LAQV, REQUIMTE, Departamento de Ciencias Químicas, Faculdade de Farmacia, Universidade do Porto, Portugal.
LAQV, REQUIMTE, Departamento de Ciencias Químicas, Faculdade de Farmacia, Universidade do Porto, Portugal; i3S - Instituto de Investigacao e Inovacao em Saúde, Universidade do Porto, Rua Alfredo Allen 208, 4200-393 Porto, Portugal; INEB - Instituto de Engenharia Biomedica, Universidade do Porto, Rua Alfredo Allen 208, 4200-393 Porto, Portugal.
Int J Pharm. 2022 Apr 5;617:121582. doi: 10.1016/j.ijpharm.2022.121582. Epub 2022 Feb 14.
TreatingHelicobacter pylori(H. pylori) infections has been a never-ending challenge, which has contributed to the high incidence of gastric cancer. The antibiotics commonly used are not reaching the infection site in its active state and in a concentration high enough to effectively kill the bacteria. In this context, amoxicillin-loaded lipid nanoparticles with carefully chosen materials were developed, namely dioleoylphosphatidylethanolamine (DOPE) as a targeting agent and Tween®80 and linolenic acid as antimicrobial agents. This work shows the ability of these nanoparticles in (i) targeting the bacteria (imaging flow cytometry) and inhibiting their adhesion to MKN-74 cells (bacteria-gastric cells adhesion model); (ii) killing the bacteria even as an antibiotic-free strategy (time-kill kineticstudies, scanning electron microscopy, and bacterial membrane permeability studies); (iii)overcoming gastrointestinal features using a newly developedin vitroinfection model that includes both physical (epithelial cells and mucus) and the chemical (acid medium) barriers; and in (iv) being incorporated in a floating system that can increase the retention time at the stomach. Overall, this work presents an effective nanosystem to deal with the ulcer-bug. Besides, it also provides two innovative tools transferable to other fields-anin vitroinfection model and a floating system to incorporate nanoparticles.
治疗幽门螺杆菌(H. pylori)感染一直是一个挑战,这导致了胃癌的高发率。常用的抗生素在活性状态下不能到达感染部位,也不能达到足够高的浓度来有效杀死细菌。在这种情况下,开发了载有阿莫西林的脂质纳米粒,选择了精心挑选的材料,即二油酰基磷脂酰乙醇胺(DOPE)作为靶向剂,以及吐温®80 和亚油酸作为抗菌剂。这项工作表明,这些纳米粒具有以下能力:(i)靶向细菌(成像流动细胞术)并抑制其与 MKN-74 细胞的黏附(细菌-胃细胞黏附模型);(ii)即使没有抗生素也能杀死细菌(时间杀伤动力学研究、扫描电子显微镜和细菌膜通透性研究);(iii)克服胃肠道特征,使用新开发的包括物理(上皮细胞和黏液)和化学(酸性介质)屏障的体外感染模型;以及(iv)整合到可增加在胃中滞留时间的漂浮系统中。总的来说,这项工作提出了一种有效的纳米系统来应对溃疡-细菌。此外,它还提供了两个可转移到其他领域的创新工具——体外感染模型和用于纳米粒的漂浮系统。