A Review for the Analysis of Antidepressant, Antiepileptic and Quinolone Type Drugs in Pharmaceuticals and Environmental Samples

Rani, Susheela; Malik, Ashok Kumar; Heena, -; Kaur, Ramandeep; Kaur, Ripneel

doi:10.1080/10408347.2016.1141670

Cited by 27 publications

(7 citation statements)

References 145 publications

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“…Moreno, Navas, and Asuero (2014) presented an overview focused on only HPLC coupled with DAD strategies to analyze antidepressants and other types of CNS-acting drugs in human biological fluids. Afterwards, Rani, Malik, Heena and Kaur (2016) compiled and discussed the findings of antidepressant quantitative research. Mainstream separation and detection instruments in combination with commonly assessed materials (biological, environmental and pharmaceutical samples) were all included in this review.…”

Section: Previous Reviews By Other Authorsmentioning

confidence: 99%

Recent advances in liquid chromatographic methods for the determination of selective serotonin reuptake inhibitors and serotonin norepinephrine reuptake inhibitors

Jia

Bartlett

2020

Biomedical Chromatography

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Depression is now the second largest public health burden throughout the world. Selective serotonin reuptake inhibitors (SSRIs) and serotonin norepinephrine reuptake inhibitors (SNRIs) have replaced older antidepressants to become first‐line medications to treat this disease with increased remission rates and markedly decreased incidence of severe adverse events. Traditional and modern bioanalytical strategies for SSRI and SNRI determination are being continuously improved. There has also been a recent increase in the use of unconventional sample preparation methods. This review critically evaluates the development of SSRI and SNRI liquid chromatographic analytical methods published between 2014 and mid‐2019, with special attention to novel sample preparation methods.

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Section: Previous Reviews By Other Authorsmentioning

confidence: 99%

Recent advances in liquid chromatographic methods for the determination of selective serotonin reuptake inhibitors and serotonin norepinephrine reuptake inhibitors

Jia

Bartlett

2020

Biomedical Chromatography

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“…It is racemic compound composed of R and S enantiomers combined in equal amounts [4]. It is also used in sleep, anxiety and eating disorders, pain syndromes, arrhythmia and some immune dysfunction cures [5].…”

Section: Introductionmentioning

confidence: 99%

Sensitive Determination of Venlafaxine in Urine Samples by Using HPLC-DAD System After Fabric Phase Sorptive Extraction

ÖZDEMİR

Ulusoy

Morgül

et al. 2022

Cumhuriyet Science Journal

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This study is focused on developing a sensitive analytical method for Venlafaxine molecule which is antidepressant drug belonging to the serotonin-noradrenaline reuptake inhibitors (SNRI) group. With this study, a separation and preconcentration method based on fabric phase sorptive extraction(FPSE) method was developed for low levels of Venlafaxine in urine samples. Experimental variables such as pH, ionic strength, desorption solvent, and other parameters were studied and optimized step by step. The linearity of method under optimized conditions is in the range of 15.00-750.00 ng mL-1 while limit of detection is 4.28 ng mL-1. The relative standard deviation (RSD %) obtained from model solutions containing 300 ng mL-1 of Venlafaxine was lower than 3.1 % and pre-concentration factor was calculated as 62.50 for target molecule. In order to test accuracy of the method, recovery tests were carried out by means of spiked urine samples. As a result of recovery tests, quantative values were obtained in the range of 97.5-104.2 % successively.

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“…A literature survey shows that several analytical methods for the quantification of CIT and SER in biological fluids have been documented either alone or with their metabolites and/or other SSRIs using various detection techniques. − The method of choice for qualitative and quantitative measurement of SSRIs and metabolites in complex biological matrices is liquid chromatography (LC) coupled with tandem mass spectrometry (MS) . Many LC-MS/MS methods have been employed for the determination of CIT and SER in various biological fluids. − These methods were developed to detect the target SSRI after oral administration in either human beings and/or laboratory animals.…”

Section: Introductionmentioning

confidence: 99%

Toxicity Profile, Pharmacokinetic, and Drug–Drug Interaction Study of Citalopram and Sertraline Following Oral Delivery in Rat: An LC-MS/MS Method for the Simultaneous Determination in Plasma

Elgawish

Ali

Moustafa

et al. 2020

Chem. Res. Toxicol.

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The burden of depression and other mental disorders is on the rise globally, and successful treatment sometimes requires modifications of drugs and/or dose regimens. The development of novel analytical methods for the determination of antidepressant drugs in biological fluids is thus urgently required. Herein, a sensitive, robust, and rapid liquid chromatographic coupled tandem mass spectrometric method was developed and validated for the determination of citalopram (CIT) and sertraline (SER) in rat plasma after oral administration. The analytes of interest and internal standard (duloxetine (DUL)) were extracted from 100 μL of plasma with solid-phase extraction on an Oasis HLB cartridge followed by the separation with gradient elution with water containing 0.1% formic acid and acetonitrile on an Agilent Eclipse Plus ODS (4.6 × 100 mm, 3.5 μm) column at flow rate 0.2 mL min −1 . The triple quadrupole mass spectrometry was applied via electrospray ionization source for detection. The fragmentation pattern of the protonated CIT, SER, and DUL was elucidated using multiple reaction monitoring of the transitions of m/z 325.2 to 109, 306.1 to 158.9, and 298.1 to 154.1 as [M + H] + for CIT, SER, and DUL, respectively. The proposed method has been validated as per US-FDA bioanalytical guidelines in terms of linearity, accuracy, precision, matrix effects, stability, selectivity, and recovery. The method was linear over the concentration range of 1−2000 and 1−1000 ng mL −1 with the lower limit of detection of 0.12 and 0.19 ng mL −1 for CIT and SER, respectively. The interday and intraday precisions and accuracy expressed by the relative standard deviation and the relative standard error were both lower than 11.1% and 2.1%, respectively. The proposed method was successfully applied for the pharmacokinetics and drug monitoring studies of CIT and SER in rat plasma after a single oral dose of 120 mg kg −1 of CIT and SER. Coadministration of SER with CIT has affected the peak plasma concentrations, maximum plasma concentration time, area under the concentration−time curve, and oral clearance of CIT. Molecular modeling study showed that SER could competitively inhibit CYP2D6, the main enzyme involved in CIT metabolism. A possible drug−drug interaction in psychiatric patients undergoing chronic SER and CIT treatment is therefore worthy of more attention in an effort to avoid side effects and serotonin syndrome.

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A Review for the Analysis of Antidepressant, Antiepileptic and Quinolone Type Drugs in Pharmaceuticals and Environmental Samples

Cited by 27 publications

References 145 publications

Recent advances in liquid chromatographic methods for the determination of selective serotonin reuptake inhibitors and serotonin norepinephrine reuptake inhibitors

Recent advances in liquid chromatographic methods for the determination of selective serotonin reuptake inhibitors and serotonin norepinephrine reuptake inhibitors

Sensitive Determination of Venlafaxine in Urine Samples by Using HPLC-DAD System After Fabric Phase Sorptive Extraction

Toxicity Profile, Pharmacokinetic, and Drug–Drug Interaction Study of Citalopram and Sertraline Following Oral Delivery in Rat: An LC-MS/MS Method for the Simultaneous Determination in Plasma

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