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. Author manuscript; available in PMC: 2016 Feb 26.
Published in final edited form as: Fertil Steril. 2014 Nov 20;103(1):281–90.e5. doi: 10.1016/j.fertnstert.2014.09.039

Figure 1. Hydrodynamic trap array images and trapping schemes.

Figure 1

(A) Images of the 8-trap hydrodynamic array: Oocytes flow in and load into the wells from right to left which is the direction of fluid flow. (B) Macroscale view of hydrodynamic trap arrays: Displays two parallel arrays bonded to a standard size microscope slide coverslip. (C) An individual trap: Consists of a trapping channel (red) and a bypass channel (blue). The resistances of each segment dictate the trapping behavior of the device. The trapping region consists of a circular trap (320 μm in diameter) and a high resistance channel (40 μm width) which connects to the ends of the bypass segment. (D) Immature sea star oocytes within the chip: Oocytes load into the chip from right to left for the six traps displayed. The nucleus and nucleolus are visible in each oocyte which is ~200 μm. Double trapping can occur with smaller oocytes, as seen in trap five. Scale bars are 200 μm. (E) Indirect trapping: Occurs when the trap resistance is greater than the bypass channel resistance (Rt/Rb=1.56) causing the first oocyte to be directed into the bypass channel. (F) Direct trapping: Occurs when the trap resistance is lower than the bypass resistance (Rt/Rb=0.8), directing the first oocyte into the trap. Subsequent oocytes can be directed into the trap causing double trapping, or directed into the bypass channel depending on the change in resistance due to the trapped oocytes for either regime.