Table 4.
Parameter | Experimental groups | P value | SEM | ||||
---|---|---|---|---|---|---|---|
On 5 dpt | Control | Commercial cream | PPE-HA-AgNPsI | PPE-HA-AgNPsII | PPE-HA-AgNPsIII | ||
TNF-α, pg/μL | 327.33a | 171.67c | 212.33b | 173.00c | 153.08d | 0.02 | 1.2 |
IL-6, pg/μL | 179.10a | 159.00b | 137.07c | 97.67d | 71.87e | < 0.001 | 1.2 |
IL-1β, pg/μL | 194.00a | 131.00c | 149.00b | 133.33c | 127.33c | 0.02 | 2.6 |
NO (µmol/ L) | 4.93a | 4.83a | 3.80b | 3.10c | 2.77c | < 0.001 | 0.06 |
NOS (µmol/ L) | 1.87a | 1.46ab | 1.40ab | 1.37ab | 1.20b | 0.04 | 0.05 |
CRP (mg/ L) | 14.50a | 11.33ab | 11.43ab | 8.57bc | 6.90c | 0.001 | 0.23 |
MPO (µmol/L) | 12.53d | 37.00b | 32.23c | 44.57a | 45.53a | < 0.001 | 0.34 |
On 10 dpt | |||||||
TNF-α, pg/μL | 374.33a | 138.00c | 164.00b | 128.00c | 109.97d | 0.03 | 3.2 |
IL-6, pg/μL | 202.77a | 147.00b | 125.33c | 95.90d | 70.50e | < 0.001 | 1.8 |
IL-1β, pg/μL | 241.00a | 131.67b | 134.00b | 121.33bc | 110.67c | 0.01 | 2.7 |
NO (µmol/ L) | 4.17a | 3.57ab | 3.23bc | 2.77cd | 2.30d | < 0.001 | 0.1 |
NOS (µmol/ L) | 1.47a | 1.33ab | 1.10ab | 1.10ab | 0.9b | 0.03 | 0.04 |
CRP (mg/ L) | 16.80a | 8.97b | 9.43b | 6.77b | 3.37c | < 0.001 | 0.17 |
MPO (µmol/L) | 9.03c | 31.33a | 27.83b | 34.27a | 33.50a | < 0.001 | 0.15 |
dpt, days post-treatment; TNF-α, tumor necrosis factor-alpha; IL-6, interleukin-6; IL-1β, interleukin-1 beta; NO, nitric oxide; NOS, nitric oxide synthase; CRP, C-reactive protein; MPO, myeloperoxidase. Control: the rats in this group had an experimental cutaneous wound with subsequent C. albicans strain infection and received no treatment, commercial cream: rats in this group had an experimental cutaneous wound with subsequent C. albicans infection and received a commercially available ketoconazole cream (2%) as a reference drug, PPE-HA-AgNPsI: the rats in this group had an experimental cutaneous wound with subsequent C. albicans infection and received a PPE-HA-AgNP formulated nanocomposite at 25% concentration, PPE-HA-AgNPsII: the rats in this group had an experimental cutaneous wound with subsequent C. albicans infection and received a PPE-HA-AgNP formulated nanocomposite at 50% concertation, PPE-HA-AgNPsIII: the rats in this group had an experimental cutaneous wound with subsequent C. albicans infection and received a PPE-HA-AgNP formulated nanocomposite at full concentration. a–eMean values with distinct letters in the same row changed significantly (p < 0.05).