Titlebook: Dermatological Phototherapy and Photodiagnostic Methods; Jean Krutmann,Helmut H?nigsmann,Paul R. Bergstress Book 20011st edition Springer-

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https://doi.org/10.1007/978-3-662-43037-8 related donors is increasingly used to cure otherwise lethal hematological malignancies, hematological and immunological disorders, and certain errors of metabolism [1, 2]. Although remarkable progress has been achieved in the past 25 years [3, 4] based on improved supportive-care techniques, molec

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https://doi.org/10.1007/978-3-658-28247-9 individual. The drugs alone are inactive, but once activated by high-intensity light usually from a laser, they are exceptionally effective at inhibiting the growth of hyperproliferative tissues. PDT was originally designed for the treatment of malignancies because of the unique property of several

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https://doi.org/10.37307/b.978-3-503-23676-3.e., UVA-1 (340–400 nm) [35]. The combination of a metal halide lamp with a novel filtering system offered, for the first time, the unique possibility to expose human skin to high doses of UVA-1 radiation without causing a sunburn reaction. Soon thereafter, UVA-1 irradiation devices proved to be use

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https://doi.org/10.1007/978-3-662-64523-9 and physical UV-blocking agents . The molecules of chemical substances (Fig. 1) such as aminobenzoates, cinnamates, salicylates, benzophenones, and camphor derivatives can absorb (Fig. 2a) quanta of UV radiation energy (i.e., photons) due to their molecular structure and, therefore, are promoted

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