Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Design, Synthesis, and Characterization of a Paclitaxel Formulation Activated by Extracellular MMP9
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4605309
Author(s) Ehrsam, Daniel; Sieber, Sandro; Oufir, Mouhssin; Porta, Fabiola; Hamburger, Matthias; Huwyler, Jörg; Meyer zu Schwabedissen, Henriette E.
Author(s) at UniBasel Porta, Fabiola
Meyer zu Schwabedissen, Henriette
Ehrsam, Daniel
Hamburger, Matthias
Huwyler, Jörg
Sieber, Sandro
Oufir, Mouhssin
Year 2020
Title Design, Synthesis, and Characterization of a Paclitaxel Formulation Activated by Extracellular MMP9
Journal Bioconjugate Chemistry
Volume 31
Number 3
Pages / Article-Number 781-793
Abstract The concept of triggered drug release offers a possibility to overcome the toxic side effects of chemotherapeutics in cancer treatment by reducing systemic exposure to the active drug. In the present work, the concept foresees the use of the extracellular enzyme MMP9 as an enzymatic trigger for drug release in the proximity of tumor cells.; A paclitaxel-hemisuccinate-peptide conjugate as a building block for self-assembling nanoparticles was synthesized using standard conjugation approaches. The building block was purified via preparative HPLC and analyzed by LC-MS. Nanoparticles were formed using the nanoprecipitation method and characterized. For selection of a suitable in vitro model system, common bioanalytical methods were used to determine mRNA expression, enzyme amount, and activity of MMP9.; The MMP9-labile prodrug was synthesized and characterized. Nanoparticles were formed out of MMP9-labile conjugate-building blocks. The nanoparticle's diameter averaged at around 120 nm and presented a spherical shape. LN-18 cells, a glioblastoma multiforme derived cell line, were chosen as an in vitro model based on findings in cancer tissue and cell line characterization. The prodrug showed cytotoxicity in LN-18 cells, which was reduced by addition of an MMP9 inhibitor.; taken together, we confirmed increased MMP9 in several cancer tissues (cervical, esophageal, lung, and brain) compared to healthy tissue and showed the effectiveness of MMP9-labile prodrug in in vitro tests.
Publisher American Chemical Society
ISSN/ISBN 1043-1802 ; 1520-4812
edoc-URL https://edoc.unibas.ch/78964/
Full Text on edoc No
Digital Object Identifier DOI 10.1021/acs.bioconjchem.9b00865
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/31894970
ISI-Number WOS:000526399100038
Document type (ISI) Journal Article
 
   

MCSS v5.8 PRO. 0.429 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
23/02/2024