2013
DOI: 10.2147/ijn.s47585
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Photothermal ablation of pancreatic cancer cells with hybrid iron-oxide core gold-shell nanoparticles

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Cited by 62 publications
(40 citation statements)
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“…The HNP preparation and characterisation has been reported previously [21,22] along with their ability to undergo triggered heating upon laser irradiation in agar phantoms [17,34], in vitro and in situ in tumour bearing mouse cadavers [35,36]. Drug attachment was carried out at three drug:HNP weight ratios (5:1, 2.5:1 and 1:1 based on Fe weight of HNP) for all four bisnaphthalamide based drugs.…”
Section: Hnp-drug Conjugation and Characterisationmentioning
confidence: 99%
“…The HNP preparation and characterisation has been reported previously [21,22] along with their ability to undergo triggered heating upon laser irradiation in agar phantoms [17,34], in vitro and in situ in tumour bearing mouse cadavers [35,36]. Drug attachment was carried out at three drug:HNP weight ratios (5:1, 2.5:1 and 1:1 based on Fe weight of HNP) for all four bisnaphthalamide based drugs.…”
Section: Hnp-drug Conjugation and Characterisationmentioning
confidence: 99%
“…The specific nanostructure of the gold nanoshells could also allow nearinfrared light to be absorbed and converted into heat whereby cancer cells are exposed to slightly higher temperatures than usual to destroy them [21]. Some studies have demonstrated the use of iron oxide gold-shell nanoparticles that are MRI-visible photothermal sensitizers during laser irradiation of pancreatic cancer cells [24]. Exposure to iron oxide gold-shell nanoparticles followed by laser irradiation led to significant improvement in the management of pancreatic cancer cell [24].…”
Section: Destruction From Inside the Cellmentioning
confidence: 99%
“…Some studies have demonstrated the use of iron oxide gold-shell nanoparticles that are MRI-visible photothermal sensitizers during laser irradiation of pancreatic cancer cells [24]. Exposure to iron oxide gold-shell nanoparticles followed by laser irradiation led to significant improvement in the management of pancreatic cancer cell [24]. There are some major disadvantages for nanoshell therapy such as drug toxicity and tumor resistance.…”
Section: Destruction From Inside the Cellmentioning
confidence: 99%
“…This oxygen is highly toxic and leads to cell death via apoptosis or necrosis [1]. Photofrin®, also known as porfimer sodium is an FDA approved photosensitizing agent, used in the management of non-small cell lung cancer and esophageal cancer [2]. Porfimer sodium has proved effective in relieving symptoms of esophageal cancer when the mass obstructs the esophagus or when it is untreatable with laser alone.…”
Section: Photodynamic Therapymentioning
confidence: 99%
“…Phototherapy could enhance Heat Shock Proteins (HSP). HSP expression in the tumor cells, in particular on the cell surface of apoptotic cells, which could be recognized by APCs through toll-like receptor (TLRs), followed by cytokine release via Myd88 and NF-kB signaling pathways [2]. In particular, phototherapy, as a promising cancer treatment strategy that uses a local, selective photothermal or photochemical interaction on target tumor to release tumor antigens, creates an antigen source that acts as an in situ cancer vaccine.…”
Section: Photothermal Therapymentioning
confidence: 99%