Microdroplets-on-chip: A review.
Aihui WangAynur AbdullaXianting DingPublished in: Proceedings of the Institution of Mechanical Engineers. Part H, Journal of engineering in medicine (2019)
Single-cell analysis serves as an important approach to study cell functions and interactions. Catering to the demand of Big Data Era, fast reactions for single cells and paralleled high-throughput analysis have become an urgent need. Microdroplet in microfluidics has advantages of modularity and integrity, as well as high throughput and sensitivity, which present great potential in the field of single-cell analysis. This review is carried out on three aspects to introduce microdroplet chips for single-cell analysis: droplet formation, droplet detection and practical functions. Structures of droplet formation are categorized into three types, including T-shaped channel, flow-involved channel and three-dimensional micro-vortice. The detection methods, including fluorescence, Raman spectroscopy, mass spectroscopy and electrochemical detection, are summarized from applications. Both pros and cons for existing techniques are reviewed and discussed. The functions of microdroplets-on-chip cover cell culture, nucleic acid test and cell identification. For each field, principles/mechanisms and/or schematic images are laconically introduced. Microdroplet in microfluidics has become a major research direction in single-cell analysis. With updated methods of droplet formation such as inertial ordering and micro-vortice, microdroplets-based biochips will expect high throughput detection and high-accuracy trace detection for clinical diagnosis in the near future.
Keyphrases
- single cell
- high throughput
- rna seq
- big data
- label free
- machine learning
- real time pcr
- artificial intelligence
- loop mediated isothermal amplification
- oxidative stress
- induced apoptosis
- cell therapy
- deep learning
- endoplasmic reticulum stress
- risk assessment
- heavy metals
- human health
- sensitive detection
- optical coherence tomography
- cell cycle arrest
- cell death
- data analysis