1. Academic Validation
  2. Improvement of pulmonary absorptions of poorly absorbable drugs using Gelucire 44/14 as an absorption enhancer

Improvement of pulmonary absorptions of poorly absorbable drugs using Gelucire 44/14 as an absorption enhancer

  • J Pharm Pharmacol. 2014 Oct;66(10):1410-20. doi: 10.1111/jphp.12274.
Hailong Zhang 1 Xiaoyan Huang Jie Mi Yayu Huo Guan Wang Jianfeng Xing Yang Gao
Affiliations

Affiliation

  • 1 School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Abstract

Objectives: This study aims to evaluate the absorption-enhancing effects of Gelucire 44/14 on the pulmonary absorption of different poorly absorbable drugs and relative mechanism of action.

Methods: Absorption-enhancing effect of Gelucire 44/14 were examined by an in-vivo pulmonary absorption experiment in rats, and the membrane toxicity of Gelucire 44/14 was evaluated by measuring levels of protein and dehydrogenase (LDH) in the bronchoalveolar lavage fluid (BALF) and morphological observation.

Key findings: Pulmonary absorptions of fluorescein isothiocyanate-dextrans, Insulin and Calcitonin were enhanced by Gelucire 44/14 (0.1-2.0%, w/v) in a concentration-dependent manner, and the maximal absorption-enhancing effect was obtained when the concentration of Gelucire 44/14 increased to 2.0% (w/v). Furthermore, Gelucire 44/14 neither increase the levels of protein and LDH in BALF nor change morphology of lung compared with control group. In addition, a well correlation between the absorption-enhancing effect and surface tension of Insulin solution in the presence of Gelucire 44/14 was observed, suggesting Gelucire 44/14-mediated decrease in the surface tension of the gas-liquid interface in alveolar tissue was possible one of the improving mechanisms of Gelucire 44/14.

Conclusion: Gelucire 44/14 was a potential and safe absorption enhancer for improving the absorption of poorly absorbable drugs including Insulin and Calcitonin by pulmonary delivery.

Keywords

Gelucire 44/14; absorption enhancer; membrane toxicity; poorly absorbable drugs; pulmonary absorption.

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