Process analytical technology applied for end-point detection of pharmaceutical blending by combining two calibration-free methods: Simultaneously monitoring specific near-infrared peak intensity and moving block standard deviation

2011 ◽  
Vol 210 (2) ◽  
pp. 122-131 ◽  
Author(s):  
Wataru Momose ◽  
Keiji Imai ◽  
Shoji Yokota ◽  
Etsuo Yonemochi ◽  
Katsuhide Terada
Keyword(s):  
Standard Deviation ◽  
Near Infrared ◽  
Process Analytical Technology ◽  
End Point ◽  
Peak Intensity ◽  
End Point Detection ◽  
Calibration Free ◽  
Point Detection ◽  
Analytical Technology

Real-time predictions of drug release and end point detection of a coating operation by in-line near infrared measurements

2011 ◽  
Vol 421 (2) ◽  
pp. 237-243 ◽  
Author(s):  
Claire Gendre ◽  
Mathieu Boiret ◽  
Muriel Genty ◽  
Pierre Chaminade ◽  
Jean Manuel Pean
Keyword(s):  
Drug Release ◽  
Real Time ◽  
Near Infrared ◽  
End Point ◽  
Infrared Measurements ◽  
End Point Detection ◽  
Point Detection

scholarly journals Acid number, viscosity and end-point detection in a multiphase high temperature polymerisation process using an online miniaturised MEMS Fabry-Pérot interferometer

Talanta ◽  
2021 ◽  
Vol 224 ◽  
pp. 121735
Author(s):  
Claudio Avila ◽  
Christos Mantzaridis ◽  
Joan Ferré ◽  
Rodrigo Rocha de Oliveira ◽  
Uula Kantojärvi ◽  
...  
Keyword(s):  
High Temperature ◽  
Acid Number ◽  
End Point ◽  
Fabry Perot ◽  
End Point Detection ◽  
Point Detection

Fluoroimmunoassay for human choriomammotropin.

1979 ◽  
Vol 25 (6) ◽  
pp. 973-975 ◽  
Author(s):  
T Chard ◽  
A Sykes
Keyword(s):  
Equipment Design ◽  
Radiation Hazard ◽  
Human Origin ◽  
End Point ◽  
End Point Detection ◽  
Purified Antigen ◽  
Point Detection

Abstract We describe an immunoassay for human choriomammo-tropin by use of the fluorescein-labeled hormone (of human origin). The technique is generally similar to the radioimmunoassay for this material, but has the advantage of stability of tracer and avoidance of radiation hazard. However, the procedure requires approximately 50-fold more tracer than does the radioimmunoassay, and this would be a disadvantage with materials for which supplies of purified antigen are scarce. Furthermore, both within-assay variation (3.9%) and between-assay variation (7.8--7.9%) were less satisfactory than that of radioimmunoassay (1.5% and 2.2--3%, respectively). This is almost certainly the result of imprecision of end-point detection and could probably be corrected by further attention to equipment design.

AEROBIC END-POINT DETECTION IN A SEQUENCING BATCH REACTOR

2005 ◽  
Vol 38 (1) ◽  
pp. 115-120
Author(s):  
Hilario López García ◽  
Iván Machón González
Keyword(s):  
Sequencing Batch Reactor ◽  
Batch Reactor ◽  
End Point ◽  
End Point Detection ◽  
Point Detection

Optical end point detection of etched YBCO films

1992 ◽  
Vol 191 (3-4) ◽  
pp. 525-529 ◽  
Author(s):  
R. Dolata ◽  
M. Fischer ◽  
W. Jutzi
Keyword(s):  
Ybco Films ◽  
End Point ◽  
End Point Detection ◽  
Point Detection
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