Temoporfin-loaded 1-tetradecanol-based thermoresponsive solid lipid nanoparticles for photodynamic therapy
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27622757
DOI
10.1016/j.jconrel.2016.09.009
PII: S0168-3659(16)30709-X
Knihovny.cz E-resources
- Keywords
- Drug delivery, Nanomedicine, Photodynamic therapy, Solid lipid nanoparticles, Temoporfin,
- MeSH
- Mammary Neoplasms, Experimental therapy MeSH
- Photochemotherapy methods MeSH
- Photosensitizing Agents administration & dosage therapeutic use MeSH
- Humans MeSH
- Lipids chemistry MeSH
- Fatty Alcohols administration & dosage therapeutic use MeSH
- Mesoporphyrins chemistry MeSH
- Mice, Nude MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Nanoparticles chemistry MeSH
- Drug Carriers chemistry MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Photosensitizing Agents MeSH
- Lipids MeSH
- Fatty Alcohols MeSH
- Mesoporphyrins MeSH
- myristyl alcohol MeSH Browser
- Drug Carriers MeSH
- temoporfin MeSH Browser
We developed fully biodegradable/metabolizable nanosystem based on polymer surfactant-stabilized thermoresponsive solid lipid nanoparticles with non-covalently bound photosensitizer temoporfin (T-SLNP) with particle size below 50nm. The efficacy of T-SLNP was compared with commercial temoporfin formulation in terms of in vitro phototoxicity in 4T1 (murine mammary carcinoma) and MDA-MB-231(human breast adenocarcinoma) cells and of in vivo anticancer effect in Nu/Nu mice bearing MDA-MB-231 tumors. In vitro study demonstrated faster accumulation kinetics in the cells for our formulation design resulting in higher phototoxicity against the tumor cells. In vivo anticancer efficacy was markedly improved by T-SLNP compared with commercial temoporfin formulation. Owing to controlled and sustained release properties, subcellular size, biocompatibility with tissue and cells, the T-SLNP nanodispersion prepared in this study represents promising drug delivery system applicable in cancer treatment.
References provided by Crossref.org
Magnetic Temperature-Sensitive Solid-Lipid Particles for Targeting and Killing Tumor Cells