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Merck KGaA
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AAT Bioquest
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Avantor
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Merck KGaA
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Image Search Results
Journal: Aaps Open
Article Title: Extraction of niclosamide from commercial approved tablets into aqueous buffered solution creates potentially approvable oral and nasal sprays against COVID-19 and other respiratory infections
doi: 10.1186/s41120-023-00072-x
Figure Lengend Snippet: Baseline-corrected, 30 s subtracted spectra over 1–180 min dissolution for 300 µM fresh Yomesan niclosamide in nominal pH 9.35 Tris Buffer. The 30 s scan is shown as the dashed orange line and this 30 s scan was subtracted from each subsequent scan for 1 – 180 min. Each spectrum is an average of three scans (note: legend is ordered as 180 min to blank; graph is blank to 180 min)
Article Snippet: Tris buffer was used mostly at 20 mM buffer concentration. pH buffers were made using the TRIZMA HCl and
Techniques: Dissolution
Journal: Aaps Open
Article Title: Extraction of niclosamide from commercial approved tablets into aqueous buffered solution creates potentially approvable oral and nasal sprays against COVID-19 and other respiratory infections
doi: 10.1186/s41120-023-00072-x
Figure Lengend Snippet: Comparison between baseline-corrected UV-Vis spectra for Yomesan at the 30 s time point for initial Yomesan niclosamide-equivalent concentrations of 300 µM, 600 µM, and 1 mM in pH 9.35 Tris buffer. A UV-Vis spectra showing the “impurity” peak indicated (black arrow) at 345 nm, and the expected double niclosamide peaks indicated (gray arrows) at 333 and 377 nm. B Relative absorbance at 333 nm vs. initial added Yomesan niclosamide-equivalent concentration (µM) reveals a linear dependence to the “impurity” absorbance with an intercept at an Absorbance of 0.0292 AU, which would be equivalent to a niclosamide concentration of 1.05 µM. C Comparison between the UV-Vis spectra for the 30s “impurity” for 1 mM Yomesan niclosamide and a 12.5 µM vanillin solution, both in pH 9.35 Tris buffer
Article Snippet: Tris buffer was used mostly at 20 mM buffer concentration. pH buffers were made using the TRIZMA HCl and
Techniques: Comparison, Concentration Assay
Journal: Aaps Open
Article Title: Extraction of niclosamide from commercial approved tablets into aqueous buffered solution creates potentially approvable oral and nasal sprays against COVID-19 and other respiratory infections
doi: 10.1186/s41120-023-00072-x
Figure Lengend Snippet: Dissolution of ~1 mM 200 °C heat-treated Yomesan in nominal pH 9.35 Tris buffer at 23 °C: A 1 to 180 min, final pH 9.32 with logarithmic fit to initial data (dashed line); B comparison between heat-treated Yomesan (black-filled symbols) and untreated Yomesan (gray-filled symbols) from Fig. C in 9.35 TB vs time after addition out to day 2 final pH 9.26. Dotted lines are to guide the eye
Article Snippet: Tris buffer was used mostly at 20 mM buffer concentration. pH buffers were made using the TRIZMA HCl and
Techniques: Dissolution, Comparison
Journal: Aaps Open
Article Title: Extraction of niclosamide from commercial approved tablets into aqueous buffered solution creates potentially approvable oral and nasal sprays against COVID-19 and other respiratory infections
doi: 10.1186/s41120-023-00072-x
Figure Lengend Snippet: Yomesan-niclosamide dissolution as a function of Tris buffer pH: Maximum niclosamide concentrations from Fig. (filled black circles) vs. supernatant pH, plotted along with pHp theory determined earlier (Needham ) (dotted black line), for anhydrous (AK Sci) niclosamide (pKa 7.12, S w = 2.53 µM). Also shown are the day 2 equilibrated concentrations (gray-filled circles) and pHp theory for the monohydrate (dotted gray line) ( S w = 1 µM) ( S w = intrinsic solubility of the protonated niclosamide acid)
Article Snippet: Tris buffer was used mostly at 20 mM buffer concentration. pH buffers were made using the TRIZMA HCl and
Techniques: Dissolution, Solubility