4.6 Article

3D spiral channels combined with flexible micro-sieve for high-throughput rare tumor cell enrichment and assay from clinical pleural effusion samples

期刊

BIO-DESIGN AND MANUFACTURING
卷 5, 期 2, 页码 358-370

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s42242-021-00167-y

关键词

Cell enrichment; High throughput; Pleural effusion; Liquid biopsy; 3D printing

资金

  1. National Key Research and Development Program of China [2018YFC2001100]
  2. National Natural Science Foundation of China [61774167, 61801477]
  3. Instrument Development Program of the Chinese Academy of Sciences, Beijing Municipal Natural Science Foundation [4192062, 4182072]
  4. Beijing Municipal Administration of Hospitals Incubating Program [PX2017050]
  5. Youth Innovation Promotion Association of Chinese Academy of Sciences

向作者/读者索取更多资源

In this paper, a three-dimensional sieving method for rare tumor cell enrichment was proposed. It effectively eliminated dead zones in traditional two-dimensional cell filters, resulting in high throughput and recovery rates. The method was able to effectively enrich rare target cells from pleural effusion samples and the purified cells exhibited significantly stronger proliferation capabilities compared to unprocessed cells.
The sieving and enrichment of rare tumor cells from large-volume pleural effusion (PE) samples is a promising technique for cell-based lung tumor diagnosis and drug tests, which features high throughput and recovery, purification, as well as viability rates of rare target cells as the prerequisites for high sensitivity, specificity, and accuracy of tumor cell analysis. In this paper, we propose a three-dimensional (3D) sieving method for rare tumor cell enrichment, which effectively eliminates the dead zones in traditional two-dimensional (2D) cell filters with a dimension-raising strategy to satisfy the requirements mentioned above. The prototype device was combined with a funnel-shaped holder, a flexible micropore membrane in the middle, and a 3D spiral fluid channel covered on the membrane as a three-layer ice-creaming cone composite structure. Driven by gravity alone, the device performed as follows: (1) 20-fold throughput compared with the 2D commercial plane cell filter, which was up to 20 mL/min for a threefold dilution of whole blood sample; (2) high recovery rates of 84.5% +/- 21%, 86% +/- 25%, 83% +/- 14% for 100, 1000, and 10 000 cells/mL, respectively, in 30 mL phosphate buffer saline (PBS) sample, and a 100% positive detection rate in the case of <= 5 A549 cells in 1 mL PBS; (3) a typical purification rate of 85.5% +/- 9.1%; and (4) a viability rate of > 93%. In the demonstration application, this device effectively enriched rare target cells from large volumes (> 25 mL) of clinical pleural effusions. The following results indicated that tumor cells were easy-to-discover in the enriched PE samples, and the proliferation capability of purified cells was (> 4.6 times) significantly stronger than that of unprocessed cells in the subsequent 6-day culture. The above evaluation indicates that the proposed easily reproducible method for the effective execution of rare cell enrichments and assays is expected to become a practical technique for clinical cell-based tumor diagnosis.

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