Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy
Prostate cancer is the second leading cause of cancer-related death among the American male population, and the cost of treating prostate cancer patients is about $10 billion/year in the United States. Current treatments are mostly ineffective against advanced-stage prostate cancer and are often ass...
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Veröffentlicht in: | Journal of the American Chemical Society 2010-12, Vol.132 (51), p.18103-18114 |
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creator | Lu, Wentong Singh, Anant Kumar Khan, Sadia Afrin Senapati, Dulal Yu, Hongtao Ray, Paresh Chandra |
description | Prostate cancer is the second leading cause of cancer-related death among the American male population, and the cost of treating prostate cancer patients is about $10 billion/year in the United States. Current treatments are mostly ineffective against advanced-stage prostate cancer and are often associated with severe side effects. Driven by these factors, we report a multifunctional, nanotechnology-driven, gold nano-popcorn-based surface-enhanced Raman scattering (SERS) assay for targeted sensing, nanotherapy treatment, and in situ monitoring of photothermal nanotherapy response during the therapy process. Our experimental data show that, in the presence of LNCaP human prostate cancer cells, multifunctional popcorn-shaped gold nanoparticles form several hot spots and provide a significant enhancement of the Raman signal intensity by several orders of magnitude (2.5 × 109). As a result, it can recognize human prostate cancer cells at the 50-cells level. Our results indicate that the localized heating that occurs during near-infrared irradiation can cause irreparable cellular damage to the prostate cancer cells. Our in situ time-dependent results demonstrate for the first time that, by monitoring SERS intensity changes, one can monitor photothermal nanotherapy response during the therapy process. Possible mechanisms and operating principles of our SERS assay are discussed. Ultimately, this nanotechnology-driven assay could have enormous potential applications in rapid, on-site targeted sensing, nanotherapy treatment, and monitoring of the nanotherapy process, which are critical to providing effective treatment of cancer. |
doi_str_mv | 10.1021/ja104924b |
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Current treatments are mostly ineffective against advanced-stage prostate cancer and are often associated with severe side effects. Driven by these factors, we report a multifunctional, nanotechnology-driven, gold nano-popcorn-based surface-enhanced Raman scattering (SERS) assay for targeted sensing, nanotherapy treatment, and in situ monitoring of photothermal nanotherapy response during the therapy process. Our experimental data show that, in the presence of LNCaP human prostate cancer cells, multifunctional popcorn-shaped gold nanoparticles form several hot spots and provide a significant enhancement of the Raman signal intensity by several orders of magnitude (2.5 × 109). As a result, it can recognize human prostate cancer cells at the 50-cells level. Our results indicate that the localized heating that occurs during near-infrared irradiation can cause irreparable cellular damage to the prostate cancer cells. Our in situ time-dependent results demonstrate for the first time that, by monitoring SERS intensity changes, one can monitor photothermal nanotherapy response during the therapy process. Possible mechanisms and operating principles of our SERS assay are discussed. Ultimately, this nanotechnology-driven assay could have enormous potential applications in rapid, on-site targeted sensing, nanotherapy treatment, and monitoring of the nanotherapy process, which are critical to providing effective treatment of cancer.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja104924b</identifier><identifier>PMID: 21128627</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Cell Line, Tumor ; Gold ; Humans ; Hyperthermia, Induced ; Male ; Metal Nanoparticles ; Monitoring, Physiologic - methods ; Nanotechnology - methods ; Phototherapy ; Prostatic Neoplasms - diagnosis ; Prostatic Neoplasms - therapy ; Spectrum Analysis, Raman - methods</subject><ispartof>Journal of the American Chemical Society, 2010-12, Vol.132 (51), p.18103-18114</ispartof><rights>Copyright © 2010 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a415t-5bd4c464eb297a076e58943797d24681f47ab6db122a7e82876ada1b6327e4193</citedby><cites>FETCH-LOGICAL-a415t-5bd4c464eb297a076e58943797d24681f47ab6db122a7e82876ada1b6327e4193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja104924b$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja104924b$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21128627$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lu, Wentong</creatorcontrib><creatorcontrib>Singh, Anant Kumar</creatorcontrib><creatorcontrib>Khan, Sadia Afrin</creatorcontrib><creatorcontrib>Senapati, Dulal</creatorcontrib><creatorcontrib>Yu, Hongtao</creatorcontrib><creatorcontrib>Ray, Paresh Chandra</creatorcontrib><title>Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Prostate cancer is the second leading cause of cancer-related death among the American male population, and the cost of treating prostate cancer patients is about $10 billion/year in the United States. Current treatments are mostly ineffective against advanced-stage prostate cancer and are often associated with severe side effects. Driven by these factors, we report a multifunctional, nanotechnology-driven, gold nano-popcorn-based surface-enhanced Raman scattering (SERS) assay for targeted sensing, nanotherapy treatment, and in situ monitoring of photothermal nanotherapy response during the therapy process. Our experimental data show that, in the presence of LNCaP human prostate cancer cells, multifunctional popcorn-shaped gold nanoparticles form several hot spots and provide a significant enhancement of the Raman signal intensity by several orders of magnitude (2.5 × 109). As a result, it can recognize human prostate cancer cells at the 50-cells level. Our results indicate that the localized heating that occurs during near-infrared irradiation can cause irreparable cellular damage to the prostate cancer cells. Our in situ time-dependent results demonstrate for the first time that, by monitoring SERS intensity changes, one can monitor photothermal nanotherapy response during the therapy process. Possible mechanisms and operating principles of our SERS assay are discussed. Ultimately, this nanotechnology-driven assay could have enormous potential applications in rapid, on-site targeted sensing, nanotherapy treatment, and monitoring of the nanotherapy process, which are critical to providing effective treatment of cancer.</description><subject>Cell Line, Tumor</subject><subject>Gold</subject><subject>Humans</subject><subject>Hyperthermia, Induced</subject><subject>Male</subject><subject>Metal Nanoparticles</subject><subject>Monitoring, Physiologic - methods</subject><subject>Nanotechnology - methods</subject><subject>Phototherapy</subject><subject>Prostatic Neoplasms - diagnosis</subject><subject>Prostatic Neoplasms - therapy</subject><subject>Spectrum Analysis, Raman - methods</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc9u2zAMxoViRZu1PewFBl12GBC3kiJL9nHNsq5A_wRpejZoi04c2JIhKYc8XN-tTtL1tBNJ8PfxI0hCvnF2zZngNxvgTOZClidkxFPBkpQL9YWMGGMi0ZmanJOvIWyGUoqMn5FzwbnIlNAj8nbnWkOfwLpk7vrKeZvcQkBDl-BXGIfkdwMr60ITxgcsrtFDv6NLjxA7tHFMwRp6b-lLE7f00dkmOt_YFXU1na9dPCg6aOnyQ7nA0Dsb8AB4FyJEpFOwFXo6xbYN9DXs9S9bX0OFycyu901DF9DBYNNjFQdZ5frdJTmtoQ149REvyOuf2XL6N3l4vruf_npIQPI0JmlpZCWVxFLkGphWmGa5nOhcGyFVxmupoVSm5EKAxkxkWoEBXqqJ0Ch5PrkgP49zq8E4eKyL3jcd-F3BWbF_QfH5goH9fmT7bdmh-ST_3XwAfhwBqEKxcVtvh9X_M-gdk0qP-A</recordid><startdate>20101229</startdate><enddate>20101229</enddate><creator>Lu, Wentong</creator><creator>Singh, Anant Kumar</creator><creator>Khan, Sadia Afrin</creator><creator>Senapati, Dulal</creator><creator>Yu, Hongtao</creator><creator>Ray, Paresh Chandra</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20101229</creationdate><title>Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy</title><author>Lu, Wentong ; Singh, Anant Kumar ; Khan, Sadia Afrin ; Senapati, Dulal ; Yu, Hongtao ; Ray, Paresh Chandra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a415t-5bd4c464eb297a076e58943797d24681f47ab6db122a7e82876ada1b6327e4193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cell Line, Tumor</topic><topic>Gold</topic><topic>Humans</topic><topic>Hyperthermia, Induced</topic><topic>Male</topic><topic>Metal Nanoparticles</topic><topic>Monitoring, Physiologic - methods</topic><topic>Nanotechnology - methods</topic><topic>Phototherapy</topic><topic>Prostatic Neoplasms - diagnosis</topic><topic>Prostatic Neoplasms - therapy</topic><topic>Spectrum Analysis, Raman - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Wentong</creatorcontrib><creatorcontrib>Singh, Anant Kumar</creatorcontrib><creatorcontrib>Khan, Sadia Afrin</creatorcontrib><creatorcontrib>Senapati, Dulal</creatorcontrib><creatorcontrib>Yu, Hongtao</creatorcontrib><creatorcontrib>Ray, Paresh Chandra</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Wentong</au><au>Singh, Anant Kumar</au><au>Khan, Sadia Afrin</au><au>Senapati, Dulal</au><au>Yu, Hongtao</au><au>Ray, Paresh Chandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2010-12-29</date><risdate>2010</risdate><volume>132</volume><issue>51</issue><spage>18103</spage><epage>18114</epage><pages>18103-18114</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Prostate cancer is the second leading cause of cancer-related death among the American male population, and the cost of treating prostate cancer patients is about $10 billion/year in the United States. Current treatments are mostly ineffective against advanced-stage prostate cancer and are often associated with severe side effects. Driven by these factors, we report a multifunctional, nanotechnology-driven, gold nano-popcorn-based surface-enhanced Raman scattering (SERS) assay for targeted sensing, nanotherapy treatment, and in situ monitoring of photothermal nanotherapy response during the therapy process. Our experimental data show that, in the presence of LNCaP human prostate cancer cells, multifunctional popcorn-shaped gold nanoparticles form several hot spots and provide a significant enhancement of the Raman signal intensity by several orders of magnitude (2.5 × 109). As a result, it can recognize human prostate cancer cells at the 50-cells level. Our results indicate that the localized heating that occurs during near-infrared irradiation can cause irreparable cellular damage to the prostate cancer cells. Our in situ time-dependent results demonstrate for the first time that, by monitoring SERS intensity changes, one can monitor photothermal nanotherapy response during the therapy process. Possible mechanisms and operating principles of our SERS assay are discussed. Ultimately, this nanotechnology-driven assay could have enormous potential applications in rapid, on-site targeted sensing, nanotherapy treatment, and monitoring of the nanotherapy process, which are critical to providing effective treatment of cancer.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>21128627</pmid><doi>10.1021/ja104924b</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Cell Line, Tumor Gold Humans Hyperthermia, Induced Male Metal Nanoparticles Monitoring, Physiologic - methods Nanotechnology - methods Phototherapy Prostatic Neoplasms - diagnosis Prostatic Neoplasms - therapy Spectrum Analysis, Raman - methods |
title | Gold Nano-Popcorn-Based Targeted Diagnosis, Nanotherapy Treatment, and In Situ Monitoring of Photothermal Therapy Response of Prostate Cancer Cells Using Surface-Enhanced Raman Spectroscopy |
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