# Pharmacokinetics of bleomycin in dogs treated with electrochemotherapy

**Authors:** Nina Milevoj, Urša Lampreht Tratar, Tina Kosjek, Mojca Kržan, Filippo Torrigiani, Gregor Serša, Maja Čemazar, Nataša Tozon

PMC · DOI: 10.1080/01652176.2026.2648249 · The Veterinary Quarterly · 2026-03-25

## TL;DR

This study examines how bleomycin behaves in dogs during electrochemotherapy, finding consistent drug levels that support current treatment protocols.

## Contribution

The study provides new pharmacokinetic data for bleomycin in dogs undergoing electrochemotherapy, supporting existing treatment timing and dosage guidelines.

## Key findings

- Bleomycin's half-life in dogs was 22.03 minutes, with no significant differences in tumour concentrations at different time points.
- The volume of distribution and clearance values suggest no need for dose adjustments based on body weight or age.
- The results validate the 8–28-minute window for applying electric pulses after drug administration.

## Abstract

Bleomycin (BLM) is a cytotoxic antibiotic used in veterinary oncology, primarily in electrochemotherapy (ECT), a local ablative therapy where electric pulses increase drug uptake in tumours. BLM is administered intravenously or intratumourally, with the standard intravenous dose for dogs being 15,000 IU/m², followed by electric pulses 8–10 minutes later. This protocol is derived from human oncology and lacks extensive pharmacological data in dogs. We studied BLM pharmacokinetics in 29 dogs with various tumours treated with intravenous BLM and ECT between 2017 and 2023. Samples were collected from serum of 15 dogs, serum and tumours of 8 dogs, and tumours of 6 dogs. The mean volume of distribution (Vd) of BLM was 224.5 ± 75.02 ml/kg, clearance (CL) was 7.04 ± 2.05 ml/kg/min, and area under the curve (AUC) was 65.87 ± 2.11 µg·min/l. The half-life (t₁/₂) of BLM in dogs was 22.03 ± 0.88 minutes. No significant difference was found in tumour BLM concentrations between 8 minutes post-administration and 2 minutes after pulse completion. These results support the recommended 8–28-minute window for applying electric pulses following intravenous BLM administration and may indicate no need for dose adjustments based on body weight or age.

## Linked entities

- **Chemicals:** bleomycin (PubChem CID 5360373), BLM (PubChem CID 5360373)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, BLMH (bleomycin hydrolase) [NCBI Gene 480635], SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, PNLIP (pancreatic lipase) [NCBI Gene 5406] {aka PL, PNLIPD, PTL}
- **Diseases:** hepatoid gland carcinoma (MESH:D004701), hepatoid gland adenoma (MESH:D000236), impaired kidney function (MESH:D007674), Solid Tumours (MESH:D009369), hyperpigmentation (MESH:D017495), reduced muscle mass (MESH:D009135), epithelial tumours (MESH:D009375), thyroid tumours (MESH:D013964), pruritic erythema (MESH:D004890), loss of liver and kidney function (MESH:D056486), oral malignant melanoma (MESH:D008545), acanthomatous ameloblastoma (MESH:D000564), ulceration (MESH:D014456), soft tissue sarcoma (MESH:D012509), cutaneous and subcutaneous mast cell tumours (MESH:D000090362), oral squamous cell carcinomas (MESH:D000077195), malignant epithelial neoplasms (MESH:D002277), oral fibrosarcoma (MESH:D005354), pulmonary fibrosis (MESH:D011658), squamous cell carcinomas (MESH:D002294), skin toxicity (MESH:D012871), STS (MESH:D016114), desquamation (MESH:D017490), basal cell carcinomas (MESH:D002280), vascular anomalies (MESH:D020785), cytotoxic (MESH:D064420), teratomas (MESH:D013724), necrosis (MESH:D009336), PD (MESH:D010300), lymphomas (MESH:D008223)
- **Chemicals:** methanol (MESH:D000432), S T S (MESH:D014316), chloride (MESH:D002712), oxygen (MESH:D010100), acetonitrile (MESH:C032159), sodium (MESH:D012964), E P (-), creatinine (MESH:D003404), isoflurane (MESH:D007530), water (MESH:D014867), deoxyribose (MESH:D003855), potassium (MESH:D011188), nitrogen (MESH:D009584), glucose (MESH:D005947), BLM (MESH:D001761), propofol (MESH:D015742), ammonium formate (MESH:C030544), Oasis (MESH:C118676), Midazolam (MESH:D008874), cellulose acetate (MESH:C005062), Epirubicin (MESH:D015251), carboplatin (MESH:D016190)
- **Species:** Felis catus (cat, species) [taxon 9685], Canis lupus familiaris (dog, subspecies) [taxon 9615], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13021021/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13021021/full.md

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Source: https://tomesphere.com/paper/PMC13021021