In Situ Colorimetric LAMP Based on One-Step Modified Filter Paper to Screen Human Papillomavirus (HPV)16/18 from Clinical Samples
Cervical cancer is among the most common malignant tumors in women. The development of rapid screening techniques plays an important role in early screening for cancer treatment. We have developed an HPV screening method, which effectively combines the high-efficiency nucleic acid enrichment of chit...
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description | Cervical cancer is among the most common malignant tumors in women. The development of rapid screening techniques plays an important role in early screening for cancer treatment. We have developed an HPV screening method, which effectively combines the high-efficiency nucleic acid enrichment of chitosan-modified filter paper and the rapid visual detectability of colorimetric LAMP, along with the enhancement of the tolerance ability of the pH-sensitive LAMP reagent to acidic original samples, making the detection of HPV 16/18 easy to carry out and reliable, which is helpful for the epidemiological prevention and control strategies of HPV-induced cancer. This technique can simultaneously exhibit the “in situ amplification” capability of chitosan-modified filter paper and the nontemperature cycle dependence of visual LAMP detection. Therefore, DNA extraction and amplification can be performed efficiently and quickly within a single reaction where all DNA is concentrated in the QF paper disc. By embedding amino-modified filter paper into the plastic chip, a simple and reliable disposable chip was prepared for rapid HPV16 and HPV18 detection from clinical endometrial samples, and the results were 100% consistent with clinical diagnosis. More importantly, even after the sample was diluted 100-fold, HPV16/18-infected cells could be accurately identified, showing the advantages of the system in early cancer screening. Moreover, for endometrial samples containing plenty of cells, the filter paper could be used to enrich cells by filtration, preventing the acidic fluid from impacting pH-induced colorimetric LAMP detection and realizing direct amplification for HPV identification without nucleic acid extraction. This easy-to-operate system that can analyze a wide range of samples will be suitable for routine on-site HPV screening, dramatically extending the applications and utility for rapid, near-patient nucleic acid testing. |
doi_str_mv | 10.1021/acs.langmuir.4c00793 |
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The development of rapid screening techniques plays an important role in early screening for cancer treatment. We have developed an HPV screening method, which effectively combines the high-efficiency nucleic acid enrichment of chitosan-modified filter paper and the rapid visual detectability of colorimetric LAMP, along with the enhancement of the tolerance ability of the pH-sensitive LAMP reagent to acidic original samples, making the detection of HPV 16/18 easy to carry out and reliable, which is helpful for the epidemiological prevention and control strategies of HPV-induced cancer. This technique can simultaneously exhibit the “in situ amplification” capability of chitosan-modified filter paper and the nontemperature cycle dependence of visual LAMP detection. Therefore, DNA extraction and amplification can be performed efficiently and quickly within a single reaction where all DNA is concentrated in the QF paper disc. By embedding amino-modified filter paper into the plastic chip, a simple and reliable disposable chip was prepared for rapid HPV16 and HPV18 detection from clinical endometrial samples, and the results were 100% consistent with clinical diagnosis. More importantly, even after the sample was diluted 100-fold, HPV16/18-infected cells could be accurately identified, showing the advantages of the system in early cancer screening. Moreover, for endometrial samples containing plenty of cells, the filter paper could be used to enrich cells by filtration, preventing the acidic fluid from impacting pH-induced colorimetric LAMP detection and realizing direct amplification for HPV identification without nucleic acid extraction. This easy-to-operate system that can analyze a wide range of samples will be suitable for routine on-site HPV screening, dramatically extending the applications and utility for rapid, near-patient nucleic acid testing.</description><identifier>ISSN: 0743-7463</identifier><identifier>ISSN: 1520-5827</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/acs.langmuir.4c00793</identifier><identifier>PMID: 39093056</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Chitosan - chemistry ; Colorimetry - methods ; DNA, Viral - analysis ; DNA, Viral - genetics ; Female ; Human papillomavirus 16 - genetics ; Human papillomavirus 16 - isolation & purification ; Human papillomavirus 18 - genetics ; Human papillomavirus 18 - isolation & purification ; Human Papillomavirus Viruses ; Humans ; Nucleic Acid Amplification Techniques - methods</subject><ispartof>Langmuir, 2024-08, Vol.40 (32), p.16722-16730</ispartof><rights>2024 The Authors. 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Published by American Chemical Society 2024 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a329t-34ed4dba6693c94fea32f991781b02dd74e78f6d911301b73678b38256fc2b963</cites><orcidid>0009-0000-0803-0392</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.langmuir.4c00793$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.langmuir.4c00793$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,315,781,785,886,2766,27081,27929,27930,56743,56793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39093056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiao, Tingting</creatorcontrib><creatorcontrib>Sun, Peng</creatorcontrib><creatorcontrib>Tian, Shuang</creatorcontrib><creatorcontrib>Tan, Yingjun</creatorcontrib><creatorcontrib>Wang, Chunyan</creatorcontrib><creatorcontrib>He, Guangjun</creatorcontrib><creatorcontrib>Shi, Liujia</creatorcontrib><creatorcontrib>Zhang, Yang</creatorcontrib><creatorcontrib>Li, Jianhua</creatorcontrib><creatorcontrib>Gu, Yin</creatorcontrib><title>In Situ Colorimetric LAMP Based on One-Step Modified Filter Paper to Screen Human Papillomavirus (HPV)16/18 from Clinical Samples</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>Cervical cancer is among the most common malignant tumors in women. The development of rapid screening techniques plays an important role in early screening for cancer treatment. We have developed an HPV screening method, which effectively combines the high-efficiency nucleic acid enrichment of chitosan-modified filter paper and the rapid visual detectability of colorimetric LAMP, along with the enhancement of the tolerance ability of the pH-sensitive LAMP reagent to acidic original samples, making the detection of HPV 16/18 easy to carry out and reliable, which is helpful for the epidemiological prevention and control strategies of HPV-induced cancer. This technique can simultaneously exhibit the “in situ amplification” capability of chitosan-modified filter paper and the nontemperature cycle dependence of visual LAMP detection. Therefore, DNA extraction and amplification can be performed efficiently and quickly within a single reaction where all DNA is concentrated in the QF paper disc. By embedding amino-modified filter paper into the plastic chip, a simple and reliable disposable chip was prepared for rapid HPV16 and HPV18 detection from clinical endometrial samples, and the results were 100% consistent with clinical diagnosis. More importantly, even after the sample was diluted 100-fold, HPV16/18-infected cells could be accurately identified, showing the advantages of the system in early cancer screening. Moreover, for endometrial samples containing plenty of cells, the filter paper could be used to enrich cells by filtration, preventing the acidic fluid from impacting pH-induced colorimetric LAMP detection and realizing direct amplification for HPV identification without nucleic acid extraction. This easy-to-operate system that can analyze a wide range of samples will be suitable for routine on-site HPV screening, dramatically extending the applications and utility for rapid, near-patient nucleic acid testing.</description><subject>Chitosan - chemistry</subject><subject>Colorimetry - methods</subject><subject>DNA, Viral - analysis</subject><subject>DNA, Viral - genetics</subject><subject>Female</subject><subject>Human papillomavirus 16 - genetics</subject><subject>Human papillomavirus 16 - isolation & purification</subject><subject>Human papillomavirus 18 - genetics</subject><subject>Human papillomavirus 18 - isolation & purification</subject><subject>Human Papillomavirus Viruses</subject><subject>Humans</subject><subject>Nucleic Acid Amplification Techniques - methods</subject><issn>0743-7463</issn><issn>1520-5827</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v2yAAxdHUaU27fYOp4tgdnILBYE5VG61NpVSNlG1XhDHuqDC4YEfacd-8REmr7rILoMd7P_48AL5iNMeoxBdKp7lT_rGfbJxTjRAX5AOY4apERVWX_AjMEKek4JSRY3CS0hNCSBAqPoFjIvIKVWwG_t55uLHjBBfBhWh7M0ar4erqfg2vVTItDB4-eFNsRjPA-9DazmbxxrrRRLhWQx7HADc6GuPhcuqV36nWudCrrY1TgufL9a9vmF3gGnYx9HDhrLdaObhR_eBM-gw-dsol8-Uwn4KfN99_LJbF6uH2bnG1KhQpxVgQalraNooxQbSgnclyJwTmNW5Q2bacGl53rBUYE4QbThivG1KXFet02QhGTsHlnjtMTW9abfwYlZNDfrSKf2RQVv674-1v-Ri2MgMzhaJMOD8QYnieTBplb5M2LrdgwpQkQTUnFatEna10b9UxpBRN93YORnJXn8z1ydf65KG-HDt7f8e30Gtf2YD2hl38KUzR5y_7P_MF-MqqIA</recordid><startdate>20240813</startdate><enddate>20240813</enddate><creator>Jiao, Tingting</creator><creator>Sun, Peng</creator><creator>Tian, Shuang</creator><creator>Tan, Yingjun</creator><creator>Wang, Chunyan</creator><creator>He, Guangjun</creator><creator>Shi, Liujia</creator><creator>Zhang, Yang</creator><creator>Li, Jianhua</creator><creator>Gu, Yin</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><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0009-0000-0803-0392</orcidid></search><sort><creationdate>20240813</creationdate><title>In Situ Colorimetric LAMP Based on One-Step Modified Filter Paper to Screen Human Papillomavirus (HPV)16/18 from Clinical Samples</title><author>Jiao, Tingting ; Sun, Peng ; Tian, Shuang ; Tan, Yingjun ; Wang, Chunyan ; He, Guangjun ; Shi, Liujia ; Zhang, Yang ; Li, Jianhua ; Gu, Yin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a329t-34ed4dba6693c94fea32f991781b02dd74e78f6d911301b73678b38256fc2b963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Chitosan - chemistry</topic><topic>Colorimetry - methods</topic><topic>DNA, Viral - analysis</topic><topic>DNA, Viral - genetics</topic><topic>Female</topic><topic>Human papillomavirus 16 - genetics</topic><topic>Human papillomavirus 16 - isolation & purification</topic><topic>Human papillomavirus 18 - genetics</topic><topic>Human papillomavirus 18 - isolation & purification</topic><topic>Human Papillomavirus Viruses</topic><topic>Humans</topic><topic>Nucleic Acid Amplification Techniques - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiao, Tingting</creatorcontrib><creatorcontrib>Sun, Peng</creatorcontrib><creatorcontrib>Tian, Shuang</creatorcontrib><creatorcontrib>Tan, Yingjun</creatorcontrib><creatorcontrib>Wang, Chunyan</creatorcontrib><creatorcontrib>He, Guangjun</creatorcontrib><creatorcontrib>Shi, Liujia</creatorcontrib><creatorcontrib>Zhang, Yang</creatorcontrib><creatorcontrib>Li, Jianhua</creatorcontrib><creatorcontrib>Gu, Yin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiao, Tingting</au><au>Sun, Peng</au><au>Tian, Shuang</au><au>Tan, Yingjun</au><au>Wang, Chunyan</au><au>He, Guangjun</au><au>Shi, Liujia</au><au>Zhang, Yang</au><au>Li, Jianhua</au><au>Gu, Yin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Situ Colorimetric LAMP Based on One-Step Modified Filter Paper to Screen Human Papillomavirus (HPV)16/18 from Clinical Samples</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2024-08-13</date><risdate>2024</risdate><volume>40</volume><issue>32</issue><spage>16722</spage><epage>16730</epage><pages>16722-16730</pages><issn>0743-7463</issn><issn>1520-5827</issn><eissn>1520-5827</eissn><abstract>Cervical cancer is among the most common malignant tumors in women. The development of rapid screening techniques plays an important role in early screening for cancer treatment. We have developed an HPV screening method, which effectively combines the high-efficiency nucleic acid enrichment of chitosan-modified filter paper and the rapid visual detectability of colorimetric LAMP, along with the enhancement of the tolerance ability of the pH-sensitive LAMP reagent to acidic original samples, making the detection of HPV 16/18 easy to carry out and reliable, which is helpful for the epidemiological prevention and control strategies of HPV-induced cancer. This technique can simultaneously exhibit the “in situ amplification” capability of chitosan-modified filter paper and the nontemperature cycle dependence of visual LAMP detection. Therefore, DNA extraction and amplification can be performed efficiently and quickly within a single reaction where all DNA is concentrated in the QF paper disc. By embedding amino-modified filter paper into the plastic chip, a simple and reliable disposable chip was prepared for rapid HPV16 and HPV18 detection from clinical endometrial samples, and the results were 100% consistent with clinical diagnosis. More importantly, even after the sample was diluted 100-fold, HPV16/18-infected cells could be accurately identified, showing the advantages of the system in early cancer screening. Moreover, for endometrial samples containing plenty of cells, the filter paper could be used to enrich cells by filtration, preventing the acidic fluid from impacting pH-induced colorimetric LAMP detection and realizing direct amplification for HPV identification without nucleic acid extraction. This easy-to-operate system that can analyze a wide range of samples will be suitable for routine on-site HPV screening, dramatically extending the applications and utility for rapid, near-patient nucleic acid testing.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39093056</pmid><doi>10.1021/acs.langmuir.4c00793</doi><tpages>9</tpages><orcidid>https://orcid.org/0009-0000-0803-0392</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Chitosan - chemistry Colorimetry - methods DNA, Viral - analysis DNA, Viral - genetics Female Human papillomavirus 16 - genetics Human papillomavirus 16 - isolation & purification Human papillomavirus 18 - genetics Human papillomavirus 18 - isolation & purification Human Papillomavirus Viruses Humans Nucleic Acid Amplification Techniques - methods |
title | In Situ Colorimetric LAMP Based on One-Step Modified Filter Paper to Screen Human Papillomavirus (HPV)16/18 from Clinical Samples |
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