Abstract |
Trilaurin-based solid lipid nanoparticles (TL-SLNs) containing paclitaxel (PTX) were prepared by hot-melt high-pressure homogenisation and subsequent freezing and thawing. PTX-containing TL-SLNs showed 160.0 ± 15.8 nm of mean particle size and -43.9 mV of zeta potential. Scanning electron microscopy also revealed the spherical shape and submicron-size of the TL-SLNs. Differential scanning calorimetry measurement presented melting transition peak of TL in SLNs indicating the solidified state of the core lipid. The prepared TL-SLNs were physically stable without significant particle size changes at 4 °C for 2 months. The amounts of uptake into the human ovarian cancer cells, SKOV-3, were similar between PTX delivered in Cremophor EL-based formulation and TL-SLNs. In vitro and in vivo antitumour activity of PTX in TL-SLNs was comparable to the commercial Cremophor EL-based formulation in SKOV-3. These results suggest that PTX-loaded TL-SLNs have promising potential as an alternative parenteral formulation for PTX.
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Authors | Wenting Xu, Soo-Jeong Lim, Mi-Kyung Lee |
Journal | Journal of microencapsulation
(J Microencapsul)
Vol. 30
Issue 8
Pg. 755-61
( 2013)
ISSN: 1464-5246 [Electronic] England |
PMID | 23594306
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Drug Carriers
- Lipids
- Triglycerides
- trilaurin
- Paclitaxel
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Topics |
- Antineoplastic Agents, Phytogenic
(administration & dosage, pharmacokinetics, pharmacology)
- Cell Line, Tumor
- Drug Carriers
(chemistry)
- Female
- Humans
- Lipids
(chemistry)
- Nanoparticles
(chemistry)
- Ovarian Neoplasms
(drug therapy, pathology)
- Ovary
(drug effects, pathology)
- Paclitaxel
(administration & dosage, pharmacokinetics, pharmacology)
- Triglycerides
(chemistry)
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