49 research outputs found
OPTIMIZATION METHOD FOR ANKLE STRENGTH TRAINING DURING EXERCISE
ABSTRACT Introduction Good ankle joint strength is a precondition for high-quality exercise and is an important factor in preventing joint injuries. Objective Explore the method of optimizing ankle strength training during exercise. Methods 40 volunteers were selected and randomly divided into an experimental group and a control group. The 20 athletes in the experimental group were trained three times a week for six weeks using a control variable method, while the control group performed only professional daily physical training. Pre-training and post-training methods were used to collect and investigate the data regarding the effect of strength training on the ankle joint and its impact on skill and strength tests submitted to the athletes. Results Ankle strength training can improve ankle muscle strength and athletes’ ability to run and jump (P > 0.05). Conclusion Ankle joint strength training may improve athletes’ baseline sporting ability, improve ankle joint muscle strength, reduce the likelihood of joint injuries, and contribute to improved outcomes of various abilities, meriting further study and replication. Level of evidence II; Therapeutic studies - investigation of treatment outcomes.</div
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
Reconfigurable Liquids Stabilized by DNA Surfactants
Polyelectrolyte
microcapsules can be produced either by the layer-by-layer
assembly technique or the formation of polyelectrolyte complexes at
the liquid–liquid interface. Here, we describe the design and
construction of DNA microcapsules using the cooperative assembly of
DNA and amine-functionalized polyhedral oligomeric silsesquioxane
(POSS-NH2) at the oil–water interface. “Janus-like”
DNA surfactants (DNASs) assemble in situ at the interface, forming
an elastic film. By controlling the jamming and unjamming behavior
of DNASs, the interfacial assemblies can assume three different physical
states: solid-like, elastomer-like, and liquid-like, similar to that
seen with thermoplastics upon heating, that change from a glassy to
a rubbery state, and then to a viscous liquid. By the interfacial
jamming of DNASs, the liquid structures can be locked-in and reconfigured,
showing promising potentials for drug delivery, biphasic reactors,
and programmable liquid constructs
