Noncontact 3D Bioprinting of Proteinaceous Microarrays for Highly Sensitive Immunofluorescence Detection within Clinical Samples

免疫荧光 DNA微阵列 材料科学 纳米技术 3D生物打印 芯片上器官 细胞生物学 计算生物学 生物医学工程 化学 生物 医学 组织工程 基因表达 微流控 生物化学 基因 抗体 遗传学
作者
Amid Shakeri,Lubna Najm,Shadman Khan,Lei Tian,Liane Ladouceur,Hareet Sidhu,Nadine Al‐Jabouri,Zeinab Hosseinidoust,Tohid F. Didar
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (45): 31506-31523 被引量:4
标识
DOI:10.1021/acsnano.4c12460
摘要

Immunofluorescence assays are extensively used for the detection of disease-associated biomarkers within patient samples for direct diagnosis. Unfortunately, these 2D microarrays suffer from low repeatability and fail to attain the low limits of detection (LODs) required to accurately discern disease progression for clinical monitoring. While three-dimensional microarrays with increased biorecognition molecule density stand to circumvent these limitations, their viscous component materials are not compatible with current microarray fabrication protocols. Herein, we introduce a platform for 3D microarray bioprinting, wherein a two-step printing approach enables the high-throughput fabrication of immunosorbent hydrogels. The hydrogels are composed entirely of cross-linked proteins decorated with clinically relevant capture antibodies. Compared to two-dimensional microarrays, these proteinaceous microarrays offer 3-fold increases in signal intensity. When tested with clinically relevant biomarkers, ultrasensitive single-plex and multiplex detection of interleukin-6 (LOD 0.3 pg/mL) and tumor necrosis factor receptor 1 (LOD 1 pg/mL) is observed. When challenged with clinical samples, these hydrogel microarrays consistently discern elevated levels of interleukin-6 in blood plasma derived from patients with systemic blood infections. Given their easy-to-implement, high-throughput fabrication, and ultrasensitive detection, these three-dimensional microarrays will enable better clinical monitoring of disease progression, yielding improved patient outcomes.
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