Search Results
1 Introduction In order to make better decisions related with crop production, precision agriculture practices information technologies to transport data from several sources, and it consists of three components: capturing data in an accurate manner
corpus of work, with an optimal balance between precision and recall when querying the larger dataset in which their corpus resides. This is especially important where bibliometrics is used for evaluation purposes. The most common problem encountered is
(HPTLC), high-performance liquid chromatography (HPLC), and capillary electrophoresis (CE). Among these methods, HPLC is the most popular method for quantitative analysis of drugs and impurities, due to its selectivity, precision, and accuracy [ 12 , 13
) equipped with quaternary pump, autosampler, and DAD detector. Intermediate precision was tested on chromatograph Agilent 1200 (Agilent Technologies, Palo Alto, CA, USA) equipped with binary pump, manual injector (20 μL loop), and DAD detector. The column
9 replicates over 3 batches. The lower limit of quantification (LLOQ) was calculated as the minimum concentration at which lutein can be reliably quantified with a precision of ≤20% and accuracy within ±20%. The intra-batch precision and
multi-ton production scale. Any future development in flow technology will of course have a direct impact in these realms as well. Figure 1. Precision polymer engineering via continuous-flow reactors
peak area of each peak was measured, a standard curve with the peak area against the concentration was drawn, and linearity of the standard curve was evaluated. The precision and accuracy of the lower limit of quantitation should be less than 20% and
analytical method was subjected to validation with respect to various parameters such as linearity, intra- and inter-day precision, accuracy, limit of quantification (LOQ), limit of detection (LOD), and reproducibility for each analyte
/mL for evaluating accuracy, precision, and stability. All the solutions were stored at 4 °C until processed. Preparation of Plasma Samples Licochalcone A and IS were simultaneously extracted from the plasma specimens
, linearity, limit of detection (LOD), limit of quantification (LOQ), accuracy, precision and robustness of drug in plasma were assessed. Selectivity The selectivity of developed method was performed by evaluating blank as well as CAP samples The RT was
