Modeling Drug-Carrier Interaction in the Drug Release from Nanocarriers
The model fit to release data. (a) Telmisartan from MSNPs with different pore sizes . (b) Synthetic retinoid Am80 from PEG-PBLA NPs with different amine additives . (c) DS from PLNPs in the release medium of various ionic strengths . (d) Estradiol from PLGA NPs . (e) Savoxepine from PLA NPs of two different sizes . (f) Steroids from various PLA/PLGA NPs (■: PLA Mw 14,000; ∆ PLA Mw 9,000; ▾: PLGA Mw 13,000; ○: PLGA Mw 8,000). BDP release (●) from PLA NPs (Mw 14,000) is a control . Solid lines represent the model prediction.