In this period when environmental pollution has become uncontrollable, the removal of drug active substances reaching the environment and the analysis of drug active substances in different matrix environments are important for both living life and a sustainable environment. Therefore, the production of multifunctional materials that can be used in these two different processes has gained importance in the literature. Based on this thought, in this study, a g-CN@TiO@FeO multifunctional nanohybrid material was synthesized and used for magnetic solid-phase extraction (MSPE) and photocatalytic degradation of trimethoprim and isoniazid, used together in tuberculosis treatment. All analyses were performed by high-performance liquid chromatography using a diode-array detection (HPLC-DAD) system. The synthesized material was characterized by X-ray diffraction spectroscopy (XRD), Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller (BET) method, ζ-potential analysis, field-emission scanning electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDX). Important analytical parameters for the MSPE method such as the pH value of the sample solution, the volume of the sample solution, the amount of the sorbent, the type and volume of the elution solvent, and extraction time were optimized. The optimized MSPE method was then applied to different environmental waters and pharmaceutical samples. The recovery percentages for these samples were found to be between 95 and 107%. For trimethoprim and isoniazid, the limit of detections (LODs) were 0.055 and 0.145 and the limit of quantifications (LOQs) were 0.167 and 0.439 ng·mL, respectively. It was observed that ∼100% of trimethoprim and isoniazid active components were photocatalytically removed from the g-CN@TiO@FeO nanohybrid material in ∼120 min under UV light.
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http://dx.doi.org/10.1021/acsomega.2c01311 | DOI Listing |
Sci Rep
October 2024
Department of Pharmaceutical Chemistry, NETES Institute of Pharmaceutical Science, Nemcare Group of Institution, Mirza, Kamrup, 781125, Assam, India.
The current study developed a method for quantifying four drugs-Sulfamethoxazole, Trimethoprim, Isoniazid, and Pyridoxine-in rabbit plasma. The method uses gradient liquid chromatography based on analytical quality by design. To achieve separation, a Eclip Plus C18 (250 mm × 5 mm, 4.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
August 2024
Laboratory of Environmental Pollution Control, Department of Chemistry, Aristotle University of Thessaloniki, 541 24, Thessaloniki, Greece.
In this study, the adsorption of a mixture of high-consumed drugs onto virgin and aged PET microplastics has been studied for the time ever. The target mixture comprised two anti-inflammatory drugs, diclofenac and ketoprofen, one anti-hypertensive, valsartan, and four common antibiotics, indomethacin, trimethoprim, isoniazid, and metronidazole. Two types of PET MPs (virgin and UV-aged) were used in the experimental procedure.
View Article and Find Full Text PDFAntibiotics (Basel)
June 2024
Croatian Veterinary Institute, Savska Cesta 143, 10000 Zagreb, Croatia.
subsp. is pathogenic mainly to birds, although cases of mycobacteriosis caused by these bacteria have also been reported in other animals and humans. Not much is known about the effects of this pathogen on otters.
View Article and Find Full Text PDFIntroduction: Longitudinal extensive transverse myelitis (LETM) has four main causes: inflammatory, malnutrition, vascular, and infectious causes. Among the commonly described viral causes leading to LETM are the family, HIV, and HTLV-1. .
View Article and Find Full Text PDFTher Drug Monit
July 2024
Department of Pharmacology, AP-HP, Jean Verdier Hospital, Sorbonne Paris Nord and Sorbonne Paris Cité University, IAME, Bobigny, France.
Background: Therapeutic drug monitoring requires a validated assay and appropriate conditions for sample shipment and storage based on the stability of the compound to be analyzed. This study evaluated the stability of 29 antimicrobial compounds in whole blood (WB) and plasma samples under various storage conditions.
Methods: The pre-analytical stability of 22 antibiotics (amoxicillin, aztreonam, cefazolin, cefepime, cefotaxime, cefoxitin, ceftazidime, ceftobiprole, ceftolozane, ceftriaxone, ciprofloxacin, clindamycin, cloxacillin, daptomycin, levofloxacin, linezolid, meropenem, metronidazole, moxifloxacin, piperacillin, sulfamethoxazole, and trimethoprim), 2 beta-lactamase inhibitors (avibactam, tazobactam), and 5 antituberculosis drugs (ethambutol, isoniazid, pyrazinamide, rifabutin, and rifampicin) was assessed by WB for up to 24 hours at room temperature (RT) and 72 hours at +4°C.
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