Evidence map›Paper›PMID 34758972›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2023

Evaluation of 30-days stability of morphine hydrochloride and clonidine at high and low concentrations in polypropylene syringes.

Emilie Catry, Marie-Lise Colsoul, Mélanie Closset, Caroline Nyssen, Justine Hubert, Laura Soumoy, Benoît Bihin, Jacques Jamart, Jean-Daniel Hecq, Laurence Galanti

Open access · greenAbstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 75% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Interpol review of forensic drug chemistry, 2022-2025.Forensic science international. Synergy · 2026
    Review
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

10 authors at 1 institution in 1 country.

Emilie CatryDepartment of Laboratory, CHU UCL, Namur, Yvoir, Belgium emilie.catry@saintluc.uclouvain.be.
Marie-Lise ColsoulDepartment of Laboratory, CHU UCL, Namur, Yvoir, Belgium.
Mélanie ClossetDepartment of Laboratory, CHU UCL, Namur, Yvoir, Belgium.
Caroline NyssenDepartment of Pharmacy, CHU UCL Namur, Yvoir, Belgium.
Justine HubertDrug Stability Research Group, CHU UCL Namur, Yvoir, Belgium.
Laura SoumoyDrug Stability Research Group, CHU UCL Namur, Yvoir, Belgium.
Benoît BihinDrug Stability Research Group, CHU UCL Namur, Yvoir, Belgium.
Jacques JamartDrug Stability Research Group, CHU UCL Namur, Yvoir, Belgium.
Jean-Daniel HecqDrug Stability Research Group, CHU UCL Namur, Yvoir, Belgium.
Laurence GalantiDepartment of Laboratory, CHU UCL, Namur, Yvoir, Belgium.
CHU Dinant Godinne UCL Namur · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesClonidine is an alpha-2 adrenoreceptor agonist and is frequently combined with opioids (ie, morphine hydrochloride (HCl)) for the management of chronic pain. In palliative care, the administration of clonidine and morphine HCl is recommended in case of tolerance effect. This study aimed to evaluate the physical and chemical stability of this admixture at high and low concentrations in 14 and 48 mL polypropylene syringes.

methodsThe stability of a low concentration admixture of clonidine (Catapressan 0.15 mg/mL, Boehringer Ingelheim, Germany) and morphine (morphine HCl 40 mg/mL, Sterop, Belgium) at 0.003 and 0.417 mg/mL, respectively, was evaluated by using five polypropylene syringes of 48 mL. The high concentration admixture consisted of 0.032 mg/mL clonidine and 4.286 mg/mL morphine HCl and was evaluated by using five polypropylene syringes of 14 mL. All syringes were stored for 30 days at 5°C±3°C. Periodic samples were visually and microscopically examined to observe any particle appearance or colour change. pH and absorbance at three wavelengths (350, 410 and 550 nm) were monitored. The concentrations were measured by ultra-high performance liquid chromatography-photodiode array detection.

resultsDuring the 30 days, there was no change in colour or appearance of opacity, turbidity or precipitation, and pH remained stable. The low and high concentration admixtures were considered chemically stable since the lower limit of the 90% CI remained superior to 90% of the initial concentration. Concentration measurements showed that the degradation rate was less than 1% over 10 days for each component in both admixtures.

conclusionsThe admixture of clonidine and morphine HCl at low and high concentrations in polypropylene syringes appeared to be physically and chemically stable throughout the study period of 30 days at 5°C±3°C. In conclusion, the admixture can be prepared in advance under aseptic conditions by a centralised intravenous additive service in the pharmacy department.

Indexed as

ClonidinePolypropylenesAnalgesics, OpioidDrug StabilityHumansMorphine DerivativesSyringesAnalgesics, OpioidClonidineMorphine DerivativesPolypropylenesanalytic sample preparation methodsdrug incompatibilityhospitalpalliative carepharmaceutical preparationspharmacy service

Identifiers

PMID34758972
PMCPMC10086706
OpenAlexW3214463606

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.