Study | Route | Mechanism of delivery | Solvent/vehicle | Groups (dosage 5Â mg/kg) | Frequency of delivery | Euthanasia endpoint | Sample size (per group) |
---|---|---|---|---|---|---|---|
Study 1: ALZET osmotic pump subcutaneous delivery (original study identification of issue) | SC | Osmotic pump | Propylene glycol | THC, CBD, CBD + THC, vehicle | Continuous/daily | Early euthanasia | N = 4a |
Study 2: ALZET osmotic pump subcutaneous delivery with provisions to reduce risk of contamination | SC | Osmotic pump | Propylene glycol | THC, CBD, CBD + THC, vehicle | Continuous/daily | Early euthanasia | N = 2a |
Study 3: Isolated THC, CBD direct subcutaneous injection | SC | 25-GA needle, 0.1 ml | THC dissolved in ethanol CBD dissolved in saline | THC (20 mg/day) CBD (20 mg/day) | Daily | 7 days | N = 2a |
Study 4: Direct injection subcutaneous delivery, histopathology | SC | 25-GA needle, 0.1 ml | Propylene glycol | THC, CBD, CBD + THC, vehicle, saline | Daily | 10 days | N = 2a |
Study 5: Intraperitoneal delivery | IP | 22-GA needle, 0.1 ml | Propylene glycol | THC, CBD, CBD + THC, vehicle | Weekly | 8 weeks | N = 12 |
Study 6: ALZET osmotic pump subcutaneous delivery with change in solvent | SC | Osmotic pump | 1:1:18 parts ethanol:Kolliphor:saline | THC, CBD, CBD + THC, vehicle | Continuous/daily | 8 weeks | N = 4 |