Evidence map›Paper›PMID 39195030›Full record

ArticleGels (Basel, Switzerland)2024

In Vitro Physicochemical and Pharmacokinetic Properties of Bevacizumab Dissolved in Silicone Oils Compared to Hydrogel-Substitutes and Porcine Vitreous Bodies.

Maximilian Hammer, Jonathan Herth, Lorenz Herbster, Manuel Ben Böhmann, Marcel Muuss, Ramin Khoramnia, Alexander Scheuerle, Walter Mier, Sabrina Wohlfart, Gerd Uwe Auffarth and 1 more

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

11 authors.

Maximilian HammerUniversity Eye Clinic Heidelberg, 69120 Heidelberg, Germany.
Jonathan HerthThe David J Apple Laboratory for Vision Research, 69120 Heidelberg, Germany.
Lorenz HerbsterInstitute for Pharmacy and Molecular Biotechnology, 69120 Heidelberg, Germany.
Manuel Ben BöhmannInstitute for Pharmacy and Molecular Biotechnology, 69120 Heidelberg, Germany.
Marcel MuussUniversity Eye Clinic Heidelberg, 69120 Heidelberg, Germany.
Ramin KhoramniaUniversity Eye Clinic Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-6237-7773
Alexander ScheuerleUniversity Eye Clinic Heidelberg, 69120 Heidelberg, Germany.
Walter MierDepartment of Nuclear Medicine, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Sabrina WohlfartThe David J Apple Laboratory for Vision Research, 69120 Heidelberg, Germany.
Gerd Uwe AuffarthUniversity Eye Clinic Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-6927-5251
Philipp UhlInstitute for Pharmacy and Molecular Biotechnology, 69120 Heidelberg, Germany.

Funding

Dr. Hans Messer Stiftung n/aJoachim Herz Foundation Add-On Fellowship
6 · The paper itself

Abstract

Anti-VEGF agents, e.g., bevacizumab, are used in retinal surgery, while their interaction with silicone oils and novel hydrogels remains unclear. This study examines the in vitro pharmacokinetics of bevacizumab in silicone oil-filled eyes compared to various hydrogel replacements and the porcine vitreous body as well as its impact on the interface tension of silicone oils. An in vitro model filled with light or heavy silicone oil, porcine vitreous bodies, or hydrogels (alginate and polyethylene glycol (PEG)-based) was equilibrated with a balanced salt solution. Monitoring of bevacizumab in the aqueous phase was conducted for up to 24 h, and its effect on interfacial tension was studied. Significant differences in bevacizumab partitioning were observed across endotamponades after 24 h. In silicone oils, bevacizumab was found exclusively in the aqueous phase, while in the other endotamponades, it accumulated in the gel phase (96.1% in porcine vitreous body, 83.5% in alginate, and 27.6% in PEG-based hydrogel). Bevacizumab significantly reduced interfacial tension (40 to 8 mN/m), possibly enhancing silicone oil emulsification. The type of endotamponade heavily influenced the bevacizumab concentration in the aqueous. The vitreous body and replacement hydrogels likely serve as a drug reservoir, highlighting the need for in vivo studies to explore these interactions prior to clinical application.

Indexed as

bevacizumabhydrogelsintravitreal injectionsilicone oilvitreoretinal surgery

Identifiers

PMID39195030
PMCPMC11353491

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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.