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Fluorescent nanoparticle probes for imaging of cancer
Author(s) -
Santra Swadeshmukul,
Malhotra Astha
Publication year - 2011
Publication title -
wiley interdisciplinary reviews: nanomedicine and nanobiotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.175
H-Index - 72
eISSN - 1939-0041
pISSN - 1939-5116
DOI - 10.1002/wnan.134
Subject(s) - nanotechnology , nanoparticle , fluorescence , biocompatibility , in vivo , quantum dot , materials science , preclinical imaging , cancer imaging , surface modification , fluorescence lifetime imaging microscopy , cancer , chemistry , medicine , biology , optics , physics , microbiology and biotechnology , metallurgy
Fluorescent nanoparticles (FNPs) have received immense popularity in cancer imaging in recent years because of their attractive optical properties. In comparison to traditional organic‐based fluorescent dyes and fluorescent proteins, FNPs offer much improved sensitivity and photostability. FNPs in certain size range have a strong tendency to enter and retain in solid tumor tissue with abnormal (leaky) vasculature—a phenomenon known as Enhanced Permeation and Retention (EPR) effect, advancing their use for in vivo tumor imaging. Furthermore, large surface area of FNPs and their usual core–shell structure offer a platform for designing and fabricating multimodal/multifunctional nanoparticles (MMNPs). For effective cancer imaging, often the optical imaging modality is integrated with other nonoptical‐based imaging modalities such as MRI, X‐ray, and PET, thus creating multimodal nanoparticle (NP)‐based imaging probes. Such multimodal NP probes can be further integrated with therapeutic drug as well as cancer targeting agent leading to multifunctional NPs. Biocompatibility of FNPs is an important criterion that must be seriously considered during FNP design. NP composition, size, and surface chemistry must be carefully selected to minimize potential toxicological consequences both in vitro and in vivo . In this article, we will mainly focus on three different types of FNPs: dye‐loaded NPs, quantum dots (Qdots), and phosphores; briefly highlighting their potential use in translational research. WIREs Nanomed Nanobiotechnol 2011 3 501–510 DOI: 10.1002/wnan.134 This article is categorized under: Diagnostic Tools > In Vivo Nanodiagnostics and Imaging