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Rapid visual identification of PCR amplified nucleic acids by centrifugal gel separation: Potential use for molecular point-of-care tests.
Hwang, Sang-Hyun; Kim, Dong-Eun; Im, Ji-Hyun; Kang, Su-Jin; Lee, Do-Hoon; Son, Sang Jun.
Afiliación
  • Hwang SH; Department of Laboratory Medicine, Center for Diagnostic Oncology, Research Institute and Hospital, National Cancer Center, Goyang-si, Gyeonggi-do 410-769, Republic of Korea; Hematologic Malignancy Branch, Research Institute and Hospital, National Cancer Center, Goyang-si, Gyeonggi-do 410-769, Repub
  • Kim DE; Department of Bioscience and Biotechnology, Konkuk University, Seoul 143-701, Republic of Korea. Electronic address: kimde@konkuk.ac.kr.
  • Im JH; Department of Laboratory Medicine, Center for Diagnostic Oncology, Research Institute and Hospital, National Cancer Center, Goyang-si, Gyeonggi-do 410-769, Republic of Korea.
  • Kang SJ; Department of Laboratory Medicine, Center for Diagnostic Oncology, Research Institute and Hospital, National Cancer Center, Goyang-si, Gyeonggi-do 410-769, Republic of Korea.
  • Lee DH; Department of Laboratory Medicine, Center for Diagnostic Oncology, Research Institute and Hospital, National Cancer Center, Goyang-si, Gyeonggi-do 410-769, Republic of Korea.
  • Son SJ; Department of Chemistry, Gachon University, Seongnam, Gyeonggi, and Gachon Medical Research Institute, Gil Medical Center, Inchon, Republic of Korea.
Biosens Bioelectron ; 79: 829-34, 2016 May 15.
Article en En | MEDLINE | ID: mdl-26774997
Recently, nucleic acid amplification and detection techniques have progressed based on advances in in microfluidics, microelectronics, and optical systems. Nucleic acids amplification based point-of-care test (POCT) in resource-limited settings requires simple visual detection methods. Several biosensing methods including lateral flow immunoassays (LFIA) were previously used to visually detect nucleic acids. However, prolonged assay time, several washing steps, and a need for specific antibodies limited their use. Here we developed a novel, rapid method to visualize amplified nucleic acids with naked eyes in clinical samples. First, we optimized conditions based on separation using very low centrifugal force and a density medium to detect human papillomavirus (HPV)-16 DNA in cervical specimens. After DNA extraction, HPV16 PCR was performed with biotin-labeled forward primer and Cy3-labeled reverse primer. PCR amplicon was mixed with streptavidin-magnetic beads, introduced into the density medium. After two-minute centrifugation, the result was visually identified. This system showed identical results with commercial HPV real-time PCR for 30 clinical samples and could detect up to 10(2)copies/mL of HPV DNA without any optical instruments. This robust and sensitive visual detection system is suitable for non-specialist personnel and point-of-care diagnosis in low-resource settings.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: ADN Viral / Centrifugación por Gradiente de Densidad / Sistemas de Atención de Punto / Infecciones por Papillomavirus / Papillomavirus Humano 16 Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Biosens Bioelectron Asunto de la revista: BIOTECNOLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ADN Viral / Centrifugación por Gradiente de Densidad / Sistemas de Atención de Punto / Infecciones por Papillomavirus / Papillomavirus Humano 16 Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Biosens Bioelectron Asunto de la revista: BIOTECNOLOGIA Año: 2016 Tipo del documento: Article