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Residual solvent (revision 8)

Old revision·02:57, 30 Nov 2024·TechnicianTeal

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Residual solvent
Governing guidanceICH Q3C; USP <467>
Determined byHeadspace gas chromatography
ClassesClass 1 avoid; Class 2 limit; Class 3 low toxicity
Topic infobox · conventions

Residual solvents are organic volatile chemicals used or produced in manufacture that remain in the finished substance. They are classified by toxicity: Class 1 solvents are to be avoided, Class 2 are limited to specified concentrations, and Class 3 are regarded as low-risk and controlled at a general limit.[1]

In peptide manufacture the solvents of interest are those used in synthesis, cleavage and purification — dimethylformamide, dichloromethane, acetonitrile, methanol, trifluoroacetic acid and diethyl ether among them. Several fall in Class 2 and are limited accordingly.[2]

Determination is by headspace gas chromatography, in which the sample is equilibrated in a sealed vial and the vapour above it sampled. The method is specific to the named solvents: a solvent not on the method's list is not looked for and will not be reported.[2]

Classes and limits

[edit]
ClassBasisExamples relevant to peptidesControl
1Known or suspected human carcinogenBenzene, carbon tetrachlorideTo be avoided
2Non-genotoxic animal carcinogen or other toxicityDichloromethane, methanol, acetonitrile, N,N-dimethylformamideLimited by specified concentration
3Low toxic potentialAcetic acid, ethanol, diethyl ether, acetoneGenerally limited at 0.5%

Limits for Class 2 solvents are derived from a permitted daily exposure and a maximum daily dose, so a concentration limit depends on how much substance is administered. A concentration expressed without reference to that basis cannot be assessed against a limit.[1]

Dimethylformamide is the solvent most characteristic of peptide synthesis and is a Class 2 solvent with a comparatively low limit. Its persistence in a dried peptide depends on the drying regime and on whether an intermediate solvent exchange was performed, and it contributes to any loss-on-drying figure obtained on the same material.[3][4]

References

  1. ^ a b International Council for Harmonisation, Q3C(R8): Impurities — Guideline for Residual Solvents (2021).
  2. ^ a b United States Pharmacopeia, General Chapter <467>, Residual Solvents.
  3. ^ United States Pharmacopeia, General Chapter <1503>, Quality Attributes of Synthetic Peptide Drug Substances.
  4. ^ United States Pharmacopeia, General Chapter <731>, Loss on Drying.