Title :
Dry powders based on mucus-penetrating nanocomposite microparticles for pulmonary delivery of antibiotics
Author :
Zimeng Wang ; Meenach, Samantha A.
Author_Institution :
Dept. of Chem. Eng., Univ. of Rhode Island, Kingston, RI, USA
Abstract :
Pulmonary antibiotic delivery is increasingly recommended as maintenance therapy for cystic fibrosis (CF) patients with chronic Pseudomonas aeruginosa infection. However, the abnormally thick and sticky mucus present in the respiratory tract of CF patients impairs efficient mucus penetration and limits the range of antibiotics for inhalation treatment. To overcome the obstacles of pulmonary antibiotic delivery, we have developed nanocomposite microparticles (nCmP) for inhalation of antibiotics in the form of dry powder aerosols, which will achieve targeted delivery, rapid mucus penetration, and controlled drug release. Azithromycin and rapamycin loaded nanoparticles were prepared via nanoprecipitation. nCmPs based on mannitol carrier were fabricated by spray drying. Scanning electron microscopy and dynamic light scattering showed 200 nm diameter nanoparticles entrapped in 1 - 2 μm sized microparticles with smooth morphology. In vitro release testing showed that both drug loaded particles have sustained drug release over 12 hours. Redispersity testing indicated that nanoparticles can be well redispersed after being released from mannitol carriers.
Keywords :
aerosols; cellular biophysics; diseases; drug delivery systems; drugs; drying; light scattering; lung; materials preparation; microfabrication; microorganisms; nanocomposites; nanofabrication; nanomedicine; nanoparticles; pneumodynamics; powders; precipitation (physical chemistry); scanning electron microscopy; spraying; CF patient therapy; abnormally sticky mucus; abnormally thick mucus; antibiotic inhalation; antibiotic range limitation; azithromycin loaded nanoparticle; chronic Pseudomonas aeruginosa infection; controlled drug release; cystic fibrosis; drug loaded particle; dry powder aerosol; dynamic light scattering; in vitro release testing; inhalation treatment; maintenance therapy; mannitol carrier; mucus-penetrating nanocomposite microparticle; nCmP fabrication; nanocomposite microparticles; nanoparticle entrapping; nanoparticle preparation; nanoparticle redispersity testing; nanoprecipitation; pulmonary antibiotic delivery; rapamycin loaded nanoparticle; rapid mucus penetration; respiratory tract; scanning electron microscopy; size 1 mum to 2 mum; size 200 nm; smooth morphology; spray drying; sustained drug release; targeted delivery; Antibiotics; Encapsulation; Nanoparticles; Powders; Scanning electron microscopy; controlled release; dry powder inhalation; mucus penetration; nanocomposite microparticles;
Conference_Titel :
Biomedical Engineering Conference (NEBEC), 2015 41st Annual Northeast
Conference_Location :
Troy, NY
Print_ISBN :
978-1-4799-8358-2
DOI :
10.1109/NEBEC.2015.7117136
