Objective: To develop a pH responsive drug delivery system (DDS) for controlled release of
therapeutic cargo, Doxazosin Mesylate (DZM) which was loaded into carrier material mesoporous silica
nanoparticle (MSN) and subsequently coated with Eudragit S-100(ES-100) to release the drug at pH 7.4.
Material and Methods: We have synthesized cylindrical MSN under acidic condition using non-ionic
surfactant (Pluronic® P 123) and Tetraethoxysilane (TEOS). After post synthesis treatment (PST) surfactant
was removed by calcination. To obtain pH sensitive release calcined MSN was coated with ES-100 (MSN-DZMES100).
The Brauner-Emmett-Teller (BET) surface area, adsorption isotherm, t-plot, pore volume of MSN were done in
surface area analyzer to characterize different MSN samples (as synthesized, calcined, and coated).
Result and Discussion: Highest surafce area (427.114 m2/g) was observed in case of calcined sample when compared to
as synthesized (3.1198m2/g) and coated MSN (8.8480m2/g). Adsorption pore width of final coated sample was 12.58 nm
whereas as synthesized and calcined samples possessed pore width 36.82 nm and 7.32 nm respectively. All uncoated and
coated MSN samples were further characterized with FESEM, TEM, FTIR. No significant interaction between drug and
MSN was found from FTIR studies. The drug loading into coated mesoporous support was found to be 43.7%. In vitro
studies were done at different pH using Franz-diffusion cell. Results showed significant release at pH 7.4 from MSNDZM-
ES100. Cumulative drug release over a period of 10 hr was 81% at this systemic pH.
Conclusion: ES-100 coated mesoporous silica nanoparticle is a smart carrier for pH responsive release of guest molecule.