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. Author manuscript; available in PMC: 2021 Jan 22.
Published in final edited form as: Mol Pharm. 2019 Apr 29;16(6):2494–2501. doi: 10.1021/acs.molpharmaceut.9b00086

Figure 2.

Figure 2

Liposomes at different positions in the microfluidic chip. A: Liposome assembly at the 6 way formation junction. A 1-octanol pocket is initially attached to the liposomes. The liposome and the octanol pocket separate further downstream in the post-junction channel. B: The liposomes experience a spontaneous exposure to a drug solute at a T-junction where the two flows mix in a controlled manner. C: The liposomes, surrounded by the autofluorescing drug (λex = 350 nm), can be monitored at different parts of the channel, corresponding to different times that the liposome has been exposed to the drug. The increase in liposome intensity as the fluorescing drug diffuses across the membrane is used to determine the permeability coefficient of the drug across the lipid membrane under investigation.