Laboratory AutomationSupplemental record

3D printing and milling a real-time PCR device for infectious disease diagnostics

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Matched by doi · retrieved 2026-07-21

Abstract

Diagnosing infectious diseases using quantitative polymerase chain reaction (qPCR) offers a conclusive result in determining the infection, the strain or type of pathogen, and the level of infection. However, due to the high-cost instrumentation involved and the complexity in maintenance, it is rarely used in the field to make a quick turnaround diagnosis. In order to provide a higher level of accessibility than current qPCR devices, a set of 3D manufacturing methods is explored as a possible option to fabricate a low-cost and portable qPCR device. The key advantage of this approach is the ability to upload the digital format of the design files on the internet for wide distribution so that people at any location can simply download and feed into their 3D printers for quick manufacturing. The material and design are carefully selected to minimize the number of custom parts that depend on advanced manufacturing processes which lower accessibility. The presented 3D manufactured qPCR device is tested with 20-μL samples that contain various concentrations of lentivirus, the same type as HIV. A reverse-transcription step is a part of the device's operation, which takes place prior to the qPCR step to reverse transcribe the target RNA from the lentivirus into complementary DNA (cDNA). This is immediately followed by qPCR which quantifies the target sequence molecules in the sample during the PCR amplification process. The entire process of thermal control and time-coordinated fluorescence reading is automated by closed-loop feedback and a microcontroller. The resulting device is portable and battery-operated, with a size of 12 × 7 × 6 cm3 and mass of only 214 g. By uploading and sharing the design files online, the presented low-cost qPCR device may provide easier access to a robust diagnosis protocol for various infectious diseases, such as HIV and malaria.

Bibliographic details

Published
2017-06-06
Journal/source
PLOS ONE
Publisher
Public Library of Science (PLoS)
DOI
10.1371/journal.pone.0179133
Type
journal-article
Language
en
Volume / issue
12 / 6
Pages
e0179133
ISSN
1932-6203

Access and metrics

Open access
Yes
OA status
gold
License
cc-by
Version
publishedVersion
Cited by
55
References
25
Retracted
No

Authors and affiliations

  1. Geoffrey MulberryUniversity of Central Florida
  2. Kevin A. WhiteUniversity of Central Florida
  3. Manjusha VaidyaUniversity of Central Florida
  4. Kiminobu SugayaUniversity of Central Florida
  5. Brian N. KimCorresponding authorUniversity of Central Florida

Topics and keywords

Virus-based gene therapy researchViral gastroenteritis research and epidemiologyHerpesvirus Infections and TreatmentsInfectious disease (medical specialty)VirologyMedicineDiseaseInternal medicine