Thomsen Hanna, Benkovics Gábor, Fenyvesi Éva, Farewell Anne, Malanga Milo, Ericson Marica B
Biomedical Photonics Group, Department of Chemistry and Molecular Biology, University of Gothenburg, Sweden; CARe, Centre for Antibiotic Resistance Research, University of Gothenburg, Sweden.
CycloLab Ltd. Budapest, Hungary; Department of Organic Chemistry, Faculty of Science, Charles University in Prague, Czech Republic.
Int J Pharm. 2017 Oct 15;531(2):650-657. doi: 10.1016/j.ijpharm.2017.06.011. Epub 2017 Jun 6.
Cyclodextrin (CD) polymers are interesting nanoparticulate systems for pharmaceutical delivery; however, knowledge regarding their applications towards delivery into complex microbial biofilm structures is so far limited. The challenge is to demonstrate penetration and transport through the biofilm and its exopolysaccharide matrix. The ideal functionalization for penetration into mature biofilms is unexplored. In this paper, we present a novel set of rhodamine labelled βCD-polymers, with different charge moieties, i.e., neutral, anionic, and cationic, and explore their potential delivery into mature Staphylococcus epidermidis biofilms using multiphoton laser scanning microscopy (MPM). The S. epidermidis biofilms, being a medically relevant model organism, were stained with SYTO9. By using MPM, three-dimensional imaging and spectral investigation of the distribution of the βCD-polymers could be obtained. It was found that the cationic βCD-polymers showed significantly higher integration into the biofilms, compared to neutral and anionic functionalized βCDs. None of the carriers presented any inherent toxicity to the biofilms, meaning that the addition of rhodamine moiety does not affect the inertness of the delivery system. Taken together, this study demonstrates a novel approach by which delivery of fluorescently labelled CD nanoparticles to bacterial biofilms can be explored using MPM. Future studies should be undertaken investigating the potential in using cationic functionalization of CD based delivery systems for targeting anti-microbial effects in biofilms.
环糊精(CD)聚合物是用于药物递送的有趣的纳米颗粒系统;然而,迄今为止,关于它们在递送至复杂微生物生物膜结构方面的应用的知识仍然有限。挑战在于证明其穿透生物膜及其胞外多糖基质并在其中运输。尚未探索用于穿透成熟生物膜的理想功能化方法。在本文中,我们展示了一组新型的罗丹明标记的β-环糊精聚合物,它们具有不同的电荷部分,即中性、阴离子和阳离子,并使用多光子激光扫描显微镜(MPM)探索它们递送至成熟表皮葡萄球菌生物膜的潜力。表皮葡萄球菌生物膜作为一种与医学相关的模式生物,用SYTO9进行了染色。通过使用MPM,可以获得β-环糊精聚合物分布的三维成像和光谱研究。结果发现,与中性和阴离子功能化的β-环糊精相比,阳离子β-环糊精聚合物在生物膜中的整合程度明显更高。所有载体对生物膜均未表现出任何固有毒性,这意味着罗丹明部分的添加不会影响递送系统的惰性。综上所述,本研究展示了一种新方法,通过该方法可以使用MPM探索将荧光标记的环糊精纳米颗粒递送至细菌生物膜的情况。未来的研究应调查使用基于环糊精的递送系统的阳离子功能化来靶向生物膜中的抗菌作用的潜力。