Thermal cycling characteristics of a 3D-printed serpentine microchannel for DNA amplification by polymerase chain reaction

被引:20
作者
Park, Jaehyun [1 ]
Park, Heesung [1 ]
机构
[1] Changwon Natl Univ, Dept Mech Engn, 20 Changwondaehak Ro, Chang Won 51140, South Korea
基金
新加坡国家研究基金会;
关键词
3D-printer; Microchannel; Polymerase chain reaction; Thermal cycling; CONTINUOUS-FLOW PCR; CHIP; DEVICE; SURFACE;
D O I
10.1016/j.sna.2017.10.044
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
A polymerase chain reaction (PCR) device with integrated heaters for DNA amplification is proposed by using 3D-printing technology, which has the advantages of fast prototyping, design flexibility, and low cost. The thermal characteristics of the 3D-printed device for PCR are reported for the first time. The overall dimensions of the PCR device are 30 mm x 40 mm where a serpentine microchannel is created to implement 27 thermal cycles. The serpentine microchannel of 260 mu m in depth, 450 pm in width and 1470 mm in length has been designed to inspect shape conformity and temperature variations. Thermal cycling experiments has showed that three temperature zones for denaturation (90-95 degrees C), annealing (55-65 degrees C) and extension (70-77 degrees C) were successfully produced for DNA amplification. The thermal cycling efficiency ranges 67.4% to 47.8% when the flow rate is changed from 5 mu L/min to 10 mu L/min. The study demonstrates the feasibility of a low-cost 3D-printed PCR device that enables DNA amplification by thermal cycling. This paper concludes that 3D-printing technology can be applied for bio-microfluidic devices that require precise temperature control. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 187
页数:5
相关论文
共 50 条
  • [41] CHARACTERIZATION OF PRIMERS FOR OPTIMAL AMPLIFICATION OF HEPATITIS-B VIRUS-DNA IN THE POLYMERASE CHAIN-REACTION ASSAY
    KANEKO, S
    MILLER, RH
    JOURNAL OF VIROLOGICAL METHODS, 1990, 29 (02) : 225 - 229
  • [42] MULTIPLE PRIMER PAIRS FOR POLYMERASE CHAIN-REACTION (PCR) AMPLIFICATION OF HUMAN PARVOVIRUS-B19 DNA
    DURIGON, EL
    ERDMAN, DD
    GARY, GW
    PALLANSCH, MA
    TOROK, TJ
    ANDERSON, LJ
    JOURNAL OF VIROLOGICAL METHODS, 1993, 44 (2-3) : 155 - 165
  • [43] Optimization of 3D Digital Microfluidic Biochips for the Multiplexed Polymerase Chain Reaction
    Li, Zipeng
    Ho, Tsung-Yi
    Chakrabarty, Krishnendu
    ACM TRANSACTIONS ON DESIGN AUTOMATION OF ELECTRONIC SYSTEMS, 2016, 21 (02)
  • [44] DIFFERENTIAL POLYMERASE CHAIN-REACTION ASSAY OF CYCLIN D1 GENE AMPLIFICATION IN ESOPHAGEAL-CARCINOMA
    GRAMLICH, TL
    FRITSCH, CR
    MAURER, D
    EBERLE, M
    GANSLER, TS
    DIAGNOSTIC MOLECULAR PATHOLOGY, 1994, 3 (04) : 255 - 259
  • [45] AMPLIFICATION BY POLYMERASE CHAIN-REACTION OF PLASMODIUM-FALCIPARUM DNA FROM GIEMSA-STAINED THIN BLOOD SMEARS
    KIMURA, M
    KANEKO, O
    INOUE, A
    ISHII, A
    TANABE, K
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 70 (1-2) : 193 - 197
  • [46] POLYMERASE CHAIN-REACTION INSITU - INTRACELLULAR AMPLIFICATION AND DETECTION OF HIV-1 PROVIRAL DNA AND OTHER SPECIFIC GENES
    BAGASRA, O
    SESHAMMA, T
    POMERANTZ, RJ
    JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 158 (01) : 131 - 145
  • [47] Polymerase chain reaction amplification specificity: Incidence of allele dropout using different DNA preparation methods for heterozygous single cells
    Gitlin, SA
    Lanzendorf, SE
    Gibbons, WE
    JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 1996, 13 (02) : 107 - 111
  • [48] EPSTEIN-BARR VIRAL-DNA IN HODGKINS-DISEASE - AMPLIFICATION AND DETECTION USING THE POLYMERASE CHAIN-REACTION
    BROCKSMITH, D
    ANGEL, CA
    PRINGLE, JH
    LAUDER, I
    JOURNAL OF PATHOLOGY, 1991, 165 (01) : 11 - 15
  • [49] A 3D-Printed Millifluidic Platform Enabling Bacterial Preconcentration and DNA Purification for Molecular Detection of Pathogens in Blood
    Kim, Yonghee
    Lee, Jinyeop
    Park, Sungsu
    MICROMACHINES, 2018, 9 (09)
  • [50] DESIGN OF POLYMERASE CHAIN-REACTION PRIMERS FOR THE SELECTIVE AMPLIFICATION OF HIV-1 RNA IN THE PRESENCE OF HIV-1 DNA
    KOLLMANN, TR
    ZHUANG, XJ
    RUBINSTEIN, A
    GOLDSTEIN, H
    AIDS, 1992, 6 (06) : 547 - 552