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Immunoliposomes provide a complementary, and in many instances advantageous, drug delivery strategy to antibody-drug conjugates.
Particulate nanocarriers have been praised for their advantageous drug delivery properties in the lung, such as avoidance of macrophage clearance mechanisms and long residence times.
Solid lipid nanoparticles (SLN) have been praised for their advantageous drug delivery properties such as biocompatibility, controlled release and passive drug targeting.
Our results demonstrate that the SIP exhibits markedly advantageous drug release performance in terms of dissolution time.
It might be possible to identify other drugs with similar pharmacological effects or advantageous drug combinations when targeting two positions in the network to get a stronger effect of the treatment, e.g. combination of Glipizide (PPARG) and Metformin (AMPK).
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Increase in MDR parasite fitness affects the mutations in the parasite population, which can establish advantageous drug-resistant genotypes [ 59– 62].
However, a high polysaccharide concentration can be advantageous for drug delivery systems.
Liposomes are potentially advantageous targeted drug carriers for such intravascular applications.
This polymer may be an advantageous implantable drug delivery system for use in acute oxidative stress prophylaxis and/or chronic oxidative stress cell therapies due to its solid/liquid reversibility in a redox environment, controlled thiolation, high loading capacity through covalent drug-addition, and simple post-synthesis modification which bound-thiols introduce.
CB[n] compounds are expected to be particularly advantageous in drug delivery studies because they bind their targets strongly (generally Ka>104 M−1) by a combination of the hydrophobic effect and ion-dipole interactions with the ureidyl C = O groups of the CB[n] portals [13], [14], [15].
The uniform mesoporous pore size along with magnetic core (Fe) are advantageous for drug delivery applications.
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