Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4
Yes === The hydrophobicity of a drug can be a major challenge in its development and prevents the clinical translation of highly potent anti-cancer agents. We have used a lipid-based nanoemulsion termed Lipid-Oil-Nanodroplets (LONDs) for the encapsulation and in vivo delivery of the poorly bioavaila...
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ndltd-BRADFORD-oai-bradscholars.brad.ac.uk-10454-185162021-08-21T05:03:58Z Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 Charalambous, A. Mico, V. McVeigh, L.E. Marston, G. Ingram, N. Volpato, M. Peyman, S.A. McLaughlan, J.R. Wierzbicki, Antonia Loadman, Paul M. Bushby, R.J. Markham, A.F. Evans, S.D. Coletta, P.L. Lipid-Oil-Nanodroplets (LONDs) Combretastatin A4 Microbubbles Targeting Ultrasound trigger Yes The hydrophobicity of a drug can be a major challenge in its development and prevents the clinical translation of highly potent anti-cancer agents. We have used a lipid-based nanoemulsion termed Lipid-Oil-Nanodroplets (LONDs) for the encapsulation and in vivo delivery of the poorly bioavailable Combretastatin A4 (CA4). Drug delivery with CA4 LONDs was assessed in a xenograft model of colorectal cancer. LC-MS/MS analysis revealed that CA4 LONDs, administered at a drug dose four times lower than drug control, achieved equivalent concentrations of CA4 intratumorally. We then attached CA4 LONDs to microbubbles (MBs) and targeted this construct to VEGFR2. A reduction in tumor perfusion was observed in CA4 LONDs-MBs treated tumors. A combination study with irinotecan demonstrated a greater reduction in tumor growth and perfusion (P = 0.01) compared to irinotecan alone. This study suggests that LONDs, either alone or attached to targeted MBs, have the potential to significantly enhance tumor-specific hydrophobic drug delivery. The work was funded by the Medical Research Council (grant number: MR/L01629X MRC Medical Bioinformatics Centre) and the EPSRC (grant number EP/P023266/1 Health Impact Partnership). EPSRC (EP/I000623/1, EP/K023845/1). Laura E. McVeigh was funded by an EPSRC PhD Studentship (EP/L504993/1). 2021-06-11T08:12:48Z 2021-06-23T15:30:39Z 2021-06-11T08:12:48Z 2021-06-23T15:30:39Z 2021-08 2021-03 2021-04-22 2021-06-11T07:13:01Z Article Published version Charalambous A, Mico V, McVeigh LE (2021) Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4. Nanomedicine: Nanotechnology, Biology, and Medicine. 36: 102401. http://hdl.handle.net/10454/18516 en https://doi.org/10.1016/j.nano.2021.102401 © 2021 The Authors. Published by Elsevier Inc. under a Creative Commons license (https://creativecommons.org/licenses/by/4.0/). |
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Lipid-Oil-Nanodroplets (LONDs) Combretastatin A4 Microbubbles Targeting Ultrasound trigger |
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Lipid-Oil-Nanodroplets (LONDs) Combretastatin A4 Microbubbles Targeting Ultrasound trigger Charalambous, A. Mico, V. McVeigh, L.E. Marston, G. Ingram, N. Volpato, M. Peyman, S.A. McLaughlan, J.R. Wierzbicki, Antonia Loadman, Paul M. Bushby, R.J. Markham, A.F. Evans, S.D. Coletta, P.L. Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
description |
Yes === The hydrophobicity of a drug can be a major challenge in its development and prevents the clinical translation of highly potent anti-cancer agents. We have used a lipid-based nanoemulsion termed Lipid-Oil-Nanodroplets (LONDs) for the encapsulation and in vivo delivery of the poorly bioavailable Combretastatin A4 (CA4). Drug delivery with CA4 LONDs was assessed in a xenograft model of colorectal cancer. LC-MS/MS analysis revealed that CA4 LONDs, administered at a drug dose four times lower than drug control, achieved equivalent concentrations of CA4 intratumorally. We then attached CA4 LONDs to microbubbles (MBs) and targeted this construct to VEGFR2. A reduction in tumor perfusion was observed in CA4 LONDs-MBs treated tumors. A combination study with irinotecan demonstrated a greater reduction in tumor growth and perfusion (P = 0.01) compared to irinotecan alone. This study suggests that LONDs, either alone or attached to targeted MBs, have the potential to significantly enhance tumor-specific hydrophobic drug delivery. === The work was funded by the Medical Research Council (grant number: MR/L01629X MRC Medical Bioinformatics Centre) and the EPSRC (grant number EP/P023266/1 Health Impact Partnership). EPSRC (EP/I000623/1, EP/K023845/1). Laura E. McVeigh was funded by an EPSRC PhD Studentship (EP/L504993/1). |
author |
Charalambous, A. Mico, V. McVeigh, L.E. Marston, G. Ingram, N. Volpato, M. Peyman, S.A. McLaughlan, J.R. Wierzbicki, Antonia Loadman, Paul M. Bushby, R.J. Markham, A.F. Evans, S.D. Coletta, P.L. |
author_facet |
Charalambous, A. Mico, V. McVeigh, L.E. Marston, G. Ingram, N. Volpato, M. Peyman, S.A. McLaughlan, J.R. Wierzbicki, Antonia Loadman, Paul M. Bushby, R.J. Markham, A.F. Evans, S.D. Coletta, P.L. |
author_sort |
Charalambous, A. |
title |
Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
title_short |
Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
title_full |
Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
title_fullStr |
Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
title_full_unstemmed |
Targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, Combretastatin A4 |
title_sort |
targeted microbubbles carrying lipid-oil-nanodroplets for ultrasound-triggered delivery of the hydrophobic drug, combretastatin a4 |
publishDate |
2021 |
url |
http://hdl.handle.net/10454/18516 |
work_keys_str_mv |
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