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The sample size for all experiments ( in vitro and in vivo ) was not chosen with consideration of adequate power to detect a prespecified effect size

All experiments were designed to minimize the use of animals and the number of experiments performed

However, they can likely go for long periods between meals

Between mild and severe patients, the AUCs of the PE-P 18:0-20:3, PE-O 16:0-20:4, and TAG 54:4-FA22:4 were 0.725, 0.763, and 0.738, respectively ( Figures 5BD )

[DOI] [PMC free article] [PubMed] [Google Scholar] 91.Cheng D., Xu Q., Wang Y., Li G., Sun W., Ma D., Zhou S., Liu Y., Han L., Ni C

[13] There are no safety data regarding the use of nicotinic acid in doses above the RDA during breast-feeding