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Neuroprotective efficacy of P7C3 compounds in primate hippocampus

Ave, Cornelius, OR, USA), controlled with proper stirring speed (100 rpm) and temperature (37 0.5 C), was used to study the in vitro release, whereas for dissolution studies a simulated gastric fluid (pH 1.2) and an intestinal fluid (pH 6.5) environment was used for 2 and 48 h thereafter, respectively

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Interindividual variability using the exponential model was estimated for K p,R and R kp , and sex and surgical treatment were tested in the covariate analysis using likelihood ratio tests