Accumulation of chemicals from the environment to clothing and other textiles can influence human uptake by several exposure routes. In this research, we demonstrate that the cloth-air equilibrium distribution ratio for species i, K can be measured relatively easily and quickly using headspace analysis of cloth dosed with two common indoor air SVOCs, diethyl phthalate (DEP) and di-n-butyl phthalate (DnBP). A known mass of a phthalate was applied to the cloth in a volatile solvent carrier. After evaporation of the solvent, the cloth was placed in a vial and allowed to equilibrate with the air in the vial. Since the volume of headspace air is small, the total mass required to transfer from cloth to air is small and also the time required for air equilibration with the fabric surface is very short (minutes). Distribution ratios for the two phthalate esters sorbed to cotton jean material, reported as the concentration in the bulk cloth divided by the air concentration, were measured at 20, 25, 32, and 40 °C. The volume-normalized distribution ratio, K [(μg/m)/(μg/m)], ranged from (0.75 ± 0.01)× 10 to (5.6 ± 0.2) × 10 for DEP and (5 ± 0.3)× 10 to (57 ± 1) × 10 for DnBP. Mass-normalized distribution ratio, K [m/g], ranged from (0.25 ± 0.01) to (1.8 ± 0.1) for DEP and (1.6 ± 0.1) to (18.5 ± 0.5) for DnBP. The cloth-air distribution ratios obtained from this study compare favorably with previously published results using other methods. Although equilibration with air in the headspace can be rapid, diffusion into the textile fibers is a slower equilibration process. Overall, this simple method has the potential to rapidly generate distribution ratios for a large number of chemical-textile pairs.
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http://dx.doi.org/10.1016/j.talanta.2018.02.061 | DOI Listing |
Pharmaceutics
January 2025
College of Pharmacy, Keimyung University, Daegu 42601, Republic of Korea.
/: Inhaler devices have been developed for the effective delivery of inhaled medications used in the treatment of pulmonary diseases. However, differing operating procedures across the devices can lead to user errors and reduce treatment efficacy, especially when patients use multiple devices simultaneously. To address this, we developed a novel dry powder inhaler (DPI), combining fluticasone propionate (FP), salmeterol xinafoate (SX), and tiotropium bromide (TB) into a single device designed for bioequivalent delivery compared to existing commercial products in an animal model.
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January 2025
Center for Pharmacy, University of Bergen, 5020 Bergen, Norway.
Polymyxin E (PME), a polymyxin antibiotic, serves as a final resort against antibiotic resistance. Nephrotoxicity is the primary concern when employing PME. To alleviate this issue, researchers have explored strategies including dosing adjustments and innovative formulations.
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January 2025
Department of Pharmaceutical Science, School of Pharmacy and Nutrition, University of Navarra, 31009 Pamplona, Spain.
Background/objectives: Colorectal cancer (CRC) holds the third and second position among cancers affecting men and women, respectively. Frequently, the first-line treatment for metastatic CRC consists of the intravenous administration of 5-fluorouracil and leucovorin in combination with oxaliplatin or irinotecan. Physiologically-based pharmacokinetic models (PBPK) aim to mechanistically incorporate body physiology and drug physicochemical attributes, enabling the description of both systemic and organ drug exposure based on the treatment specificities.
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December 2024
Department of Obstetrics and Gynecology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, SP, Brazil.
: Fluoxetine (FLX) is the inhibitor of serotonin reuptake most prescribed in pregnant women with depression. This study evaluates the influence of gestational diabetes mellitus (GDM) on the enantioselective pharmacokinetics and transplacental distribution of FLX and its metabolite norfluoxetine (norFLX). : Ten pregnant women diagnosed with GDM (GDM group) were investigated in the third trimester of gestation after they achieved good glycemic control.
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December 2024
Department of Pharmaceutical Technology, Faculty of Natural Sciences I, Institute of Pharmacy, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3, 06120 Halle/Saale, Germany.
Background/objectives: Bringing small interfering RNA (siRNA) into the cell cytosol to achieve specific gene silencing is an attractive but also very challenging option for improved therapies. The first step for successful siRNA delivery is the complexation with a permanent cationic or ionizable compound. This protects the negatively charged siRNA and enables transfection through the cell membrane.
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