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1.
J Adv Vet Anim Res ; 10(1): 103-112, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37155541

RESUMO

Objectives: This study aimed to pinpoint the universality of extracellular antimicrobial resistance elements (eAREs) and compare the contents of eAREs with those of intracellular AREs (iAREs) in animal feces, thus laying a foundation for the further analysis of the horizontal transfer of antimicrobial resistance genes (ARGs) in the animal guts. Materials and Methods: Extracellular DNAs were isolated from the fecal samples of Pavo cristatus (n = 18), Ursus thibetanus (n = 2), two breeds of broilers (n = 21 and 11, respectively), and from the contents of rabbit intestines (n = 5). eAREs were detected by PCR technology. iAREs in P. cristatus and broiler feces were also detected and compared with the corresponding eAREs. In addition, some gene cassettes of class 1 integrons were sequenced and analyzed. Results: The results showed that eAREs exist in animal feces and intestinal contents. In this study, different eAREs were detected from animal feces and intestinal contents, and tetA, tetB, sul1, sul2, class 1 integron, and IncFIB presented the highest detection rates. The detection rates of certain eAREs were significantly higher than those of parallel iAREs. The integral cassettes with intact structures were found in eAREs, and the cassettes carried ARGs. Conclusions: The presented study here sheds light on the presence of eAREs in animal feces or guts, and eAREs may play an important role in the horizontal gene transfer of ARGs.

2.
Adv Mater ; 33(29): e2100943, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34076317

RESUMO

Quasi-solid-state polymer electrolytes are one of the most promising candidates for long-life lithium-metal batteries. However, introduction of plasticizers for high ion conductivity at room temperature inevitably gives rise to poor mechanical strength and requires a very thick electrolyte membrane, which is detrimental to safety and energy density of the batteries. Herein, inspired by tube brushes coupling hardness with softness, a novel superstructured polymer bottlebrush BC-g-PLiSTFSI-b-PEGM (BC = bacterial cellulose; PLiSTFSI = poly(lithium 4-styrenesulfonyl-(trifluoromethylsulfonyl) imide); PEGM = poly(diethylene glycol monomethyl ether methacrylate)) with a hard nanofibril backbone and soft functional polymer side-chains is reported as an effective strategy to well balance the mechanical strength and ion conductivity of quasi-solid-state polymer electrolytes. The resulting single lithium-ion conducting quasi-solid-state polymer-brush electrolytes (SLIC-QSPBEs) integrate the features of the ultrathin membrane thickness (10 µm), the nanofibril backbone-strengthened porous nanonetwork (Young's modulus = 1.9 GPa), and the high-rate single lithium-ion conducting diblock copolymer brushes. As a result, the ultrathin yet robust SLIC-QSPBEs enable ultralong-term (over 3300 h) reversible and stable lithium plating/stripping in Li/Li symmetrical cell at a current density of 1 mA cm-2 for lithium anode. This work affords a promising strategy to develop advanced electrolytes for solid-state lithium-metal batteries.

3.
J R Soc Interface ; 17(168): 20200174, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32693747

RESUMO

The progression of game theory from classical to evolutionary and spatial games provided a powerful means to study cooperation, and enabled a better understanding of general cooperation-promoting mechanisms. However, current standard models assume that at any given point players must choose either cooperation or defection, meaning that regardless of the spatial structure in which they exist, they cannot differentiate between their neighbours and adjust their behaviour accordingly. This is at odds with interactions among organisms in nature who are well capable of behaving differently towards different members of their communities. We account for this natural fact by introducing a new type of player-dubbed link players-who can adjust their behaviour to each individual neighbour. This is in contrast to more common node players whose behaviour affects all neighbours in the same way. We proceed to study cooperation in pure and mixed populations, showing that cooperation peaks at moderately low densities of link players. In such conditions, players naturally specialize in different roles. Node players tend to be either cooperators or defectors, while link players form social insulation between cooperative and defecting clusters by acting both as cooperators and defectors. Such fairly complex processes emerging from a simple model reflect some of the complexities observed in experimental studies on social behaviour in microbes and pave a way for the development of richer game models.


Assuntos
Comportamento Cooperativo , Teoria dos Jogos , Evolução Biológica , Dinâmica Populacional , Comportamento Social
4.
Int J Pharm ; 535(1-2): 325-332, 2018 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-29051121

RESUMO

Three dimensional (3D) extrusion-based printing is a paste-based rapid prototyping process, which is capable of building complex 3D structures. The aim of this study was to explore the feasibility of 3D extrusion-based printing as a pharmaceutical manufacture technique for the fabrication of gastro-floating tablets. Novel low-density lattice internal structure gastro-floating tablets of dipyridamole were developed to prolong the gastric residence time in order to improve drug release rate and consequently, improve bioavailability and therapeutic efficacy. Excipients commonly employed in the pharmaceutical study could be efficiently applied in the room temperature 3D extrusion-based printing process. The tablets were designed with three kinds of infill percentage and prepared by hydroxypropyl methylcellulose (HPMC K4M) and hydroxypropyl methylcellulose (HPMC E15) as hydrophilic matrices and microcrystalline cellulose (MCC PH101) as extrusion molding agent. In vitro evaluation of the 3D printed gastro-floating tablets was performed by determining mechanical properties, content uniformity, and weight variation. Furthermore, re-floating ability, floating duration time, and drug release behavior were also evaluated. Dissolution profiles revealed the relationship between infill percentage and drug release behavior. The results of this study revealed the potential of 3D extrusion-based printing to fabricate gastro-floating tablets with more than 8h floating process with traditional pharmaceutical excipients and lattice internal structure design.


Assuntos
Dipiridamol/química , Composição de Medicamentos/métodos , Excipientes/química , Impressão Tridimensional , Disponibilidade Biológica , Celulose/química , Preparações de Ação Retardada/química , Liberação Controlada de Fármacos , Mucosa Gástrica/metabolismo , Derivados da Hipromelose/química , Comprimidos
5.
Int J Pharm ; 525(1): 5-11, 2017 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-28377316

RESUMO

The purpose of this study was to explore the feasibility of combining fused deposition modeling (FDM) 3D printing technology with hot melt extrusion (HME) to fabricate a novel controlled-release drug delivery device. Glipizide used in the treatment of diabetes was selected as model drug, and was successfully loaded into commercial polyvinyl alcohol (PVA) filaments by HME method. The drug-loaded filaments were printed through a dual-nozzle 3D printer, and finally formed a double-chamber device composed by a tablet embedded within a larger tablet (DuoTablet), each chamber contains different contents of glipizide. The drug-loaded 3D printed device was evaluated for drug release under in vitro dissolution condition, and we found the release profile fit Korsmeyer-Peppas release kinetics. With the double-chamber design, it is feasible to design either controlled drug release or delayed drug release behavior by reasonably arranging the concentration distribution of the drug in the device. The characteristics of the external layer performed main influence on the release profile of the internal compartment such as lag-time or rate of release. The results of this study suggest the potential of 3D printing to fabricate controlled-release drug delivery system containing multiple drug concentration distributions via hot melt extrusion method and specialized design configurations.


Assuntos
Preparações de Ação Retardada , Glipizida/administração & dosagem , Impressão Tridimensional , Tecnologia Farmacêutica , Comprimidos
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