Metadata

Dataset ID: 10
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Study Design
Study Design Background To investigate if ultrasound-mediated blood-brain barrier opening or drug formulation in polymetic nanoparticles can increase the acuumulation of cabazitazel in the brain or theapeutic effect for glioblastoma.
Study Description FUS for BBB opening
Study Type preclinical
Study Subtype in vivo
Publication
Paper Linked https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427936/
Paper Title Therapeutic Effect of Cabazitaxel and Blood-Brain Barrier opening in a Patient-Derived Glioblastoma Model
Paper Authors Sulheim, Einar, Mørch, Yrr, Snipstad, Sofie, Borgos, Sven Even, Miletic, Hrvoje, Bjerkvig, Rolf, de Lange Davies, Catharina, Åslund, Andreas K.O.
Affiliation Department of Physics, Norwegian University of Science and Technology (NTNU), Trondheim, Norway ; Department of Biotechnology and Nanomedicine, SINTEF AS, Trondheim Norway ; Department of Biotechnology and Nanomedicine, SINTEF AS, Trondheim Norway ; Cancer Clinic, St.Olav’s University Hospital, Trondheim Norway ; Department of Pathology, Haukeland University Hospital, Bergen, Norway ; Department of Biomedicine, University of Bergen, Norway ; Department of Oncology, Luxembourg Institute of Health, Luxembourg ; Stroke Unit, Department of internal medicine, St. Olav's University Hospital, Trondheim, Norway
Paper Journal Nanotheranostics
Paper Year 2019
Paper Doi https://doi.org/10.7150/ntno.31479
Open Access yes
Updated Year 2023
Study Component
Multi Modality Images no
Imaging Modality MRI
Imaging Sub Modality T2W, DCE
Radiation no
Imaging Coverage brain
Imaging Target anatomy, vascular permeability
Dataset Information
Institution NTNU
Pi Andreas K.O. Åslund
Country Of Institution Norway
Imaging Facility MR Core
Euro Bio Imaging Node NORMOLIM
Country Of Imaging Facility Norway
In Vivo Experimental Parameters
Number Of Groups 4
Types Of Groups cab-NPMB and FUS; cab, empty NPMB and FUS; cab; saline control
Overall Sample Size 15
Disease Model cancer
Organ Or Tissue brain
Sample Size For Each Group 3 for cab-NPMB and FUS; 4 for cab, empty NPMB and FUS; 4 for cab; 4 for saline control
Power Calculation none
Inclusion Criteria none
Exclusion Criteria none
Randomization yes mice were randomly divided into four groups
Blinding no
Outcome Measures tumor growth, cab accumulation using mass spectrometry, signal ratio of treated/non-treated hemisphere
Statistical Methods Not stated
Species Mice
Strain NOD/SCID, Balb/c nudes
Immune Status immunedeficient
Sex female
Age older than 8 weeks
Age At Start Experiment older than 8 weeks
Age At Scanning Experiment S older than 11 weeks, weekly scanning
Weight About 20 g
Weight At Start Experiment About 20 g
Weight At End Experiment About 20 g
Source Of Animals Janvier Labs
Experimental Procedures
Pharmacological Drug Jevtana® (Cabazitaxel), and poly(2-ethyl butylcyanoacrylate) (PEBCA) NPs (cab-NPs, diameter 153 nm) and NP stabilized microbubbles (NPMBs, diamter > 1000 nm) (experimental)
Company Sanofi-Aventis
Drug Dose 10
Volume 0,05
Site Route Of Administration intravenous
Frequency Of Administration two times, with a week apart
Vehicle Or Carrier Solution Formulation saline
Blood Sampling no
Surgical Procedures Including Sham Surgery yes
Description Of The Surgical Procedure Intracranial inoculation of glioma cells. The skin was sterilized by ethanol and a 1 cm sagittal incision was made to expose the bregma. A hole was drilled at the coordinates A +1, L -2 and V -3.5 mm in relation to bregma. 5 ?l cell suspension (200 000 cells) was aspirated into a 25 ?l Hamilton syringe (Model 1702 N). The syringe was mounted onto a stereotactic frame and inserted into the brain slowly for 4 mm and then retracted 0.5 mm, before the injection. The injection was performed over 3 minutes and 2 minutes later the syringe was slowly retracted.
Target Organ Tissue brain
Pathogen Infection Intervention And Control no
Analgesic Plan To Relieve Pain Suffering And Distress yes
Analgesic Name Marcain
Route subcutaneous injection
Analgesic Dose 1:5, 0.04 ml/20g
Anesthesia Type gas
Duration ~30 minutes
Anesthesia Drugs Isoflurane
Anesthesia Dose ~2% in 78% medical air/20% O2
Euthanasia yes
Method cervical dislocation
Histology yes
Tissues Collected Post Euthanasia brain
Timing Of Collection after the last scanning
Histological Procedure formalin fixed
Name Of Reagent S anti-P-gp antibody
Catalogue Number EPR10364-57, Abcam
Frequency Of Imaging weekly
Timing Of Imaging three weeks after inoculation
Overall Scan Length ~ 6 minutes (for tumour development evaluation)
Contrast Agent Or Radio Isotope Or Challenge With Gas Molecule yes
Contrast Agent Commercial Drug Omniscan
Contrast Agent Chemical Drug gadolinium
Route Of Administration intravenous
Cell Line P3, patient derived
Modified Cell Line no
Cell Injection Route intracranial
Number Of Cells 200 000 cells
Housing Room SPF
Dietary Intervention no
Respiration Rate only during scanning
Body Tempurature Etc only during scanning
Food Intake Measured no
Image Acquisition
Instrument Vendor Bruker
Instrument Type BioSpec 70/20
Instrument Specifics 7T
Raw Data yes
Qa Qc yes, annual QC
Image Correlation
Image Type Primary image
Format Compression DICOM, raw
Dimensions 2D
Overall Number Of Images T2-RARE for anatomy, FLASH to evaluate BBB-opening,3x FLASH acquired
Field Of View 20mm x 20mm
Dimension Extents 200 x 200 x 1mm
Size Description 20mm x 20mm x 9mm
Pixel Voxel Size Description 100um x 100 um x 1mm
Ai Enhanced Algorithm no
Analyzed Data
Analysis Result Type Numerical
Data Used For Analysis volume measurements, ratio of signal from treated and untreated hemispheres
Analysis Method And Details HOROS
Status complete
Ontology Terms
Ncit Imaging NCIT:C16809
Ncit Imaging Submodality NCIT:C180729,NCIT:C62665
Doid DOID:162
Ncit Anatomy NCIT:C12439
Ncit Species NCIT:C14238
Ncit Strain NCIT:C15167,NCIT:C15159,NCIT:C37357,NCIT:C14239
Chebi Pharmaco CHEBI:63584
Chebi Anesthesia CHEBI:6015
Chebi Contrast Agent Commercial Name CHEBI:31642
Chebi Contrast Agent Chemical Name CHEBI:31642
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