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Table 3 Ex vivo stability data for doxorubicin (DOX)

From: Enhancement of oral bioavailability of doxorubicin through surface modified biodegradable polymeric nanoparticles

Conditions

LQC (2.90 ng/ml)

HQC (2000.00 ng/ml)

Long term stability; recovery (ng) after storage (− 40 °C)

 Previous day

2.83 ± 0.05

1989.04 ± 5.16

 30th day

2.79 ± 0.04 (98.59%)

1951.78 ± 19.12 (98.13%)

Freeze–thaw stress; recovery (ng) after freeze–thaw cycles (− 40 to 25 °C)

 Pre-cycle

2.84 ± 0.03

1988.10 ± 4.19

 First cycle

2.80 ± 0.04 (98.59%)

1976.19 ± 12.91 (99.40%)

 Second cycle

2.78 ± 0.04 (97.88%)

1972.54 ± 13.16 (99.22%)

 Third cycle

2.74 ± 0.05 (96.48%)

1966.44 ± 13.67 (98.91)

Heating–cooling stress; recovery (ng) after heating–cooling cycles (50–4 °C)

 Pre-cycle

2.85 ± 0.03

1989.09 ± 5.90

 First cycle

2.80 ± 0.04 (98.25%)

1981.61 ± 11.95 (99.62%)

 Second cycle

2.76 ± 0.03 (96.84%)

1974.01 ± 12.04 (99.24%)

 Third cycle

2.72 ± 0.03 (95.44%)

1963.02 ± 13.02 (98.69%)

Bench top stability; recovery (ng) at room temperature (25 °C)

 0 h

2.84 ± 0.03

1988.49 ± 11.01

 24 h

2.80 ± 0.05 (98.59%)

1969.10 ± 12.31 (99.02%)

Post processing stability; recovery (ng) after storage in auto sampler (4 °C)

 0 h

2.85 ± 0.03

1979.02 ± 7.91

 24 h

2.81 ± 0.04 (99.60%)

1962.01 ± 14.02 (99.14%)

  1. Values (Mean ± SD) are derived from six replicates. Figures in parenthesis represent analyte concentration (%) relative to time zero. Theoretical contents; LOQQC: 1.01 ng/ml, LQC: 2.9 ng/ml; MQC: 1000 ng/ml; and HQC: 2000 ng/ml