All-in-One Centrifugal Microfluidic Device for Size-Selective Circulating Tumor Cell Isolation with High Purity

循环肿瘤细胞 化学 全血 微流控 色谱法 癌症 分离(微生物学) 生物医学工程 纳米技术 免疫学 内科学 生物 材料科学 生物信息学 医学 转移
作者
Ada Lee,Juhee Park,Minji Lim,Vijaya Sunkara,Shine Young Kim,Gwang Ha Kim,Mi Hyun Kim,Yoon‐Kyoung Cho
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:86 (22): 11349-11356 被引量:112
标识
DOI:10.1021/ac5035049
摘要

Circulating tumor cells (CTCs) have gained increasing attention owing to their roles in cancer recurrence and progression. Due to the rarity of CTCs in the bloodstream, an enrichment process is essential for effective target cell characterization. However, in a typical pressure-driven microfluidic system, the enrichment process generally requires complicated equipment and long processing times. Furthermore, the commonly used immunoaffinity-based positive selection method is limited, as its recovery rate relies on EpCAM expression of target CTCs, which shows heterogeneity among cell types. Here, we propose a centrifugal-force-based size-selective CTC isolation platform that can isolate and enumerate CTCs from whole blood within 30 s with high purity. The device was validated using the MCF-7 breast cancer cell line spiked in phosphate-buffered saline and whole blood, and an average capture efficiency of 61% was achieved, which is typical for size-based filtration. The capture efficiency for whole blood samples varied from 44% to 84% under various flow conditions and dilution factors. Under the optimized operating conditions, a few hundred white blood cells per 1 mL of whole blood were captured, representing a 20-fold decrease compared to those obtained using a commercialized size-based CTC isolation device. In clinical validation, normalized CTC counts varied from 10 to 60 per 7.5 mL of blood from gastric and lung cancer patients, yielding a detection rate of 50% and 38%, respectively. Overall, our CTC isolation device enables rapid and label-free isolation of CTCs with high purity, which should greatly improve downstream molecular analyses of captured CTCs.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
高挑的萤完成签到 ,获得积分10
1秒前
风中映冬发布了新的文献求助10
1秒前
科研通AI5应助D.Z采纳,获得10
1秒前
1秒前
刘星发布了新的文献求助10
2秒前
半颗星辰发布了新的文献求助10
2秒前
尼可刹米洛贝林完成签到,获得积分10
2秒前
doctorwang完成签到,获得积分10
2秒前
谦让的雍发布了新的文献求助10
3秒前
田様应助阿珍采纳,获得10
4秒前
湘玉给你溜肥肠完成签到,获得积分10
5秒前
lee发布了新的文献求助10
5秒前
iNk应助起名好难采纳,获得20
5秒前
5秒前
5秒前
6秒前
7秒前
123456完成签到,获得积分10
8秒前
8秒前
8秒前
伍秋望完成签到,获得积分10
8秒前
9秒前
细心的不乐完成签到,获得积分10
9秒前
pihril完成签到,获得积分10
10秒前
Murmures发布了新的文献求助10
10秒前
时尚的归尘完成签到,获得积分10
11秒前
11秒前
Jiawww完成签到,获得积分10
11秒前
11秒前
胡萝卜发布了新的文献求助10
12秒前
斯文败类应助reeeveb采纳,获得10
12秒前
快乐冰绿完成签到,获得积分10
12秒前
博林发布了新的文献求助10
12秒前
hecarli完成签到,获得积分0
12秒前
立刻睡大觉完成签到,获得积分20
12秒前
贺小刚发布了新的文献求助10
13秒前
cong发布了新的文献求助10
13秒前
CodeCraft应助sdnihbhew采纳,获得10
13秒前
sn完成签到,获得积分10
14秒前
dildil完成签到,获得积分10
14秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
CRC Handbook of Chemistry and Physics 104th edition 1000
Izeltabart tapatansine - AdisInsight 600
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 500
An International System for Human Cytogenomic Nomenclature (2024) 500
Introduction to Comparative Public Administration Administrative Systems and Reforms in Europe, Third Edition 3rd edition 500
Distinct Aggregation Behaviors and Rheological Responses of Two Terminally Functionalized Polyisoprenes with Different Quadruple Hydrogen Bonding Motifs 450
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3767565
求助须知:如何正确求助?哪些是违规求助? 3312194
关于积分的说明 10162593
捐赠科研通 3027488
什么是DOI,文献DOI怎么找? 1661538
邀请新用户注册赠送积分活动 794088
科研通“疑难数据库(出版商)”最低求助积分说明 755998