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Biomedical Engineering – From Theory to Applications

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<strong>Biomedical</strong> <strong>Engineering</strong> <strong>–</strong> <strong>From</strong> <strong>Theory</strong> <strong>to</strong> <strong>Applications</strong><br />

Fig. 6. General frame of the porphyrin type structures involved in biomedical studies<br />

Porphyrinoid pho<strong>to</strong>sensitizers are classified as belonging <strong>to</strong> the first, second or third<br />

generation of pho<strong>to</strong>sensitizers as shown in Figure 6, or depending on the platform <strong>to</strong> which<br />

they belong (porphyrin, chlorophyll, dyes) (Allison R.R. et al., 2004). They could also be<br />

classified according <strong>to</strong> their primary mechanism of action and/or according <strong>to</strong> their use<br />

(type of cancer, pho<strong>to</strong>diagnosis or therapy).<br />

The first generation of pho<strong>to</strong>sensitizers consists only of hema<strong>to</strong>porphyrin derivatives and<br />

was developed during the 70’s. Pho<strong>to</strong>sensitizers belonging <strong>to</strong> the second generation are<br />

porphyrin derivatives or synthetics made from the late ‘80s on. Second generation 10<br />

pho<strong>to</strong>sensitizers are improved compared <strong>to</strong> the first generation: they have a definite<br />

structure (which means they are no more a combination of monomers, dimers and<br />

oligomers), absorb light at longer wavelengths and cause less skin pho<strong>to</strong>sensitization.<br />

Third generation pho<strong>to</strong>sensitizers use available drugs and then modify them with different<br />

carriers in order <strong>to</strong> obtain tailored characteristics.<br />

Examples of clinically available porphyrin sensitizers are presented in Table 2.

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