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This in vitro pilot study was designed to determine the accuracy of addition silicone impressions made with custom trays or made with either passive or stressed dual-arch trays.
This in vitro pilot study prior to in vivo experiments suggests that on-stent cell delivery of EPCs may be novel therapeutic devices for re-endothelialization or endothelium lining or paving at an atherosclerotic arterial wall, resulting in the prevention of on-stent thrombus formation and in-stent restenosis, as well as the rapid formation of normal tissue architecture.
Our in vitro pilot study yielded promising results; however, additional animal studies are required to confirm these findings.
In an in vitro pilot study, the combination of ciprofloxacin and colistin has yielded promising results in killing P. aeruginosa biofilms based on the novel concept of combining antibiotics that target the different metabolic states of the biofilm cells.
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After evaluating the ability of 9 to bind to its targets in vitro, a pilot in vivo study was necessary to test the ability of the HtBv probe to be useful for delivering imaging agents to tumors that may express different levels of PSMA and/or αvβ3 integrin.
Feasibility was demonstrated with computer simulations (treating acoustically induced displacements, concomitant heating, and US displacement-estimation algorithms) and pilot in vitro experimental studies, which agree qualitatively in differentiating HIFU lesions from normal tissue.
In addition to its direct effects on MCT by KIT inhibition, in vitro and in vivo, pilot studies indicate that masitinib also has a potential for chemosensitisation to classic chemotherapeutic agents including gemcitabine, vinblastine and doxorubicin [ 15- 17].
Animal sizes for our experiments were determined according to our in vitro assays and a pilot test without previous statistical calculation.
The sufficiently high specific absorption rate (SAR) (∼256.4 W/g in an agar solution) achieved at the biologically safe range of applied AC magnetic field and frequency as well as the superior biocompatibility of EMZF-SPNPA, which were confirmed from both in-vitro and in-vivo animal pilot studies, allowing it to be considered as a potential localized HSPs agent.
In a pilot study in vitro with porcine macrophages, we obtained similar results (data not shown).
After determining the in vitro thrombolytic activity in equine thrombi, pilot pharmacokinetic data were obtained in healthy horses.
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CEO of Professional Science Editing for Scientists @ prosciediting.com