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The chemical structures of microPCM and each of its components (i.e., PLA and PA) were analyzed using Fourier transform infrared (FTIR) spectroscopy (Bruker Alpha-P FT-IR Spectrophotometer).
In a single spot urine sample from each man, phthalate metabolites, including mono-butyl phthalate (MBP), mono-ethyl phthalate (MEP), mono- 2-ethylhexyl) phthalate (mono- 2-ethylhexyl phthalate (mono- 2-ethylhexylid (phthalatetotal PA were analyzed using solid phase extraction and coupled with high-perforMEHPe liquid chromatography and detection by tandem mass spectrometry.
After various times (0 250 min) blood samples were collected and plasma levels of PA were analyzed using ELISA, as described in the methods.
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Protease activity (PA) was analyzed using digestive organ samples according to Kader et al. [ 23].
When plasma levels of PAI-1, PC, and t-PA were analyzed using peak values, patients with complications showed higher maximum plasma PAI-1 levels than those without complications during the observation weeks (P < 0.05).
The thin films of the HAP and HAP 30% PA plates were analyzed using an XRD instrument (Ultima IV; Rigaku, Osaka, Japan).
The characteristics of the participants, HRQoL scores, and PA levels were analyzed using descriptive statistics (means ± SD).
The surface morphology and presence of various functional groups in PA doped PPy films were analyzed using scanning electron microscopy, FTIR and Raman spectroscopy.
In order to obtain the accuracy and precision of the method, several synthetic mixtures with different concentration ratios of PA, MP, PP, CH and PS were analyzed using the proposed method.
The online PA interest survey responses were analyzed using Survey Monkey analytical tools [ 34].
In order to obtain the accuracy and precision of the ILS method, several synthetic mixtures with different concentration ratios of PA, MP, PP, CH and PS were analyzed using the proposed method.
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