Back to Search Start Over

Inhalable particulate drug delivery systems for lung cancer therapy: Nanoparticles, microparticles, nanocomposites and nanoaggregates

Authors :
Kadria A. Elkhodairy
Sana Mohamed Mortada
Mohamed Gaber
Jia-You Fang
May S. Freag
Mahmoud M. Abd-Elwakil
Mayada M. Elgohary
Hadeer M. Abdelaziz
Magda W. Samaha
Ahmed O. Elzoghby
Nayra M Kamel
Moustafa T. Mabrouk
Dalia M. Kabary
Source :
Journal of Controlled Release. 269:374-392
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

There is progressive evolution in the use of inhalable drug delivery systems (DDSs) for lung cancer therapy. The inhalation route offers many advantages, being non-invasive method of drug administration as well as localized delivery of anti-cancer drugs to tumor tissue. This article reviews various inhalable colloidal systems studied for tumor-targeted drug delivery including polymeric, lipid, hybrid and inorganic nanocarriers. The active targeting approaches for enhanced delivery of nanocarriers to lung cancer cells were illustrated. This article also reviews the recent advances of inhalable microparticle-based drug delivery systems for lung cancer therapy including bioresponsive, large porous, solid lipid and drug-complex microparticles. The possible strategies to improve the aerosolization behavior and maintain the critical physicochemical parameters for efficient delivery of drugs deep into lungs were also discussed. Therefore, a strong emphasis is placed on the approaches which combine the merits of both nanocarriers and microparticles including inhalable nanocomposites and nanoaggregates and on the optimization of such formulations using the proper techniques and carriers. Finally, the toxicological behavior and market potential of the inhalable anti-cancer drug delivery systems are discussed.

Details

ISSN :
01683659
Volume :
269
Database :
OpenAIRE
Journal :
Journal of Controlled Release
Accession number :
edsair.doi.dedup.....7b8f9320a8930750e064de2915990257
Full Text :
https://doi.org/10.1016/j.jconrel.2017.11.036