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. 2020 Dec 10;148(5):566–575. doi: 10.1017/S0031182020002310

Table 1.

In vitro BNZ dissolution efficiency and stability of BNZ-MP stored at room temperature up to 36 months

Sample Dissolution efficiency (±s.d.) (%) Drug content (±s.d.)
Time (min) Time (month)
10 15 20 30 45 60 90 120 0 6 9 12 24 36
BNZ-MP-RLa 83.56**** (9.97) 86.68**** (8.03) 89.64**** (7.41) 92.28**** (6.37) 91.51**** (5.67) 91.52*** (4.98) 91.31** (5.28) 92.73* (4.98) 22.90 (0.55) 22.88 (0.57) 22.76 (0.48) 22.92 (0.41) 21.52 (0.96) 21.86 (1.44)
BNZ-MP-RSb 58.95*** (6.83) 71.13*** (6.01) 78.92*** (8.05) 80.00**** (3.42) 81.88*** (3.63) 82.59** (3.05) 83.59 (2.37) 83.80 (2.01) 23.09 (1.47) 23.05 (0.40) 22.00 (0.81) 21.63 (0.29) 21.53 (1.28) 21.64 (0.83)
BNZc 15.57 (2.61) 22.82 (2.62) 29.62 (3.89) 38.59 (4.43) 51.37 (4.11) 60.36 (4.48) 74.40 (3.58) 81.79 (3.31)
a

BNZ-MP-RL: microparticles of Eudragit® RL PO loaded with benznidazole.

b

BNZ-MP-RS: microparticles of Eudragit® RS PO loaded with benznidazole.

c

BNZ: raw benznidazole.

Difference is statistically significant with respect to BNZ: *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.