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Furthermore, dose range finding may be useful because effective concentrations achieved upon nebulization and dilution with resident lung fluid are not known but were estimated conservatively in the present study with many studies conducted at 25% strength
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Endotoxin contamination from poor manufacturing conditions Incorrect or degraded peptide sequences Residual solvents left over from synthesis Heavy metal contamination from unregulated production Microbial contamination due to non-sterile handling Mislabeled vials with little or no active ingredient This is not a minor labeling issue
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