Table 1.
Sample |
SBET, m2/g |
VT, cm3/g Exp |
CBET |
Drug Loaded,* μg/mg |
pSi† | 458 ± 4 | 1.30 | 31 | NA |
pSi-COOH | 385 ± 2 | 1.31 | 52 | NA |
pSi-C12 | 356 ± 2 | 0.82 | 27 | NA |
pSiO2-C8 | 260 ± 2 | 0.62 | 32 | NA |
pSiO2‡ | 217 ± 1 | 0.61 | 80 | NA |
pSi-COOH-RAP | 268 ± 1 | 0.92 | 48 | 68 ± 8 |
pSi-C12-RAP | 236 ± 2 | 0.56 | 24 | 36 ± 6 |
pSiO2-C8-RAP | 204 ± 1 | 0.48 | 27 | 105 ± 18 |
CBET, constant related to the affinity between the N2 adsorbate molecules and the pSi surface; SBET, specific surface area calculated at (P/P0) 0.03–0.24; VT, total pore volume at relative pressure (P/P0) equal to 0.99.
Drug-loading capacity calculated by LC-MS analysis.
Freshly etched pSi.
Porous Si converted to fully oxidized to porous silica (SiO2) by thermal oxidation in air at 800°C for 1 hour.