Drug Delivery Properties of Nanocomposite Particles for Inhalation: Comparison of Drug Concentrations in Lungs and Blood

In Vivo. 2020 Mar-Apr;34(2):543-547. doi: 10.21873/invivo.11806.

Abstract

Background/aim: Nanocomposite particles are suitable for inhalation; however, their systemic migration has not been confirmed. The aim of this study was to compare drug concentrations in lungs and blood after inhalation of nanocomposite particles.

Materials and methods: Rifampicin (RFP) was used as a model drug. Nanocomposite particles were prepared from dichloromethane with RFP and poly(DL-lactic acid-co-glycolic acid) (PLGA) dissolved in an amino acid aqueous solution using a spray dryer. Measurement of RFP concentrations in lung and blood of mice was performed by in vivo tests.

Results: Compared with the oral administration group as a control, the RFP concentration in the lungs was significantly higher in the inhalation group. In addition, studies with a fluorescent substance suggested sustained release of drugs from nanocomposite particles in the lungs.

Conclusion: Nanocomposite particles deliver pulmonary drug in an efficient and sustained manner.

Keywords: Nanocomposite particles; PLGA; drug concentration; inhalation; nanoparticles; rifampicin.

MeSH terms

  • Administration, Inhalation
  • Animals
  • Drug Carriers / chemistry*
  • Drug Delivery Systems*
  • Mice
  • Nanocomposites / chemistry*
  • Nanocomposites / ultrastructure
  • Nanoparticles / chemistry*
  • Nanoparticles / ultrastructure
  • Polylactic Acid-Polyglycolic Acid Copolymer / chemistry
  • Rifampin / administration & dosage
  • Rifampin / pharmacokinetics
  • Tissue Distribution

Substances

  • Drug Carriers
  • Polylactic Acid-Polyglycolic Acid Copolymer
  • Rifampin