Didarian, RezaOzbek, Hatice K.Ozalp, Veli C.Erel, OzcanYildirim-Tirgil, NimetBasic Sciences2024-09-102024-09-10202401073-60851559-030510.1007/s12033-024-01256-w2-s2.0-85201435224https://doi.org/10.1007/s12033-024-01256-whttps://hdl.handle.net/20.500.14411/7305Yildirim, Nimet/0000-0002-5973-8830This review delves into the advancements in molecular recognition through enhanced SELEX (Systematic Evolution of Ligands by Exponential Enrichment) platforms and post-aptamer modifications. Aptamers, with their superior specificity and affinity compared to antibodies, are central to this discussion. Despite the advantages of the SELEX process-encompassing stages like ssDNA library preparation, incubation, separation, and PCR amplification-it faces challenges, such as nuclease susceptibility. To address these issues and propel aptamer technology forward, we examine next-generation SELEX platforms, including microfluidic-based SELEX, capillary electrophoresis SELEX, cell-based aptamer selection, counter-SELEX, in vivo SELEX, and high-throughput sequencing SELEX, highlighting their respective merits and innovations. Furthermore, this article underscores the significance of post-aptamer modifications, particularly chemical strategies that enhance aptamer stability, reduce renal filtration, and expand their target range, thereby broadening their utility in diagnostics, therapeutics, and nanotechnology. By synthesizing these advanced SELEX platforms and modifications, this review illuminates the dynamic progress in aptamer research and outlines the ongoing efforts to surmount existing challenges and enhance their clinical applicability, charting a path for future breakthroughs in this evolving field.eninfo:eu-repo/semantics/closedAccessAptamersSELEXChemical modificationsPost-aptamer modificationsNext-generation SELEX platformsReviewQ3Q3WOS:00129191000000139152308