Laser-induced drug release for local tumor control--a proof of concept.

Abstract

BACKGROUND:

The systemic palliative chemotherapy of locally extended gastrointestinal and hepatobiliary tumors is associated with a considerable burden for the patient. The aim of this project was to develop a new drug release system to improve the local stent therapy in these patients as a proof of concept study. For this purpose, polymer filaments were modified with drug-loaded polymer microgels that allow selective release of the active substance by photochemical triggering using laser radiation. Integrated into a stent system, the better local tumor control could thus contribute to a significant increase in the quality of life of patients.

METHODS:

A standard mammalian cell line and two carcinoma cell lines were established. By Fluorescence activated cell sorting (FACS), the cytotoxicity of the different materials was determined in vitro before and after drug loading with the chemotherapeutic agent 5-Fluorouracil (5-FU). For this purpose, the locally applied 5-FU concentration was previously determined by Bromdesoxyuridin assay. 5-FU dimer was synthesized by photo-induced dimerization of 5-FU in the presence of benzophenone in methanol. The chemical structure of 5-FU dimer was confirmed with Hydrogen-1 nuclear magnetic resonance and Fluorine-19 nuclear magnetic resonance. 5-FU dimer is nonsoluble in water and can be easily incorporated in polymer microgels modified with hydrophobic binding domains (cyclodextrin). After laser irradiation, 5-FU dimer decomposes and 5-FU can be released from microgels. Finally, the measurements were repeated after this laser-induced drug release.

RESULTS:

In FACS analysis, neither the microgels nor the microgel cumarin complexes showed a significant difference in comparison with the negative control with H2O and therefore no toxic effect on the cell lines. After loading with the 5-FU dimer, there was no significant cell death (contrary to the pure 5-FU monomer, which dose had been previously tested as highly toxic). After laser-induced dissociation back to monomer and the associated drug release, FACS analysis showed cytotoxicity.

CONCLUSIONS:

It was possible to develop 5-FU dimerloaded microgels, which show no cytotoxic effect on cell lines before laser irradiation. After dissociation back to 5-FU monomer by selective photochemical triggering using laser irradiation, the active substance was released. Thus, a new drug release system has been created and tested in vitro. For further development, integration into a stent system and for in vivo follow-up evaluation more studies need to be conducted.

• Authors: Andreas Lambertz, Christian D Klink, Anjali Röth, Dominik Schmitz, Andrij Pich, Katalin Feher, Elke Bremus-Köbberling, Ulf P Neumann, Karsten Junge
• Journal: The Journal of surgical research (J Surg Res) Vol. 192 Issue 2 Pg. 312-6 (Dec 2014) ISSN: 1095-8673 [Electronic] United States
• PMID: 25145903 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2014 Elsevier Inc. All rights reserved.

Chemical References

• Antimetabolites, Antineoplastic
• beta-Cyclodextrins
• Bromodeoxyuridine
• betadex
• Fluorouracil

Topics

• Adenocarcinoma (pathology)
• Animals
• Antimetabolites, Antineoplastic (chemistry, pharmacokinetics)
• Bromodeoxyuridine (metabolism)
• Cell Line, Tumor
• Dimerization
• Drug Delivery Systems (methods)
• Fibroblasts (cytology, metabolism)
• Flow Cytometry
• Fluorouracil (chemistry, pharmacokinetics)
• Hydrophobic and Hydrophilic Interactions
• Lasers
• Palliative Care (methods)
• Pancreatic Neoplasms (pathology)
• Solubility
• Stents
• beta-Cyclodextrins (pharmacokinetics)