Development and Validation of A Spectrofluorimetric Determination of Calf Thymus DNA Using a Terbium-Danofloxacin Probe

Background: Analysis of biomolecules is required in many biomedical research areas. A spectrofluorimetric method is proposed for determination of calf thymus DNA (ctDNA) based on the fluorescence enhancement of terbium-danofloxacin (Tb3+-Dano) in the presence of ctDNA. Methods: A probe with maximum...

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Main Authors: Naser Soltani (Author), Jamshid Manzoori (Author), Mohammad Amjadi (Author), Farzaneh Lotfipour (Author)
Format: Book
Published: Tabriz University of Medical Sciences, 2016-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Naser Soltani  |e author 
700 1 0 |a Jamshid Manzoori  |e author 
700 1 0 |a Mohammad Amjadi  |e author 
700 1 0 |a Farzaneh Lotfipour  |e author 
700 1 0 |a Farzaneh Lotfipour  |e author 
245 0 0 |a Development and Validation of A Spectrofluorimetric Determination of Calf Thymus DNA Using a Terbium-Danofloxacin Probe 
260 |b Tabriz University of Medical Sciences,   |c 2016-03-01T00:00:00Z. 
500 |a 10.15171/PS.2016.02 
500 |a 2383-2886 
500 |a 2383-2886 
520 |a Background: Analysis of biomolecules is required in many biomedical research areas. A spectrofluorimetric method is proposed for determination of calf thymus DNA (ctDNA) based on the fluorescence enhancement of terbium-danofloxacin (Tb3+-Dano) in the presence of ctDNA. Methods: A probe with maximum excitation and emission wavelengths of 347 nm and 545 nm, respectively, was developed. The enhanced fluorescence intensity of Tb3+-Dano system was proportional to the concentration of ctDNA. The effective factors and the optimum conditions for the determination of ctDNA were studied. Under the optimum conditions of [Tris buffer]= 0.01 mol L-1 (pH 7.8), [ Tb3+]= 1×10-5 mol L-1 and [Dano]= 5×10-5 mol L-1, the maximum response was achieved. The developed method was evaluated in terms of accuracy, precision and limit of detection. Results: The linear concentration range for quantification of ctDNA was 36-3289 ng mL-1 and the detection limit (S/N=3) was 8 ng mL-1. The concentration of DNA extracted from Escherichia coli as an extracted sample was also determined using the developed probe. The concentration of DNA in extracted sample was determined using UV assay and developed method, the results were satisfactory. Conclusion: The proposed method is a simple, practical and relatively interference free method to follow up the concentrations of ctDNA. 
546 |a EN 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutical Sciences, Vol 22, Iss 1, Pp 2-8 (2016) 
787 0 |n http://journals.tbzmed.ac.ir/PHARM/Abstract/PHARM_1041_20150813105958 
787 0 |n https://doaj.org/toc/2383-2886 
787 0 |n https://doaj.org/toc/2383-2886 
856 4 1 |u https://doaj.org/article/99e40f7ff6b544a0a89e7ccf83d7879a  |z Connect to this object online.