Extraction Of Carbamazepine Research Articles

Molecularly imprinted polymer membranes based on single template for recognition and extraction of carbamazepine and its structurally analogues

In this work, a novel molecularly imprinted polymer membrane (MIPM) using oxcarbazepine (OXC) as the single template and polyvinylidene difluoride membrane as the subtract was fabricated for recognition and extraction of carbamazepine (CBZ) and its analogues including OXC, carbamazepine-10,11-epoxide (CBZE), and monohydroxy derivative 10, 11-dihydro-10-hydroxy carbamazepine (MHD). The prepared MIPMs were characterized by scanning electron microscope, Fourier transform infrared spectroscopy, Brunaner-emmet-teller measurements and X-ray photoelectron spectroscopy, showing the successful construction of uniform and porous polymers on the surface of membranes. A series of adsorption affinity tests were investigated, indicating the prepared materials had specific recognition capacity and excellent stability as novel sorbents. The maximum static adsorption capacities of MIPMs towards OXC, CBZ, MHD or CBZE was 4.246, 3.621, 2.316, or 4.877 mg·g−1, respectively. The MIPMs showed reusability and reproducibility. The usability of MIPMs was evaluated by combining MIPMs extraction and high performance liquid chromatography detection for the determination of CBZ, CBZE, OXC and MHD in different matrices including methanol, normal saline, phosphate buffer solution, and plasma. The mean recovery of four target compounds in methanol, normal saline and phosphate buffer solution was more than 75 %, while the mean recovery of CBZ and CBZE in plasma was more than 80 %. The results demonstrated that the proposed MIPMs is very suitable for the determination of OXC, CBZ, MHD and/or CBZE in different matrices.

Application of a Small Protein-Coated Column to Trap, Extract and Enrich Carbamazepine Directly from Human Serum for Direct Chromatographic Analysis

An automated solid phase extraction (SPE) protocol to determine carbamazepine in human serum has been developed and validated using a simple, rabid and sensitive liquid chromatography-based bio-analytical method. Extraction of carbamazepine was carried out using an on-line SPE tool of a short protein-coated (PC) ODS silica pre-column (PC-ODS-pre-column) and phosphate buffer saline (PBS) with a pH of 7.4 as an extraction solvent. There are two distinct chromatographic modes used by PC-ODS-pre-column. While carbamazepine trapping required reversed-phase liquid chromatography, proteins were extracted from serum samples using PBS by size-exclusion liquid chromatography. Then, carbamazepine was eluted from the PC-ODS-pre-column onto the quantification position using a mixture of methanol-distilled deionized water (50:50, v/v) as an eluent and ODS analytical column. At room temperature (22 ± 1 °C), carbamazepine was completely separated from the co-eluted matrix components and detected at 230 nm. Carbamazepine’s linearity was obtained at concentrations ranging from 50 to 10,000 ng/mL. With good accuracy and precision, carbamazepine recoveries in serum samples ranged from 86.14 to 97.82%. The extraction step was conducted using PBS as a safe and green extraction solvent, making this protocol both cost-effective and ecologically safe.

A new molecular imprinted PEDOT glassy carbon electrode for carbamazepine detection

An electrochemical sensor for the detection of carbamazepine was fabricated by the electropolymerization of PEDOT on glassy carbon electrodes. Molecular imprinted polymer sites were synthesized by cyclic voltammetry on the electrodes' surfaces providing high selectivity and sensitivity towards carbamazepine molecules. Scanning electron microscopy validated the formation of the polymer. Extraction of carbamazepine from the polymer was performed by immersion in acetonitrile and validated by ultraviolet–visible spectroscopy along with cyclic voltammetry experiments comparing pre- and post-template extraction data. Further cyclic voltammetry and square-wave voltammetry tests aided in characterizing the electrodes’ response to carbamazepine concentration in PBS solution with [Fe(CN)6]3−/4− as a redox pair/mediator. The limits of detection and quantification were found to be 0.98 x 10−3 M and 2.97 x 10−3 M respectively. The biosensor was highly sensitive to carbamazepine molecules in comparison to non-imprinted electrodes, simple to construct and easy to operate.

Synthesis and Preliminary Assays of a Novel Molecularly Imprinted Polymer Dedicated to the Extraction of Carbamazepine from River Water

Monitoring of trace organic contaminants in aquatic media has become a major concern today. The presence of Carbamazepine (CBZ), anticonvulsant and analgesic used in the treatment of pain associated with trigeminal neuralgia, has been reported in effluents from sewage treatment plants due to its low biodegradability. To monitor its content in waters, a Molecularly Imprinted Polymer (MIP) of CBZ was synthesized to extract this molecule from river waters by Solid Phase Extraction (SPE).

Development of Molecularly Imprinted Polymers (MIPs) Nano Particles for the Selective Determination of Carbamazepine in Human Serum and Plasma

A new, simple, rapid, and sensitive solid-phase extraction with molecularly imprinted polymer (SPE-MIP) for determination of Carbamazepine in biological samples was developed. These nano particle polymers were synthesized via a non-covalent molecular imprinting approach through precipitation polymerization method using methacrylic acid (MAA) as a functional monomer, ethylene glycol dimethacrylate (EGDMA) as a cross-linker agent, carbamazepine as a target template molecule and azobisisobutyronitrile (AIBN) as an initiator. The optimal conditions for SPE consisted of conditioning the cartridge using a pH=3.0 water, loading 5.0 ml of the sample under basic aqueous conditions, clean-up using 2×2ml acetonitrile and elution with 3.0 ml methanol. After optimization of SPE procedure, an aliquot of extracted template was injected to the ACE, 5μm 250×4.6 mm analytical column with the mobile phase as the same as elution solvent. This method was used for extraction of carbamazepine from an anticonvulsant aqueous solution and the results revealed an extraction recovery of more than 90%. HPLC chromatograms show an efficient clean up, which supports the potential of MISPE for clean-up of trace amounts of carbamazepine from the drug formulation.