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. 2020 Feb 4;8:50. doi: 10.3389/fchem.2020.00050

Table 4.

Clinical observation of control and hydrogel treated rats for acute oral toxicity study.

Observation Group A Group B
Mean ± SEM Mean ± SEM
Body weight (g)
Pre–treatment 205 ± 0.86 207 ± 1.06
Day 1 210 ± 1.52 212 ± 1.30
Day 7 215 ± 1.93 218 ± 2.06
Day 14 225 ± 2.13 226 ± 1.80
Water Intake (mL/animal/day)
Pre–treatment 30 ± 1.40 28 ± 1.61
Day 1 28 ± 1.35 30 ± 1.35
Day 7 39 ± 1.36 40 ± 1.25
Day 14 41 ± 1.11 39 ± 1.24
Food Intake (g/animal/day)
Pre–treatment 13 ± 1.65 16 ± 0.96
Day 1 15 ± 1.24 14 ± 0.80
Day 7 17 ± 1.35 16 ± 0.50
Day 14 19 ± 1.53 19 ± 0.38
Signs of illness
Dermal toxicity
Dermal irritation
Ocular toxicity
Eye Irritation
Lacrimation
Salivation
Convulsions
Hyperactivity
Touch response + +
Corneal reflex + +
Righting reflex + +
Gripping strength + +
Alertness + +
Mortality

Results are expressed as Mean ± SEM of 5 rats in each group. Group A-Control, Group B -FCX6 hydrogel. Both at a dose of 5g/kg bodyweight. -Sign indicates lack or absence of specified observation. + Sign indicates presence of specified observations. All values have p>0.05, indicating statistically insignificant results.