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For dissolution of extracts, an aqueous solution of methyl hydroxypropyl cellulose (MHPC, 0.5 %, methocel™ E4M prem) was prepared.
Modification included dissolution of extracts in DMSO instead of water.
The modification included dissolution of extracts in DMSO instead of methanol.
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We compared re-dissolution of extracts in either a 1 M or a 10 M NaOH solution.
We also showed that re-dissolution of extracts from natural samples into 1 M NaOH solution makes P signals more visible by 31P-NMR spectroscopy than when a stronger alkaline solution is used.
However, as discussed in detail elsewhere [17], other dissimilarities exist among groups with respect to sample extraction (e.g. soil:extractant ratios), dissolution of lyophilized extracts for NMR analysis, NMR acquisition parameters, and methods to identify and quantify specific P forms.
In particular, approximately 17.0 mg kg−1 of organic P and 63.6 mg kg−1 of inorganic P were lost during re-dissolution of extract from forest soil with 10 M NaOH.
The coating solution was prepared by dissolution of the extracted lignin or modified lignin powder in adequate solvent and sprayed into the granular urea via a nozzle.
In equilibrium, the flow gradient is balanced by the rate of dissolution of the extracted volatile matter (VM): frac{partial }{partial r}left( {Dnabla c4pi r^{2} } right) = 4pi r^{2} rhowhere r is the distance from the center of the particle, c is the concentration of extracted VM, ρ is the characteristic rate of dissolution, and D is a diffusion coefficient.
Dissolution of the dried extracts in a common vehicle was a challenge; therefore, two negative controls were used; distilled water (5 ml/kg) for FPR extract treated group and 3% Tween 20 for FPL extract treated group.
In order to enhance the dissolution of Ginkgo biloba extract (GBE), a process for the micronization of GBE by supercritical antisolvent (SAS) was developed.
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