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IGF-1 DES Nasal Spray certificate of analysis, lot PL-2610-103

Certificate PL-26-00217 reports the release tests for IGF-1 DES Nasal Spray lot PL-2610-103: 99.36% purity by reverse-phase HPLC and identity confirmed by LC-MS, tested October 6, 2026. The lot number printed on each unit matches this certificate.

Certificate numberPL-26-00217
Lot numberPL-2610-103
CompoundIGF-1 DES Nasal Spray 1 mg
SequenceH-TLCGAELVDALQFVCGDRGFYFNKPTGYGSSSRRAPQTGIVDECCFRSCDLRRLEMYCAPLKPAKSA-OH (67 residues; three intrachain disulfides; free N- and C-termini)
Molecular formulaC 319 H 501 N 91 O 96 S 7 (reduced-chain calculation)
CAS number112603-35-7
Purity (RP-HPLC)99.36%
Identity (LC-MS)Conforms (7,365.34 Da) · expected 7365.4 Da, found 7365.34 Da
MethodRP-HPLC (UV 214 nm) + LC-MS
TestedOctober 6, 2026
Retest byOctober 5, 2028
Tested byManufacturer’s in-house laboratory (not an independent third-party test)
ConclusionConforms

Tests run on this lot

TestMethodSpecificationResult
Identity (mass)LC-MS, ESI positiveTheoretical ± 1.0 Da7,365.34 Da (PASS)
PurityRP-HPLC, UV 214 nm, area%≥ 99.0%99.36% (PASS)
Largest impurityRP-HPLC, area%≤ 1.0%0.32% (RT 16.30) (PASS)
Assay (label claim)Assay vs label claim1.9–2.1 mg/bottle1.98 mg/bottle (PASS)
Bacterial endotoxinLAL, kinetic≤ 5.0 EU/mg0.403 EU/mg (PASS)
Aerobic count (TAMC)USP <61>< 10 CFU/mL< 10 CFU/mL (PASS)
Yeast & mold (TYMC)USP <61>< 10 CFU/mL< 10 CFU/mL (PASS)
E. coliUSP <62>AbsentAbsent (PASS)

What these results mean

HPLC purity is the share of UV-detectable material that elutes as the target compound; it is not the same as net peptide content, which also accounts for water and counter-ions. Identity means the measured mass matched the mass calculated for the compound. A certificate reports only the tests run on this lot; endotoxin, sterility and contaminant panels are not part of standard lot release. How to read a certificate of analysis.

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