Preparation, characterization and anti-proliferative effects of sclareol-loaded solid lipid nanoparticles on A549 human lung epithelial cancer cells
| Autor: | Ailar Nakhlband, Masoud Eskandani, Hamed Hamishehkar, Somayeh Vandghanooni, Mir Babak Bahadori, Morteza Eskandani |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Chemistry
Sclareol Pharmaceutical Science 02 engineering and technology 021001 nanoscience & nanotechnology medicine.disease_cause 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Apoptosis 030220 oncology & carcinogenesis Solid lipid nanoparticle Zeta potential medicine Biophysics DNA fragmentation MTT assay 0210 nano-technology Cytotoxicity Genotoxicity |
| Zdroj: | Journal of Drug Delivery Science and Technology. 45:272-280 |
| ISSN: | 1773-2247 |
| DOI: | 10.1016/j.jddst.2018.02.017 |
| Popis: | Here, sclareol-loaded solid lipid nanoparticles (sclareol-SLNs) was formulated and tested for potential geno-cytotoxicity upon A549 lung cancer cells. Sclareol-SLNs was formulated using hot homogenization. Different physicochemical features including size, zeta potential, dispersity, drug loading (DL), and encapsulation efficiency (EE) as well as in vitro drug release behavior were determined. Genotoxicity and cytotoxicity of the developed sclareol-SLNs were evaluated using DNA ladder and MTT assay, respectively. The cell death types were determined by detection of phosphatidylserine, dsDNA integrity, and proportion of different amounts in the associated cell cycle. Electron microscopy and particle size analysis showed dispersed and homogenous NPs with an average diameter of 88 nm and a high percent of EE (89%) and drug loading (42.47 mg/g). Sustained drug release was achieved at a physiologic pH, and long-term stability in terms of the size, zeta, dispersity, and EE of NPs was achieved. Cytotoxicity assay results showed that the plain sclareol inhibited A549 growth with an IC50 value of 19 μg/mL after 24 h, yet sclareol-SLNs inhibition was perceived after 48 h. DNA fragmentation assay using gel electrophoresis showed clear fragmentation in the chromatin within the cell's treated by sclareol and NPs. Flow cytometry analyses determined early and late apoptosis in sclareol and sclareol-SLNs treated cells. |
| Databáze: | OpenAIRE |
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