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Compounds were quantified using a standard calibration curve.
All compounds were quantified by refractive index detection (Shimadzu, Kyoto, Japan).
All compounds were quantified by refractive index detection (Waters, Massachusetts, USA).
The unidentified compounds were quantified and labeled as derivatives of polyphenol standards with similar UV spectra.
Arginine and related compounds were quantified in plasma, wound fluids and multiple tissues.
Three different compounds were quantified by stable isotope dilution assay (SIDA): β-damascenone, β-ionone and α-ionone.
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Tars are collected, and six compounds are quantified.
The cell viability of these compounds was quantified by MTT assay.
Attomoles of labeled compounds are quantified in milligram‐sized samples, such as 20 μl of blood.
The ferric reducing antioxidant power of the compounds was quantified by the method described by [36] with slight modifications.
The total covalency of the compounds was quantified using covalent bond density (CBD), defined by the number of bonds and the bond overlap populations computed in this study.
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