Unique challenges of providing bioanalytical support for biological therapeutic pharmacokinetic programs

被引:22
作者
Nowatzke, William L. [1 ]
Rogers, Kathryn [1 ]
Wells, Edward [1 ]
Bowsher, Ronald R. [2 ,4 ]
Ray, Chad [3 ]
Unger, Steve [1 ]
机构
[1] Worldwide Clin Trials, Drug Dev Solut, Bioanalyt Sci, Austin, TX 78754 USA
[2] EMD Millipore Corp, BioPharma Serv, St Charles, MO 63304 USA
[3] Pfizer Global Res & Dev, Dept Pharmacokinet Dynam & Metab, San Diego, CA 92121 USA
[4] B2S Consulting, Indianapolis, IN 46237 USA
关键词
MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; ELECTROSPRAY-IONIZATION; METHODS VALIDATION; HOST ANTIBODIES; RECOMMENDATIONS; IMMUNOASSAYS; DESIGN; ASSAYS; OPTIMIZATION;
D O I
10.4155/BIO.11.2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Regulatory recommendations for providing bioanalytical support for biological therapeutics have co-evolved with the increasing success of these unique pharmaceuticals. Immunoassays have been used to quantify biological macromolecules for more than SO years. These assays rely on the use of antigen-specific antibodies. More recently, LC-MS methods have being adapted to quantitate biologics. LC-MS has attributes that complement the limitations encountered by immunoassays. Whether employing immunoassay or LC-MS methods, compared with traditional chemical-based therapeutics, biological therapeutics present unique analytical challenges to analysts. In this article, we review bioanalytical strategies for supporting biologics and discuss the regulatory and analytical challenges that must be met.
引用
收藏
页码:509 / 521
页数:13
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