Industry Perspectives on Process Analytical Technology: Tools and Applications in API Development

被引:122
|
作者
Chanda, Arani [1 ]
Daly, Adrian M. [2 ]
Foley, David A. [3 ]
LaPack, Mark A. [4 ]
Mukherjee, Samrat [5 ]
Orr, John D. [1 ]
Reid, George L., III [3 ]
Thompson, Duncan R. [6 ]
Ward, Howard W., II [3 ]
机构
[1] Eisai Inc, Analyt Res Labs, Andover, MA 01810 USA
[2] Pfizer Global Supply, Proc Analyt Sci Grp, Ringaskiddy, Cork, Ireland
[3] Pfizer Worldwide Res & Dev, Analyt Res & Dev, Groton, CT 06340 USA
[4] Eli Lilly & Co, Small Mol Design & Dev, Indianapolis, IN 46285 USA
[5] AbbVie Inc, Dept R452, GPRD, Proc R&D, N Chicago, IL 60064 USA
[6] GlaxoSmithKline Med Res Ctr, Prod Dev, Analyt Sci, Stevenage SG1 2NY, Herts, England
关键词
NEAR-INFRARED SPECTROSCOPY; SCALE-UP; RAMAN-SPECTROSCOPY; MASS-SPECTROMETRY; MANUFACTURING ROUTE; REACTION-KINETICS; NMR-SPECTROSCOPY; IR-ANALYSIS; ONLINE NMR; CRYSTALLIZATION;
D O I
10.1021/op400358b
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The IQ Consortium reports on the current state of process analytical technology (PAT) for active pharmaceutical ingredient (API) development in branded pharmaceutical companies. The article uses an API process workflow (process steps from raw material identification through to finished API) to provide representative examples, including why and how the pharmaceutical industry uses PAT tools in API development. The use of PAT can improve R&D efficiency and minimize personnel hazards associated with sampling hazardous materials for in-process testing. Although not all steps or chemical processes are readily amenable to the use of the PAT toolbox, when appropriate, PAT enables reliable and rapid (real or near time) analyses of processes that may contain materials that are highly hazardous, transient, or heterogeneous. These measurements can provide significant data for developing process chemistry understanding, and they may include the detection of previously unknown reaction intermediates, mechanisms, or relationships between process variables. As the process becomes defined and understanding is gained through these measurements, the number of parameters suspected to be critical is reduced. As the process approaches the commercial manufacturing stage and the process design space is established, a simplification of the monitoring and control technology, as much as is practical, is desired. In many cases, this results in controls being either off-line, or if in situ control is required, the results from PAT are correlated with simple manufacturing measurements such as temperature and pressure.
引用
收藏
页码:63 / 83
页数:21
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