School of Electronics and Computer Science, University of Southampton, Southampton, UK.
Integr Biol (Camb). 2009 Jun;1(5-6):345-62. doi: 10.1039/b905502a. Epub 2009 May 7.
The requirement for analysis of large numbers of biomolecules for drug discovery and clinical diagnostics has driven the development of low-cost, flexible and high-throughput methods for simultaneous detection of multiple molecular targets in a single sample (multiplexed analysis). The technique that seems most likely to satisfy all of these requirements is the multiplexed suspension (bead-based) assay, which offers a number of advantages over alternative approaches such as ELISAs and microarrays. In a bead based assay, different probe molecules are attached to different beads (of a few tens of microns in size), which are then reacted in suspension with the target sample. After reaction, the beads must be identifiable in order to determine the attached probe molecule, and thus each bead must be labelled (encoded) with a unique identifier. A large number of techniques have been proposed for encoding beads. This critical review analyses each technology on the basis of its ability to fulfil the practical requirements of assays, whilst being compatible with low-cost, high-throughput manufacturing processes and high-throughput detection methods. As a result, we identify the most likely candidates to be used for future integrated device development for practical applications.
对大量生物分子进行分析是药物发现和临床诊断的要求,这推动了低成本、灵活和高通量的方法的发展,以便在单个样本中同时检测多个分子靶标(多重分析)。似乎最有可能满足所有这些要求的技术是多重悬浮(基于珠)分析,它相对于 ELISA 和微阵列等替代方法具有许多优势。在基于珠的分析中,不同的探针分子连接到不同的珠子(大小为几十微米),然后在悬浮液中与靶样品反应。反应后,为了确定连接的探针分子,必须能够识别珠子,因此每个珠子都必须用唯一的标识符进行标记(编码)。已经提出了许多用于编码珠子的技术。本综述分析了每种技术根据其满足分析实际要求的能力,同时与低成本、高通量制造工艺和高通量检测方法兼容的能力。因此,我们确定了最有可能被用于未来实用应用的集成设备开发的候选者。