Modeling Drug-Carrier Interaction in the Drug Release from Nanocarriers
Figure 3
The model fit into release data. (a) Carboxylfluorescein from thermosensitive liposomes with different PEG addition [24]. (b, c) Verapamil and doxorubicin from liposomes [25]. (d) Amiodarone from LNC [26]. (e) BSA from PLLA nanocapsules [29]. (f) Indomethacin from PECL nanocapsules [27]. Solid lines represent the model prediction.