UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Novel paclitaxel formulations solubilized by parenteral nutrition nanoemulsions for application against glioma cell lines

Najlah, M; Kadam, A; Wan, K-W; Ahmed, W; Taylor, KMG; Elhissi, AMA; (2016) Novel paclitaxel formulations solubilized by parenteral nutrition nanoemulsions for application against glioma cell lines. International Journal of Phamaceutics , 506 (1-2) pp. 102-109. 10.1016/j.ijpharm.2016.04.027. Green open access

[thumbnail of Taylor_1-s2.0-S0378517316303118-main.pdf]
Preview
Text
Taylor_1-s2.0-S0378517316303118-main.pdf

Download (1MB) | Preview

Abstract

The aim of this study is to investigate using nanoemulsion formulations as drug-delivery vehicles of paclitaxel (PX), a poor water-soluble anticancer drug. Two commercially available nanoemulsion fat formulations (Clinoleic 20% and Intralipid 20%) were loaded with PX and characterised based on their size, zeta potential, pH and loading efficiency. The effect of formulation on the cytotoxicity of PX was also evaluated using MTT assay. The droplet size of the Clinoleic emulsion increased from 254.1 nm to 264.7 nm when paclitaxel (6 mg/ml) was loaded into the formulation, compared to the drug-free formulation. Similarly, the droplet size of Intralipid increased from 283.3 to 294.6 nm on inclusion of 6 mg/ml paclitaxel. The Polydispersity Indexes (PDIs) of all the nanoemulsion formulations (Clinoleic and Intralipid) were less than 0.2 irrespective of paclitaxel concentration indicating that all nanoemulsion formulations used were homogeneously sized. The pH range for the Clinoleic formulations (7.1–7.5) was slightly higher than that of the Intralipid formulations (6.5–6.9). The zeta potential of linoleic had a greater negative value than that of Intralipid. Loading efficiencies for paclitaxel were 70.4–80.2% and 44.2–57.4% for Clinoleic and Intralipid formulations, respectively. Clinoleic loaded with paclitaxel decreased the viability of U87-MG cell to 6.4 ± 2.3%, compared to Intralipid loaded with paclitaxel (21.29 ± 3.82%). Both nanoemulsions were less toxic to the normal glial cells (SVG-P12), decreasing the cell viability to 25–35%. This study suggests that nanoemulsions are useful and potentially applicable vehicles of paclitaxel for treatment of glioma.

Type: Article
Title: Novel paclitaxel formulations solubilized by parenteral nutrition nanoemulsions for application against glioma cell lines
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.ijpharm.2016.04.027
Publisher version: http://dx.doi.org/10.1016/j.ijpharm.2016.04.027
Language: English
Additional information: Copyright © The Authors 2016. This is an Open Access article published under a Creative Commons Attribution 4.0 International licence (http://creativecommons.org/licenses/by/4.0/).
Keywords: Droplet size; Nanoemulsion; Paclitaxel; Stability; Anticancer; MTT assay
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy > Pharmaceutics
URI: https://discovery.ucl.ac.uk/id/eprint/1485826
Downloads since deposit
132Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item