Body
fluids flow all over the body and affect the biological processes
at biointerfaces. To simulate such a case, sum frequency generation
(SFG) vibrational spectroscopy and a self-designed microfluidic chip
were combined together to investigate the interaction between a pH-responsive
polymeric drug, poly(α-propylacrylic acid) (PPAAc), and the
model cell membranes in different liquid environments. By examining
the SFG spectra under the static and flowing conditions, the drug–membrane
interaction was revealed comprehensively. The interfacial water layer
was screened as the key factor affecting the drug–membrane
interaction. The interfacial water layer can prevent the side propyl
groups on PPAAc from inserting into the model cell membrane but would
be disrupted by numerous ions in buffer solutions. Without flowing,
at pH 6.6, the interaction between PPAAc and the model cell membrane
was strongest; with flowing, at pH 5.8, the interaction was strongest.
Flowing was proven to substantially affect the interaction between
PPAAc and the model cell membranes, suggesting that the fluid environment
was of key significance for biointerfaces. This work demonstrated
that, by combining SFG and microfluidics, new information about the
molecular-level interaction between macromolecules and the model cell
membranes can be acquired, which cannot be obtained by collecting
the normal static SFG spectra.