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The analytical HPLC column for the optimized quality control (XBridge® Shield RP-18; 2.5 μm; 3.0 50 mm) and C18plus SepPak® cartridges for solid phase extraction (SPE) were purchased from Waters (Waters® Associates Milford, MA, USA).
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The utility of numerical models and optimized solutions for quality control, tailor-made concrete mixtures and selection of constituent materials is highlighted.
The influences of different parameters such as reaction time, temperature, initial gel concentration, mechanical stirring and drying conditions on the improvement of the final products were experienced and the procedure for the efficient synthesis of zeolite NaA was optimized with available quality control tests.
These results indicated the necessity of a complete evaluation for possible processing effects on physicochemical and nutritional characteristics of WBR grains within the entire process extending immediate treatments to its prolonged storage and consumption, in order to achieve better quality control using the optimized processing parameters.
The processes were optimized to obtain a product approved to quality control according to a radiopharmaceutical to be administered in a context of a clinical routine.
These models allow the quality control of these medicines to be optimized using simple, fast, low-cost techniques that produce no chemical waste.
An exact amount was subsequently prepared as dilutions in the optimized mobile phase to make a set of calibration and quality control solutions.
Finally, using a set of 3 samples, the optimized model was successfully transferred to a secondary instrument located in a quality control (QC) laboratory.
Samples that passed EHV1 DNA extraction quality control testing were screened for respiratory viruses using previously optimized and described PCR and reverse transcriptase PCR assays.
Optimized probes were present on the arrays in triplicate; one set of standardized probes (Agilent Technologies, Palo Alto, CA) used for quality control and background subtraction was also present on the arrays.
The entire quality control process (except for tests for residual solvents, endotoxins and sterility) was completed within 3 min using the optimized analytical HPLC system.
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