{"title":"Conditions for a microfluidic creep experiment for microparticles using a cross-slot extensional flow device.","authors":"Sara Ghanbarpour Mamaghani, Joanna B Dahl","doi":"10.1063/5.0239475","DOIUrl":null,"url":null,"abstract":"<p><p>The micromechanical measurement field has struggled to establish repeatable techniques because the deforming stresses can be difficult to model. A recent numerical study [Lu <i>et al.</i>, J. Fluid Mech. <b>962</b>, A26 (2023)] showed that viscoelastic capsules flowing through a cross-slot can achieve a quasi-steady strain near the extensional flow stagnation point that is equal to the equilibrium static strain, thereby implying that the capsule's elastic behavior can be captured in continuous device operation. However, no experimental microfluidic cross-slot studies have reported quasi-steady strains for suspended cells or particles to our knowledge. Here, we demonstrate experimentally the conditions necessary for the cross-slot microfluidic device to replicate a uniaxial creep test at the microscale and at relatively high throughput. By using large dimension cross-slots relative to the microparticle diameter, our cross-slot implementation creates an extensional flow region that is large enough for agarose hydrogel microparticles to achieve a strain plateau while dwelling near the stagnation point. This strain plateau will be key for accurately and precisely measuring viscoelastic properties of small microscale biological objects. We propose an analytical mechanical model to extract linear viscoelastic mechanical properties from observed particle strain histories. Particle image velocimetry measurements of the unperturbed velocity field is used to estimate where in the device particles experienced extensional flow and where the mechanical model might be applied to extract mechanical property measurements. Finally, we provide recommendations for applying the cross-slot microscale creep experiment to other biomaterials and criteria to identify particles that likely achieved a quasi-steady strain state.</p>","PeriodicalId":8855,"journal":{"name":"Biomicrofluidics","volume":"19 2","pages":"024102"},"PeriodicalIF":2.6000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11888784/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomicrofluidics","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1063/5.0239475","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The micromechanical measurement field has struggled to establish repeatable techniques because the deforming stresses can be difficult to model. A recent numerical study [Lu et al., J. Fluid Mech. 962, A26 (2023)] showed that viscoelastic capsules flowing through a cross-slot can achieve a quasi-steady strain near the extensional flow stagnation point that is equal to the equilibrium static strain, thereby implying that the capsule's elastic behavior can be captured in continuous device operation. However, no experimental microfluidic cross-slot studies have reported quasi-steady strains for suspended cells or particles to our knowledge. Here, we demonstrate experimentally the conditions necessary for the cross-slot microfluidic device to replicate a uniaxial creep test at the microscale and at relatively high throughput. By using large dimension cross-slots relative to the microparticle diameter, our cross-slot implementation creates an extensional flow region that is large enough for agarose hydrogel microparticles to achieve a strain plateau while dwelling near the stagnation point. This strain plateau will be key for accurately and precisely measuring viscoelastic properties of small microscale biological objects. We propose an analytical mechanical model to extract linear viscoelastic mechanical properties from observed particle strain histories. Particle image velocimetry measurements of the unperturbed velocity field is used to estimate where in the device particles experienced extensional flow and where the mechanical model might be applied to extract mechanical property measurements. Finally, we provide recommendations for applying the cross-slot microscale creep experiment to other biomaterials and criteria to identify particles that likely achieved a quasi-steady strain state.
微机械测量领域一直在努力建立可重复的技术,因为变形应力很难建模。最近的一项数值研究[Lu et al., J. Fluid Mech. 962, A26(2023)]表明,粘弹性胶囊在穿过交叉槽时,在拉伸流动滞止点附近可以获得准稳态应变,该应变等于平衡静态应变,这意味着在装置连续运行时,胶囊的弹性行为可以被捕获。然而,据我们所知,没有实验微流体交叉槽研究报道悬浮细胞或颗粒的准稳定菌株。在这里,我们通过实验证明了交叉槽微流体装置在微尺度和相对高通量下复制单轴蠕变试验所需的条件。通过使用相对于微粒直径的大尺寸交叉槽,我们的交叉槽实现创建了一个足够大的拉伸流动区域,使琼脂糖水凝胶微粒在停留在停滞点附近时达到应变平台。该应变平台将是精确测量微小生物物体粘弹性特性的关键。我们提出了一个解析力学模型,从观察到的颗粒应变历史中提取线性粘弹性力学特性。无扰动速度场的粒子图像测速测量用于估计装置中粒子经历拉伸流动的位置,以及可以应用力学模型提取力学性能测量的位置。最后,我们提出了将交叉槽微尺度蠕变实验应用于其他生物材料和标准的建议,以识别可能达到准稳态应变状态的颗粒。
期刊介绍:
Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications.
BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics.
Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary)
Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification)
Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation)
Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles)
Cell culture and analysis(single cell assays, stimuli response, stem cell transfection)
Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays)
Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers)
Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...