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The filter paper activity of Accellerase™ 1000 was ~40 FPU/mL, which was measured using a method developed by the National Renewable Energy Laboratory NRELL, US) [ 50].
One kind of measurement is electrophysiologic, and most of these are measured using a method called black lipid membranes, where you paint lipid in decade onto a partition separating two aqueous chambers, and then you you put your channel in lipid vesicles, you fuse them with this bilayer membrane, the channels end up in there.
The intraparticle diffusion coefficient was measured using a method based on the fitting of a set of experimental chromatographic profiles to the lumped pore diffusion model.
The proline content in the honey samples was measured using a method established by the IHC [15].
Flumazenil concentrations in blood were measured using a method published previously, based on HPLC coupled to tandem mass spectrometry (LC-MS/MS) [16].
The DPPH radical-scavenging activities of the compounds isolated from G. paraguayens were measured using a method described previously (Chen et al. [2008]).
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Albumin was measured using a colorimetric method (Jaffe method).
Ferrous iron was measured on site using a 1,10 phenanthroline method and total iron was measured using a FerroZine method with a Hach portable digital spectrophotometer.
Solvent activities were measured using a gravimetric method in the range 48 70°C.
The reducing power of the samples was measured using a previous method [21].
The TS and VS concentrations were measured using a standard method (Clesceri et al. 2012).
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