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1.
Molecules ; 26(2)2021 Jan 16.
Artigo em Inglês | MEDLINE | ID: mdl-33467083

RESUMO

Chitosan is the only cationic polysaccharide found in nature. It has broad application prospects in biomaterials, but its application is limited due to its poor solubility in water. A novel chitosan derivative was synthesized by amidation of chitosan with 18ß-glycyrrhetinic acid and sialic acid. The chitosan derivatives were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and measurement of the zeta potential. We also investigated the solubility, cytotoxicity, and blood compatibility of chitosan derivatives. 18ß-glycyrrhetinic acid and sialic acid could be grafted onto chitosan molecular chains. The thermal stability of the synthesized chitosan derivatives was decreased and the surface was positively charged in water and phosphate-buffered saline. After chitosan had been modified by 18 ß-glycyrrhetinic acid and sialic acid, the solubility of chitosan was improved greatly in water and phosphate-buffered saline, and percent hemolysis was <5%. Novel amphiphilic chitosan derivatives could be suitable polymers for biomedical purposes.


Assuntos
Quitosana , Ácido Glicirretínico/análogos & derivados , Teste de Materiais , Ácido N-Acetilneuramínico , Linhagem Celular , Quitosana/análogos & derivados , Quitosana/síntese química , Quitosana/química , Quitosana/farmacologia , Ácido Glicirretínico/química , Ácido Glicirretínico/farmacologia , Humanos , Ácido N-Acetilneuramínico/química , Ácido N-Acetilneuramínico/farmacologia , Solubilidade
2.
Molecules ; 24(14)2019 Jul 16.
Artigo em Inglês | MEDLINE | ID: mdl-31315269

RESUMO

Mussel adhesive proteins (MAPs) have a unique ability to firmly adhere to different surfaces in aqueous environments via the special amino acid, 3,4-dihydroxyphenylalanine (DOPA). The catechol groups in DOPA are a key group for adhesive proteins, which is highly informative for the biomedical domain. By simulating MAPs, medical products can be developed for tissue adhesion, drug delivery, and wound healing. Hydrogel is a common formulation that is highly adaptable to numerous medical applications. Based on a discussion of the adhesion mechanism of MAPs, this paper reviews the formation and adhesion mechanism of catechol-functionalized hydrogels, types of hydrogels and main factors affecting adhesion, and medical applications of hydrogels, and future the development of catechol-functionalized hydrogels.


Assuntos
Bivalves/química , Catecóis/química , Animais , Bivalves/metabolismo , Di-Hidroxifenilalanina/química , Sistemas de Liberação de Medicamentos , Hidrogéis , Proteínas/metabolismo , Aderências Teciduais , Cicatrização
3.
Food Chem ; 264: 277-283, 2018 Oct 30.
Artigo em Inglês | MEDLINE | ID: mdl-29853377

RESUMO

The mechanism of the thermal degradation and the toxicity of the thermal degradation products of agar were studied using TG/DTA, Fourier-transform infrared spectroscopy and pyrolysis gas chromatography/mass spectrometry. It was found that the thermal degradation of agar is a single-step reaction, the thermal degradation temperature (T0, Tp, Tf) increases with increasing gel strength (P) and the influence of P on the thermal degradation rate is modest. The thermal degradation of agar is an exothermic reaction, and the activation energy of the reaction increases with increasing P. In the thermal degradation, agar is first decomposed into 3,6-anhydropyran galactopyranose and galactopyranose, then 3,6-anhydropyran galactopyranose, and finally furyl hydroxymethyl ketone, through loop opening, dehydration and hydrogen transfer. Galactopyranose follows three degradation pathways, and its final degradation products are 3,4-atrosan, d-allose, furfural and 5-(hydroxymethyl)-2-furancarboxaldehyde. Of the degradation products, furyl hydroxymethyl ketone, furfural, and 5-(hydroxymethyl)-2-furancarboxaldehyde show some toxicity to humans.


Assuntos
Ágar/química , Ágar/toxicidade , Furaldeído/química , Galactose/química , Cromatografia Gasosa-Espectrometria de Massas , Glucose/química , Espectroscopia de Infravermelho com Transformada de Fourier , Temperatura , Termogravimetria
4.
Int J Biol Macromol ; 112: 1191-1198, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29408210

RESUMO

The purpose of this study was to develop a promising burns dressing. Chiosan (CS) has been widely used as biomaterials, in combination with marine peptides (MPs) extracted from seawater cultured Tilapia, the newly developed material Chitosan-Marine Peptides hydrogels (CSMP) in this study showed antibacterial activity, pro-cell proliferation and migration, well burning healing. Pathological examinations by HE staining demonstrated that CSMP had pronounced wound healing efficiencies. In burn wounds treated with CSMP, reepithelialization and collagen fiber deposition were observed on day 7, the epithelium was completely regenerated by day 14, and the wounds were completely healed by day 21. Furthermore, CSMP can up-regulate the expression of FGF2 and VEGF. Collectively, these results suggest that CSMP may enhance cell migration and promote the skin regeneration, which demonstrates the potential application of CSMP in burning healing.


Assuntos
Queimaduras/tratamento farmacológico , Queimaduras/patologia , Quitosana/uso terapêutico , Hidrogéis/uso terapêutico , Peptídeos/uso terapêutico , Tilápia/metabolismo , Cicatrização/efeitos dos fármacos , Animais , Antibacterianos/farmacologia , Morte Celular/efeitos dos fármacos , Linhagem Celular , Movimento Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Quitosana/farmacologia , Feminino , Fator 2 de Crescimento de Fibroblastos/metabolismo , Hidrogéis/farmacologia , Masculino , Camundongos , Testes de Sensibilidade Microbiana , Peptídeos/farmacologia , Coelhos , Pele/patologia , Espectroscopia de Infravermelho com Transformada de Fourier , Fator A de Crescimento do Endotélio Vascular/metabolismo
5.
Mar Drugs ; 15(11)2017 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-29112116

RESUMO

Classic hypotheses of Alzheimer's disease (AD) include cholinergic neuron death, acetylcholine (ACh) deficiency, metal ion dynamic equilibrium disorder, and deposition of amyloid and tau. Increased evidence suggests neuroinflammation and oxidative stress may cause AD. However, none of these factors induces AD independently, but they are all associated with the formation of Aß and tau proteins. Current clinical treatments based on ACh deficiency can only temporarily relieve symptoms, accompanied with many side-effects. Hence, searching for natural neuroprotective agents, which can significantly improve the major symptoms and reverse disease progress, have received great attention. Currently, several bioactive marine products have shown neuroprotective activities, immunomodulatory and anti-inflammatory effects with low toxicity and mild side effects in laboratory studies. Recently, chitosan (CTS), chitooligosaccharide (COS) and their derivatives from exoskeletons of crustaceans and cell walls of fungi have shown neuroprotective and antioxidative effects, matrix metalloproteinase inhibition, anti-HIV and anti-inflammatory properties. With regards to the hypotheses of AD, the neuroprotective effect of CTS, COS, and their derivatives on AD-like changes in several models have been reported. CTS and COS exert beneficial effects on cognitive impairments via inhibiting oxidative stress and neuroinflammation. They are also a new type of non-toxic ß-secretase and AChE inhibitor. As neuroprotective agents, they could reduce the cell membrane damage caused by copper ions and decrease the content of reactive oxygen species. This review will focus on their anti-neuroinflammation, antioxidants and their inhibition of ß-amyloid, acetylcholinesterase and copper ions adsorption. Finally, the limitations and future work will be discussed.


Assuntos
Doença de Alzheimer/tratamento farmacológico , Quitina/análogos & derivados , Quitosana/análogos & derivados , Quitosana/uso terapêutico , Quitina/química , Quitina/uso terapêutico , Inibidores da Colinesterase/química , Inibidores da Colinesterase/uso terapêutico , Cobre , Humanos , Oligossacarídeos
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