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Exact(20)
For glycosyl linkage analysis, EV polysaccharide fractions (500 μg - 1 mg) were suspended in 200 300 μl of dimethyl sulfoxide (DMSO) and left to stir for one week.
The particles (about 2 mg) were suspended in deionized water before measurement.
Accurately weighted aliquots of drug-loaded nanoparticles (15 mg) were suspended in 5 ml release medium (PBS pH 7.4 containing 0.1% w/v Tween 80).
The different concentrations of the seed powder (50, 100 and 150 mg) were suspended in the distilled water to obtain 10,000, 20,000 and 30,000 mg/L (Alo et al. 2012).
In preparation of coupled SLNs, the drug-loaded formulations (100 mg) were suspended in a PBS (pH 7.4; 10 ml) containing Lf (10 mg) and EDC (10 mg) and then incubated for 2 h at room temperature.
GNPs (900 mg) were suspended and refluxed in a mixture of concentrated acid H2SO4/HNO3 (30 ml/30 ml) at 140°C for 1 h, followed by diluting with deionized water (3,000 ml).
Similar(40)
GO (200 mg) was suspended in DI water for approximately 2 mg/mL.
A weighed quantity of the fibers (20 mg) was suspended in PBS of pH 7.4.
The white Ag/ACD powder (200 mg) was suspended in xylene (30 mL) and refluxed for 1 h.
pH tuned Pseudomonas fluorescens lipase (1 mg) was suspended in different solvents (100 μl each) and ultrasonicated at 110W periodically.
pH tuned Burkholderia cepacia lipase (1 mg) was suspended in different solvents (100 μl each) and ultrasonicated at 110W continually.
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