Affiliation:
1. Skolkovo Institute of Science and Technology
2. G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences
3. Institute of Biological Instrumentation, Russian Academy of Sciences
Abstract
Lignin polymers and their derivatives are actively used in various fields of biomedicine to create biocompatible materials, as medications, and to form nanoparticles. However, natural polymeric compounds derived from plant materials or monomers are defined as a mixture of compounds having a high heterogeneity in chemical structure, which greatly complicates the determination of their biological activity. This paper describes a new method of controlled synthesis using the enzyme laccase, which can be applied to obtain polymers with a specific structure. Based on enzymatically synthesized lignin-like polymers from ferulic and gentisiс phenolic monomers, nanoparticles with stable properties under physiological conditions were formed. The nanoparticles can differ in morphology from globular to fibrillar structures, depending on monomers used in the enzymatic reaction and the method of their formation. Nanoparticles obtained from lignin-like polymers of ferulic and gentisic acids can be loaded with low molecular weight hydrophobic compounds, including the anticancer drug doxorubicin. It has been shown that polyferulic nanoparticles are actively penetrate in tumor cells growing both in a monolayer culture and as part of spheroids, and, compared with a free compound, doxorubicin in the composition of nanoparticles has a greater cytotoxic effect on breast cancer cells. These data indicate the possibility of effective use of these carriers as passive targeted drug delivery in the treatment of tumors.
Publisher
The Russian Academy of Sciences
Reference24 articles.
1. Brigger I., Dubernet C., Couvreur P. // Adv. Drug Deliv. Rev. 2002. V. 54. P. 631–651. https://doi.org/10.1016/s0169-409x(02)00044-3
2. Bozzuto G., Molinari A. // Int. J. Nanomed. 2002. V. 10. P. 975–999.
3. Sharma A., Goyal A.K., Rath G. // J. Drug Target. 2017. V. 15. P. 1–16. https://doi.org/ 10.1080/1061186X.2017.1400553
4. Cho C.F., Shukla S., Simpson E.J., Steinmetz N.F., Luyt L.G., Lewis J.D. // Methods Mol. Biol. 2014. V. 1108. P. 211–230. https://doi.org/10.1007/978-1-62703-751-8_16
5. Lomis N., Westfall S., Farahdel L., Malhotra M., Shum-Tim D., Prakash S. // Nanomaterials (Basel). 2016. V. 6. P. 116. https://doi.org/10.3390/nano6060116