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The molecular diffusion is uniquely assessed by diffusion weighted imaging (DWI) techniques [ 1, 3].
The potential functional significance of these microstructural changes suggests that this line of investigation may lead to improved understanding of the origins of common gastrointestinal symptoms and perhaps development of novel treatments.— Shulamit Babitz Frøkjær et al. Altered brain microstructure assessed by diffusion tensor imaging in patients with diabetes and gastrointestinal symptoms.
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The successful formation of the graft-copolymer structures and the absence of residual mPEG-azide homopolymer in the final products were further assessed by diffusion-ordered NMR spectroscopy (DOSY).
ODN dissociation from the carrier was assessed by comparing diffusion constants of CL-ODN complexes and ODNs before complexation and after release.
Antimicrobial susceptibility to β-lactams was assessed by disk diffusion following Clinical Laboratory Standards Institute recommendations (http://www.clsi.org).org
Coresistance to other antibiotics was assessed by disk diffusion and interpreted according to the Clinical Laboratory Standards Institute criteria [ 16].
The in vitro skin permeation and deposition behavior of tetrandrine loaded in the ethosomes were assessed by Franz diffusion cells and confocal laser scanning microscopy.
As assessed by disk diffusion assay, all isolates were also susceptible to trimethoprim/sulfamethoxazole, ceftazidime, chloramphenicol, azithromycin, aztreonam, ciprofloxacin, imipenem, and tetracycline.
The toxicity of combinations of antibiotics with AgNPs was assessed by the disc diffusion method.
Antibacterial activities of the aqueous (PBS) and organic extractions were assessed by the well diffusion method.
The antibacterial activity of the samples was assessed by the agar diffusion method.
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