Simultaneous determination of citalopram and tadalafil by the second derivative synchronous fluorescence method in biological fluids; application of Box-Behnken optimization design

被引:7
作者
Abdel-Raoof, Ahmed M. [1 ]
Hasan, Mohamed A. [1 ]
Madkour, Ahmed W. [1 ]
Abdel-Fattah, Ashraf [1 ]
Eissa, Maya S. [2 ]
机构
[1] Al Azhar Univ, Fac Pharm, Pharmaceut Analyt Chem Dept, Cairo, Egypt
[2] Egyptian Russian Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo, Egypt
关键词
Box-Behnken design; citalopram; second derivative synchronous; tadalafil; PERFORMANCE LIQUID-CHROMATOGRAPHY; VALIDATED SPECTROFLUOROMETRIC METHOD; PHARMACEUTICAL-PREPARATIONS; ERECTILE DYSFUNCTION; BULK; HPLC; DESMETHYLCITALOPRAM; VOLTAMMETRY; METABOLITES; INHIBITORS;
D O I
10.1002/bio.3913
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This is the first study focusing solely on that determination of tadalafil in the presence of citalopram as an antidepressant drug. The determination in biological fluids of a co-administered antidepressant drug and a sexual stimulation drug is a very critical and important step for psychotic and ischaemic heart disease patients, especially in cases of emergency and this requires therapeutic drug monitoring. A sensitive, efficient and rapid assay was selected satisfactorily and applied for simultaneous determination of citalopram and tadalafil either in their pure forms, in tablet dosage forms or in spiked human plasma. There was a large overlap for both drugs, forming the broad band found in conventional fluorescence spectra and their related synchronous fluorescence intensity. Therefore, the development of a highly sensitive second derivative synchronous fluorescence method was demonstrated that removed this overlap. The proposed method depended on measuring the amplitudes of the second derivative of synchronous fluorescence intensity at suitable wavelengths of 301 nm and 367 nm for citalopram and tadalafil at Delta lambda = 60 nm, respectively. Box-Behnken design as a response surface methodology was used to fit models and create an optimization process encompassing a set of factors and resulting in an optimum response value specifically designed for this method. Under optimum conditions, the linear dynamic ranges for citalopram and tadalafil estimation were 20-900 and 5-400 ng ml(-1)with detection limits of 5.40 and 1.43 ng ml(-1), respectively.
引用
收藏
页码:57 / 65
页数:9
相关论文
共 53 条
  • [1] D-optimal design as a useful tool response surface methodology for the optimization of signals from synchronous fluorescence prior to simultaneous determination of avanafil and tadalafil
    Abdel-Raoof, Ahmed M.
    Said, Ragab A. M.
    Emara, Mohamed S.
    El-Desouky, Ebrahim A.
    Abdelzaher, Ahmed M.
    Hasan, Mohamed A.
    Osman, Ayman E.
    [J]. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2020, 235 (235)
  • [2] Optimization of Highly Sensitive Screen Printed Electrode Modified With Cerium (IV) Oxide Nanoparticles for Electrochemical Determination of Oxymetazoline Hydrochloride Using Response Surface Methodology
    Abdel-Raoof, Ahmed M.
    Abdel-Monem, Ahmed H.
    Almrasy, Ahmed A.
    Mohamed, Tahany F.
    Nasr, Zeinab A.
    Mohamed, Ghada F.
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2020, 167 (04)
  • [3] Determination of tadalafil in pharmaceutical preparation by HPLC using monolithic silica column
    Aboul-Enein, HY
    Ali, I
    [J]. TALANTA, 2005, 65 (01) : 276 - 280
  • [4] Validated spectrofluorimetric method for determination of two phosphodiesterase inhibitors tadalafil and vardenafil in pharmaceutical preparations and spiked human plasma
    Abu El-Enin, Mohammed Abu Bakr
    Hammouda, Mohammed El-Sayed Abd Al-Ghaffar
    El-Sherbiny, Dina Tawfik
    El-Wasseef, Dalia Rashad
    El-Ashry, Saadia Mahmoud
    [J]. LUMINESCENCE, 2016, 31 (01) : 173 - 178
  • [5] SPECTROPHOTOMETRIC DETERMINATION OF TADALAFIL IN PURE AND DOSAGE FORMS
    Al Kaf, Ali
    Gouda, Ayman A.
    [J]. CHEMICAL INDUSTRY & CHEMICAL ENGINEERING QUARTERLY, 2011, 17 (02) : 125 - 132
  • [6] Validated method for tadalafil analysis in pharmaceutical preparations by capillary electrophoresis
    Ali, I
    Aboul-Enein, HY
    [J]. CHROMATOGRAPHIA, 2004, 60 (3-4) : 187 - 191
  • [7] [Anonymous], 2005, ICH HARM TRIP GUID V
  • [8] Box G., 2005, STAT EXPT DESIGN INN
  • [9] Bruns RE, 2006, DATA HANDL SCI TECHN, V25, P1
  • [10] Budavari S., 2007, MERCK INDEX