Prostate tissue ablation and drug delivery by an image-guided injectable ionic liquid in ex vivo and in vivo models

Author:

Demirlenk Yusuf M.1ORCID,Albadawi Hassan1ORCID,Zhang Zefu1ORCID,Atar Dila1,Cevik Enes1,Keum Hyeongseop1ORCID,Kim Jinjoo1ORCID,Rehman Suliman1,Gunduz Seyda12ORCID,Graf Erin3,Mayer Joseph L.1,Dos Santos Pedro R.14ORCID,Oklu Rahmi15ORCID

Affiliation:

1. Laboratory for Patient-Inspired Engineering, Mayo Clinic, 13400 East Shea Blvd., Scottsdale, AZ 85259, USA.

2. Department of Medical Oncology, Istinye University, Bahcesehir Liv Hospital, Istanbul 34517, Turkey.

3. Department of Laboratory Medicine and Pathology, Mayo Clinic, 5777 E Mayo Blvd., Phoenix, AZ 85054, USA.

4. Department of Cardiothoracic Surgery, Mayo Clinic, 5777 E Mayo Blvd., Phoenix, AZ 85054, USA.

5. Division of Vascular and Interventional Radiology, Mayo Clinic, 5777 E Mayo Blvd., Phoenix, AZ 85054, USA.

Abstract

Benign prostatic hyperplasia and prostate cancer are often associated with lower urinary tract symptoms, which can severely affect patient quality of life. To address this challenge, we developed and optimized an injectable compound, prostate ablation and drug delivery agent (PADA), for percutaneous prostate tissue ablation and concurrently delivered therapeutic agents. PADA is an ionic liquid composed of choline and geranic acid mixed with anticancer therapeutics and a contrast agent. The PADA formulation was optimized for mechanical properties compatible with hand injection, diffusion capability, cytotoxicity against prostate cells, and visibility of an x-ray contrast agent. PADA also exhibited antibacterial properties against highly resistant clinically isolated bacteria in vitro. Ultrasound-guided injection, dispersion of PADA in the tissue, and tissue ablation were tested ex vivo in healthy porcine, canine, and human prostates and in freshly resected human tumors. In vivo testing was conducted in a murine subcutaneous tumor model and in the canine prostate. In all models, PADA decreased the number of viable cells in the region of dispersion and supported the delivery of nivolumab throughout a portion of the tissue. In canine survival experiments, there were no adverse events and no impact on urination. The injection approach was easy to perform under ultrasound guidance and produced a localized effect with a favorable safety profile. These findings suggest that PADA is a promising therapeutic prostate ablation strategy to treat lower urinary tract symptoms.

Publisher

American Association for the Advancement of Science (AAAS)

Reference41 articles.

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