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Pharm Res. 2016 May;33(5):1289-303. doi: 10.1007/s11095-016-1872-x. Epub 2016 Feb 22.

Lomustine Nanoparticles Enable Both Bone Marrow Sparing and High Brain Drug Levels - A Strategy for Brain Cancer Treatments.

Author information

1
UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
2
School of Physics, University of Exeter, Exeter, EX4 4QL, UK.
3
Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, 69978, Israel.
4
Nanomerics Ltd. Euro House, 1394 High Road, London, N20 9YZ, UK.
5
UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK. Ijeoma.uchegbu@ucl.ac.uk.
6
Nanomerics Ltd. Euro House, 1394 High Road, London, N20 9YZ, UK. Ijeoma.uchegbu@ucl.ac.uk.

Abstract

PURPOSE:

The blood brain barrier compromises glioblastoma chemotherapy. However high blood concentrations of lipophilic, alkylating drugs result in brain uptake, but cause myelosuppression. We hypothesised that nanoparticles could achieve therapeutic brain concentrations without dose-limiting myelosuppression.

METHODS:

Mice were dosed with either intravenous lomustine Molecular Envelope Technology (MET) nanoparticles (13 mg kg(-1)) or ethanolic lomustine (6.5 mg kg(-1)) and tissues analysed. Efficacy was assessed in an orthotopic U-87 MG glioblastoma model, following intravenous MET lomustine (daily 13 mg kg(-1)) or ethanolic lomustine (daily 1.2 mg kg(-1) - the highest repeated dose possible). Myelosuppression and MET particle macrophage uptake were also investigated.

RESULTS:

The MET formulation resulted in modest brain targeting (brain/ bone AUC0-4h ratios for MET and ethanolic lomustine = 0.90 and 0.53 respectively and brain/ liver AUC0-4h ratios for MET and ethanolic lomustine = 0.24 and 0.15 respectively). The MET formulation significantly increased mice (U-87 MG tumours) survival times; with MET lomustine, ethanolic lomustine and untreated mean survival times of 33.2, 22.5 and 21.3 days respectively and there were no material treatment-related differences in blood and femoral cell counts. Macrophage uptake is slower for MET nanoparticles than for liposomes.

CONCLUSIONS:

Particulate drug formulations improved brain tumour therapy without major bone marrow toxicity.

KEYWORDS:

glioblastoma multiforme; lomustine; molecular envelope technology (MET); myelosuppression; nanoparticles

PMID:
26903051
PMCID:
PMC4820487
DOI:
10.1007/s11095-016-1872-x
[Indexed for MEDLINE]
Free PMC Article

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