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Kaplan-Meier estimates of time to and duration of first integument-related toxicity were prepared.
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Inocula for toxicity studies were prepared as described above but reaction phases were diluted into 320 mM Sucrose at two different concentrations (25 µg and 0.25 µg total protein/50 µl) and only non infected MBM was used.
To replace toxic and nonvolatile solvents for use with different MWCNTs, eight solvent mixtures with low toxicity and volatility were prepared.
In this study, thermoplastic polyurethane (TPU) scaffolds containing carbon nanotubes (CNTs) or nanofibrillated cellulose fibers (NFCs) were prepared using low toxicity dimethyl sulfoxide (DMSO) as a solvent.
For the determination of 'dark' toxicity of the compounds, well plates were prepared in the same manner as above but without irradiation.
In the present study, felodipine loaded PLGA nanoparticles were prepared, characterized and evaluated for in vivo toxicity study in animal model.
The aconitine-encapsulated GP nanoparticles (238.2 ± 1.2 nm) were prepared following the same procedure and tested for its toxicity by intraperitoneal injection on ICR mouse (n = 8).
PEG-NRs were prepared from stock CTAB-coated gold nanorods to minimize toxicity and extend particle circulation time as previously described.
were prepared.
Samples were prepared in 96 well plates and analyzed by flow cytometry, which allowed for rapid, inexpensive and precise assessment of compound's toxicity associated with cell death.
The partially purified plaunotol extract (PPE) used in this acute and chronic toxicity study was prepared from the leaves of C. stellatopilosus.
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