CSIR Central

Inhalable microparticles containing large payload of antituberculosis

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

View Archive Info
 
 
Field Value
 
Contributor Muttil, Pavan
 
Creator Kaur, Jatinder
Kumar, Kaushlendra
Yadav, A B
Sharma, Rolee
Misra, Amit

 
Date 2007-12-26T10:57:24Z
2007-12-26T10:57:24Z
2007
 
Identifier EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES 32 (2007) 140-150
http://hdl.handle.net/123456789/56
 
Description Microparticles containing large payloads of two anti-tuberculosis (TB) drugs were prepared and evaluated for suitability as a dry powder inhalation targeting alveolar macrophages. A solution containing one part each of isoniazid and rifabutin, plus two parts poly(lactic acid) (L-PLA) was spraydried. Drug content and in vitro release were assayed by HPLC, and DSC was used to elucidate release behaviour. Particle size was measured by laser scattering and aerosol characteristics by cascade impaction using a Lovelace impactor. Microparticles were administered to mice using an inhouse inhalation apparatus or by intra-tracheal instillation. Drugs in solution were administered orally and by intra-cardiac injection. Flow cytometry and HPLC were used to investigate the specificity and magnitude of targeting macrophages. Microparticles having drug content -50% (w/w), particle size -5 m and satisfactory aerosol characteristics (median mass aerodynamic diameter, MMAD = 3.57 m; geometric standard deviation, GSD = 1.41m; fine particle fraction, FPF <4.6"", = 78.91:1: 8.4%) were obtained in yields of >60%. About 70% of the payload was released in vitro in 10 days. Microparticles targeted macrophages and not epithelial cells on inhalation. Drug concentrations in macrophages were -20 times higher when microparticles were inhaled rather than drug solutions administered. Microparticles were thus deemed suitable for enhanced targeted drug delivery to lung macrophages.
 
Format 582825 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No 6857
 
Subject Dry powder inhalation
Respirable microspheres
Targeting
Macrophages
Pulmonary delivery
Tuberculosis
 
Title Inhalable microparticles containing large payload of antituberculosis
 
Type Article