<abstract xmlns="http://www.w3.org/1999/xhtml">The co-administration of several drugs in multidrug therapy may alter the binding of each drug to human serum albumin (HSA) and, thus, their pharmacology effect. Therefore, in this study, the interaction mechanism between HSA and two fluoroquinolones (FQs), sparfloxacin (SPF) and levofloxacin (LVF), was investigated using fluorescence and absorption methods in the absence and presence of the competing drugtigecycline (TGC). The the UV-Vis and fluorescence spectroscopy results showed that the fluorescence quenching of HSA was a result of the formation of the HSA-SPF and HSA-LVF complexes. The fluorescence quenching of HSA-TGC revealed that tigecycline can regulate the binding sites, binding mode and binding affinity of fluoroquinolones. The binding constants (KA) and binding sites (n) of the interaction systems were calculated. The results confirmed that the KA values of the HSA-FQ system decreased in the presence of TGC, indicating that TGC can affect the binding ability of FQ for HSA. This interaction may increase the free plasma concentration of unbound FQ and enhance their pharmacology effect.</abstract>

The co-administration of several drugs in multidrug therapy may alter the binding of each drug to human serum albumin (HSA) and, thus, their pharmacology effect. Therefore, in this study, the interaction mechanism between HSA and two fluoroquinolones (FQs), sparfloxacin (SPF) and levofloxacin (LVF), was investigated using fluorescence and absorption methods in the absence and presence of the competing drugtigecycline (TGC). The the UV-Vis and fluorescence spectroscopy results showed that the fluorescence quenching of HSA was a result of the formation of the HSA-SPF and HSA-LVF complexes. The fluorescence quenching of HSA-TGC revealed that tigecycline can regulate the binding sites, binding mode and binding affinity of fluoroquinolones. The binding constants (KA) and binding sites (n) of the interaction systems were calculated. The results confirmed that the KA values of the HSA-FQ system decreased in the presence of TGC, indicating that TGC can affect the binding ability of FQ for HSA. This interaction may increase the free plasma concentration of unbound FQ and enhance their pharmacology effect.

The Effect of Tigecycline on the Binding of Fluoroquinolones to Human Serum Albumin

Experimental and Applied Biomedical Research (EABR)

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

The co-administration of several drugs in multidrug therapy may alter the binding of each drug to human serum albumin (HSA) and, thus, their pharmacology...

The Effect of Tigecycline on the Binding of Fluoroquinolones to Human Serum Albumin

Publicado en línea: 11 abr 2018

Páginas: 17 - 25

Recibido: 17 ene 2017

Aceptado: 03 feb 2017

DOI: https://doi.org/10.1515/sjecr-2017-0006

Palabras clave
Fluorescence, Human serum albumin, Fluoroquinolones, Tigecycline

© 2018 Ratomir M. Jelic et al., published by De Gruyter Open

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

The Effect of Tigecycline on the Binding of Fluoroquinolones to Human Serum Albumin

Publicado en línea: 11 abr 2018

Páginas: 17 - 25

Recibido: 17 ene 2017

Aceptado: 03 feb 2017

DOI: https://doi.org/10.1515/sjecr-2017-0006

Palabras claveFluorescence, Human serum albumin, Fluoroquinolones, Tigecycline

© 2018 Ratomir M. Jelic et al., published by De Gruyter Open

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Palabras clave
Fluorescence, Human serum albumin, Fluoroquinolones, Tigecycline