Liu Qi, Chen Xirui, Li Jiangao, Tan Linjie, Wang Kenian, Zhang Jinming, Dong Hangming, Li Ying, Tang Ben Zhong
Innovation Research Center for AIE Pharmaceutical Biology, Guangzhou Municipal and Guangdong Provincial Key Laboratory of Molecular Target & Clinical Pharmacology, The NMPA and State Key Laboratory of Respiratory Disease, School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, Guangdong, 511436, China.
Strait Institute of Flexible Electronics (SIFE, Future Technologies), Fujian Key Laboratory of Flexible Electronics, Fujian Normal University and Strait Laboratory of Flexible Electronics (SLoFE), Fuzhou, Fujian, 350117, China.
Biosens Bioelectron. 2025 Mar 1;271:117068. doi: 10.1016/j.bios.2024.117068. Epub 2024 Dec 14.
Krebs von den Lungen-6 (KL-6) has been recognized as an effective serum biomarker for interstitial lung disease (ILD). The KL-6 accurate detection is of great significance for evaluating the severity of ILD and the prognosis of patients. In this study, a bright aggregation-induced emission luminogen (AIEgen) N, N'-((1,2-diphenylethene-1,2-diyl)bis(4,1-phenylene))bis(N-phenylnaphthalen-1-amine) (TPETN) with a high quantum yield of 87.57% was designed and synthesized, which was subsequently encapsulated into polystyrene nanoparticles (PSNPs) for construction of ultrahigh fluorescent nanoparticle (TPNPs). The obtained TPNPs was found to be 128 times and 16 times higher sensitivity than traditional gold nanoparticles (AuNPs) and tetramethyl 4',4''',4''''',4'''''''-(ethene-1,1,2,2-tetrayl) tetrakis([1,1'-biphenyl]-4-carboxylate) (TCBPE) embedded nanoparticles (TCNPs), respectively. Then, TPNPs were employed as signal output to construct a lateral flow immunoassay platform (TPNP-LFIA) for KL-6 detection. TPNP-LFIA achieved a limit of detection (LOD) of 0.0534 ng/mL, which was 77.15 times and 7.69 times lower than those of AuNP- and TCNP- based LFIA, respectively. The dynamic linearity of TPNP-LFIA for detecting KL-6 ranged from 0.15 to 333.33 ng/mL. The recovery rates of TPNP-LFIA in serum samples varied from 99.96% to 108.13%, with coefficients of variation ≤6.24%. Hence, TPNP-LFIA has promising potential as a rapid and quantitative method for detecting KL-6.
肺表面活性物质相关蛋白6(KL-6)已被公认为间质性肺疾病(ILD)的一种有效血清生物标志物。KL-6的准确检测对于评估ILD的严重程度及患者预后具有重要意义。在本研究中,设计并合成了一种具有87.57%高量子产率的明亮聚集诱导发光荧光团(AIEgen)N, N'-((1,2-二苯乙烯-1,2-二基)双(4,1-亚苯基))双(N-苯基萘-1-胺)(TPETN),随后将其封装到聚苯乙烯纳米颗粒(PSNPs)中以构建超高荧光纳米颗粒(TPNPs)。结果发现,所制备的TPNPs的灵敏度分别比传统金纳米颗粒(AuNPs)和嵌入四甲基4',4''',4''''',4'''''''-(乙烯-1,1,2,2-四基)四( [1,1'-联苯]-4-羧酸酯)(TCBPE)的纳米颗粒(TCNPs)高128倍和16倍。然后,将TPNPs用作信号输出构建用于检测KL-6的侧向流动免疫分析平台(TPNP-LFIA)。TPNP-LFIA的检测限(LOD)为0.0534 ng/mL,分别比基于AuNP和TCNP的LFIA低77.15倍和7.69倍。TPNP-LFIA检测KL-6的动态线性范围为0.15至333.33 ng/mL。TPNP-LFIA在血清样品中的回收率在99.96%至108.13%之间,变异系数≤6.24%。因此,TPNP-LFIA作为一种快速定量检测KL-6的方法具有广阔的应用前景。