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. Author manuscript; available in PMC: 2016 Mar 24.
Published in final edited form as: Biomaterials. 2010 May 15;31(23):6031–6038. doi: 10.1016/j.biomaterials.2010.04.009

Table 2.

Pharmacokinetic parameters of the different formulations injected to rats (n = 8). Cmax is the maximal value of the rivastigmine plasmatic concentration and tmax the corresponding time. t1ng corresponds to the time when the rivastigmine concentration was less than 1 ng mL−1. AUC corresponds to the area under the plasma concentration vs. time curve between days 0 and the last day of the study.

Formulation Cmax (ng mL−1) tmax (h) t1ng (day) AUC ± SD (h ng mL−1)
PK-Oil-300-5 4077 0.25 2 4100 ± 1900
PK-BTM-300-15 397 0.25 9 8100 ± 6600
PK-BTM-300-25 482 8 14 11,600 ± 10,100
PK-BTM-500-25 334 8 >35 14,700 ± 7000
PK-SAM-300-15 758 12 11 20,300 ± 17,600