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Biodesix provided blinded serum proteomic assay determinations.
Data are presented as mean ± SE obtained from three assay determinations for each treatment group for each sex.
HPLC-UV assay determinations of plasma LPV and RTV concentrations of participants from the cohort study were performed at the Dept.
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This solution was diluted further volumetrically to 100 μg mL−1 with diluent for assay determination in pharmaceutical dosage forms.
The developed simple LC method for assay determination of diacerein and aceclofenac is linear, precise, accurate and specific.
Amniotic fluid analysis included Gram stain examination, white blood cell count, and matrix metalloproteinase 8 (enzyme-linked immunosorbent assay) determination.
The present research provides the ion chromatographic method for the assay determination of the castanospermin and celgosivir as active pharmaceutical ingredients.
The accuracy of the method for assay determination was checked at three concentration levels of FEX; 0.1, 10.0, and 50 μg/ml (n = 3) for 3 consecutive days.
A selective stability indicating HPLC method was developed and validated for quantification of impurities (process related and degradants) and assay determination of Exemestane.
The objective of the ion chromatographic method is to develop the novel isocratic method for assay determination in Aza sugars having polyhydroxyl compounds such as 1-deoxynojirimycin, miglitol, castanospermin, and celgosivir.
Neutrophil and monocyte viability was analyzed by MTT assay (determination of 3- 4, 5-dimethyl-2-thiazolyl -2, 5-dimethyl-2-thiazolyl -2 5-dimethyl-2-thiazolyl -2o formazan) as described before [24].
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