Growth Effects of Caffeic Acid and Thioglycolic Acid Modified Chitosans in U937 Cells
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 33122
Growth Effects of Caffeic Acid and Thioglycolic Acid Modified Chitosans in U937 Cells

Authors: Aytekin A.O., Morimura S.

Abstract:

Chitosan is a biopolymer composed of glucosamine and N-acetyl glucosamine. Solubility and viscosity pose problems in some applications. These problems can be overcome with unique modifications. In this study, firstly, chitosan was modified by caffeic acid and thioglycolic acid, separately. Then, growing effects of these modified polymers was observed in U937 cell line. Caffeic acid is a phenolic compound and its modifications act carcinogenic inhibitors in drugs. Thiolated chitosans are commonly being used for drugdelivery systems in various routes, because of enhancing mucoadhesiveness property. U937 cell line was used model cell for leukaemia. Modifications were achieved by 1 – 15 % binding range. Increasing binding ratios showed higher radical-scavenging activity and reducing cell growth, in compared to native chitosan. Caffeic acid modifications showed higher radical-scavenging activity than thiolated chitosans at the same concentrations. Caffeic acid and thioglycolic acid modifications inhibited growth of U937, effectively.

Keywords: Chitosan, U937 cell, caffeic acid, thioglycolic acid

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1054745

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 1874

References:


[1] Kumar, M., Muzzarelli, R., Muzzarelli, C., Sashiwa, H., Domb, A., (2004). Chitosan chemistry and pharmaceutical perspectives. Chem. Rev 104, 6017-6084.
[2] Shahidi, F., Arachchi, J., Jeon, Y., (1999). Food applications of chitin and chitosans. Trends in food science & Technology 10, 37-51.
[3] Kafedjiiski, K., Krauland, A., Hoffer, M., Bernkop-Schn├╝rch, A., (2005). Synthesis and in vitro evaluation of a novel thiolated chitosan. Biomaterials 26, 819-826.
[4] Rice-Evans, C., Miller, N., Paganga, G., (1997). Antioxidant properties of phenolic compounds. Trends in plant science 2, 152-159.
[5] Rajan, P., Vedernikova, I., Cos, P., Vanden Berghe, D., Augustyns, K., Haemers, A., (2001). Synthesis and evaluation of caffeic acid amides as antioxidants. Bioorganic & Medicinal Chemistry Letters 11, 215-217.
[6] Kumar, G., Bristow, J., Smith, P., Payne, G., (2000). Enzymatic gelation of the natural polymer chitosan. Polymer 41, 2157-2168.
[7] Harris, P., Ralph, P., (1985). Human leukemic models of myelomonocytic development: a review of the HL-60 and U937 cell lines. Journal of leukocyte biology 37, 407.
[8] Rusjan, D., Korosec-Koruza, Z., (2007). A comparison of extraction methods for selected phenolic compounds from grape berry skins using liquid chromatography and spectrophotometry. Acta chimica slovenica 54, 114.
[9] Lee, D., Zhang, W., Shirley, S.A., Kong, X., Hellermann, G.R., Lockey, R.F., Mohapatra, S.S., (2007). Thiolated chitosan/DNA nanocomplexes exhibit enhanced and sustained gene delivery. Pharm Res 24, 157-167.
[10] Mao, S., Shuai, X., Unger, F., Simon, M., Bi, D., Kissel, T., (2004). The depolymerization of chitosan: effects on physicochemical and biological properties. International journal of pharmaceutics 281, 45-54.
[11] Shimada, K., Fujikawa, K., Yahara, K., Nakamura, T., (1992). Antioxidative properties of xanthan on the autoxidation of soybean oil in cyclodextrin emulsion. Journal of Agricultural and Food Chemistry 40, 945-948.
[12] Inagaki, S., Morimura, S., Gondo, K., Tang, Y., Akutagawa, H., Kida, K., (2007). Isolation of Tryptophol as an Apoptosis-Inducing Component of Vinegar Produced from Boiled Extract of Black Soybean in Human.