Evidence map›Paper›PMID 37003312›Full record

ArticleInternational journal of pharmaceutics2023

In depth characterization of physicochemical critical quality attributes of a clinical drug-dendrimer conjugate.

Silvia Sonzini, Fanny Caputo, Dora Mehn, Luigi Calzolai, Sven Even Borgos, Astrid Hyldbakk, Kevin Treacher, Weimin Li, Mark Jackman, Najet Mahmoudi and 5 more

Abstract read
In one paragraph

Article in International journal of pharmaceutics, 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
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

15 authors.

Silvia SonziniAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Cambridge, UK. Electronic address: silvia.sonzini@astrazeneca.com.
Fanny CaputoDepartment of Biotechnology and Nanomedicine, SINTEF Industry, Trondheim, Norway; Univ. Grenoble Alpes, CEA, LETI, F-38000 Grenoble, France.
Dora MehnEuropean Commission, Joint Research Centre (JRC), Ispra, Italy.
Luigi CalzolaiEuropean Commission, Joint Research Centre (JRC), Ispra, Italy.
Sven Even BorgosDepartment of Biotechnology and Nanomedicine, SINTEF Industry, Trondheim, Norway.
Astrid HyldbakkDepartment of Biotechnology and Nanomedicine, SINTEF Industry, Trondheim, Norway.
Kevin TreacherNew Modalities & Parenteral Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, UK.
Weimin LiAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Cambridge, UK.
Mark JackmanAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Cambridge, UK.
Najet MahmoudiRutherford Appleton Laboratory, ISIS Facility, Science and Technology Facilities Council, Didcot OX11 0QX, UK.
M Jayne LawrenceDivision of Pharmacy & Optometry and the North West Centre for Advanced Drug Delivery (NoWCADD), School of Health Sciences, University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Claire PattersonAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Macclesfield, UK.
David OwenStarpharma Pty Ltd., 4-6 Southampton Cresent, Abbotsford, Victoria 3067, Australia.
Marianne AshfordAdvanced Drug Delivery, Pharmaceutical Sciences, R&D, AstraZeneca, Macclesfield, UK.
Nadim AkhtarNew Modalities & Parenteral Development, Pharmaceutical Technology & Development, Operations, AstraZeneca, Macclesfield, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A deep and detailed understanding of drug-dendrimer conjugates key properties is needed to define the critical quality attributes that affect drug product performance. The characterization must be executed both in the formulation media and in biological matrices. This, nevertheless, is challenging on account of a very limited number of suitable, established methods for characterizing the physicochemical properties, stability, and interaction with biological environment of complex drug-dendrimer conjugates. In order to fully characterize AZD0466, a drug-dendrimer conjugate currently under clinical development by AstraZeneca, a collaboration was initiated with the European Nanomedicine Characterisation Laboratory to deploy a state-of-the-art multi-step approach to measure physicochemical properties. An incremental complexity characterization approach was applied to two batches of AZD0466 and the corresponding dendrimer not carrying any drug, SPL-8984. Thus, the aim of this work is to guide in depth characterization efforts in the analysis of drug-dendrimer conjugates. Additionally, it serves to highlight the importance of using the adequate complementary techniques to measure physical and chemical stability in both simple and biological media, to drive a complex drug-dendrimer conjugate product from discovery to clinical development.

Indexed as

DendrimersNanomedicineDendrimersDrug deliveryDrug-dendrimer conjugateNanomedicineNanoparticlePhysicochemical properties

Identifiers

PMID37003312
PMCPMC10157317

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.