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Indeed, subtle differences in pharmacokinetic parameters between two formulations can produce clinically important differences in seizure control [ 14].
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Each of the six formulations can be identified by their unique combination of absorption peaks/bands to identify major components of the formulation [48].
It can be seen that the difference between two formulations is distinctive as the parameter α1 increases to unity.
Scientists have edged closer to an effective Zika virus vaccine after demonstrating that three different formulations can protect monkeys from the disease.
The two types of formulations can be described as projecting expansion relevance and closing relevance, respectively.
The connection between those two formulations, however, has never been entirely clear.
The difference in Tmax values between the two formulations was assessed using nonparametric Wilcoxon signed rank test using SAS Enterprise guide 5.1.
Free drug and drug-loaded nanoparticles were tested to discriminate between the two formulations.
Pharmacodynamically, no significant differences in SDMT scores between the two formulations were found.
Paclitaxel pharmacokinetics and tissue distribution were evaluated, and differences were observed between the two formulations.
The maximum ratio between the two formulations in Model D is 1.8 for silicate and 2.2 for carbonaceous dust.
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