2018
DOI: 10.1016/j.bios.2018.03.065
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Isothermal exponential amplification techniques: From basic principles to applications in electrochemical biosensors

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Cited by 100 publications
(50 citation statements)
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“…In recent years, owing to the advantages of simplicity and versatility, DNA amplification technology has emerged as an attractive tool in biology field and plays an important role in biomedical research [69][70][71][72][73]. The nucleic acid amplification techniques can be divided into two categories: thermal cycling amplification strategies, like polymerase chain reaction (PCR) [74][75][76], and isothermal amplification strategies, such as rolling circle amplification (RCA) and hybridization chain reaction (HCR) [77][78][79][80][81]. The characteristics of typical DNA amplification technologies as well as the representative works are comprehensively introduced in this section.…”
Section: Dna Amplification Technologymentioning
confidence: 99%
“…In recent years, owing to the advantages of simplicity and versatility, DNA amplification technology has emerged as an attractive tool in biology field and plays an important role in biomedical research [69][70][71][72][73]. The nucleic acid amplification techniques can be divided into two categories: thermal cycling amplification strategies, like polymerase chain reaction (PCR) [74][75][76], and isothermal amplification strategies, such as rolling circle amplification (RCA) and hybridization chain reaction (HCR) [77][78][79][80][81]. The characteristics of typical DNA amplification technologies as well as the representative works are comprehensively introduced in this section.…”
Section: Dna Amplification Technologymentioning
confidence: 99%
“…Detection of this damage and exploring DNA repair systems are important; hence, more attention is paid to the innovation and development of highly precise techniques. On the other hand, classic methodologies such as PCR cannot recognize type of detected DNA damage, other techniques give chance to detect single cells with DNA damage in a given population (comet assay), analyze the ratio of apoptotic to necrotic cells (FCM and FISH) or detect oxidative damage, and quantify thymine dimers (HPLC-electrospray tandem mass spectrometry and GC-MS) [5,[87][88][89]. Methodology is crucial for sensitive detection of genome DNA damage, characterization of damage type, and quantification of DNA damage and repair mechanisms.…”
Section: Discussionmentioning
confidence: 99%
“…Nevertheless, the need for temperature cycles and precise control thereof for proper PCR operation requires sophisticated instrumentation, making its integration with biosensing devices difficult. More recently, nucleic acid amplification techniques that run at a constant temperature have been reported to facilitate the design and development of biosensing platforms with the required sensitivity [29]. Among the different isothermal amplification techniques described, those that work at cellular temperatures (≈37 ºC) are particularly convenient, since they require less energy, which translates into simpler instrumentation and therefore adequate for use at the point of need.…”
Section: Quantified This Technique Is Referred To As Reverse Transcrmentioning
confidence: 99%
“…One of the most prominent aspects of RPA technology is its high reaction speed, even superior to PCR. In this regard, given the absence of thermal cycles, amplification kinetics is conditioned by the activity of the enzymes that work in concert, and RPA has been reported to be faster than other isothermal exponential variants such as Loop-mediated isothermal AMPlification (LAMP) or Helicase-Dependent Amplification (HDA) that occur at 60-65ºC [29]. Here again, RNA targets should be previously retro-transcribed into DNA by a reverse transcriptase and the generated 14 DNA strand, complementary to the RNA target, is subsequently amplified by RPA.…”
Section: Quantified This Technique Is Referred To As Reverse Transcrmentioning
confidence: 99%