Klučáková Martina, Závodská Petra
Faculty of Chemistry, Brno University of Technology, Purkyňova 118/464, 612 00 Brno, Czech Republic.
Molecules. 2024 Dec 16;29(24):5937. doi: 10.3390/molecules29245937.
The presence of pharmaceuticals in nature systems poses a threat to the environment, plants, animals, and, last but not least, human health. Their transport in soils, waters, and sediments plays important roles in the toxicity and bioavailability of pharmaceuticals. The mobility of pharmaceuticals can be affected by their interactions with organic matter and other soil and water constituents. In this study, a model agarose hydrogel enriched by humic acid as a representative of organic matter is used as a transport medium for pharmaceuticals. Sulphapyridine (as a representative of sulphonamide antibiotics) and diclofenac (as a representative of widely used non-steroidal anti-inflammatory drugs) were chosen for experiments in diffusion cells. Pharmaceuticals were passed through the hydrogel from the donor solution to the acceptor compartment and could interact with humic acids incorporated in the hydrogel. The lag time was prolonged if the hydrogel was enriched by humic acids from 134 to 390 s for sulphapyridine and from 323 to 606 s for diclofenac. Similarly, the incorporation of humic acids in the hydrogel resulted in a decrease in the determined diffusion coefficients. The decrease was stronger in the first stage of the experiment when diffusing particles could interact with vacant binding sites.
天然系统中药物的存在对环境、植物、动物,以及最后但同样重要的人类健康构成威胁。它们在土壤、水体和沉积物中的迁移在药物的毒性和生物利用度方面起着重要作用。药物的迁移性会受到其与有机物以及其他土壤和水体成分相互作用的影响。在本研究中,一种用腐殖酸(作为有机物的代表)富集的模型琼脂糖水凝胶被用作药物的传输介质。选择磺胺吡啶(作为磺胺类抗生素的代表)和双氯芬酸(作为广泛使用的非甾体抗炎药的代表)在扩散池中进行实验。药物从供体溶液穿过水凝胶到达受体隔室,并可能与水凝胶中所含的腐殖酸相互作用。如果水凝胶用腐殖酸富集,磺胺吡啶的滞后时间从134秒延长至390秒,双氯芬酸的滞后时间从323秒延长至606秒。同样,水凝胶中腐殖酸的掺入导致测定的扩散系数降低。在实验的第一阶段,当扩散颗粒能够与空的结合位点相互作用时,这种降低更为明显。