| Literature DB >> 26361572 |
Ying-Ying Huang1, Sulbha K Sharma2, Tianhong Dai3, Hoon Chung3, Anastasia Yaroslavsky4, Maria Garcia-Diaz5, Julie Chang6, Long Y Chiang7, Michael R Hamblin8.
Abstract
Photodynamic therapy (PDT) uses the combination of non-toxic dyes and harmless visible light to produce reactive oxygen species that can kill cancer cells and infectious microorganisms. Due to the tendency of most photosensitizers (PS) to be poorly soluble and to form nonphotoactive aggregates, drug-delivery vehicles have become of high importance. The nanotechnology revolution has provided many examples of nanoscale drug-delivery platforms that have been applied to PDT. These include liposomes, lipoplexes, nanoemulsions, micelles, polymer nanoparticles (degradable and nondegradable), and silica nanoparticles. In some cases (fullerenes and quantum dots), the actual nanoparticle itself is the PS. Targeting ligands such as antibodies and peptides can be used to increase specificity. Gold and silver nanoparticles can provide plasmonic enhancement of PDT. Two-photon excitation or optical upconversion can be used instead of one-photon excitation to increase tissue penetration at longer wavelengths. Finally, after sections on in vivo studies and nanotoxicology, we attempt to answer the title question, "can nano-technology potentiate PDT?"Entities:
Keywords: ORMOSIL; dendrimer; fullerene; graphene; lipoplex; lipoprotein; liposome; magnetic nanoparticle; micelle; nanocell; nanoparticle; polymeric nanoparticle; porphysome; quantum dot; single-walled carbon nanotube; two-photon excitation; upconversion
Year: 2012 PMID: 26361572 PMCID: PMC4562697 DOI: 10.1515/ntrev-2011-0005
Source DB: PubMed Journal: Nanotechnol Rev ISSN: 2191-9089 Impact factor: 7.848