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. 2018 Sep 6;13:5127–5138. doi: 10.2147/IJN.S161240

Table 2.

PK parameters of insulin following the administration (oral or subcutaneous) of different formulations to diabetic rats

PK parameters Simple insulin solution (SC) Insulin-loaded NPs from Cs in enteric capsules Insulin-loaded NPs from CPP-g-Cs in enteric capsules
Dose (IU/kg) 5 30 30
Cmax (μIU/mL) 110.4±8 21.3±2.2 37.6±3.2
Tmax (hours) 1 4 6
AUC (μIUh/mL) 220.8±5.3 103.6±4.1 259.3±6
BAR (%) 100 7.8±0.7 19.6±1.3

Notes: PK parameters following the administration of three different formulations to diabetic rats: subcutaneous (SC) administration of simple insulin solution, oral administration of insulin-loaded NPs from chitosan filled in enteric protective capsules, and oral administration of insulin-loaded NPs from peptide-grafted derivative of chitosan (CPP-g-Cs) NPs filled in enteric protective capsules.

Abbreviations: AUC, area under the curve; BAR, relative bioavailability; CPP, cell-penetrating peptide; Cs, chitosan; NPs, nanoparticles; PK, pharmacokinetic.