Supporting informations Microfluidic with integrated microfilter of conical-shaped holes for high efficiency and high purity capture of circulating tumor cells Yadong Tang 1+, Jian Shi 2+, Sisi Li 1, Li Wang 3, Yvon E.Cayre 2,4 and Yong Chen 1,5,6 * 1 Ecole Normale Supérieure-PSL Research University, Département de Chimie, Sorbonne Universités - UPMC Univ Paris 06, CNRS UMR 8640 PASTEUR, 24, rue Lhomond, 75005 Paris, France 2 BiocareCell, 249, rue Saint-Denis, 75002 Paris, France 3 Curie Institute, 12 rue Lhomond, 75005 Paris, France 4 Sorbonne Universités - UPMC Univ Paris 06, 4 place Jussieu 75005 Paris, France 5 Institute for Integrated Cell-Material Science, Kyoto University, Kyoto 606-8507, Japan 6 Institute for Interdisciplinary Research, Jianghan University, 430056 Wuhan, China +Authors contributed equally to this work *Corresponding author: E-mail:yong.chen@ens.fr 1
Supplementary Methods Fabrication of PEGDA microfilters The fabrication procedure of PEGDA microfilter is shown in Supplementary Fig.S1. Briefly, chromium mask of holes arrays of 5.5, 6.5, 8.0 μm diameter and 30 µm period was produced by micro pattern generator (μpg 101, Heidelberg Instruments). 30 µm AZ40XT resist layer was spin-coated on the mask and backside exposed with UV light at an incident angle of 20 (for a final of half conical angle of 13 ) and a rotation speed of 3 rpm. After development, conical holes of bottom and top diameters of 5.5, 6.5, 8.0μm and 19.4, 20.4, 21.9 μm were obtained, followed by evaporation of TMCS for anti-sticking surface treatment. A PDMS solution was prepared using GE RTV 615 PDMS components A and B at a ratio of 10:1 and then poured on the top of the resist master. After curing at 80 C for 2 h, the PDMS layer was peeled off and placed on a glass slide. Then, the PDMS-glass assembly was placed in a desiccator for degasing during 15 min. Meanwhile, a PEGDA solution mixed with 1v/v%2-hydroxy-2-methylpropiophenone as photo-initiator was prepared and used to fill the PDMS-glass cavity by degasing induced micro-aspiration, followed by UV exposure at 9.1mW/cm 2 for 30s. Finally, the solidified PEGDA filter was peeled off, resulting in a microfilter with conical holes and a porosity of 3.6%. To increase the mechanical strength, 100 µm thick PEGDA rings of 13 mm outer diameter and 6 or 9 mm inner diameter were prepared in a similar manner. Briefly, a 100 µm thick SU8-3050 resist was exposed with a Cr mask defining the ring geometry. After development and trimethylchlorosilane (TMCS) evaporation, the PDMS mold was produced by soft lithography and placed on a glass slide. Then, the PEGDA solution was injected into the mold and solidified by UV exposure. Finally, the ring was mounted on the filter, using pre-cured PEGDA solution as 2
binder for UV curing. For comparison, filters of cylindrical holes were obtained using UV lithography at normal incident angle without rotation. Integration of PEGDA filter into microfluidic devices The layouts of the upper and bottom PDMS layers are shown in Supplementary Fig.S2. Here the upper PDMS was produced by soft lithography with a mold fabricated by a CNC milling system. First, a two level pattern was produced on a PMMA plate. The first level is a cavity of 13 mm diameter and 130 µm in depth, designed for embedment of PEGDA filter. The second level includes a 6 mm or 9 mm chamber, 8 radial channels of 400 µm width, the inlet, the outlet and the ring channels of 1 mm width, all having a depth of 400 µm. After machining, the mold was ultrasonic washed with isopropanol. Then, the pattern was replicated twice into PDMS by soft lithography and both inlet and outlet holes were punched, resulting in the desired upper layer. The bottom was fabricated by standard soft lithography with a mold fabricated by UV lithography. First, a chromium mask was produced and then replicated into a 100 µm thick photoresist (SU8-3050, Micro resist). After development and evaporation of TMCS, PDMS was poured on the SU8 mold with a thickness of ~ 1 mm and cured at 80 C for 1 h. After peeling off, the main chamber of diameter of 6 mm or 9 mm was punched. The surfaces of upper and bottom PDMS layers were treated by plasma shortly and the PEGDA filter was sandwiched between the two PDMS layer, following by a thermal bonding at 80 C for 30 min. Finally, the inlet and outlet of the bottom later were punched and the PDMS-PEGDA assembly was irreversibly bonded to a glass slide after plasma treatment of the PDMS later. 3
Hydrodynamic simulation Numerical simulation has been performed with commercial software (COMSOL Multiphysics). For simplicity, cylindrical- and conical-holes were replaced by a linear array of rectangular or trapezoidal slits, respectively, keeping the other geometrical parameters as the same of two-dimensional filters (6.5 µm entrance size, 30 µm thickness, and 30 µm pitch size). The results were obtained with a transfilter pressure of 100 Pa and water viscosity of without cells. Figure S7 shows the flow velocity over the interesting area, indicating a higher flow rate across the conical holes than across the cylindrical ones. Streamlines are also shown, illustrating a flow focusing effect, i.e., no flow goes to the areas at equidistance of neighboring holes. Definition of capture efficiency, WBC clearance efficiency and cell viability The capture efficiency of the device for the targeting tumor cells was defined as the ratio of tumor cells found on the filter,, to the initial tumor cells injected into the device,, (S1) The leukocyte clearance efficiency of the filter was defined as the ratio of the number of unclogged holes,, and the number of total holes of the filter,, per milliliter blood sample (S2) where is the number WBCs found on the filter. The cell viability of the tumor cells captured by the filter was defined as the ratio of live tumor cells,, and dead tumor cells, both being found on the filter 4
(S3) 5
Supplementary Figure S1. Fabrication procedure of conical-hole filters. (a) Fabrication of PDMS mold with conical pillars; (b) Replication of PDMA pattern into PEGDA thin membrane, the same replication process is used for the fabrication of PEGDA ring; (c) UV assisted bonding of PEGDA membrane and ring. Supplementary Figure S2. Layout for the fabrication of upper (a) and bottom (b) PDMS layers. The filter is sandwiched between the PDMS layers and the sample is loaded from inlet 1 and collected from outlet 2, passing through the radical channels for cross-flow injection and then the filter for tumor cell capture. Supplementary Figure S3. PEGDA filter with conical-hole array. (a, b) Bottom and top view of SEM images of conical-hole array, respectively; (c) Top view SEM image of a single conical hole. Scale bar: (a, b) 100 µm (c) 5 µm. Supplementary Figure S4. Fluorescence images of WBCs isolated from a healthy donor on the filter. (a) Fluorescence of nuclei staining with DAPI (blue). (b, c) Fluorescence after staining with anti-ck-alexafluor 488 (green) and anti-cd45-pe (red), respectively. (d) Merge image of (a-c). Scale bar: (a-d) 30 µm. Supplementary Figure S5. Fluorescence images of WBCs on the filter. Blood samples of a healthy person were diluted in PBS at 1:1 (v/v%). After filtration and anti-cd45 staining, 6
fluorescence images were taken, showing a much reduced WBC retention by conical holes (a) than cylindrical ones (b). Scale bar: 100 μm. Supplementary Figure S6. SEM image of tumor cells on the filter. HT-29 cells were spiked in PBS at a 10 4 cells/ml concentration. After filtration, cells were fixed by dehydration and coated by 2nm thick gold. Scale bar: 100µm. Supplementary Figure S7. Hydrodynamic simulation of flow focusing. The same transfilter pressure (100 Pa) were applied, showing both flow focusing but a higher flow rate through trapezoidal slits than through rectangular ones. 7
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