Grant: Travel Awards - Institute Community Support
University of Toronto
$960.00
Quantifying cancer targeting nanoparticle interaction with tumour microenvironment
FY 2015-16
Summary
In nanoparticle cancer targeting, researchers decorate the surface of nano-scale drug carriers with molecules that can recognize cancer cells in the tumour. Although effective in the diagnosis and treatment in animal tumor models, only a small percentage of these designs actually makes it into the drug market for human. The reason behind the lack of success is because we don't have a comprehensive understanding of how many injected nanoparticles actually get to the cancer cells within the tumour. In this research we showed that even by decorating the surface of the nanoparticles with cancer cell recognition molecules, these nanoparticles do not end up at the cancer cells. Instead, most of the nanoparticles are residing in the tumour scaffold matrix. The implication of this finding is that we need to change our nanoparticle engineering strategies in order to better target tumour and increase clinical efficacy.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
344942
Name
Dai Qin
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Institute of Cancer Research
Projecttitle
Quantifying cancer targeting nanoparticle interaction with tumour microenvironment
Programtype2
Undefined
Orgnameinp2
University of Toronto
Cihramount2
$960
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Animal Model; Cancer; Delivery; Flow Cytometry; Immunology; Nanoparticle; Targeting; Therapy
Abstract
In nanoparticle cancer targeting, researchers decorate the surface of nano-scale drug carriers with molecules that can recognize cancer cells in the tumour. Although effective in the diagnosis and treatment in animal tumor models, only a small percentage of these designs actually makes it into the drug market for human. The reason behind the lack of success is because we don't have a comprehensive understanding of how many injected nanoparticles actually get to the cancer cells within the tumour. In this research we showed that even by decorating the surface of the nanoparticles with cancer cell recognition molecules, these nanoparticles do not end up at the cancer cells. Instead, most of the nanoparticles are residing in the tumour scaffold matrix. The implication of this finding is that we need to change our nanoparticle engineering strategies in order to better target tumour and increase clinical efficacy.
Competitiondate
201601
Approvedterm2
1 yr 0 mth
Pinamesdelim
Dai, Qin
Approvedterm
1 an 0 mois
Cihrcontribution2
Inst of Cancer Research~ $960~ $0~