Evidence map›Paper›PMID 38637597›Full record

ArticleScientific reports2024

Physicochemical stability of bortezomib solutions for subcutaneous administration.

Ángela Gómez, Mª Cristina Benéitez García, Nélida Barrueco, Mª Amparo Lucena-Campillo, Elena López-Lunar, Benito García-Díaz, Marta Vicario-de-la-Torre, Ismael Escobar-Rodríguez, María Esther Gil-Alegre

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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
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.

  1. 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

9 authors.

Ángela GómezDepartment of Pharmaceutical and Food Technology, Complutense University of Madrid, 28040, Madrid, Spain.
Mª Cristina Benéitez GarcíaDepartment of Basic Health Sciences, Area of Pharmacy and Pharmaceutical Technology, Faculty of Health Sciences, Rey Juan Carlos University, Madrid, Spain.ORCID 0000-0003-3139-9045
Nélida BarruecoPharmacy Service, Infanta Leonor Hospital, Madrid, Spain.
Mª Amparo Lucena-CampilloSevero Ochoa Hospital, Madrid, Spain.
Elena López-LunarDepartment of Pharmacy Jose Germain Psychiatric Institute. Department of Pharmacy and Pharmaceutical Technology, Complutense University of Madrid, Madrid, Spain.
Benito García-DíazPharmacy Service, Severo Ochoa Hospital, Madrid, Spain.
Marta Vicario-de-la-TorreDepartment of Pharmaceutical and Food Technology, Complutense University of Madrid, 28040, Madrid, Spain.
Ismael Escobar-RodríguezPharmacy Service, Infanta Leonor Hospital, Madrid, Spain.
María Esther Gil-AlegreDepartment of Pharmaceutical and Food Technology, Complutense University of Madrid, 28040, Madrid, Spain. megil@ucm.es.ORCID 0000-0002-8313-8261

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For the majority of cytotoxic drug preparations, such as bortezomib, the unit dose information is not available. In addition, there is a lack of information on the physicochemical stability of the pharmaceutical preparation after opening; this information is crucial for its administration to patients in successive visits, and the per-patient cost can be affected. The purpose of our proposed physicochemical stability study is to determine the shelf life of the reconstituted liquid product under refrigeration and clinical practice conditions. This evaluation was extended to both vials and ready-to-use syringes prefilled with the contents of the open vial. The stability test design includes the specified storage conditions and the critical physicochemical parameters of reconstituted injectable bortezomib. Furthermore, this approach includes the determination of impurities, the monitoring of the purity of the mean peak using a photodiode array, the control of the mass balance, the monitoring of subvisible particles using a laser diffraction analyser, and the setting of stability specifications. For the chemical stability study, the amount of bortezomib and its degradation products were determined using a stability-indicating HPLC method. The physical inspection of the samples was performed throughout the stability study, and their pH values were also monitored. Bortezomib (2.5 mg/mL) in 0.9% sodium chloride remained stable for 7 days when stored in both polypropylene syringes and vials at 5 ± 3 °C (refrigeration) and shielded from light. Additionally, it exhibits stability for 24 h under storage conditions simulating clinical use (20-30 °C and protected from light). The proposed protocol provides the stability in the vials once reconstituted and in prefilled refrigerated syringes; this protocol can be used to reduce waste and increase cost savings.

Indexed as

Antineoplastic AgentsDrug PackagingBortezomibChromatography, High Pressure LiquidDrug StabilityHumansPharmaceutical SolutionsPolypropylenesSyringesAntineoplastic AgentsBortezomibPharmaceutical SolutionsPolypropylenesAnd open vialsBortezomibPhysicochemical stabilityPrefilled syringesReady-to-administer subcutaneous injectionStability study protocol

Identifiers

PMID38637597
PMCPMC11026495

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Registered trials

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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.