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However, the efficacy was insufficient for drug registration

[168] showed that the ability of PET fragments to interact with cell membranes is strongly size-dependent: PET monomers readily inserted into phospholipid bilayers from the aqueous phase, whereas PET tetramers did not penetrate the membrane, implying higher passive-diffusion potential and thus greater bioavailability for smaller particles

Transcriptomic Profiling Unravels Novel Deregulated Gene Signatures Associated with Acute Myocardial Infarction: A Bioinformatics Approach

Independent laboratory verification of molecular weight and structure is performed on every production run

Filardo G, et al

Alternative and Complementary Therapies, 19 (4), 217-230