Published January 1, 2025 | Version v1
Journal article Open

Generation of continuous production of polymeric nanoparticles via microfluidics for aerosolised localised drug delivery

  • 1. Univ Lyon 1, CNRS, UMR 5007, LAGEPP, Villeurbanne, France
  • 2. Ctr Hosp Lyon Sud, Dept Surg Oncol, Hosp Civils Lyon, Lyon, France
  • 3. Univ Lyon, Univ Jean Monnet, Ecole Natl Super Mines St Etienne, Ctr CIS,INSERM,U1059 Sainbiose,Mines St Etienne, 158 Cours Fauriel,CS 62362, F-42023 St Etienne 2, France
  • 4. Univ Lyon, Univ Claude Bernard Lyon 1, Lab CarMeN IRIS Team, INSERM,INRA,INSA Lyon, Bron, France

Description

Transferring the production of nanoparticles from laboratory batches to large-scale production for preclinical and clinical applications represents a challenge due to difficulties in scaling up formulations and lack of suitable preclinical models for testing. Here, we transpose the production of hyaluronic acid and polyarginine-based nanoparticles encapsulating the platinum-derivative dichloro(1,2 diaminocyclohexane)platinum(II), from conventional bulk method to continuous production using microfluidics. The microfluidic-based drug delivery system is then tested in a customised preclinical setup to assess its suitability for pressurised intraperitoneal aerosol chemotherapy (PIPAC), a locoregional chemotherapy used to treat peritoneal carcinomatosis. PIPAC consists of the aerosolization of drugs under pressure using laparoscopy. In our preclinical setup, two clinical aerosol devices, CapnoPen (R) and TOPOL (R), are used in conjunction with syringe pump to achieve the clinically optimal aerosol droplet size range (25-50 mu m). Aerosol droplet sizes of 38 and 64 mu m are obtained at upstream pressures of 14.7 and 7.4 bar and flow rates of 0.4 and 1.1 mL/s, for CapnoPen (R) and TOPOL (R), respectively. To study the spatial distribution of the aerosol, our preclinical setup is then coupled to an ex-vivo model (inverted porcine urinary bladder) that mimics the physiological peritoneal cavity environment. The smaller droplet size obtained with CapnoPen (R) provided more homogeneous aerosol distribution in the bladder cavity, crucial for maximising treatment coverage within the peritoneal cavity. Furthermore, stability studies reveal that nanoparticles maintained their physicochemical properties and anticancer activity post-aerosolization. Overall, this study provides a scalable approach for the production of platinum-derivative-loaded polymeric nanoparticles and demonstrates the suitability of this DDS for PIPAC.

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