Supercritical Fluid-Assisted Porous Microspheres for Efficient Delivery of Insulin and Inhalation Therapy of Diabetes

Adv Healthc Mater. 2019 Jun;8(12):e1800910. doi: 10.1002/adhm.201800910. Epub 2018 Oct 3.

Abstract

Pulmonary delivery of drugs has attracted increasing attention in healthcare, as the lungs are an easily accessible site for noninvasive systemic delivery of drugs. Although pulmonary inhalation of porous microparticles has been shown to sustain drug delivery, there are limited reports on efficient delivery of insulin and inhalation therapy of diabetes based on supercritical carbon dioxide (SC-CO2 ) technology. Herein, this study reports the fabrication of insulin-loaded poly-l-lactide porous microspheres (INS-PLLA PMs) by using the SC-CO2 technology, and their use as an inhalation delivery system potentially for diabetes therapy. Biocompatibility and delivery efficiency of the PLLA PMs in the lungs are investigated. The PLLA PMs show negligible toxicity to lung-derived cells, resulting in no significant reduction in cell viability, as well as levels of various inflammatory mediators such as interleukin (IL)-6, IL-8, and tumor necrosis factor-α, compared with the negative control group. INS-PLLA PMs are further efficiently deposited in the trachea and the bronchi of superior lobes of the lungs, which exhibit pronounced hypoglycemic activity in induced diabetic rats. Together, the results demonstrate that the INS-PLLA PMs have a strong potential as an effective strategy for inhalation treatment of diabetes.

Keywords: inhalation therapy; insulin; porous microspheres; supercritical carbon dioxide technology; type II diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • A549 Cells
  • Administration, Inhalation
  • Alkaline Phosphatase / metabolism
  • Animals
  • Carbon Dioxide / chemistry
  • Chemical Precipitation
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / metabolism
  • Humans
  • Insulin / administration & dosage*
  • Insulin / therapeutic use*
  • L-Lactate Dehydrogenase / metabolism
  • Lung / metabolism
  • Male
  • Microspheres*
  • Polyesters / chemistry
  • Porosity
  • Rats, Sprague-Dawley
  • Solvents / chemistry
  • Tissue Distribution

Substances

  • Insulin
  • Polyesters
  • Solvents
  • Carbon Dioxide
  • poly(lactide)
  • L-Lactate Dehydrogenase
  • Alkaline Phosphatase