Biomedical Engineering Reference
In-Depth Information
Table 1
(continued)
2. cyanuric chloride (trichloro-s-triazine)
3. diisocyanate
4. cyanogen bromide [CNBr]
5. azlactone
6. dialdehyde
7. glycidol-modification and periodate-activation (aldehyde generation)
are demonstrated in Table 1B with the specific reagents of divinylsulfone,
cyanuric chloride (trichloro-s-triazine), diisocyanate, cyanogen bromide
[CNBr], azlactone, dialdehyde, glycidol (epoxy)-modification-and-periodate-
activation, and epoxy resin, etc. Typical examples of combined strategies are
indicated in Table 1C [113-124]. Some coupling reagents are radio-(photo-)
reactive. Typical radio-reactive cross-linkers include photo-sensitive azo,
benzophenone, and (meth)acrylate, etc. [121-123].
