Rapid Lymph Accumulation of Polystyrene Nanoparticles Following Pulmonary Administration

• Published in: Pharmaceutical research Vol. 30; no. 2; pp. 424 - 434
• Main Authors: Mohammad, Abdul Khader, Amayreh, Lenah K., Mazzara, John M., Reineke, Joshua J.
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.02.2013; Springer; Springer Nature B.V
• Subjects: Administration, Inhalation; Animals; Biochemistry; Biological and medical sciences; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Biomedicine; Drug delivery systems; General pharmacology; Lung - metabolism; Lung - ultrastructure; Lungs; Lymph - metabolism; Lymph Nodes - metabolism; Lymph Nodes - ultrastructure; Lymphatic system; Male; Medical Law; Medical sciences; Mice; Mice, Inbred BALB C; Nanoparticles; Nanoparticles - administration & dosage; Nanoparticles - analysis; Nanoparticles - chemistry; Particle Size; Pharmaceutical sciences; Pharmaceutical technology. Pharmaceutical industry; Pharmacology. Drug treatments; Pharmacology/Toxicology; Pharmacy; Polystyrene; Polystyrenes - administration & dosage; Polystyrenes - chemistry; Polystyrenes - pharmacokinetics; Research Paper; Tissue Distribution; Toxicity; pharyngeal aspiration; biodistribution; pulmonary delivery; polystyrene nanoparticle; lymph node; Pharmaceutical technology; Lymph node; Nanoparticle; Intrapulmonary administration; Distribution; Microparticle; Styrene polymer; Pharmacokinetics; Lymph
• ISSN: 0724-8741; 1573-904X
• DOI: 10.1007/s11095-012-0884-4

ABSTRACT Purpose Pulmonary administration of polymeric nanoparticle drug delivery systems is of great interest for both systemic and local therapies. However, little is understood about the relationship of particle size and pulmonary absorption. We investigated uptake and biodistribution of polystyrene nanoparticles (PN) of 50 nm, 100 nm, 250 nm, and 900 nm diameters in mice following administration to lungs via pharyngeal aspiration. Methods The amount of PN in tissues was analyzed by gel permeation chromatography (GPC). Results At 1 h, larger diameter PN (250 nm and 900 nm) had the highest total uptake at around 15% of administered dose, whereas the smaller diameter PN (50 nm and 100 nm) had uptake of only 5–6%. However, at 3 h, the 50 nm PN had the highest total uptake at 24.4%. For each size tested, the highest nanoparticle deposition was observed in the lymph nodes (LN) as compared to other tissues accounting for a total of about 35–50% of absorbed nanoparticles. Conclusion PN size impacts the rate and extent of uptake from lungs and, further, the extent of LN deposition. The extent of uptake and lymph distribution of the model, non-degradable PN lends potential to pulmonary administered, biodegradable polymeric nanoparticles for delivery of therapeutics to regional lymph nodes.