Pharmacokinetics of Ethionamide Delivered in Spray-Dried Microparticles to the Lungs of Guinea Pigs

• Published in: Journal of pharmaceutical sciences Vol. 106; no. 1; pp. 331 - 337
• Main Authors: Garcia-Contreras, Lucila, Padilla-Carlin, Danielle J., Sung, Jean, VerBerkmoes, Jarod, Muttil, Pavan, Elbert, Katharina, Peloquin, Charles, Edwards, David, Hickey, Anthony
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2017
• Subjects: Administration, Inhalation; Administration, Intravenous; Administration, Oral; Aerosols - administration & dosage; Aerosols - chemistry; Aerosols - pharmacokinetics; Animals; Antitubercular Agents - administration & dosage; Antitubercular Agents - chemistry; Antitubercular Agents - pharmacokinetics; bioavailability; Desiccation; Dry Powder Inhalers; ethionamide; Ethionamide - administration & dosage; Ethionamide - chemistry; Ethionamide - pharmacokinetics; Guinea Pigs; Lung - metabolism; Male; Particle Size; pharmacokinetics and pulmonary absorption; Porosity; porous particles; Powders; tuberculosis; PRO; MRT; AUC; pharmacokinetics and pulmonary absorption; DPAG; GSD; MDR; DPPC; MIC; tuberculosis; MMAD; CL; FMO; BAL; IV; TB; ethionamide; PPs; porous particles; CV; bioavailability; ETH; MTB; PK; FPF
• ISSN: 0022-3549; 1520-6017; 1520-6017
• DOI: 10.1016/j.xphs.2016.09.033

The use of ethionamide (ETH) in treating multidrug-resistant tuberculosis is limited by severe side effects. ETH disposition after pulmonary administration in spray-dried particles might minimize systemic exposure and side effects. To explore this hypothesis, spray-dried ETH particles were optimized for performance in a dry powder aerosol generator and exposure chamber. ETH particles were administered by the intravenous (IV), oral, or pulmonary routes to guinea pigs. ETH appearance in plasma, bronchoalveolar lavage, and lung tissues was measured and subjected to noncompartmental pharmacokinetic analysis. Dry powder aerosol generator dispersion of 20% ETH particles gave the highest dose at the exposure chamber ports and fine particle fraction of 72.3%. Pulmonary ETH was absorbed more rapidly and to a greater extent than orally administered drug. At Tmax, ETH concentrations were significantly higher in plasma than lungs from IV dosing, whereas insufflation lung concentrations were 5-fold higher than in plasma. AUC(0-t) (area under the curve) and apparent total body clearance (CL) were similar after IV administration and insufflation. AUC(0-t) after oral administration was 6- to 7-fold smaller and CL was 6-fold faster. Notably, ETH bioavailability after pulmonary administration was significantly higher (85%) than after oral administration (17%). These results suggest that pulmonary ETH delivery would potentially enhance efficacy for tuberculosis treatment given the high lung concentrations and bioavailability.