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nuclei from sample and internal standard source plants or cells were prepared; n represents the number of times each nuclei preparation was sampled by cell flow cytometry.
Forty experimentally produced HA disks sintered at 870 to 920 °C were prepared (n = 20 × 2).
Spray-dried melatonin-loaded nanocapsules were prepared (n = 3) using an MSD® 1.0 spray dryer (Labmaq, São Paulo, Brazil).
Porcine colon explants from 2 pigs were prepared (n = 20) and cultured for 0h, 8h, 18h and 24h using the device.
Melatonin-loaded polymeric nanocapsules (NC) were prepared (n = 3) by interfacial deposition of the preformed polymer according to the method described by Fessi and co-workers [36].
Four photoelastic models were prepared (n = 1): Model 1 – conventional EH cylindrical implant (Ø 4.0 mm × 11 mm - Neodent®), Model 2 – modified EH cylindrical implant, Model 3 – conventional MT Conical implant (Ø 4.3 mm × 10 mm - Neodent®) and Model 4 – modified MT conical implant.
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Alternatively, Jeong et al. prepared N-doped graphene by a modified Hummer's method followed by a nitrogen plasma process [30].
Hence, we prepared N-carboxymethyl chitosan (MCC) coated carvedilol loaded SLN to protect the rapid release of carvedilol in acidic environment.
Prepared N-halamine polymers were designed to contain multi-available positions for halogenation and quaternarization and to tune the stability of halogens attached to the polymers.
These properties show that the as synthesized S-doped microporous carbon material can be more effective than similarly prepared N-doped microporous carbons in CO2 capture.
Following this strategy we designed and prepared N-hydroxylactam molecules of different size through a synthetic protocol based on a ring closing metathesis amenable to a fragment-based approach potentially leading to a large molecular diversity.
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