Biocompatible chemical network of α-cellulose-ESBO (epoxidized soybean oil) scaffold for tissue engineering application.

Carbohydr Polym

Department of Chemical Engineering, University of South Carolina, Columbia, SC, 29208, United States; Biomedical Engineering Program, University of South Carolina, Columbia, SC, 29208, United States.

Published: August 2020

Despite many desirable properties, the use of α-cellulose in biomedical applications is limited because of its poor processability. Here we demonstrate that the chemical network of α-cellulose and epoxidized soybean oil (ESBO) can be adequately processed into biocompatible, self-standing, highly-porous scaffolds for tissue engineering applications. First, α-cellulose was dissolved in N-Methylmorpholine N-oxide monohydrate (NMMO.MH) and chemically crosslinked by ESBO. Then, the porous scaffolds of α-cellulose-ESBO were fabricated by solvent exchange and freeze-drying techniques. The scaffolds were evaluated for morphology, thermal and mechanical stability, and in vitro cell attachment and cell viability. Scanning electron microscopy images and Brunauer-Emmett-Teller results suggested that porous scaffolds provide a good surface and internal structure for cell adhesion and growth. Specifically, the α-cellulose-ESBO scaffolds support the homogeneous attachment and proliferation of MG63 cells. Overall, our results suggest that α-cellulose-ESBO chemically crosslinked networks are biocompatible and demonstrate a remarkable capacity for the development of tissue engineering platforms.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.carbpol.2020.116322DOI Listing

Publication Analysis

Top Keywords

tissue engineering
12
chemical network
8
epoxidized soybean
8
soybean oil
8
chemically crosslinked
8
porous scaffolds
8
scaffolds
5
biocompatible chemical
4
α-cellulose-esbo
4
network α-cellulose-esbo
4

Similar Publications

Cardiovascular disease (CVD) is the leading cause of death in the United States. Damage in the cardiovascular system can be due to environmental exposure, trauma, drug toxicity, or numerous other factors. As a result, cardiac tissue and vasculature undergo structural changes and display diminished function.

View Article and Find Full Text PDF

For noninvasive light-based physiological monitoring, optimal wavelengths of individual tissue components can be identified using absorption spectroscopy. However, because of the lack of sensitivity of hardware at longer wavelengths, absorption spectroscopy has typically been applied for wavelengths in the visible (VIS) and near-infrared (NIR) range from 400 to 1,000 nm. Hardware advancements in the short-wave infrared (SWIR) range have enabled investigators to explore wavelengths in the ~1,000 nm to 3,000 nm range in which fall characteristic absorption peaks for lipid, protein, and water.

View Article and Find Full Text PDF

Patterning soft materials with cell adhesion motifs can be used to emulate the structures found in natural tissues. While patterning in tissue is driven by cellular assembly, patterning soft materials in the laboratory most often involves light-mediated chemical reactions to spatially control the presentation of cell binding sites. Here we present hydrogels that are formed with two responsive crosslinkers-an anthracene-maleimide adduct and a disulfide linkage-thereby allowing simultaneous or sequential patterning using force and UV light.

View Article and Find Full Text PDF

Aim: To evaluate in vitro the antibacterial efficacy and cytocompatibility of different implant-decontamination methods, using both 2D and 3D peri-implant mucosa models.

Methods: Four decontamination methods [chlorhexidine (CHX), electrolytic treatment (GS), curcumin (CUR), xanthohumol (XN)] were compared in four independent experiments, three with a 2D peri-implant mucosa model on titanium surfaces and another on a 3D peri-implant mucosa model. These decontamination procedures were tested for their antibacterial effect using a multispecies biofilm model with Streptococcus oralis, Actinomyces naeslundii, Veillonella dispar, and Porphyromonas gingivalis for 24 h.

View Article and Find Full Text PDF

Intelligent Design of Lipid Nanoparticles for Enhanced Gene Therapeutics.

Mol Pharm

January 2025

ZJU-Hangzhou Global Scientific and Technological Innovation Canter, Zhejiang University, Hangzhou, Zhejiang 311215, China.

Lipid nanoparticles (LNPs) are an effective delivery system for gene therapeutics. By optimizing their formulation, the physiochemical properties of LNPs can be tailored to improve tissue penetration, cellular uptake, and precise targeting. The application of these targeted delivery strategies within the LNP framework ensures efficient delivery of therapeutic agents to specific organs or cell types, thereby maximizing therapeutic efficacy.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!