Trimethoprim-Based multicomponent solid Systems: Mechanochemical Screening, characterization and antibacterial activity assessment

甲氧苄啶 抗菌剂 化学 抗菌活性 表征(材料科学) 药理学 医学 材料科学 抗生素 纳米技术 生物 细菌 生物化学 遗传学
作者
Giusi Piccirillo,Rafael T. Aroso,João A. Baptista,Ricardo A. E. Castro,Gabriela Silva,Mário J. F. Calvete,Mariette M. Pereira,João Canotilho,M. Ermelinda S. Eusébio
出处
期刊:International Journal of Pharmaceutics [Elsevier]
卷期号:661: 124416-124416
标识
DOI:10.1016/j.ijpharm.2024.124416
摘要

In this work, multicomponent trimethoprim-based pharmaceutical solid systems were developed by mechanochemistry, using coformers from the GRAS list and other active pharmaceutical ingredients. The choice of coformers took into account their potential to increase the aqueous solubility/dissolution rate of TMP or its antibacterial activity. All the binary systems were characterized by thermal analysis, powder X-ray diffraction and infrared spectroscopy, and 3 equimolar systems with FTIR pointing to salts, and 4 eutectic mixtures were identified. The intrinsic dissolution rate of TMP in combination with nicotinic acid (a salt) and with paracetamol (eutectic mixture) were 25% and 5% higher than for pure TMP, respectively. For both Gram-positive and −negative strains, the antibacterial activity of TMP with some of the coformers was improved, since the dosage used was lower than the TMP control. A significant increase in antibacterial activity against E. coli was found for the eutectic mixture with curcumin, with the best results being obtained for the eutectic and equimolar mixtures with ciprofloxacin. Combining trimethoprim with coformers offers an interesting alternative to using trimethoprim alone: multicomponent forms with enhanced TMP dissolution rates were identified, as well as combinations showing enhanced antibacterial activity relatively to the pure drug.

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