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. Author manuscript; available in PMC: 2019 Oct 28.
Published in final edited form as: J Control Release. 2018 Sep 6;288:111–125. doi: 10.1016/j.jconrel.2018.09.003

Table 1.

Physicochemical properties and portal vein PK parameters following intraluminal injection of salmon calcitonin or Exenatide with PIP 640 or without (control) into rat jejunum.

Peptide drug MW (kDa) Hydrodynamic size (Å)(calculated) AUC(t 0–60) (ng/ml*min) Cmax (ng/ml)
Control PIP 640 Control PIP 640
Calcitonin 3.4 11 155±2.7 1680±540 3.3±0.36 55.6±6.7
Exenatide 4.2 11 237.6±38 1577±72.3 6.5±0.75 53±5.8

MW = molecular weight. The hydrodynamic radius was calculated using the relationship established between the MW and the hydrodynamic radius of a protein. PK parameters for area under the curve between 0–60 min (AUC t 0–60) and maximum concentration achieved (Cmax) were calculated with the trapezoid rule using Microsoft Excel add-in program, PK-Solver [24].

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