Journalartikel

Synthesis of beta-cyclodextrin dimers as carrier systems for photodynamic therapy of cancer


AutorenlisteRuebner, A; Moser, JG; Kirsch, D; Spengler, B; Andrees, S; Roehrs, S

Jahr der Veröffentlichung1996

Seiten35-38

ZeitschriftJournal of Inclusion Phenomena and Macrocyclic Chemistry

Bandnummer25

Heftnummer1-3

ISSN0923-0750

DOI Linkhttps://doi.org/10.1007/BF01041531

VerlagSpringer


Abstract
The aim of our investigation was the development of carrier systems for an application of inert drugs in polyphasic photodynamic tumor therapy. As carrier systems, beta-cyclodextrin dimers linked at their primary and secondary faces by spacers of varying lengths were synthesized. Cyclodextrins are known to form stable inclusion complexes with porphyrinoid photosensitizers. The influence of spacer length on the P-cyclodextrin dimer inclusion complexes with porphyrinoid photosensitizers was studied.



Zitierstile

Harvard-ZitierstilRuebner, A., Moser, J., Kirsch, D., Spengler, B., Andrees, S. and Roehrs, S. (1996) Synthesis of beta-cyclodextrin dimers as carrier systems for photodynamic therapy of cancer, Journal of Inclusion Phenomena and Macrocyclic Chemistry, 25(1-3), pp. 35-38. https://doi.org/10.1007/BF01041531

APA-ZitierstilRuebner, A., Moser, J., Kirsch, D., Spengler, B., Andrees, S., & Roehrs, S. (1996). Synthesis of beta-cyclodextrin dimers as carrier systems for photodynamic therapy of cancer. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 25(1-3), 35-38. https://doi.org/10.1007/BF01041531


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