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Simultaneous detection of two growth factors from human single-embryo culture medium by a bead-based digital microfluidic chip
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Simultaneous detection of two growth factors from human single-embryo culture medium by a bead-based digital microfluidic chip

Meng-Shiue Lee, Wensyang Hsu, Hong-Yuan Huang, Hsueh-Yang Tseng, Chia-Tung Lee, Chung-Yu Hsu, Yi-Chueh Shieh, Shih-Hung Wang, Da-Jeng YaoCheng-Hsien Liu
Biosensors and Bioelectronics, 111851
2019
PMID: 31740257

摘要

Culture medium Digital microfluidic Growth factor Immunoassay In vitro fertilization IVF Biotechnology Biophysics Biomedical Engineering Electrochemistry
The measurement of growth factors released in a culture medium is considered to be an attractive non-invasive approach, apart from the embryo morphology, to identify the condition of an embryo development after fertilization in vitro (IVF), but the available embryo culture medium in the current method is only a few microlitres. This small sample volume, also of small concentration, makes difficult the application of a conventional detection method, such as an enzyme-linked immunosorbent assay (ELISA). A reliable detection of the growth factor from each embryo culture medium of such a small concentration hence remains a challenge. Here for the first time we report the results of measurement of not just one, but two, growth factors, human IL-1β and human TNF-α, from an individual droplet of embryo culture medium with a bead-based digital microfluidic chip. The required sample volume for a single measurement is only 520 nL; the total duration of the on-chip process is less than 40 min. Using the culture media of human embryos with normal morphologic features, we found that the concentrations of TNF-α change little from day 3 to day 5–6, but the concentrations of IL-1β for some embryos might double from day 3 to day 5–6. For other embryos even with similar normal morphologic features, some growth factors, such as IL-1β, might exhibit different expressions during the culture period. Those growth factors could serve to distinguish the development conditions of each embryo, not merely from an observation of embryo morphology.

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