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Furthermore, surface functionalization, nanotopography, responsive drug release, motion-based responses, and permeation enhancers have been incorporated into such platforms to further enhance drug uptake.
Magnetically responsive drug carriers can be magnetite (Fe3O4) or maghemite (Fe2O3).
These nanocomposites possess high heat-generating ability, pH and NIR responsive drug delivery, and heat-induced high drug release as well.
These nanocomposites possess high heat-generating ability, pH responsive drug delivery, and heat-induced high drug release as well.
This study describes the design of an MSN-based carrier for use in a heat shock responsive drug delivery system.
The drug loading experiment of Zn-HAp nanoparticles was then confirmed with 1 mol% Zn-HAp (which had the maximum drug loading efficiency with pH responsive drug interaction).
So a non-selective redox responsive drug delivery system may result in an undesired drug release in normal cells and relevant side-effects.
Therefore, the DOX-MMS can be optimized as powerful delivery system for efficient magnetic responsive drug release and chemo-thermal therapy.
Taken together, these findings suggest that MBC-MSN are a strong candidate to act as a carrier in heat shock responsive drug delivery.
Magnetic field induced thermo-responsive and pH responsive drug release studies were carried out and it was found that MCP nanogels have a good on-demand drug release properties.
Prodrug-based self-assembled hydrogels represent a new class of active biomaterials that can be harnessed for medical applications, in particular the design of stimuli responsive drug delivery devices.
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