Literature DB >> 26909544

Transport mechanisms at the pulmonary mucosa: implications for drug delivery.

Sabrina Nickel1, Caoimhe G Clerkin1, Mohammed Ali Selo1,2, Carsten Ehrhardt1.   

Abstract

INTRODUCTION: Over the past years, a significant number of papers have substantiated earlier findings proposing a role for drug transporter proteins in pulmonary drug disposition. Whilst the majority of reports present data from in vitro models, a growing number of publications advance the field by introducing sophisticated ex vivo and in vivo techniques. In a few cases, evidence from clinical studies in human volunteers is complementing the picture. AREAS COVERED: In this review, recent advances in pulmonary drug transporter research are critically evaluated. Transporter expression data in tissues and cell-based in vitro models is summarized and information on transport activity assessed. Novel techniques allowing for better quantification of transporter-related effects following pulmonary delivery are also described. EXPERT OPINION: Different tissue and cell populations of the lung have distinct transporter expression patterns. Whether these patterns are affected by disease, gender and smoking habits requires further clarification. Transporters have been found to have an impact on drug absorption processes, at least in vitro. Recent ex vivo experiments using isolated, perfused lung models, however, suggest that mainly efflux pumps have significant effects on absorption into the pulmonary circulation. Whether these rodent-based ex vivo models predict the human situation is basis for further research.

Entities:  

Keywords:  BCRP; Drug transporters; Inhalation; MRP1; Organic cation transporters; P-glycoprotein; Peptide transporters; Pulmonary drug disposition

Mesh:

Substances:

Year:  2016        PMID: 26909544     DOI: 10.1517/17425247.2016.1140144

Source DB:  PubMed          Journal:  Expert Opin Drug Deliv        ISSN: 1742-5247            Impact factor:   6.648


  11 in total

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7.  OCTN2-Mediated Acetyl-l-Carnitine Transport in Human Pulmonary Epithelial Cells In Vitro.

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