Dissociation Kinetics and Antimicrobial Activity of Ofloxacin Antibiotic in Artificial Tears Via 1H-NMR, Raman, and UV-Vis Spectroscopic Analysis.

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY
Ahmad Telfah, M-Ali Al-Akhras, Haya AlShheamat, Marwan S Mousa, Inshad Jum'h, Abdel Qader Albawab, Elen Tolstik, Johann Dierks, Roland Hergenröder
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引用次数: 0

Abstract

Introduction: The hydrogen-bonded networks play a significant role in influencing several physicochemical properties of ofloxacin in artificial tears (ATs), including density, pH, viscosity, and self-diffusion coefficients. The activities of the ofloxacin antibiotic with Ats mixtures are not solely determined by their concentration but are also influenced by the strength of the hydrogen bonding network which highlight the importance of considering factors such as excessive tear production and dry eye conditions when formulating appropriate dosages of ofloxacin antibiotics for eye drops. Objectives: Investigating the physicochemical properties of ofloxacin-ATs mixtures, which serve as a model for understanding the impact of hydrogen bonding on the antimicrobial activity of ofloxacin antibiotic eye drops. Determine the antimicrobial activities of the ofloxacin-Ats mixture with different concentration of ofloxacin. Methods: The ofloxacin-ATs mixtures were analyzed using 1H-NMR, Raman, and UV-Vis spectroscopies, with variation of ofloxacin concentration to study its dissociation kinetics in ATs, mimicking its behavior in human eye tears. The investigation includes comprehensive analysis of 1H-NMR spectral data, self-diffusion coefficients, Raman spectroscopy, UV-Vis spectroscopy, liquid viscosity, and acidity, providing a comprehensive assessment of the physicochemical properties. Results: Analysis of NMR chemical shifts, linewidths, and self-diffusion coefficient curves reveals distinct patterns, with peaks or minima observed around 0.6 ofloxacin mole fraction dissociated in ATs, indicating a strong correlation with the hydrogen bonding network. Additionally, the pH data exhibits a similar trend to viscosity, suggesting an influence of the hydrogen bonding network on protonic ion concentrations. Antibacterial activity of the ofloxacin-ATs mixtures is evaluated through growth rate analysis against Salmonella typhimurium, considering varying concentrations with mole fractions of 0.1, 0.4, 0.6, 0.8, and 0.9. Conclusions: The antibiotic-ATs mixture with a mole fraction of 0.6 ofloxacin exhibited lower activity compared to mixtures with mole fractions of 0.1 and 0.4, despite its lower concentration. The activities of the mixtures are not solely dependent on concentration but are also influenced by the strength of the hydrogen bonding network. These findings emphasize the importance of considering tear over-secretion and dry eye problems when designing appropriate doses of ofloxacin antibiotics for eye drop formulations.

通过 1H-NMR、拉曼和紫外可见光谱分析人工泪液中氧氟沙星抗生素的解离动力学和抗菌活性。
导言:氢键网络在影响人工泪液(ATs)中氧氟沙星的多种理化性质(包括密度、pH 值、粘度和自扩散系数)方面发挥着重要作用。氧氟沙星抗生素与人工泪液(Ats)混合物的活性不仅取决于其浓度,还受氢键网络强度的影响,这凸显了在配制适当剂量的氧氟沙星抗生素滴眼液时考虑泪液分泌过多和干眼症等因素的重要性。研究目的研究氧氟沙星-ATs 混合物的理化性质,作为了解氢键对氧氟沙星抗生素滴眼液抗菌活性影响的模型。确定不同浓度的氧氟沙星-Ats 混合物的抗菌活性。方法使用 1H-NMR、拉曼和紫外-可见光谱分析氧氟沙星-ATs 混合物,并根据氧氟沙星浓度的变化研究其在 ATs 中的解离动力学,模拟其在人眼泪液中的行为。这项研究包括对 1H-NMR 光谱数据、自扩散系数、拉曼光谱、紫外-可见光谱、液体粘度和酸度的综合分析,从而对其理化性质进行全面评估。研究结果对核磁共振化学位移、线宽和自扩散系数曲线的分析揭示了不同的模式,在 ATs 中离解的氧氟沙星摩尔分数为 0.6 左右观察到峰值或最小值,表明与氢键网络密切相关。此外,pH 值数据呈现出与粘度相似的趋势,表明氢键网络对质子离子浓度有影响。通过对鼠伤寒沙门氏菌的生长率分析,评估了氧氟沙星-ATs 混合物的抗菌活性,考虑了不同浓度的分子分数 0.1、0.4、0.6、0.8 和 0.9。结论氧氟沙星摩尔分数为 0.6 的抗生素-ATs 混合物的活性低于摩尔分数为 0.1 和 0.4 的混合物,尽管其浓度较低。混合物的活性不仅取决于浓度,还受到氢键网络强度的影响。这些发现强调了在设计适当剂量的氧氟沙星抗生素滴眼剂配方时考虑泪液过度分泌和干眼症问题的重要性。
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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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