Development and assessment of countermeasure formulations for treatment of lung injury induced by chlorine inhalation

被引:14
作者
Hoyle, Gary W. [1 ]
Chen, Jing [1 ]
Schlueter, Connie F. [1 ]
Mo, Yiqun [1 ]
Humphrey, David M., Jr. [1 ]
Rawson, Greg [2 ]
Nino, Joe A. [2 ]
Carson, Kenneth H. [2 ]
机构
[1] Univ Louisville, Sch Publ Hlth & Informat Sci, Dept Environm & Occupat Hlth Sci, 701 HSC-A,319 Abraham Flexner Way, Louisville, KY 40202 USA
[2] SW Res Inst, Chem & Chem Engn Div, Microencapsulat & Nanomat Dept, San Antonio, TX USA
基金
美国国家卫生研究院;
关键词
Acute lung injury; Pulmonary edema; Airway hyperreactivity; Microencapsulation; CONTROLLED DRUG-DELIVERY; PULMONARY-FIBROSIS; ACUTE EXPOSURE; TRIPTOLIDE; GAS; INFLAMMATION; INHIBITION; CORTICOSTEROIDS; BUDESONIDE; TOXICITY;
D O I
10.1016/j.taap.2016.03.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chlorine is a commonly used, reactive compound to which humans can be exposed via accidental or intentional release resulting in acute lung injury. Formulations of rolipram (a phosphodiesterase inhibitor), triptolide (a natural plant product with anti-inflammatory properties), and budesonide (a corticosteroid), either neat or in conjunction with poly(lactic:glycolic acid) (PLGA), were developed for treatment of chlorine-induced acute lung injury by intramuscular injection. Formulations were produced by spray-drying, which generated generally spherical microparticles that were suitable for intramuscular injection. Multiple parameters were varied to produce formulations with a wide range of in vitro release kinetics. Testing of selected formulations in chlorine exposed mice demonstrated efficacy against key aspects of acute lung injury. The results show the feasibility of developing microencapsulated formulations that could be used to treat chlorine-induced acute lung injury by intramuscular injection, which represents a preferred route of administration in a mass casualty situation. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 18
页数:10
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