Elbashir Abdalla A, Dsugi Nuha Fathi Ali, Aboul-Enein Hassan Y
Chemistry Department, Faculty of Science, University of Khartoum, Khartoum, 11115, Sudan.
Pharmaceutical and Medicinal Chemistry Department, Pharmaceutical and Drug Industries Research Division, National Research Centre, Dokki, Cairo, 12311, Egypt.
J Fluoresc. 2014 Mar;24(2):355-61. doi: 10.1007/s10895-013-1300-0. Epub 2013 Sep 21.
The supramolecular interaction of ofloxacin (Oflo) and methyl β-cyclodextrin (Mβ-CD) has been examined by UV-vis, IR and fluorescence spectroscopy. The formation of inclusion complex has been confirmed based on the changes of the spectral properties. The results showed that Mβ-CD reacted with Oflo to form an inclusion complex. The Oflo and Mβ-CD complex formed a host-guest complex in 1:1 stoichiometry and inclusion constant (K = 7.8 × 10(-3) L mol(-1)) was ascertained by the typical double reciprocal plots. Furthermore, the thermodynamic parameters (∆H°, ∆S° and ∆G°) associated with the inclusion process were also determined. In addition, solid inclusion complex was synthesized. Based on the significant enhancement of the fluorescence intensity of Oflo produced through complex formation, a simple, accurate, rapid and highly sensitive spectrofluorometric method for the determination of Oflo in pharmaceutical formulation was developed. The measurement of relative fluorescence intensity was carried out at 497 nm with excitation at 296 nm. The factors affecting the inclusion complex formation were studied and optimized. Under the optimum reaction conditions, linear relationships with good correlation coefficients (0.9995) were in the concentration range of 50-350 ng/mL for spectrofluorimetry. The limit of detection (LOD) was 11.5 ng/mL. The proposed method was successfully applied to the analysis of Oflo in pharmaceutical preparation.
通过紫外可见光谱、红外光谱和荧光光谱研究了氧氟沙星(Oflo)与甲基β-环糊精(Mβ-CD)的超分子相互作用。基于光谱性质的变化证实了包合物的形成。结果表明,Mβ-CD与Oflo反应形成包合物。Oflo与Mβ-CD复合物以1:1化学计量比形成主客体复合物,并通过典型的双倒数图确定了包合常数(K = 7.8×10⁻³ L mol⁻¹)。此外,还测定了与包合过程相关的热力学参数(∆H°、∆S°和∆G°)。另外,合成了固体包合物。基于包合形成后Oflo荧光强度的显著增强,开发了一种简单、准确、快速且高度灵敏的荧光光谱法用于测定药物制剂中的Oflo。在296 nm激发波长下,于497 nm处测量相对荧光强度。研究并优化了影响包合物形成的因素。在最佳反应条件下,荧光光谱法在50 - 350 ng/mL浓度范围内具有良好的线性关系,相关系数为0.9995。检测限(LOD)为11.5 ng/mL。所提出的方法成功应用于药物制剂中Oflo的分析。