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Intratracheal Administration of Dry Powder Formulation in Mice
Published on: July 25, 2020
Design and Characterization of Atorvastatin Dry Powder Formulation as a potential Lung Cancer Treatment
1Department of Pharmaceutics, College of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.
Abstract:
Lung cancer is the leading cause of cancer death. Many studies have shown the beneficial effects of Atorvastatin in decreasing the mortality risk and improving survival among patients with lung cancer. This research paper focuses on improving AVT cytotoxic activity and cellular uptake by developing mannitol microcarriers as a promising drug delivery system for lung cancer treatment and, studying the impact of improving inhalation deposition on the delivery and Dry Powder formulations efficiency. The AVT loaded mannitol (AM) microparticles (AVT-AM) formulation was prepared by spray drying and characterized for its physicochemical properties and aerodynamic deposition. The results revealed that the AVT-AM formulation has good flow properties and aerosol deposition with a particle size of 3418 nm ± 26.86. The formulation was also assessed in vitro for cytotoxicity effects (proliferation, apoptosis, and cell cycle progression) on A549 human lung adenocarcinoma. Compared with free AVT, the AVT-AM formulation has significantly higher cellular uptake and anti-cancer properties by disrupting cell cycle progression via either apoptosis or cell cycle arrest in the G2/M phase. This study shows that AVT loaded mannitol microcarriers may provide a potentially effective and sustained pulmonary drug delivery for lung cancer treatment.
Insights
Mannitol microcarriers enhance Atorvastatin (AVT) delivery for lung cancer, improving cellular uptake and anti-cancer effects. This novel pulmonary drug delivery system shows promise for sustained treatment and reduced mortality.
Area of Science:
- Pharmacology
- Biotechnology
- Oncology
Background:
- Lung cancer is a leading cause of cancer mortality.
- Atorvastatin (AVT) has demonstrated beneficial effects in reducing mortality and improving survival in lung cancer patients.
- Optimizing drug delivery systems is crucial for enhancing therapeutic efficacy.
Purpose of the Study:
- To develop mannitol microcarriers for improved Atorvastatin (AVT) delivery in lung cancer treatment.
- To enhance AVT's cytotoxic activity and cellular uptake via a pulmonary drug delivery system.
- To evaluate the impact of improved inhalation deposition on dry powder formulation efficiency.
Main Methods:
- Atorvastatin-loaded mannitol (AM) microparticles (AVT-AM) were prepared using spray drying.
- Physicochemical properties, including particle size (3418 nm ± 26.86), and aerodynamic deposition were characterized.
- In vitro cytotoxicity assays (proliferation, apoptosis, cell cycle) were performed on A549 lung adenocarcinoma cells.
Main Results:
- The AVT-AM formulation exhibited good flow properties and aerosol deposition.
- Compared to free AVT, the AVT-AM formulation showed significantly higher cellular uptake.
- The formulation demonstrated enhanced anti-cancer properties by disrupting cell cycle progression through apoptosis or G2/M phase arrest.
Conclusions:
- Mannitol microcarriers represent a promising strategy for improving Atorvastatin (AVT) delivery for lung cancer.
- The developed AVT-AM formulation offers potential for effective and sustained pulmonary drug delivery.
- This approach may lead to improved therapeutic outcomes and reduced mortality in lung cancer patients.
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