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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: J Neurochem. 2016 Dec 20;140(2):334–346. doi: 10.1111/jnc.13892

Table 2. Content of activated lovastatin in sera of rats receiving lovastatin-encapsulating PLGA nanoparticles.

Healthy male Lewis rats received a single peri-neural injection of lovastatin-encapsulating PLGA nanoparticles and one week later sera levels of active lovastatin were analyzed by HPLC and found to be below the level of detection. For comparison, levels of activated lovastatin in sera of rats that received lovastatin prodrug as a single intraperitoneal bolus or by oral gavage, as indicated, are shown. In all cases, levels of the inactive lovastatin prodrug were below the level of detection. Data shown are the means ± SEM, n=3–6.

Dose and Route of Administration Time Lovastatin Hydroxy Acid (ng/ml)
10 mg/kg, intraperitoneal 1h 937.5 ± 50.4
100 mg/kg, oral gavage 1h 385.3 ± 53.7
20 mg of 25% w/w lovastatin-encapsulating nanoparticles 1 week undetectable