CD BioGlyco provides high-quality and custom production services for luzonicosides, which are cyclic steroid glycosides derived from the starfish Echinaster luzonicus. Luzonicoside A and D exhibit strong anticancer properties, effectively inhibiting the proliferation, colony formation, and migration of human melanoma cells. The production process at CD BioGlyco includes the meticulous extraction of glycosides from the starfish, followed by advanced fractionation and purification techniques using chromatography. To ensure the highest quality, these compounds' structural characterization and quality control are carried out with nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and bioassays, guaranteeing their purity and bioactivity. This comprehensive approach highlights CD BioGlyco's commitment to delivering High-quality Marine Glycosides for research applications.
Fig.1 Structures of luzonicoside A (LuzA) (1) and luzonicoside D (LuzD) (2) isolated from the starfish E. luzonicus. (Malyarenko, et al., 2017)
Our detailed workflow ensures we deliver high-quality luzonicosides, particularly in the development of anticancer treatments. The use of advanced extraction, purification, and characterization techniques underscores the company's commitment to excellence in marine-derived bioactive compounds. Moreover, we also offer comprehensive Marine Biomolecule Production solutions for clients worldwide.
The process begins with the collection of the starfish E. luzonicus from their natural habitats. The collected starfish are cleaned and their tissues are prepared for extraction by homogenizing them into a uniform mixture.
The homogenized starfish tissues are extracted using a suitable solvent system, typically involving organic solvents like methanol or ethanol.
The concentrated fractions undergo purification through advanced chromatographic techniques.
High-performance liquid chromatography (HPLC) is used to assess the purity of the isolated luzonicosides.
DOI: 10.3390/md15070227
Technology: Cytotoxicity assays, Cell proliferation assays, Cell cycle analysis
Journal: Marine Drugs
IF: 4.9
Published: 2017
Results: The study highlights the potent anticancer activity of luzonicosides A and D. These compounds significantly inhibit the proliferation, colony formation, and migration of human melanoma cells, specifically in the RPMI-7951 and SK-Mel-28 cell lines. Luzonicoside A demonstrated greater efficacy compared to luzonicoside D. The research further elucidated the molecular mechanisms underlying these effects, involving the regulation of cell cycle arrest and apoptosis. Key molecular targets include cleaved caspase-3, PARP, Survivin, Bcl-2, p21, and Cyclin D1, indicating a comprehensive modulation of cell death pathways and cell cycle control.
Can CD BioGlyco customize luzonicoside production to specific research needs?
Yes, CD BioGlyco offers customized production services tailored to the specific needs of researchers and developers, including different purity levels, quantities, and additional analytical services.
What quality control measures are in place for luzonicoside production?
Quality control includes rigorous testing for purity using HPLC, structural verification with NMR and MS, and bioactivity assays to ensure the Luzonicosides meet high standards for research and therapeutic use.
At CD BioGlyco, our luzonicoside production service provides valuable tools for advancing cancer research, leveraging cutting-edge technology and scientific expertise to deliver top-quality marine glycosides. Please do not hesitate to
for more details about our service and feel free to get in touch for your solution.References