Zhang Xuemei, Liu Qing, Hu Junhua, Xu Ling, Tan Wen
School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, China.
Key-Pharma Biomedical Inc., Dongguan 523000, China.
Acta Pharm Sin B. 2014 Feb;4(1):79-85. doi: 10.1016/j.apsb.2013.12.010. Epub 2014 Jan 18.
An aerosol formulation containing 7.5 mg of R-salbutamol sulfate was developed. The aerosol was nebulized with an air-jet nebulizer, and further assessed according to the new European Medicines Agency (EMA) guidelines. A breath simulator was used for studies of delivery rate and total amount of the active ingredient at volume of 3 mL. A next generation impactor (NGI) with a cooler was used for analysis of the particle size and in vitro lung deposition rate of the active ingredient at 5 °C. The anti-asthmatic efficacy of the aerosol formulation was assessed in guinea pigs with asthma evoked by intravenous injection of histamine compared with racemic salbutamol. Our results show that this aerosol formulation of R-salbutamol sulfate met all the requirements of the new EMA guidelines for nebulizer. The efficacy of a half-dose of R-salbutamol equaled that of a normal dose of racemic salbutamol.
开发了一种含有7.5毫克R - 硫酸沙丁胺醇的气雾剂制剂。该气雾剂用射流雾化器进行雾化,并根据新的欧洲药品管理局(EMA)指南进行进一步评估。使用呼吸模拟器研究活性成分在3毫升体积时的递送速率和总量。带有冷却器的下一代撞击器(NGI)用于分析5℃时活性成分的粒径和体外肺部沉积率。与消旋沙丁胺醇相比,在静脉注射组胺诱发哮喘的豚鼠中评估气雾剂制剂的抗哮喘疗效。我们的结果表明,这种R - 硫酸沙丁胺醇气雾剂制剂符合EMA关于雾化器的新指南的所有要求。半剂量R - 硫酸沙丁胺醇的疗效等同于正常剂量消旋沙丁胺醇的疗效。