Atorvastatin-loaded lipid nanoparticles: antitumor activity studies on MCF-7 breast cancer cells
Autor: | Shital M Salunkhe, Vaishali M Gambhire, Makarand S Gambhire |
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Rok vydání: | 2018 |
Předmět: |
Statin
medicine.drug_class Atorvastatin Pharmaceutical Science Nanoparticle Antineoplastic Agents Breast Neoplasms 02 engineering and technology 03 medical and health sciences 0302 clinical medicine Drug Discovery Solid lipid nanoparticle medicine Humans cardiovascular diseases Particle Size Cytotoxicity Pharmacology Antitumor activity Drug Carriers Cell growth Chemistry Organic Chemistry nutritional and metabolic diseases 021001 nanoscience & nanotechnology Lipids MCF-7 030220 oncology & carcinogenesis MCF-7 Cells Cancer research Nanoparticles Female lipids (amino acids peptides and proteins) 0210 nano-technology medicine.drug |
Zdroj: | Drug Development and Industrial Pharmacy. 44:1685-1692 |
ISSN: | 1520-5762 0363-9045 |
Popis: | Atorvastatin is a synthetic statin commonly used in the treatment of hypercholesterolemia. Apart from this, statins appear to have pleiotropic effects, including modulation of cell growth, apoptosis. Through modulation of these pathways, statins have the potential to influence a wide range of disease processes, including cancer. However, poor aqueous solubility (0.1 mg/mL) and poor oral bioavailability has limited therapeutic application of atorvastatin. Present work is an attempt to improve tumor targeting of atorvastatin by incorporating in nanostructured lipid carriers (NLCs) and studying its anticancer activity on MCF-7 cell lines. NLCs of atorvastatin were formulated by high-speed homogenization followed by probe sonication method. The optimized batch of NLCs had a mean size of 130.02 ± 3.1 nm and entrapment efficiency of 90.42 ± 3.7%. The in vitro drug release study by dialysis method indicated that drug entrapped in the NLCs remains entrapped at acidic pH as well as in phosphate buffer of pH 7.4 for a prolonged period of time as compared to plain drug. In vitro cytotoxicity studies on MCF-7 (mammary adenocarcinoma human cell lines) cell lines showed that concentration of drug required for total growth inhibition (TGI) and 50% growth inhibition (GI50) of MCF-7 cells was found to be 27.4 µg/mL and10 µg/mL respectively, in case of atorvastatin- NLCs which is less than that required in case of plain atorvastatin and almost similar to that of adriamycin. All these findings reinforce the fact that atorvastatin loaded NLCs are promising novel delivery system for treating breast cancer. |
Databáze: | OpenAIRE |
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