A simple, accurate, and sensitive microextraction by packed sorbent-gas chromatography-mass spectrometry method has been developed for the simultaneous quantification of four antiepileptic drugs; oxcarbazepine, carbamazepine, phenytoin, and alprazolam in human plasma and urine as a tool for drug monitoring. Caffeine was used as internal standards for the electron ionization mode. An original pretreatment procedure on biological samples, based on microextraction in packed syringe using C(18) as packing material gave high extraction yields (69.92-99.38%), satisfactory precision (RSD < 4.7%) and good selectivity. Linearity was found in the 0.1-500 ng/mL range for these drugs with limits of detection (LODs) between 0.0018 and 0.0036 ng/mL. Therefore, the method has been found to be suitable for the therapeutic drug monitoring of patients treated with oxcarbazepine, carbamazepine, phenytoin, and alprazolam. After validation, the method was successfully applied to some plasma samples from patients undergoing therapy with one or more of these drugs. A comparison of the detection limit with similar methods indicates high sensitivity of the present method over the earlier reported methods. The present method is applied for the analysis of these drugs in the real urine and plasma samples of the epileptic patients.

In the present work, a high‐efficiency and solvent minimized microextraction technique, fabric phase sorptive extraction followed by gas chromatography and mass spectrometry analysis is proposed for the rapid determination of four organophosphorus pesticides (terbufos, malathion, chlorpyrifos, and triazofos) in vegetable samples including beans, tomato, brinjal, and cabbage. Fabric phase sorptive extraction combines the beneficial features of sol‐gel derived microextraction sorbents with the rich surface chemistry of cellulose fabric substrate, which collectively form a highly efficient microextraction system. Fabric phase sorptive extraction membrane, when immersed directly into the sample matrix, may extract target analytes even when high percentage of matrix interferents are present. The technique also greatly simplifies sample preparation workflow. Most important fabric phase sorptive extraction parameters were investigated and optimized. The developed method displayed good linearity over the concentration range 0.5–500 ng/g. Under optimum experimental conditions, the limits of detection were found in the range of 0.033 to 0.136 ng/g. The relative standard deviations for the extraction of organophosphorus pesticides were < 5%. Subsequently, the new method was applied to beans, tomato, brinjal, and cabbage samples. The results from the real sample analysis indicate that the method is green, rapid, and economically feasible for the determination of organophosphorus pesticides in vegetable samples.

A method for the simultaneous determination of the antiepileptic drugs, phenobarbital (PHB), phenytoin (PTN), carbamazepine (CBZ), primidone (PRM) and oxcarbazepine (OXC) in human plasma and urine samples by using micro-extraction in a packed syringe as the sample preparation method connected with LC/UV (MEPS/LC/UV) is described. Micro-extraction in a packed syringe (MEPS) is a new miniaturized, solid-phase extraction technique that can be connected online to gas or liquid chromatography without any modifications. In MEPS approximately 1 mg of the solid packing material is inserted into a syringe (100-250 μL) as a plug. Sample preparation takes place on the packed bed. The bed can be coated to provide selective and suitable sampling conditions. The new method is very promising, easy to use, fully automated, inexpensive and quick. The standard curves were obtained within the concentration range 1-500 ng/mL in both plasma and urine samples. The results showed high correlation coefficients (R(2) >0.988) for all of the analytes within the calibration range. The extraction recovery was found to be between 88.56 and 99.38%. The limit of quantification was found to be between 0.132 and 1.956 ng/mL. The precision (RSD) values of quality control samples (QC) had a maximum deviation of 4.9%. A comparison of the detection limits with similar methods indicates high sensitivity of the present method. The method is applied for the analysis of these drugs in real urine and plasma samples of epileptic patients.

A simple, fast, selective and very sensitive method based on sample preparation by the relatively new technique of microextraction in a packed syringe (MEPS) and analysis by liquid chromatography (LC) and gas chromatography-mass spectrometry (GC-MS) for the simultaneous determination of antidepressant drugs (amitriptyline, imipramine, clomipramine, mirtazapine and citalopram) was developed. MEPS is a new miniaturized, solid-phase extraction (SPE) technique that can be connected to LC or GC without any modifications. It is very easy to use, fully automated, inexpensive, quick and uses very small amounts (in lL) of organic solvents. Drugs are extracted using the MEPS technique followed by their analysis using LC-UV and GC-MS. Limits of detection were in the range of 0.088-0.284 ng mL -1 on GC-MS and between 0.133 and 0.360 ng mL -1 on LC-UV. The purpose of this study is to develop and validate MEPS as a new sample preparation technique for antidepressant drugs using chromatographic methods to detect these drugs in human plasma and urine samples.

High-performance liquid chromatography (HPLC) has several advantages over the conventional methods due to their operational simplicity. It is a vital tool to determine metal ions having same mass but different electronic configuration, to separate complex mixtures and to resolve ions that may be indistinguishable by mass spectrometry alone. Metal ions play vital role in many biological processes and involved in setting up of many diseases. Therefore, the development of simple methods for the detection and quantification of metals in real samples might serve as diagnostic tools for various diseases. This review article focuses on the recent main feature of this technique, i.e. speciation of metal ions and their applications to series of problem of metal ion chemistry in different environmental matrixes. Speciation of metals is of increasing interest and has a great importance because of bioavailability, environmental mobility, toxicity and potential risk of metals. With the capability of partitioning the complex species of different metal ions, HPLC is an efficient technique for this task. This review summarizes recent advances in the development of HPLC to the fundamental understanding of metal ion chemistry in the environment and discusses all the issues that still need a lot of consideration. It has been classified into different sections depending on the role of HPLC in separation used and metal speciation; furthermore, the underlying sample preconcentration techniques and detection systems involved for the determination of metal ions and their applications were discussed.