Szöllősi Dávid, Hajdrik Polett, Tordai Hedvig, Bergmann Ralf, Horváth Ildikó, Mihály Judith, Gaál Anikó, Jezsó Bálint, Shailaja Kanni Das, Felföldi Tamás, Padmanabhan Parasuraman, Zoltán Gulyás Balázs, Máthé Domokos, Varga Zoltán, Szigeti Krisztián
Department of Biophysics and Radiation Biology, Semmelweis University, Budapest 1094, Hungary.
Biological Nanochemistry Research Group, HUN-REN Research Centre for Natural Sciences, Institute of Materials and Environmental Chemistry, Budapest 1117, Hungary.
ACS Omega. 2024 Oct 11;9(42):42808-42813. doi: 10.1021/acsomega.4c04632. eCollection 2024 Oct 22.
Bacterial outer membrane vesicles (OMVs) are emerging as important players in the host-microbiome interaction, while also proving to be a promising platform for vaccine development and targeted drug delivery. The available methods for measuring their biodistribution, however, are limited. We aimed to establish a high-efficiency radiolabeling method for the treatment of OMVs. Tc-HYNIC-duramycin was incubated with OMVs isolated from BL21(DE3) ΔnlpI ΔlpxM. Radiolabeling efficiency (RLE) and radiochemical purity (RCP) were measured with size-exclusion high-performance liquid chromatography. The biodistribution was quantitatively measured in mice using SPECT/CT imaging. RLE was 81.84 ± 2.03% for undiluted OMV suspension and 56.17 ± 2.29% for 100× dilution. Postlabeling purification with a spin-desalting column results in 100% radioactivity in the OMV fraction according to HPLC, indicating 100% RCP of the final product. The biodistribution was found to be in line with previous data reported in the literature using other OMV tracking attempts. Our findings illustrate that using HYNIC-duramycin for labeling of the OMVs enhances efficiency and is easily implementable for in vivo imaging studies, significantly improving upon earlier methods.
细菌外膜囊泡(OMVs)正在成为宿主-微生物组相互作用中的重要参与者,同时也被证明是一个有前景的疫苗开发和靶向药物递送平台。然而,现有的测量其生物分布的方法有限。我们旨在建立一种用于OMVs处理的高效放射性标记方法。用锝-六氢吡啶肼-短杆菌肽与从BL21(DE3) ΔnlpI ΔlpxM分离的OMVs孵育。使用尺寸排阻高效液相色谱法测量放射性标记效率(RLE)和放射化学纯度(RCP)。使用SPECT/CT成像在小鼠中定量测量生物分布。未稀释的OMV悬浮液的RLE为81.84±2.03%,100倍稀释时为56.17±2.29%。根据HPLC,用旋转脱盐柱进行标记后纯化,OMV部分的放射性为100%,表明最终产品的RCP为100%。发现生物分布与文献中使用其他OMV追踪方法报道的先前数据一致。我们的研究结果表明,使用六氢吡啶肼-短杆菌肽标记OMVs可提高效率,并且易于用于体内成像研究,显著改进了早期方法。