Table I.
Formulation code | Drug/polymer (mg) | Concentration of cross-linker (ml) | Drug loading (% w/w)a | Encapsulation efficiency (% w/w)b |
---|---|---|---|---|
F 1 | 100:500 | 0 | 4.92 ± 0.05 | 24.5 ± 0.38 |
F 2 | 100:300 | 5.05 ± 0.07 | 15.15 ± 0.30 | |
F 3 | 250:500 | 8.63 ± 0.05 | 14.38 ± 0.23 | |
F 4 | 100:500 | 0.25 | 4.74 ± 0.21 | 21.34 ± 0.94 |
F 5 | 100:300 | 4.77 ± 0.40 | 12.87 ± 1.08 | |
F 6 | 250:500 | 8.70 ± 0.54 | 26.11 ± 1.62 | |
F 7 | 100:500 | 0.5 | 5.25 ± 0.34 | 23.58 ± 1.53 |
F 8 | 100:300 | 4.28 ± 0.37 | 11.56 ± 1.01 | |
F 9 | 250:500 | 6.67 ± 0.55 | 20.02 ± 1.66 | |
F 10 | 100:500 | 1 | 4.79 ± 0.45 | 21.54 ± 2.06 |
F 11 | 100:300 | 4.38 ± 0.66 | 11.82 ± 1.77 | |
F 12 | 250:500 | 6.85 ± 0.56 | 20.53 ± 1.68 |
aDrug loading (percent weight/weight) = amount of drug in microspheres/amount of microspheres taken
bEncapsulation efficiency (percent weight/weight) = amount of drug in microspheres/drug initially added