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1.
Int J Biol Macromol ; 274(Pt 2): 133499, 2024 Jun 27.
Artículo en Inglés | MEDLINE | ID: mdl-38944085

RESUMEN

Two chitosan Schiff bases were synthesized by condensation of chitosan with 2-(4-formylphenoxy)-N-phenylacetamide and N-(4-bromophenyl)-2-(4-formylphenoxy) acetamide denoted as Cs-SBA and Cs-SBBr, respectively. The molecular structures of the resulting chitosan derivatives were characterized using FTIR and 1HNMR and their thermal properties were investigated by TGA. These derivatives were treated with sodium tripolyphosphate (TPP) to produce Cs Schiff base nanoparticles. The nanoparticles physicochemical properties were determined by FTIR, XRD, TEM, and zeta potential analysis. The antimicrobial action against Helicobacter pylori (H. pylori) was evaluated and the results indicated that the anti-H. pylori activity had minimal inhibitory concentration MIC values of 15.62 ± 0.05 and 3.9 ± 0.03 µg/mL for Cs-SBA and Cs-SBBr nanoparticles (Cs-SBA NPs and Cs-SBBr NPs), respectively. The better biologically active nanoparticles, Cs-SBBr NPs, were tested for their cyclooxygenases (COX-1 and COX-2) inhibitory potential. Cs-SBBr NPs demonstrated COX enzyme inhibition activity against COX-2 (IC50 4.5 ± 0.165 µg/mL) higher than the conventional Indomethacin (IC50 0.08 ± 0.003 µg/mL), and Celecoxib (IC50 0.79 ± 0.029 µg/mL). Additionally, the cytotoxicity test of Cs-SBBr NPs showed cytotoxic effect on Vero cells (CCL-81) with IC50 = 17.95 ± 0.12 µg/mL which is regarded as a safe compound. Therefore, Cs-SBBr NPs may become an alternative to cure H. pylori and prevent gastric cancer.

2.
Int J Biol Macromol ; 257(Pt 2): 128742, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-38092112

RESUMEN

The production of novel natural medicines for the treatment of Helicobacter pylori (H. pylori) has lately attracted a lot of interest. Some bacterial infections have traditionally been alleviated by terpenes. The present work intended to examine the impact of several chitosan menthone Schiff base nanocomposites on the treatment of H. pylori infection as well as on its anti-inflammatory capacity. Chitosan (Cs) was condensed with menthone with different molar ratios of Cs:menthone (1:0.5, 1:1, and 1:2) to produce chitosan Schiff bases namely; Cs-SB1, Cs-SB2, and Cs-SB3, respectively. Cs-SB3 Schiff base nanocomposites were prepared individually by adding 2%Ag, 2%Se, (1%Ag + 1%Se), and 2%Fe2O3 nanoparticles to produce compounds denoted as Cs-SB-Ag, Cs-SB-Se, Cs-SB-Ag/ Se, and Cs-SB-Fe, respectively. The anti-H. pylori activity of Cs-SB-Se was detected at a minimal inhibitory concentration MIC of 1.9 µg/mL making it the most biologically active compound in our study. Cs-SB-Se nanocomposite was tested for its cyclooxygenases (COX-1 and COX-2) inhibitory potential which demonstrated inhibitory efficacy towards COX enzymes with inhibition value against COX-1 (IC50 = 49.86 ± 1.784 µg/mL) and COX-2 (IC50 = 12.64 ± 0.463 µg/mL) which were less than the well-known Celecoxib (22.65 ± 0.081 and 0.789 ± 0.029 µg/mL) and Indomethacin (0.035 ± 0.001 and 0.08 ± 0.003 µg/mL) inhibitors. The selectivity index SI = 3.94 for tested nanocomposites indicated higher selectivity for COX-1. The cytotoxicity of the Cs-SB-Se nanocomposite was evaluated in Vero cells (CCL-81) and it showed that at a concentration of 62.5 µg/mL, cell viability was 85.43 %.


Asunto(s)
Quitosano , Helicobacter pylori , Mentol , Nanocompuestos , Nanopartículas , Animales , Chlorocebus aethiops , Quitosano/farmacología , Bases de Schiff/farmacología , Células Vero , Ciclooxigenasa 2 , Antibacterianos/farmacología
3.
Int J Biol Macromol ; 208: 1029-1045, 2022 May 31.
Artículo en Inglés | MEDLINE | ID: mdl-35378157

RESUMEN

Chitosan (Cs) bis-aldehyde Schiff base derivatives were synthesized by condensation of Cs with three bis-aldehydes namely; butane-1,4-diyl bis(4-formylbenzoate), N,N'-(butane-1,4-diyl)bis(2-(4-formylphenoxy)acetamide) and 4,4'-(butane-1,4-diylbis(oxy))dibenzaldehyde. The prepared Cs derivatives were blended with carboxymethyl chitosan(CMC) and graphene quantum dots (GQDs) to produce semi-IPNs polyelectrolyte complexes (PECs). and characterized with respect to their molecular structure and physio-chemical properties. The antibacterial activity against H. pylori (and in vitro Inosine 5'-monophosphate dehydrogenase IMPDH inhibitory assay) was evaluated. Additionally, a preliminary in vitro assessment for wound healing was performed against PECs in which wound closure percentages, and rates were investigated indicating an accelerated wound healing compared with untreated cells. The PEC based on Schiff base PEC containing amide linkage showed the highest wound healing ability. A minimal inhibitory concentration (MIC) was obtained for the PEC sample containing Cs Schiff base derived from 4,4'-(butane-1, 4-diylbis(oxy))dibenzaldehyde at a dose of 0.98 µg/ml inhibiting H. pylori growth by 100%. Additionally, the selected above-mentioned compound was selected to test its inhibitory activity against the HpIMPDH enzyme in addition to its selectivity towards the hIMPDH2 enzyme and was found to have promising activity against the HpIMPDH enzyme with IC50 value of 0.65 µM, and to be safer and less active against the hIMPDH2 enzyme with IC50 > 10 µM, reflecting its selectivity.


Asunto(s)
Quitosano , Grafito , Helicobacter pylori , Puntos Cuánticos , Antibacterianos/química , Antibacterianos/farmacología , Butanos , Quitosano/química , IMP Deshidrogenasa , Polielectrolitos , Estudios Prospectivos , Bases de Schiff/química
4.
Int J Biol Macromol ; 154: 683-697, 2020 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-32194112

RESUMEN

Chitosan has been termed as the most well-known among biopolymers, receiving widespread attention from researchers in various fields mainly, agriculture, food, and health. Chitosan is a deacetylated derivative of chitin, mainly isolated from waste shells of the phylum Arthropoda after their consumption as food. Chitosan molecules can be easily modified for adsorption and slow release of plant growth regulators, herbicides, pesticides, and fertilizers, etc. Chitosan as a carrier and control release matrix that offers many benefits including; protection of biomolecules from harsh environmental conditions such as pH, light, temperatures and prolonged release of active ingredients from its matrix consequently protecting the plant's cells from the hazardous effects of burst release. In the current review, tends to discuss the recent advances in the area of chitosan application as a control release system. Also, future recommendations will be made in light of current advancements and major gaps.


Asunto(s)
Agricultura/métodos , Quitosano/química , Portadores de Fármacos/química , Nanoestructuras/química , Control de Plagas , Agroquímicos , Plantas
5.
Int J Biol Macromol ; 153: 492-501, 2020 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-32112843

RESUMEN

Three heteroaryl pyrazole derivatives; namely 1-phenyl-3-(thiophene-2-yl)-1H-pyrazole-4-carbaldehyde, 1-phenyl-3-(furan-2-yl)-1H-pyrazole-4-carbaldehyde and 1-phenyl-3-(pyridine-3-yl)-1H-pyrazole-4-carbaldehyde were synthesized and reacted with chitosan to form Schiff bases of chitosan. All newly synthesized compounds have been characterized by solubility tests, elemental analysis, spectral (FTIR, 1H NMR) analyses, thermogravimetric analysis and X-ray diffraction (XRD). The Schiff bases were screened for their biological activity against gram-negative bacteria (Escherichia coli and Klebsiella pneumonia), gram-positive bacteria (Staphylococcus aureus and Streptococcus mutans) and fungi (Asperagillus fumigatus and Candida albican). The results indicated that the antimicrobial activity was dependent on the type of the Schiff base moiety. Cytotoxicity of the prepared chitosan derivatives was evaluated by MTT assay and the results indicated the absence of cytotoxic activity.


Asunto(s)
Antibacterianos , Antifúngicos , Aspergillus fumigatus/crecimiento & desarrollo , Bacterias/crecimiento & desarrollo , Candida albicans/crecimiento & desarrollo , Quitosano/química , Antibacterianos/síntesis química , Antibacterianos/química , Antibacterianos/farmacología , Antifúngicos/síntesis química , Antifúngicos/química , Antifúngicos/farmacología , Bases de Schiff/química , Bases de Schiff/farmacología
6.
Int J Biol Macromol ; 121: 889-904, 2019 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-30340012

RESUMEN

Chitosan is obtained from chitin, which could be considered to be the most abundant polymer after cellulose. Owing to these properties, chitosan alone or chitosan-based composite film production is attaining huge attention in terms of applications from researchers and industrialists coming from divergent fields. To enhance the biological (mainly antimicrobial and antioxidant) and physiological (mainly mechanical, thermal and barrier) attributes of the chitosan-based films, a vast medley of plant extracts and supporting polymers has been blended into chitosan films. Considering the up to date literature reports based on chitosan film production and applications, it can be stated that still, the research ratio is low in this field. Chitosan blend/composite films with specific properties (superhydrophobicity, excellent mechanical strength, acceptable barrier properties) can be produced only for specific applications in food technology. In the current review, we tried to summarize the advancements made in the last 5-7 years in the field of chitosan film technology for its application in the food industry.


Asunto(s)
Materiales Biocompatibles/química , Quitosano/química , Tecnología de Alimentos , Fenómenos Químicos , Humanos
7.
Int J Biol Macromol ; 70: 199-207, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25002014

RESUMEN

Three acyl derivatives of chitosan (CS) with different side chains were synthesized and their structures were characterized. Their swelling behavior was investigated. The antifungal behavior of these chitosan derivatives was investigated in vitro on the mycelial growth, sporulation and germination of conidia or sclerotia of the sugar-beet pathogens, Rhizoctonia solani K"uhn (AG2-2) and Sclerotium rolfsii Sacc. All the prepared derivatives had a significant inhibiting effect on the different stages of development on the germination of conidia or sclerotia of all the investigated fungi. In the absence of chitosan and its derivative, R. solani exhibited the fastest growth of the fungi studied.


Asunto(s)
Quitosano/química , Desinfectantes/química , Desinfectantes/farmacología , Tiourea/química , Antifúngicos/química , Antifúngicos/farmacología , Quitosano/síntesis química , Pruebas de Sensibilidad Microbiana , Espectroscopía Infrarroja por Transformada de Fourier , Termogravimetría , Difracción de Rayos X
8.
Mater Sci Eng C Mater Biol Appl ; 33(4): 1819-41, 2013 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-23498203

RESUMEN

Chitosan is a biodegradable biocompatible polymer derived from natural renewable resources with numerous applications in various fields, and one of which is the area of edible films and coatings. Chitosan has antibacterial and antifungal properties which qualify it for food protection, however, its weak mechanical properties, gas and water vapor permeability limit its uses. This review discusses the application of chitosan and its blends with other natural polymers such as starch and other ingredients for example essential oils, and clay in the field of edible films for food protection. The mechanical behavior and the gas and water vapor permeability of the films are also discussed. References dealing with the antimicrobial behavior of these films and their impact on food protection are explored.


Asunto(s)
Quitosano/farmacología , Materiales Biocompatibles Revestidos/farmacología , Almacenamiento de Alimentos , Antibacterianos/farmacología , Quitosano/química , Electricidad , Humanos , Aceites Volátiles/farmacología
9.
Mater Sci Eng C Mater Biol Appl ; 32(7): 1711-1726, 2012 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-34062651

RESUMEN

Chitin and chitosan are natural polymers with a huge potential in numerous fields, namely, biomedical, biological, and many industrial applications such as waste water treatment due to the fact that they can absorb and chelate many metal cations. Electrospinning is a growing field of research to produce submicron fibers with promising applications in biomedical fields like tissue engineering scaffolds and wound healing capabilities. Both chitin and chitosan polymers were found to be hard to electrospun, however, many researchers manage to produce nano-fibers using special solvents; for example, 90% acetic acid was found to reduce the surface tension making electrospinning feasible. Mixtures of organic acids were also experimented to produce homogenous and uniform fibers. Bigger attention was given to electrospinning of their soluble derivatives such as dibutyryl and carboxymethyl chitin. More derivatives of chitosan were investigated to produce nano-fibers such as hexanoyl, polyethyleneglycol, carboxymethyl, and a series of quaternized chitosan derivatives. The obtained nano-fibers were found to have much better qualities than normal chitosan fibers. Several polymer blends of chitin/chitosan with many commercial polymers were found to be amenable for electrospinning producing uniform beads free fibers. The review surveys the various approaches for successful electrospinning of chitin, chitosan, their derivatives, and blends with several other polymers.

10.
Colloids Surf B Biointerfaces ; 74(1): 1-16, 2009 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-19682870

RESUMEN

This review discusses the definition of surface active agents and specifically natural polymeric surface active agents. Chitosan by itself was found to have weak surface activity since it has no hydrophobic segments. Chemical modifications of chitosan could improve such surface activity. This is achieved by introducing hydrophobic substituents in its glucosidic group. Several examples of chitosan derivatives with surfactant activity have been surveyed. The surface active polymers form micelles and aggregates which have enormous importance in the entrapment of water-insoluble drugs and consequently applications in the controlled drug delivery and many biomedical fields. Chitosan also interacts with several substrates by electrostatic and hydrophobic interactions with considerable biomedical applications.


Asunto(s)
Quitosano/análogos & derivados , Quitosano/química , Tensoactivos/química , Humanos , Interacciones Hidrofóbicas e Hidrofílicas , Surfactantes Pulmonares/química , Soluciones , Propiedades de Superficie
11.
Bioresour Technol ; 99(5): 1359-67, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17383869

RESUMEN

Chitin has been extracted from six different local sources in Egypt. The obtained chitin was converted into the more useful soluble chitosan by steeping into solutions of NaOH of various concentrations and for extended periods of time, then the alkali chitin was heated in an autoclave which dramatically reduced the time of deacetylation. Chitin from squid pens did not require steeping in sodium hydroxide solution and showed much higher reactivity towards deacetylation in the autoclave that even after 15 min of heating a degree of deacetylation of 90% was achieved. The obtained chitin and chitosan were characterized by spectral analysis, X-ray diffraction and thermo gravimetric analysis.


Asunto(s)
Quitina/química , Quitosano/química , Egipto , Calor , Hidróxido de Sodio/química , Espectroscopía Infrarroja por Transformada de Fourier , Factores de Tiempo , Difracción de Rayos X
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