bozica Kovacevic , Susbin Raj Wagle , Corina Mihaela Ionescu , Thomas Foster , Maja Đanić , Momir Mikov , Armin Mooranian , Hani Al-Salami
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引用次数: 0

Abstract

This study presents novel thermoresponsive nanogels composed of chenodeoxycholic acid and Tyloxapol for potential inner ear drug delivery. The nanogels exhibit non-Newtonian, shear-thinning fluid behaviour and rapid gelation at body temperature. Biocompatibility studies were conducted on auditory and macrophage cell lines. Nanogels had a minimal impact on cellular viability, glycolysis, and mitochondrial respiration of auditory cells after 24 h of exposure. However, mitochondrial function analysis in macrophages revealed a significant decrease in oxidative phosphorylation and coupling efficiency after nanogel exposure, accompanied by increased proton leakage. Despite these metabolic disruptions, glycolysis remained unaffected. The Poloxamer matrix appears to be responsible for these effects, independent of the presence of bile acids or Tyloxapol. This study highlights the potential of bile acid-enriched nanogels in drug delivery, particularly their biocompatibility and injectability while acknowledging challenges related to mitochondrial dysfunction in immune cells. These findings suggest that thermoresponsive bile acid and Tyloxapol nanogels have the potential to be safe and effective drug delivery vehicles for inner ear applications.

Abstract Image

新设计的胆汁酸-泰乐菌素纳米凝胶对生物制药的调节作用,可减轻听觉细胞的细胞毒性
本研究介绍了由苯去氧胆酸和泰乐菌素组成的新型热致伸缩性纳米凝胶,可用于内耳给药。这种纳米凝胶具有非牛顿、剪切稀化流体特性,并能在体温下快速凝胶化。对听觉细胞系和巨噬细胞系进行了生物相容性研究。暴露 24 小时后,纳米凝胶对听觉细胞的细胞活力、糖酵解和线粒体呼吸的影响极小。然而,对巨噬细胞线粒体功能的分析表明,接触纳米凝胶后氧化磷酸化和耦合效率显著下降,同时质子泄漏增加。尽管出现了这些代谢紊乱,但糖酵解仍未受到影响。Poloxamer基质似乎是造成这些影响的原因,而与胆汁酸或泰乐菌素的存在无关。这项研究强调了富含胆汁酸的纳米凝胶在给药方面的潜力,特别是其生物相容性和可注射性,同时也承认了与免疫细胞线粒体功能障碍有关的挑战。这些研究结果表明,热致伸缩性胆汁酸和泰乐菌素纳米凝胶有可能成为安全有效的内耳给药载体。
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来源期刊
CiteScore
8.00
自引率
8.00%
发文量
879
审稿时长
94 days
期刊介绍: The Journal of Drug Delivery Science and Technology is an international journal devoted to drug delivery and pharmaceutical technology. The journal covers all innovative aspects of all pharmaceutical dosage forms and the most advanced research on controlled release, bioavailability and drug absorption, nanomedicines, gene delivery, tissue engineering, etc. Hot topics, related to manufacturing processes and quality control, are also welcomed.
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