Department of Plant Biology, Institute of Biology, University of Campinas/UNICAMP, Campinas, SP, Brazil.
Department of Environmental Engineering & Oral Biopathology Graduate Program, São José dos Campos Institute of Science & Technology, São Paulo State University - UNESP, SP, Brazil.
Future Microbiol. 2019 Jul;14:957-967. doi: 10.2217/fmb-2019-0107. Epub 2019 Aug 2.
To investigate biopharmaceutical and antifungal properties of pure and complexed ellagic acid. Caco-2 cells cultured in a Transwell inserts were infected with to develop an model. Ellagic acid was complexed with cyclodextrins. Microbial compositions, ellagic acid concentration as function of time and characterization studies of complexes were evaluated. Ellagic acid presented ability to reduce invasion, although this was not statistically significant. Its poor water solubility and absorption probably limited this ability. Water solubility was increased after complexation with hydroxypropyl-β-CD; however, ellagic acid/hydroxypropyl-β-CD did not improve the antifungal activity. Although ellagic acid presented a promising antifungal activity, its biopharmaceutical properties limit such activity and should be improved.
研究鞣花酸的纯品和包合物的生物制药学和抗真菌性质。在 Transwell 小室中培养的 Caco-2 细胞被感染以建立 模型。鞣花酸与环糊精复合。评估了微生物组成、鞣花酸浓度随时间的变化以及复合物的特性研究。鞣花酸具有降低侵袭的能力,尽管这在统计学上并不显著。其较差的水溶性和吸收能力可能限制了这种能力。与羟丙基-β-环糊精复合后,水溶性增加;然而,鞣花酸/羟丙基-β-环糊精并没有提高抗真菌活性。虽然鞣花酸具有有前景的抗真菌活性,但它的生物制药学性质限制了这种活性,应该加以改善。