Nualnoi Teerapat, Wongwitwichot Paweena, Kaewmanee Siriluk, Chanchay Pornchanan, Wongpanti Nattapong, Ueangsuwan Tossapol, Siangsanor Rattikarn, Chotirouangnapa Wannittaya, Saechin Tanatchaporn, Thungtin Suwanna, Szekely Jidapa, Wattanachant Chaiyawan, Saechan Vannarat
Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai 90110, Songkhla, Thailand.
Drug Delivery System Excellence Center (DDSEC), Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai 90110, Songkhla, Thailand.
Diagnostics (Basel). 2024 May 16;14(10):1033. doi: 10.3390/diagnostics14101033.
Early diagnosis is essential for the successful management of infection, but it cannot be achieved by the current gold standard culture technique. Therefore, this study aimed to develop a lateral flow immunoassay (LFIA) targeting capsular polysaccharide. The development was performed by varying nitrocellulose membrane reaction pads and chase buffers. The prototype LFIA is composed of Unisart CN95 and chase buffer containing tris-base, casein, and Surfactant 10G. The assay showed no cross-reactivity with , , and The limit of detections (LODs) of the prototype LFIA was 10 and 10 CFU/mL in hemoculture medium and artificial urine, respectively. These LODs suggest that this prototype can detect melioidosis from positive hemoculture bottles but not straight from urine. Additionally, these LODs are still inferior compared to Active Melioidosis Detect (AMD). Overall, this prototype holds the potential to be used clinically with hemoculture bottles. However, further improvements should be considered, especially for use with urine samples.
早期诊断对于感染的成功管理至关重要,但目前的金标准培养技术无法实现这一点。因此,本研究旨在开发一种针对荚膜多糖的侧向流动免疫测定法(LFIA)。通过改变硝酸纤维素膜反应垫和追踪缓冲液来进行开发。原型LFIA由Unisart CN95和含有三羟甲基氨基甲烷碱、酪蛋白和表面活性剂10G的追踪缓冲液组成。该测定法与[具体物质1]、[具体物质2]、[具体物质3]和[具体物质4]均无交叉反应。原型LFIA在血液培养基和人工尿液中的检测限(LOD)分别为10和10 CFU/mL。这些检测限表明,该原型可以从阳性血液培养瓶中检测到类鼻疽,但不能直接从尿液中检测到。此外,与活性类鼻疽检测(AMD)相比,这些检测限仍然较低。总体而言,该原型有在临床中与血液培养瓶一起使用的潜力。然而,应考虑进一步改进,特别是用于尿液样本时。