Üçer Asiye, Ertekіn Zehra Ceren, Dіnç Erdal
Department of Analytical Chemistry, Faculty of Pharmacy, Ankara University, Yenimahalle, Ankara, Ankara, 06560, Turkey.
Department of Analytical Chemistry, Faculty of Pharmacy, Ankara Yıldırım Beyazıt University, Keçiören, Ankara, 06010, Turkey.
J Fluoresc. 2024 Dec 5. doi: 10.1007/s10895-024-04056-2.
Ofloxacin (OFL) and its (S)-enantiomer, levofloxacin (LEV), are among members of the fluoroquinolone antibiotic class, renowned for their broad-spectrum efficacy against both gram-negative and gram-positive bacteria. These potent drugs have been widely used in both human and veterinary medicine, working as bactericidal agents by binding to DNA gyrase, an essential enzyme for bacterial DNA replication. Understanding the binding constants of these drugs to DNA is vital for elucidating their interaction mechanisms and enhancing our grasp of gene expression regulation. The interactions of LEV and OFL with calf thymus DNA under a physiological medium (0.02 M tris-HCl buffer, pH 7.4) using UV spectrophotometry and spectrofluorimetry were investigated. The assay results obtained by applying two spectroscopic approaches confirmed the presence of the interaction of LEV and OFL antibiotics with DNA. In the LEV-DNA and OFL-DNA interactions, hyperchromic effect and fluorescence quenching were observed for UV spectrophotometric and spectrofluorometric measurements, respectively. In the spectrophotometric analysis, the binding constants for the LEV-DNA and OFL-DNA complexes at 298 K were determined as (1.24 ± 0.047) x 10 and (1.39 ± 0.040) x 10 M, respectively. In the spectrofluorimetric analysis of the interaction of LEV and OFL with DNA, the thermodynamic properties were examined at three distinct temperatures. Based on the fluorescence signal changes the binding constants at 293, 298, and 310 K were calculated as (8.91 ± 0.161) x 10, (7.62 ± 0.098) x 10, and (6.08 ± 0.041) x 10 M for LEV-DNA and, (3.14 ± 0.053) x 10, (3.04 ± 0.031) x 10, and (2.78 ± 0.023) x 10 M for OFL-DNA, respectively. In these assays, the Gibbs free energy (ΔG), entropy (ΔS), and enthalpy (ΔH) were determined using the Van't Hoff equation. The negative ΔG⁰ values indicate that both LEV-DNA and OFL-DNA interactions are spontaneous. Furthermore, the positive ΔS⁰ and negative ΔH⁰ values revealed that electrostatic forces played a significant role in the binding LEV and OFL to DNA.
氧氟沙星(OFL)及其(S)-对映体左氧氟沙星(LEV)属于氟喹诺酮类抗生素,以其对革兰氏阴性菌和革兰氏阳性菌的广谱抗菌效力而闻名。这些强效药物已广泛应用于人类医学和兽医学,通过与DNA旋转酶结合发挥杀菌作用,DNA旋转酶是细菌DNA复制所必需的一种酶。了解这些药物与DNA的结合常数对于阐明它们的相互作用机制以及增强我们对基因表达调控的理解至关重要。采用紫外分光光度法和荧光分光光度法研究了在生理介质(0.02 M Tris-HCl缓冲液,pH 7.4)中LEV和OFL与小牛胸腺DNA的相互作用。应用两种光谱方法获得的测定结果证实了LEV和OFL抗生素与DNA之间存在相互作用。在LEV-DNA和OFL-DNA相互作用中,紫外分光光度法和荧光分光光度法测量分别观察到增色效应和荧光猝灭。在分光光度分析中,298 K时LEV-DNA和OFL-DNA复合物的结合常数分别测定为(1.24±0.047)×10和(1.39±0.040)×10 M。在LEV和OFL与DNA相互作用的荧光分光光度分析中,在三个不同温度下研究了热力学性质。根据荧光信号变化,计算出293、298和310 K时LEV-DNA的结合常数分别为(8.91±0.161)×10、(7.62±0.098)×10和(6.08±0.041)×10 M,OFL-DNA的结合常数分别为(3.14±0.053)×10、(3.由于篇幅限制,这里翻译了一部分,完整翻译为:(3.04±0.031)×10和(2.78±0.023)×10 M。在这些测定中,使用范特霍夫方程确定了吉布斯自由能(ΔG)、熵(ΔS)和焓(ΔH)。负的ΔG⁰值表明LEV-DNA和OFL-DNA相互作用都是自发的。此外,正的ΔS⁰和负的ΔH⁰值表明静电力在LEV和OFL与DNA的结合中起重要作用。