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We analysed their chemical stability and plasma enzymatic hydrolysis, and we also evaluated the release of the antitumoral drug in the presence of the tyrosinase.
We evaluated the release characteristics using a novel in vitro model that simulates the dynamic intestinal environment by employing bicarbonate buffers representative of the conditions and contents of the gastrointestinal lumen.
We designed and fabricated a poly(D,L -lactide-co-glycolide (PLGA)-baseD,L -lactide-co-glycolidevery system anD,L -lactide-co-glycolidef antibiotics both in vitro anD,L -lactide-co-glycolide
The present study investigated the degradation and loading capability of bioresorbable microspheres with an anti-angiogenic agent, sunitinib, and then evaluated the release profiles in different media (PBS, 10 μg/mL and 4 mg/mL lysozyme solutions), and tested catheter deliverability as well as potential antiangiogenic effects of the loaded microspheres.
Numerous in vitro and in vivo studies have evaluated the release of metals from orthodontic appliances in biologic fluids such as saliva, blood, and urine.
In order to evaluate if the results obtained in the rat are transferrable to humans we evaluated the release of LTB4 and cysLTs from A23187-stimulated human neutrophils and monocytes, respectively.
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The pH dependence leaching test with continuous pH-control evaluates the release of constituents as a function of the pH.
In order to evaluate the release capacity of the heparin-conjugated scaffolds, lysozyme was used as a model protein for conjugation.
To evaluate the release of calcium and hydroxide ions from the pulp-capping materials Hydro C, NuCap, Life, and Ultrablend Plus.
Simulation results confirmed that assuming homogeneous materials to evaluate the release of contaminants from porous waste materials may result in erroneous long-term field performance assessment.
Finally, an in vitro elution method coupled with high-performance liquid chromatography was used to evaluate the release behavior of prepared formulations.
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