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. Author manuscript; available in PMC: 2024 Mar 7.
Published in final edited form as: Biomaterials. 2023 Jan 3;294:121985. doi: 10.1016/j.biomaterials.2022.121985

Table 2. Pharmacokinetic parameters of Ex-POEGMAopt.

Pharmacokinetic parameters were calculated from the data given in Figure 4. Data were fitted to a one-phase exponential decay curve and analyzed via non-compartmental pharmacokinetic analysis using GraphPad Prism 8 software and MRT values were calculated within WinNonlin software. Absorption phase pharmacokinetics of Ex-PEGRh in immunized mice were not calculated (N/C) due to its low goodness-of-fit values. Data showed the mean ± SEM.

Treatment t1/2 absorption (h−1) t1/2 elimination (h−1) MRT (h) tmax (h)* Cmax (nM)* AUC (h × nM)
Naïve Mice Exendin 0.65 ± 0.04 2.12 ± 0.3 4.2 ± 0.1 1.6 ± 0.1 31.7 ± 7.5 118 ± 9
Ex-PEGRh 6.59 ± 0.27 23.14 ± 3.2 29.8 ± 2.4 16.6 ± 1.1 34.6 ± 1.2 1585 ± 56
Ex-PEGMw 6.6 ± 0.9 34.91 ± 4.5 38.1 ± 2.2 19.5 ± 2.5 35.3 ± 2.2 2206 ± 42
Ex-POEGMAopt 9.1 ± 0.9 97.3 ± 3.2 59.8 ± 6.6 32.1 ± 2.9 35.8 ± 1.3 3664 ± 83
Immunized Mice Exendin 0.77 ± 0.07 1.88 ± 0.2 4.9 ± 0.4 1.72 ± 0.1 36.9 ± 3.4 159 ± 9
Ex-PEGRh N/C 11.9 ± 2.7 24.0 ± 2.5 N/C N/C 424 ± 17
Ex-POEGMAopt 12.1 ± 1.0 105.7 ± 6 70.8 ± 0.2 42.6 ± 3.2 30.3 ± 2.0 3664 ± 83