期刊文献+

影响干粉吸入剂肺部给药过程的因素 被引量:8

Influence factors of the pulmonary drug delivery process of dry powder inhalers
原文传递
导出
摘要 干粉吸入剂(DPI)是最具发展潜力的肺部给药制剂,临床上被广泛用于肺部局部疾病的治疗,还为某些作用于全身的药物提供了新的给药途径。DPI肺部给药过程直接决定DPI的临床疗效,该过程包括干粉的分散、雾化和肺部沉积,其受多因素共同影响,主要包括干粉的粉体学性质、给药装置和吸入气流速率三方面。临床应用中,需要平衡各影响因素,以实现药物最大的分散、雾化和肺部沉积。本文对DPI肺部给药过程的影响因素及研究进展进行综述。 As the most promising preparation for pulmonary administration,dry powder inhaler( DPI) is widely employed to deliver drugs to the respiratory epithelium,predominantly for the treatments of local disorders recently. This delivery system has also become an attractively non-invasive way for systemic administration of the biologically active components. In addition,the clinical efficacy of DPIs depends on the pulmonary drug delivery process,which involves powder dispersion,aerosolization and lung deposition. However,the process is influenced by a variety of factors,especially particles engineering,drug inhaler devices and inspiration flow rate. Thus,it is indispensable to balance the various factors in order to achieve maximum dispersion,aerosolization and lung deposition of the drug in the clinical application. The focus of this article is exclusively on the latest progress in the factors impacting the pulmonary drug delivery process of DPIs,to provide a reference for the development of the delivery of fine drug particles to the bottom of the lung.
出处 《中国新药杂志》 CAS CSCD 北大核心 2015年第21期2459-2466,共8页 Chinese Journal of New Drugs
基金 国家“重大新药创制”科技重大专项(2014ZX09507005-001)
关键词 干粉吸入剂 肺部给药 肺部沉积 粉体学性质 给药装置 吸入气流速率 dry powder inhaler pulmonary administration pulmonary deposition particles engineering inhaler drug device inspiration flow rate
  • 相关文献

参考文献40

  • 1QASEEM A, WILT TJ, WEINBERGER SE, et al. Diagnosis and management of stable chronic obstructive pulmonary disease: a clinical practice guideline update from the American College of Physicians, American College of Chest Physicians, American Thoracic Society, and European Respiratory Society[ J]. Ann In- tern Med, 2011, 155(3) : 179 -191. 被引量:1
  • 2HOPPENTOCHT M, HAGEDOORN P, FRIJLINK HW, et al. Technological and practical challenges of dry powder inhalers and formulations [ J ]. Adv Drug Deliver Rev, 2014,75 ( 2 ) : 18 - 31. 被引量:1
  • 3STEGEMANN S, KOPP S, BORCHARD G, et al. Developing and advancing dry powder inhalation towards enhanced therapeu- tics[J]. Eur JPharm Sci, 2013, 48(1): 181 -194. 被引量:1
  • 4GRADON L, SOSNOWSKI TR. Formation of particles for dry powder inhalers[ J]. Adv Powder Technol, 2014, 25 ( 1 ) : 43 - 55. 被引量:1
  • 5YANG MY, CHAN JG, CHAN HK. Pulmonary drug delivery by powder aerosols[ J]. J Control Release, 2014,193:228 -240. 被引量:1
  • 6王晓波,袭荣刚,杨晓波,潘卫三,石焱,王一楠.影响干粉吸入剂肺沉积的制剂因素[J].中国新药杂志,2010,19(7):580-583. 被引量:9
  • 7ABDELRAHIM M, SHARAF MA. Nanosized rods agglomerates as a new approach for formulation of a dry powder inhaler[ J]. Int J Nanomedicine, 2011, 6:311 -320. 被引量:1
  • 8CARVALHO TC, PETERR JI, WILLIAMS RO 3rd. Influence of particle size on regional lung deposition-what evidence is there? [J]. lnt JPharm, 2011, 406(1-2): 1-10. 被引量:1
  • 9ANDRADE-LIMA M, PERE1RA LF, FERNANDES AL. Phar- maceutical equivalence of the combination formulation of budes- onide and formoterol in a single capsule with a dry powder inhaler [J]. JBrasPneumol, 2012, 38(6): 748-756. 被引量:1
  • 10DEMOLY P, HAGEDOORN P, DE BOER AH, et al. The clini-cal relevance of dry powder inhaler performance for drug delivery [J]. Resp Med, 2014,108(8):1195-1203. 被引量:1

二级参考文献74

  • 1DE KONING JP,VAN DER MARK TW,COENEGRACHT PM,et al. Effect of an external resistance to airflow on the inspiralory flow curve [ J ]. lnt J Pharm,2002,234 ( 1-2 ) :257 - 266. 被引量:1
  • 2CLARKE MJ,TOBYN MJ,STANIFORTH JN. The formulation of powder inhalation systems containing a high mass of nedocromil sodium trihydrate[ J ]. J Pharm Sci,2001,90( 2 ) :213 -223. 被引量:1
  • 3TANG P,CHAN HK,TAM E,et al. Preparation of NaCl powder suitable for inhalation [ J ]. lnd Eng Chem Res, 2006,45 ( 12 ) : 4188 -4192. 被引量:1
  • 4BAKHBAKHI Y, CHARPENTIER PA, ROHANI S. Experimental study of the GAS process for producing micropartlcles of beclomethasone-17-21-dipropionate suitable for pulmonary delivery[J], lnt J Pharm,2006,309(1-2 ) :71 -80. 被引量:1
  • 5CHAN HK. Dry powder aerosol drug delivery-opportunities for colloid and surface scientists[ J ]. Colloids Surf A Physicochem Eng Asp,2006,284 - 285:50 - 55. 被引量:1
  • 6VANBEVER R,MINTZES JD,WANG J,et al. Formulation and physical characterization of large porous particles for inhalation [J]. Pharm Res,1999,16( 11) :1735 -1742. 被引量:1
  • 7NEWMAN SP,HOLLINGWORTH A,CLARK AR,etal. Effect of different modes of inhalation on drug delivery from a dry powder inhaler[J]. Int J Pharm,1994 ,102( 2 ) :127 -132. 被引量:1
  • 8HARRIS JA, STEIN SW, MYRDAL PB. Evaluation of the TSI aerosol impactor 3306/3321 system using a redesigned impactor stage with solution and suspension metered-dose inhalers [ J ]. AAPS Pharm Sci Tech,2006,7 ( 1 ) :138 - 145. 被引量:1
  • 9OSKOUIE AK,NOLL KE,WANG HC. Minimizing the effect of density in determination of particle aerodynamic diameter using a time of flight instrument[ J ]. J Aerosol Sci,2003,34(4) :501 -506. 被引量:1
  • 10DE BOER AH,GJALTEMA D,HAGEDOORN P,et al. Characterization of inhalation aerosols: A critical evaluation of cascade impactor and laser diffraction technique[ J ]. lnt J Pharm,2002, 249 (1-2) :219 -231. 被引量:1

共引文献29

同被引文献131

引证文献8

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部