Life sciences · Journal article
Bioengineering & Translational Medicine · September 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Journal article.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Abstract Early detection of primary tumors and metastatic processes increases the success of anti‐tumor therapies and favors good prognoses. Within the current range of methods available to detect the presence of tumors, liquid biopsy is receiving particular attention as it is a minimally invasive and quick procedure. Identification of cancer elements such as circulating tumor cells (CTCs) constitutes valuable information about tumor biology. However, this is a challenging process due to the rarity of those cells in corporal fluids such as blood (CTCs <10 cell/10 mL blood). Microfluidics, an affordable, sensitive, user‐friendly and rapidly evolving technology, has significantly provided advances in the detection and isolation of rare cancer cells. One of the main strategies currently employed is the development of inertial focusing devices with spiral geometries. In these systems, hydrodynamic forces are used to focus particles as a function of their size without additional mechanical or electronic equipment. Specifically, the interactions between inertial lift forces and Dean vortices determine the equilibrium position of particles as a function of their size, enhancing their sorting. Here, by combination of viscoelastic and inertial microfluidics approaches, we have developed a spiral device for isolation of CTCs from liquid biopsies. Our device was able to isolate and enrich with high efficiency osteosarcoma cells presented in a low number from whole blood samples. This device constitutes a promising tool for isolation, characterization and potential culture of tumor cells from patient samples and improve personalized medicine.