Pharmacokinetic Delivery and Metabolizing Rate of Nicardipine Incorporated in Hydrophilic and Hydrophobic Cyclodextrins Using Two-Compartment Mathematical Model

Figure 1

Loading of long-range GI and plasma concentration-time profiles from a dosage regime for NC (a), NC/HP𝛽CD (b), and NC/TA𝛽CD (c) compounds after oral administration.

(a)

(b)

(c)