Journal article
Authors list: Ruebner, A; Moser, JG; Kirsch, D; Spengler, B; Andrees, S; Roehrs, S
Publication year: 1996
Pages: 35-38
Journal: Journal of Inclusion Phenomena and Macrocyclic Chemistry
Volume number: 25
Issue number: 1-3
ISSN: 0923-0750
DOI Link: https://doi.org/10.1007/BF01041531
Publisher: Springer
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.
Citation Styles
Harvard Citation style: Ruebner, 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 Citation style: Ruebner, 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