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hi,
i am working in the area of enhanced drug delivery thru' BBB using
insulin fragments as delivery enhancers. my problem is how to characterize
the insulin-drug conjugate, other than chemical characterization. i am
specifically interested in physical methods like XRD and DSC etc.
kindly suggest other possible modes to define the prepared conjugate,
including literature .
thanx
pankaj
Pankaj V. Paranjpe
131 Biomedical Education Bldg. 121 Heath Street
School of Medicine and Biomedical Sciences Buffalo, NY 14214
State University of New York at Buffalo Ph: (716) 838 8482
Buffalo, NY 14214
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Pankaj:
XRD and DSC are normally very useful solid phase techniques for
interaction studies (although I have my doubts about DSC measurements on
peptides, due to their thermal instability). Suggest you also consider
isothermal reaction calorimetry (either batch mode or flow; solution
interactions) infra-red spectroscopy (solid and solution interactions)
and NMR nuclear Overhauser effect enhancement (solution interactions).
Depending on the size of the fragments and availability of material, you
may see some effects from careful viscosity measurements. Other
possibilities include circular dichroism or optical rotatory dispersion,
dielectric spectroscopy and ligand concentration dependent shifts of UV
absorption or fluorescence bands.
regards
Richard
PharmPC Discussion List Archive Index page
David Bourne (david@boomer.org)