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Reconstitution of lyophilised peptides (revision 13)

Old revision·13:52, 12 Nov 2024·DeadSpaceDot

This is an old revision of this page, as it stood at 13:52, 12 Nov 2024, saved by DeadSpaceDot with the summary give the worked example to two significant figures throughout. It may differ substantially from the current revision, and any error it contains may since have been corrected.
For the calculator, see Reconstitution calculator. For the drying process this reverses, see Lyophilisation.
Reconstitution of lyophilised peptidesPreparation
cakeheadspacecrimp5 mg
Diluent is directed down the vial wall rather than onto the cake.
ReversesLyophilisation
Common diluentsBacteriostatic water, Sterile water for injection
ConsequenceSolution stability is far shorter than powder stability
Analytical method infobox · conventions

Reconstitution is the dissolution of a lyophilised peptide cake in a liquid diluent. The dried solid is the stable form: once in solution the peptide is exposed to hydrolysis, deamidation, oxidation and aggregation, all of which proceed far faster in the liquid phase.[1]

Two quantities determine the resulting concentration: the mass of peptide actually present in the vial, and the volume of diluent added. The first is not the number printed on the label unless content, water and fill mass are known — a vial nominally containing 5 mg may contain appreciably less peptide. See Underfilling.[2]

The choice of diluent determines how long the resulting solution can be regarded as usable. Bacteriostatic water contains a preservative and is used where a container will be entered more than once; Sterile water for injection contains none. Neither confers sterility on a non-sterile powder.[3]

Mechanics

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Diluent is directed against the vial wall rather than onto the cake. A jet striking the cake dissolves it violently, generating the air–liquid interfaces and shear at which peptides unfold and aggregate; running the liquid down the wall lets the cake dissolve from beneath.[1]

Dissolution is completed by gentle swirling or by leaving the vial to stand. Shaking is the practice most likely to produce visible haze, for the same interfacial reason. A cake that has not fully dissolved after several minutes should be given time rather than agitation.

Visual inspection after dissolution is informative. A clear, colourless solution free of visible particles is the expected result; haze, particles or fibrous material indicate that the material has changed, whatever the certificate said about the powder. See Peptide aggregation.[2]

References

  1. ^ a b Manning MC, Chou DK, Murphy BM, Payne RW, Katayama DS. "Stability of protein pharmaceuticals: an update." Pharmaceutical Research 27(4):544–575 (2010). PMID 20143256.
  2. ^ a b United States Pharmacopeia, General Chapter <1503>, Quality Attributes of Synthetic Peptide Drug Substances.
  3. ^ United States Pharmacopeia, General Chapter <797>, Pharmaceutical Compounding — Sterile Preparations.