Youf Raphaëlle, Nasir Adeel, Müller Mareike, Thétiot Franck, Haute Tanguy, Ghanem Rosy, Jonas Ulrich, Schönherr Holger, Lemercier Gilles, Montier Tristan, Le Gall Tony
INSERM, Univ Brest, EFS, UMR 1078, GGB-GTCA, 29200 Brest, France.
Physical Chemistry I & Research Center of Micro- and Nanochemistry and (Bio)Technology (Cμ), Department of Chemistry and Biology, University of Siegen, 57076 Siegen, Germany.
Pharmaceutics. 2022 Aug 10;14(8):1664. doi: 10.3390/pharmaceutics14081664.
Antimicrobial photodynamic therapy (aPDT) depends on a variety of parameters notably related to the photosensitizers used, the pathogens to target and the environment to operate. In a previous study using a series of Ruthenium(II) polypyridyl ([Ru(II)]) complexes, we reported the importance of the chemical structure on both their photo-physical/physico-chemical properties and their efficacy for aPDT. By employing standard in vitro conditions, effective [Ru(II)]-mediated aPDT was demonstrated against planktonic cultures of and strains notably isolated from the airways of Cystic Fibrosis (CF) patients. CF lung disease is characterized with many pathophysiological disorders that can compromise the effectiveness of antimicrobials. Taking this into account, the present study is an extension of our previous work, with the aim of further investigating [Ru(II)]-mediated aPDT under in vitro experimental settings approaching the conditions of infected airways in CF patients. Thus, we herein studied the isolated influence of a series of parameters (including increased osmotic strength, acidic pH, lower oxygen availability, artificial sputum medium and biofilm formation) on the properties of two selected [Ru(II)] complexes. Furthermore, these compounds were used to evaluate the possibility to photoinactivate while preserving an underlying epithelium of human bronchial epithelial cells. Altogether, our results provide substantial evidence for the relevance of [Ru(II)]-based aPDT in CF lung airways. Besides optimized nano-complexes, this study also highlights the various needs for translating such a challenging perspective into clinical practice.
抗菌光动力疗法(aPDT)取决于多种参数,这些参数尤其与所使用的光敏剂、靶向的病原体以及操作环境有关。在之前一项使用一系列钌(II)多吡啶配合物([Ru(II)])的研究中,我们报道了化学结构对其光物理/物理化学性质以及aPDT疗效的重要性。通过采用标准体外条件,证实了有效的[Ru(II)]介导的aPDT对从囊性纤维化(CF)患者气道中分离出的 和 菌株的浮游培养物有效。CF肺部疾病的特征是多种病理生理紊乱,这可能会影响抗菌药物的有效性。考虑到这一点,本研究是我们之前工作的扩展,旨在进一步研究在接近CF患者感染气道条件的体外实验环境下[Ru(II)]介导的aPDT。因此,我们在此研究了一系列参数(包括渗透压增加、酸性pH值、较低的氧气可用性、人工痰液培养基和生物膜形成)对两种选定的[Ru(II)]配合物性质的单独影响。此外,这些化合物用于评估在保留人支气管上皮细胞底层上皮的同时使 光灭活的可能性。总之,我们的结果为基于[Ru(II)]的aPDT在CF肺部气道中的相关性提供了大量证据。除了优化的纳米配合物外,本研究还强调了将这种具有挑战性的观点转化为临床实践的各种需求。