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1.
J Biomed Mater Res A ; 105(2): 547-556, 2017 02.
Article in English | MEDLINE | ID: mdl-27750379

ABSTRACT

Today, there is a need for the development of biomaterials with novel properties for biomedical purposes. The biocompatibility of materials is a key factor in determining its possible use in biomedicine. In this study, composite cryogels were obtained based on pectin and chitosan using ionic cryotropic gelation. For cryogel preparation, apple pectin (AP), Heracleum L. pectin (HP), and chitosan samples with different physical and chemical characteristics were used. The properties of pectin-chitosan cryogels were found to depend on the structural features and physicochemical characteristics of the pectin and chitosan within them. The addition of chitosan to cryogels can increase their mechanical strength, cause change in surface morphology, increase the degradation time, and enhance adhesion to biological tissues. Cryogels based on AP were less immunogenic when compared with cryogels from HP. Cryogels based on AP and HP were hemocompatible and the percentage of red blood cells hemolysis was less than 5%. Unlike cryogels based on HP, which exhibited moderate cytotoxicity, cryogels based on AP exhibited light cytotoxicity. Based on the results of low immunogenicity, light cytotoxicity data as well as a low level of hemolysis of composite cryogels based on AP and chitosan are biocompatible and can potentially be used in biomedicine. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 547-556, 2017.


Subject(s)
Chitosan , Cryogels , Materials Testing , Pectins , Animals , Chitosan/chemistry , Chitosan/pharmacology , Cryogels/chemistry , Cryogels/pharmacology , Humans , Malus/chemistry , Mice , NIH 3T3 Cells , Pectins/chemistry , Pectins/pharmacology
2.
PLoS One ; 9(10): e109914, 2014.
Article in English | MEDLINE | ID: mdl-25333971

ABSTRACT

In this study, the optimized method for designing IgG-binding magnetosomes based on integration of IgG-binding fusion proteins into magnetosome membrane in vitro is presented. Fusion proteins Mbb and Mistbb consisting of magnetosome membrane protein MamC and membrane associating protein Mistic from Bacillus subtilis as anchors and BB-domains of Staphylococcus aureus protein A as IgG-binding region were used. With Response Surface Methodology (RSM) the highest level of proteins integration into magnetosome membrane was achieved under the following parameters: pH 8.78, without adding NaCl and 55 s of vortexing for Mbb; pH 9.48, 323 mM NaCl and 55 s of vortexing for Mistbb. Modified magnetosomes with Mbb and Mistbb displayed on their surface demonstrated comparable levels of IgG-binding activity, suggesting that both proteins could be efficiently used as anchor molecules. We also demonstrated that such modified magnetosomes are stable in PBS buffer during at least two weeks. IgG-binding magnetosomes obtained by this approach could serve as a multifunctional platform for displaying various types of antibodies.


Subject(s)
Immunoglobulin G/metabolism , Magnetite Nanoparticles/chemistry , Magnetosomes/chemistry , Bacterial Proteins/metabolism , Membrane Proteins/metabolism , Protein Binding , Staphylococcal Protein A/metabolism , Staphylococcus aureus/metabolism
3.
Mar Biotechnol (NY) ; 13(3): 402-10, 2011 Jun.
Article in English | MEDLINE | ID: mdl-20632197

ABSTRACT

Unique skeletal formations of marine invertebrates, including representatives of Echinodermata, have the unique potential to serve as templates for bio-inspired materials chemistry, biomimetics, and materials science. The sand dollar Scaphechinus mirabilis (Agassiz, 1983) is widely distributed in the northwest of the Pacific Ocean from southern Japan to the Aleutian Islands. This animal is the main source of naphtochinone-based substances. These compounds have recently drawn medical attention for their use as cardiological and ophthalmological drugs. Unfortunately, after extraction of the naphtochinones, the residual skeletons and spines of the sand dollars were usually discarded. Here, we report the first method for the preparation of nanostructurally organized spines of S. mirabilis, using a simple enzymatic and hydrogen peroxide-based treatment. Application of this method opens the way for development of non-wasteful environmentally clean technology of sand dollars as well-known industrial marine invertebrates.


Subject(s)
Animal Structures/anatomy & histology , Biomimetic Materials/isolation & purification , Biotechnology/methods , Nanostructures/ultrastructure , Sea Urchins/anatomy & histology , Animals , Hydrogen Peroxide , Microscopy, Electron, Scanning , Microscopy, Fluorescence , Naphthoquinones/isolation & purification , Sea Urchins/chemistry , Spectroscopy, Fourier Transform Infrared
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