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药物发现与开发中的质谱创新

Mass spectrometry innovations in drug discovery and development.

作者信息

Papac D I, Shahrokh Z

机构信息

Department of Development Research, NPS Pharmaceuticals, Inc., Salt Lake City, Utah 84108, USA.

出版信息

Pharm Res. 2001 Feb;18(2):131-45. doi: 10.1023/a:1011049231231.

DOI:10.1023/a:1011049231231
PMID:11405282
Abstract

This review highlights the many roles mass spectrometry plays in the discovery and development of new therapeutics by both the pharmaceutical and the biotechnology industries. Innovations in mass spectrometer source design, improvements to mass accuracy, and implementation of computer-controlled automation have accelerated the purification and characterization of compounds derived from combinatorial libraries, as well as the throughput of pharmacokinetics studies. The use of accelerator mass spectrometry, chemical reaction interface-mass spectrometry and continuous flow-isotope ratio mass spectrometry are promising alternatives for conducting mass balance studies in man. To meet the technical challenges of proteomics, discovery groups in biotechnology companies have led the way to development of instruments with greater sensitivity and mass accuracy (e.g., MALDI-TOF, ESI-Q-TOF, Ion Trap), the miniaturization of separation techniques and ion sources (e.g., capillary HPLC and nanospray), and the utilization of bioinformatics. Affinity-based methods coupled to mass spectrometry are allowing rapid and selective identification of both synthetic and biological molecules. With decreasing instrument cost and size and increasing reliability, mass spectrometers are penetrating both the manufacturing and the quality control arenas. The next generation of technologies to simplify the investigation of the complex fate of novel pharmaceutical entities in vitro and in vivo will be chip-based approaches coupled with mass spectrometry.

摘要

本综述强调了质谱在制药和生物技术行业新疗法发现与开发中所发挥的诸多作用。质谱仪源设计的创新、质量精度的提高以及计算机控制自动化的实施,加速了源自组合文库的化合物的纯化与表征,以及药代动力学研究的通量。加速器质谱、化学反应界面质谱和连续流动同位素比率质谱的使用是在人体中进行质量平衡研究的有前景的替代方法。为应对蛋白质组学的技术挑战,生物技术公司的发现团队引领了具有更高灵敏度和质量精度的仪器(如基质辅助激光解吸电离飞行时间质谱、电喷雾四极杆飞行时间质谱、离子阱)、分离技术和离子源的小型化(如毛细管高效液相色谱和纳喷雾)以及生物信息学利用的发展。基于亲和力的方法与质谱联用能够快速且选择性地鉴定合成分子和生物分子。随着仪器成本降低、尺寸减小以及可靠性提高,质谱仪正渗透到制造和质量控制领域。下一代简化新型药物实体在体外和体内复杂命运研究的技术将是基于芯片的方法与质谱联用。

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