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Hydrogel-magnetic nanoparticles were suspended into Falcon tubes containing 10 mL PBS (pH 7.2 at 37 °C).
The fresh bacterial cultures were suspended into normal saline and compared the turbidity with 0.5 McFarland standards.
100 mg Fe3O4/PCC MNPs were suspended into 100 mL 0.1 mM solutions of adsorbates, and then shaken at 180 rpm under pH 6.0 and 30 °C.
Samples collected were suspended into the 0.01 % (w/v) mercuric chloride for 2 3 min for surface sterilization followed by washing with distilled water.
The natural untreated estuarine particles, which contained intrinsic OM, were subjected to a range of salinity (0 – 17.5 psu) as they were suspended into the mixture of milli-Q water and ASW.
After that, the silver nanoparticles were suspended into de-ionized water with concentrations of 0.5 w/v% mixed with oleic acid surfactant concentration of 0.5, 1, and 1.5 w/v%, respectively.
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The crude ethanol extract (1026 g) of D. heterophyllum was suspended into 500 mL water.
Furthermore, the solution was suspended into the template medium and kept static for 48 h.
In general, 100 mg of ZnO nanocrystals was suspended into 20 mL of ethanol (pH = 10.8) under sonication.
100 mg modified ZnO was suspended into 20 mL pH 7.0 0.1 M phosphate buffers, and then 750 μL of 25% glutaraldehyde solution was added to the mixture.
The dialyzer tube was suspended into a 200 mL glass beaker containing release media, which was magnetically stirred continually at 500 rpm at room temperature.
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