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Updated: Jun 28, 2026

Direct Tracheal Instillation of Solutes into Mouse Lung
Published on: August 29, 2010
Inhalable Nano-Astaxanthin for Radiation-Induced Lung Injury via Enhanced Lung Retention and Inflammation Suppression
Dongxiao Zhang1,2,3,4, Jian He1,2, Jiarong Cui1,2
1Eye Center, The Second Affiliated Hospital, School of Medicine, and Liangzhu Laboratory, Zhejiang University, Hangzhou 310000, P. R. China.
Inhalable nanoparticles carrying astaxanthin (ASX) effectively prevent radiation-induced lung injury (RILI) by improving drug delivery and reducing inflammation and fibrosis. This novel nano-astaxanthin platform shows promise for clinical lung protection after radiotherapy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Radiotherapy Research
Background:
- Radiation-induced lung injury (RILI) is a serious complication of radiotherapy, involving oxidative stress, inflammation, and fibrosis.
- Astaxanthin (ASX), a natural antioxidant, is limited by poor solubility and bioavailability for RILI treatment.
Purpose of the Study:
- To develop an inhalable nanoformulation of astaxanthin (ASX@P@CS) to enhance pulmonary delivery and prevent RILI.
- To improve ASX solubility and bioavailability for effective RILI prevention.
Main Methods:
- Created inhalable chitosan-modified PLGA nanoparticles loaded with astaxanthin (ASX@P@CS).
- Evaluated the nanoformulation's intrapulmonary distribution, anti-inflammatory, and anti-fibrotic effects in mouse models of RILI.
Main Results:
- ASX@P@CS demonstrated improved ASX solubility and enhanced pulmonary permeability and retention.
- The nanoformulation significantly reduced acute oxidative damage and inflammation.
- Chronic fibrotic remodeling in RILI mouse models was effectively prevented.
Conclusions:
- Chitosan-modified nano-astaxanthin is a biocompatible and safe inhalable platform for RILI prevention.
- This strategy offers a promising approach for clinical application in protecting lungs from radiation damage.
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