Papers by Keyword: Glutaraldehyde

Abstract: Tissue engineering provides a promising approach to addressing the global shortage of organ and tissue donors by developing biological substitutes that can restore or enhance tissue function. This study presents the development and characterization of PEG-PVA biodegradable hydrogels, synthesized through chemical crosslinking with varying concentrations of glutaraldehyde, for tissue engineering applications. Mechanical, thermal, and structural properties were systematically analyzed to determine the optimal formulation for different applications. Hydrogels synthesized with 0.10g and 0.15g of glutaraldehyde were selected for detailed evaluation. The hydrogel with 0.10g glutaraldehyde exhibited a tensile strength of 1200 MPa, a glass transition temperature (Tg) of ～50°C, and a swelling ratio of 7.65, demonstrating superior mechanical robustness and thermal stability for load-bearing applications such as bone and cartilage regeneration. In contrast, the hydrogel with 0.15g glutaraldehyde, with a tensile strength of 1000 MPa, a Tg of 45°C, and a swelling ratio of 4.49, showed greater flexibility and a denser microstructure, making it more suitable for soft tissue applications requiring controlled degradation. These results underscore the importance of tailoring crosslinking density to optimize hydrogel performance for specific biomedical applications. Future studies should explore the behavior of these hydrogels in biologically relevant environments, including enzymatic degradation and in vivo testing. With further development, PEG-PVA hydrogels could play a key role in regenerative medicine, offering customizable mechanical and degradation properties for diverse clinical applications.

Abstract: Response surface methodology (RSM) was used to determine the optimal blend of alginate (ALG), poly (vinyl alcohol) (PVA) and graphene oxide (GO), as well as glutaraldehyde (GA) crosslinking solution concentration for the synthesis of dual-crosslinked ALG/PVA/GO nanocomposite hydrogel adsorbent beads for methylene blue (MB) removal. Statistical analyses show that PVA concentration contributes the largest effect to the adsorption capacity response, attributed to improved accessibility of MB molecules to adsorption sites. The optimal blend was determined to be 3% polymer with 50% PVA, 383.8384 ppm GO, crosslinked in 1% CaCl₂ and 5% GA. These results were validated, and the experimental value of the adsorption capacity deviated by only 1.702% from the RSM model prediction, suggesting good model predictability. Adsorption isotherm models were tested to provide a description of the adsorption process. The Sips isotherm model, suggesting monolayer adsorption over heterogeneous surface with action of cooperative adsorbate-adsorbate interactions, was the best fit to the experimental equilibrium data, with an R² of 0.9782. Furthermore, the ALG/PVA/GO beads demonstrated a maximum monolayer adsorption capacity of 1081.62 mg/g, showing superior performance compared to known biosorbents of MB.

Abstract: The glutaraldehyde (GA)-crosslinked carboxymethyl cellulose (CMC)-polyvinyl alcohol (PVA) film had been synthesized and used as a methylene blue adsorbent. The films were prepared using a solution casting technique and characterized using FTIR spectrophotometer, SEM. Adsorption studies include pH, contact time, methylene blue initial concentration. Furthermore, the desorption study of films was carried out using NaCl, HCl and distilled water. The results of FTIR characterization showed similarities between the spectra of CMC-PVA-GA films with their component materials. The SEM image of CMC-PVA-GA films showed a non-porous surface. In the adsorption study, GA-crosslinked CMC-PVA films (1:2 w/w) exhibited the largest adsorption capacity of methylene blue at optimum conditions for adsorption at pH 7, contact time 200 min, methylene blue concentration of 200 mg L^–1 which was 194 mg g^–1. Methylene blue adsorption kinetic followed the pseudo second-order kinetic model and the Langmuir adsorption isotherm model. The desorption studies show that adsorption takes place through an ion exchange mechanism.

Abstract: Based on data from Indonesian Health Ministry in 2009, osteoporosis case reached 19,7 % of the populations in Indonesia, especially women in menopause period. The treatment was performed by consuming bisphosphonate drugs per oral which was not effective since the absorption intake of the drug was only less than 55% of the intake dosage. Because of that, the bone filler which also has a function as drug delivery system was developed. The hydroxyapatite-gelatin bone filler with the addition of alendronate was studied. To increase the characteristics of this bone filler, glutaraldehyde was introduced in the composite as a crosslinking agent. The concentration of 0.25%, 0.5%, and 0.75% were used. The bone filler was then characterized based on FTIR test, morphology test, compressive strength test, cytotoxicity test, and degradation test. The FTIR result showed that there was no significant difference between the sample with and without glutaraldehyde since the crosslinking bond of glutaraldehyde and gelatin was C=N bond which also presented in the gelatin. The morphology of the samples depicted a bigger pore size for higher glutaraldehyde concentration which also supported by lower compressive strength. All the samples were non-toxic based on the cytotoxicity test which had cell viability more than 100%. The degradation tests showed that with the presence of glutaraldehyde in the bone filler could maintain its form longer than the bone filler without glutaraldehyde. In conclusion, the presence of glutaraldehyde could increase the characteristics of the hydroxyapatite-gelatin composite with the addition of alendronate as a bone filler candidate for osteoporotic bone.

Abstract: Glutaraldehyde cross-linked silk sericin films were successfully prepared. FTIR was applied to characterize the chemical structure of films. Compared to pure silk sericin, cross-linked silk sericin film with 3% glutaraldehyde was found a new peak at 1620 cm^-1 and the peak intensity of cross-linked film decreased markedly, which indicating cross-linking reaction has been occurred. Thermal and swelling behavior of cross-linked films was investigated. The cross-linking reaction increased the thermal decomposition temperature. The swelling ratio of glutaraldehyde cross-linked silk sericin films went up with increasing glutaralehyde loading to 3wt%.

Abstract: The aim of this study was to investigate the toxicity level of chromium and glutaraldehyde. This research was conducted by testing the resistance level of fungi (Aspergillus niger sp.) toward glutaraldehyde and chromium in the medium of Potato Dextrose Agar (PDA). Variable of this experiment was the growth of Aspergillus niger sp. that indicates the resistance level of Aspergillus niger sp. The growth rate of Aspergillus niger sp. was classified on four scales. They were, (I) scale 1: zero growth; (II) scale 2: low growth (+); (III) scale 3: medium growth (++); (IV) Scale: 4 high growth (+++). All collected data were analysed by One Way ANOVA. The result showed that the toxicity of chromium and glutaraldehyde tanning material were highly significantly different toward Aspergillus niger (P<0,01). The Aspergillus niger sp. growth rate scale in chromium medium was high (scale 4: 4.00±0.00). Meanwhile, the growth rate scale of the Aspergillus niger sp. in glutaraldehyde medium was low (scale 2: 1.33 ± 0.58). Based on the fungi growth rate, it can be concluded that glutaraldehyde was more toxic than chromium tanning material toward Aspergillus niger sp. Furthermore, it can be said that glutaraldehyde is not quite ideal to be used as an alternative of chromium as a tanning material.

Abstract: The wound dressing which have good mechanical properties, non toxic, anti inflammation, anti infection and has potency to accelerate wound healing are important to be found. This study aimed to determine the effect of glutaraldehyde on the human amniotic membrane cross linking, tensile strength, material toxicity and tissue response to a biomaterial which could be applied as an ideal wound dressing. Human amniotic membrane used was derived from one individual and was obtained from the Biomaterial Center and Tissue Bank in Dr. Soetomo General Hospital Surabaya Indonesia while the glutaraldehyde used was a commercial product. The wound dressing from human amniotic membrane-glutaraldehyde was made by dipping the human amniotic membrane with a solution of different variation of glutaraldehyde compositions, ie 0:25%, 0.5%, 0.75%, 1%, and 1.25%. The results of the research also found the pH measurements on human amnion membrane-glutaraldehyde according to skin balance range (4.0-7.0) by adding 0.25%, 0.5%, 0.75%, 1%, and 1.25% glutaraldehid to human amniotic membrane. FTIR characterization test results indicate the change of intensity of tertiary amine group (C-N) in the human amniotic membrane–glutaraldehyde by 0,25%, 0,5%, 0.75%, 1%, and 1.25% glutaraldehyde concentration. The best concentration of glutaraldehyde to be applied as wound dressing was at a concentration of 1%, which was based on the results of tensile test 26.67 MPa, percentage of living cell in the cytotoxicity assay of 113.483%, and Histopathology Anatomy test that shows 100% of wound re-epithelialization on the mice’s skins.

Abstract: The main objective of the present work was to evaluate the degradation levels of the glutaraldehyde and xylol, after use at the General Hospital (GH) of the University of Caxias do Sul, Rio Grande do Sul State, Brazil. The degradation levels were evaluated by Gas Chromatography with Flame Ionization Detection (GC/FID). Sixteen samples were collected over an experimental period of 8 months. The degradations of glutaraldehyde and xylol were 9.19 and 1.52, respectively. Besides suggestions to improve management, the present study also suggests possible replacers for the target compounds.

Abstract: Sericin is a natural protein which is removed from silk in a process called degumming. In India, 250-300 tons of sericin is extracted per year and goes as waste, it has wide range of application because of its properties like antioxidant, antibacterial, UV resistant, anticoagulant and moisture retention capacity. This paper is concerned with the application of sericin on polyester fabrics using cross linking agents like di-methylol di-hydroxy ethylene urea (DMDHEU) and glutaraldehyde. The Polyester fabrics are pretreated with sodium hydroxide (NaOH) and low temperature plasma (Oxygen gas). This pretreated sericin applied polyester fabrics show the better improvement in the wicking (moistureabsorbency) and good dye uptake properties on acid dyed fabric and it will be used for medical application.

Abstract: A Cellulase and amylase are important enzymes for hydrolysis of cellulose and starchy material into the glucose. The performance of the mixed cellulose-amylase immobilized on polysulfone membrane (PSF) by cross-linked with glutaraldehyde was investigated. PSF membrane consists of 1-methyl-2-pyrolidone (NMP) as a solvent and using polyvinylpyrolidone (PVP) as an additive was developed. The study highlighted in the surface structure of PSF membrane, stability of the immobilized enzyme and reusability of the immobilized enzyme. Morphology studied using FESEM analysis indicated a good distribution of the pores was formed on the surface of the PSF membrane. The immobilization process shown no effect on the membrane structure and it was stable to be used as a support in immobilization process. The optimum operating condition for enzymatic hydrolysis of mixed cellulase-amylase on PSF membrane was 50°C and pH 5. The maximum glucose produced at the optimum condition was 4.843g/ml. The study also indicated that immobilized mixed cellulase-amylase achieved a maximum rate of reaction at first recycle of reusable before the rate of reaction decreased rapidly after 5 reusable hydrolysis cycles.