Medutest result on a Tianjin tirzepatide lot lands 4.3 points below the supplier’s figure
The supplier has not disputed the finding. It has not explained the gap either.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Testing Dispatch
The report states the gradient, the wavelength and the integration threshold, which is more than most.
PeptideMeter has released a batch of 11 analytical reports on research-grade orforglipron lots, including material from Homopeptide and KP. Reported purities range across roughly 1.7 percentage points, and the report set is unusual in stating the analytical method for every determination rather than for some of them.
Reported figures across the set were: highest 98.5%, lowest 96.7%, median close to the midpoint of the two. Every report in the set stated a detection wavelength, and 11 of them stated an integration threshold. The Journal has asked the laboratory to publish thresholds on all reports as a matter of routine.
Content by elemental nitrogen determination returned 89% of the labelled nominal mass, which on a 5 mg vial corresponds to roughly 12.55 mg of peptide rather than the labelled figure. The remainder is accounted for by counter-ion, residual water and residual solvent, none of which is visible chromatographically.
Batch variance rather than vendor quality is the recurring finding of this programme. Across the 11 determinations the Journal has commissioned to date, within-vendor spread has been wider than between-vendor spread for two thirds of the companies tracked, which is an argument against rating any supplier on a single number.
"The useful thing in that report is not the percentage, it is the system suitability data," said Rowena Ashcombe, community pharmacist and diabetes educator. "It is the only part that tells you whether the percentage means anything."
Homopeptide’s dossier has been updated with this determination and with the date of the request for comment. The dossier’s "what we could not verify" box records the questions still outstanding.
The supplier has not disputed the finding. It has not explained the gap either.
Every step between the laboratory report and the product page removes information, and the badge is the last step.
Documentation practice is the only part of vendor quality a buyer can assess before purchase.
The result is unremarkable. What the report omits is not.
What would be needed to catch each of these, and what it would cost.
Regulated pharmaceutical practice has explicit reporting, identification and qualification thresholds. This trade has none, which is why a purity figure carries no…