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Varnish PV3 (15%) designed a release curve of 20% during the first 8 hours, thereafter stopping and restarting after 24 hours, becoming steady for 8 weeks.
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Hori et al. [ 15] designed a sustained release system for ophthalmic application of EGF using cationized gelatin hydrogel (CGH) as the carrier.
To improve it, avoiding efficiency loss, we have designed a controlled-release system, in which PZQ was encapsulated in β-cyclodextrin (β-CD).
In order to design a controlled release system with specified release characteristics, values of diffusion coefficient and solubility are required.
We designed a growth factor release system to potentially stabilize neovascularization in the treatment of ischemic tissue.
The purpose of the present research was to design a controlled release porous collagen-microbead hybrid scaffold with controlled pore structure capable of releasing insulin for application to cartilage tissue regeneration.
The aim of this study was to design a controlled release vehicle for insulin to preserve its stability and biological activity during fabrication and release.
The goal of this study was to design a prolonged release system of the hypnotic agent zolpidem (ZP) useful for the treatment of insomnia.
It has also been reported that the silica gel adsorbs the methanol and its addition is effective for designing a prolonged release system for methanol [ 58].
Determining the intracellular fate of the p AA- co-AAm) NPs is essential to designing a drug release process, due to the importance of the local chemical environment inside the cells.
Inspired by this well-established, naturally occurring mechanism, we designed a nanocomplex with the release of a stimulating motif controlled by Schiff base formation and hydrolysis.
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CEO of Professional Science Editing for Scientists @ prosciediting.com