What a reference standard is, and what an in-house standard is not
Matching a retention time against a standard is evidence of consistency, not proof of identity. Two different species can elute at the same time on one method.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 2 of 8 of this archive, newest first.
Matching a retention time against a standard is evidence of consistency, not proof of identity. Two different species can elute at the same time on one method.
Chain of custody, in a regulated setting, begins at sampling. Here it begins when the package arrives.
The Journal submitted split samples from single lots to three assay services, under names unconnected to this publication, and published each method alongside each result.
Aggregates dissociate in the mobile phase and are recorded as monomer. Only a size-based separation reports them.
A badge asserts that something was tested. It does not assert what, when, on whose sample, by what method, or whether the lot on sale is the lot that was tested.
This piece takes the measurement apart into the decisions it is made of, because each decision moves the answer.
The condition on arrival is recorded by some services and not others, and it is one of the more informative lines in a report.
A badge asserts that something was tested. It does not assert what, when, on whose sample, by what method, or whether the lot on sale is the lot that was tested.
Two years ago we ran an anonymised version of this comparison and promised a named one. This is it, with every method printed in full.
A chromatogram is silent on everything that does not absorb: counter-ions, water, inorganic salts and non-chromophoric excipients all contribute mass to the vial and nothing…
Every third-party report in this market describes a sample somebody chose to send. That choice is outside the laboratory’s control and outside its records.
Chain of custody, in a regulated setting, begins at sampling. Here it begins when the package arrives.
Lot-level verification with a public report is a real and achievable thing. It exists in this market, on a minority of listings.
The most useful single addition to any purity determination is a second separation under a different pH or on a different stationary phase, and the second-most useful is a…
Every third-party report in this market describes a sample somebody chose to send. That choice is outside the laboratory’s control and outside its records.
The condition on arrival is recorded by some services and not others, and it is one of the more informative lines in a report.
Chromatographic software does not integrate every fluctuation in the baseline. It applies a threshold, and the threshold changes the reported purity by amounts that matter…
Every step between the laboratory report and the product page removes information, and the badge is the last step.
Peptide bonds absorb strongly near 214 nm; aromatic side chains absorb near 280 nm. A method reading at 280 is blind to any fragment lacking an aromatic residue.
Ion-pairing additives sharpen peptide peaks and suppress ionisation in the mass spectrometer, which is why the purity method and the identity method are often not the same…