2019
DOI: 10.1021/acs.langmuir.8b03460
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Comprehensive Evaluation of Degradable and Cost-Effective Plasmonic Nanoshells for Localized Photothermolysis of Cancer Cells

Abstract: Integrating the concept of biodegradation and light-triggered localized therapy in a functional nanoformulation is the current approach in onco-nanomedicine. Morphology control with an enhanced photothermal response, minimal toxicity, and X-ray attenuation of polymer-based nanoparticles is a critical concern for image-guided photothermal therapy. Herein, we describe the simple design of cost-effective and degradable polycaprolactone-based plasmonic nanoshells for the integrated photothermolysis as well as loca… Show more

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Cited by 23 publications
(12 citation statements)
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“…Fluorescence imaging of biological cells and tissues and real‐time monitoring of biosamples reveal information of biological structures, providing accurate diagnostic tools and treatment of disease . Luminogens or AIEgens which can lit up under the influence of bio‐environment are regarded as prospective candidates to be used as fluorescent bioprobes.…”
Section: Resultsmentioning
confidence: 99%
“…Fluorescence imaging of biological cells and tissues and real‐time monitoring of biosamples reveal information of biological structures, providing accurate diagnostic tools and treatment of disease . Luminogens or AIEgens which can lit up under the influence of bio‐environment are regarded as prospective candidates to be used as fluorescent bioprobes.…”
Section: Resultsmentioning
confidence: 99%
“…The absorbance of the supernatant was recorded with an ELISA microplate reader at 540 nm. The hemolysis percentage of the samples was calculated using the following equation (Chauhan et al, 2019 ):…”
Section: Methodsmentioning
confidence: 99%
“…[53][54][55] After the confirmation of cellular uptake, ac ellular localisation study was carriedo ut on L929 cells by using confocal laser imaging to determine the extento fi nternalisation in the cell and the effect on cell morphology. [56] The cellular uptake of S4 in MD-MB-231 cancer cells was analysed by seedingt he cancer cells on sterile coverslips in 12-well plates (50 000 cells per well) and incubating for 24 h. Next, 25 mgmL À1 S4 was added to the well plates and incubation performed for af urther 24 h. The excessm ateriali nt he cells was washed gently with phosphate-buffered saline (PBS), and then 4% paraformaldehydew as used to fix the cells for 15 min, followed by washing with PBS. 4',6-Diamidino-2-phenylindole( DAPI;2mgmL À1 ) was used for nuclear staining over ap eriod of 5min.…”
Section: Circular Dichroism Spectra Of S3 and S4mentioning
confidence: 99%