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Octa-Ad-grafted polyamidoamine dendrimer, CD-grafted branched polyethylenimine, and Ad-grafted poly ethylene glycol) were prepared by the same methods reported previously.
A list of primers used to create first-generation libraries beyond those reported in ref (15) is shown in Table 4. Second- and third-generation libraries were prepared by the same methods, with the appropriate mutant OYE 2.6 gene replacing the wild-type as the template in PCR amplifications.
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Compound 4 was prepared by the same method as described in the preparation of compound 3 using n-octylbenzene and 3-nitropropanoyl chloride (making from 3-nitropropanoic acid [18] and thionyl chloride) as starting material.
The results suggested that there were significant differences in the catalytic activities for metal DENs of different structures: the catalysts of bimetallic nanoparticles via dendrimer-encapsulated preparation were often improved in performance over those of monometallic nanoparticle catalysts prepared by the same method, which should be due to the synergistic electronic effect.
Blank NPs were also prepared by the same method without adding gemcitabine at any stage of the preparation.
DMAB-modified PLGA nanoparticles were prepared by the same method.
The (FA + PEG -CS-NPs were PEG -CS-NPs the same method.
Docetaxel-loaded PCL nanoparticles and empty PCL/Pluronic F68 nanoparticles were prepared by the same method.
The metal masks are prepared by the same method as of that used for catalyst pattern.
Their homopolymers PMMA and PTEVS were also prepared by the same method.
These nanocomposites also exhibited enhanced thermal stability relative to the virgin polystyrene prepared by the same method.
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