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1.
Virol Sin ; 39(2): 290-300, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38331038

RESUMO

Coxsackievirus B3 (CVB3) is the pathogen causing hand, foot and mouth disease (HFMD), which manifests across a spectrum of clinical severity from mild to severe. However, CVB3-infected mouse models mainly demonstrate viral myocarditis and pancreatitis, failing to replicate human HFMD symptoms. Although several enteroviruses have been evaluated in Syrian hamsters and rhesus monkeys, there is no comprehensive data on CVB3. In this study, we have first tested the susceptibility of Syrian hamsters to CVB3 infection via different routes. The results showed that Syrian hamsters were successfully infected with CVB3 by intraperitoneal injection or nasal drip, leading to nasopharyngeal colonization, acute severe pathological injury, and typical HFMD symptoms. Notably, the nasal drip group exhibited a longer viral excretion cycle and more severe pathological damage. In the subsequent study, rhesus monkeys infected with CVB3 through nasal drips also presented signs of HFMD symptoms, viral excretion, serum antibody conversion, viral nucleic acids and antigens, and the specific organ damages, particularly in the heart. Surprisingly, there were no significant differences in myocardial enzyme levels, and the clinical symptoms resembled those often associated with common, mild infections. In summary, the study successfully developed severe Syrian hamsters and mild rhesus monkey models for CVB3-induced HFMD. These models could serve as a basis for understanding the disease pathogenesis, conducting pre-trial prevention and evaluation, and implementing post-exposure intervention.


Assuntos
Modelos Animais de Doenças , Enterovirus Humano B , Doença de Mão, Pé e Boca , Macaca mulatta , Mesocricetus , Animais , Doença de Mão, Pé e Boca/virologia , Doença de Mão, Pé e Boca/patologia , Enterovirus Humano B/patogenicidade , Anticorpos Antivirais/sangue , Cricetinae , Feminino , Eliminação de Partículas Virais , Nasofaringe/virologia , Masculino
2.
Int J Pharm ; 591: 119990, 2020 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-33075467

RESUMO

Herein, a polyoxometalate (POM)-based blend hydrogel system was in situ constructed by incorporating cetyltrimethylammoniumbromide (CTAB)-encapsulated POM cationic micelles to bare hydrogel matrixes followed by copolymerization of multivalent crosslinking groups. It was demonstrated that the fabricated blend hydrogel possessed tunable physicochemical properties, good swelling behavior (maximum swelling rate of 229% in buffer solution of pH 8.0), excellent local action and sustained release of POM component (release ratio achieved nearly 100% at the time of 120 min). Antibacterial activity study revealed that the introduction of POM greatly improved the bioavailability of itself, namely, leading to a more effective enhancement of therapeutic effects (survival ratio of both strains less than 5%). Besides, bactericidal rates (ca. 51%) were achieved even after six runs repeated, thereby verifying the biological application potential of this material. Finally, the practical application potentials were investigated and future prospects in relevant research areas were forecasted.


Assuntos
Hidrogéis , Compostos de Tungstênio , Antibacterianos , Hidrogel de Polietilenoglicol-Dimetacrilato
3.
Int J Biol Macromol ; 154: 732-738, 2020 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-32194111

RESUMO

This paper reported a facile strategy to fabricate ionically crosslinked supramolecular film, in which an in situ formed chitosan ionic film was produced by post-crosslinking the chitosan chains using negatively charged anion polyoxometalate. The incorporation of polyoxometalate into the chitosan ionic system accelerated the crosslinked degree, as evidenced by an increase in surface wrinkle via scanning electron microscopy. Interestingly, the resultant supramolecular film realized the combination of prominent antimicrobial effect and excellent biocompatibility, which was considered to have enormous application potential range from biomedical to environmental science.


Assuntos
Antibacterianos/farmacologia , Quitosana/farmacologia , Reagentes de Ligações Cruzadas , Compostos de Tungstênio/química , Antibacterianos/síntese química , Linhagem Celular , Quitosana/química , Escherichia coli/efeitos dos fármacos , Humanos , Polietilenoglicóis/química , Staphylococcus aureus/efeitos dos fármacos
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