Evidence map›Paper›PMID 23567484›Full record

ArticleEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V2013

Lyophilization of a triply unsaturated phospholipid: effects of trace metal contaminants.

N M Payton, M F Wempe, J L Betker, T W Randolph, T J Anchordoquy

Open access · greenAbstract read
In one paragraph

Article in European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Long-term storage of lyophilized liposomal formulations.Journal of pharmaceutical sciences · 2014
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

N M PaytonDepartment of Pharmaceutical Sciences, University of Colorado Denver, USA. Electronic address: Nicole.payton@ucdenver.edu.
M F Wempe
J L Betker
T W Randolph
T J Anchordoquy
University of Colorado Denver · USUniversity of Colorado Boulder · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Exploiting Cholesterol Nanodomains to Improve TargetingR01GM093287 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ANCHORDOQUY, THOMAS · 2011 to 2014
$1.1M
NCATS NIH HHS UL1 TR001082NCRR NIH HHS 5UL1RR025780NCRR NIH HHS UL1 RR025780NIBIB NIH HHS R01 EB006398NIGMS NIH HHS R01 GM093287NIGMS NIH HHS R01GM093287-01A1
6 · The paper itself

Abstract

As liquid liposomal formulations are prone to chemical degradation and aggregation, these formulations often require freeze drying (e.g., lyophilization) to achieve sufficient shelf-life. However, liposomal formulations may undergo oxidation during lyophilization and/or during prolonged storage. The goal of the current study was to characterize the degradation of 1,2-dilinolenoyl-sn-glycero-3-phosphocholine (DLPC) during lyophilization and to also probe the influence of metal contaminants in promoting the observed degradation. Aqueous sugar formulations containing DLPC (0.01 mg/ml) were lyophilized, and DLPC degradation was monitored using HPLC/UV and GC/MS methods. The effect of ferrous ion and sucrose concentration, as well as lyophilization stage promoting lipid degradation, was investigated. DLPC degradation increased with higher levels of ferrous ion. After lyophilization, 103.1 ± 1.1%, 66.9 ± 0.8%, and 28.7 ± 0.7% DLPC remained in the sucrose samples spiked with 0.0 ppm, 0.2 ppm, and 1.0 ppm ferrous ion, respectively. Lipid degradation predominantly occurs during the freezing stage of lyophilization. Sugar concentration and buffer ionic strength also influence the extent of lipid degradation, and DLPC loss correlated with degradation product formation. We conclude that DLPC oxidation during the freezing stage of lyophilization dramatically compromises the stability of lipid-based formulations. In addition, we demonstrate that metal contaminants in sugars can become highly active when lyophilized in the presence of a reducing agent.

Indexed as

BuffersCarbohydratesDrug ContaminationFerrous CompoundsFreeze DryingFreezingLipidsMetalsOsmolar ConcentrationPhosphatidylcholinesPhospholipidsSucroseSulfitesTrace Elements1,2-linoleoylphosphatidylcholineBuffersCarbohydratesFerrous CompoundsLipidsMetalsPhosphatidylcholinesPhospholipidssodium sulfiteSucroseSulfitesTrace ElementsChemical stabilityDLPCFreeze-dryingFreezingLiposomesLyophilizationMetal contaminationOxidationUnsaturated lipids

Identifiers

PMID23567484
PMCPMC3797213
OpenAlexW1976988946

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.