Evidence map›Paper›PMID 41711506›Full record

ArticleInvestigative ophthalmology & visual science2026

In-Depth Analysis of the Intravitreal Biocompatibility of Polyethylene Glycol of Different Molecular Weight in an In Vivo Porcine Model.

Maximilian Hammer, Ludwig Geisweid, Niklas Junker, Sabrina Wohlfart, Lea Skrzypczyk, Bryan Calder Ackermann, Jonathan Herth, Alexander Studier-Fischer, Walter Mier, Gerd U Auffarth and 2 more

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Maximilian HammerUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Ludwig GeisweidUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Niklas JunkerUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Sabrina WohlfartDavid J. Apple Laboratory for Vision Research, Heidelberg, Germany.
Lea SkrzypczykUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Bryan Calder AckermannUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Jonathan HerthInstitute of Pharmacy and Molecular Biotechnology, Heidelberg, Germany.
Alexander Studier-FischerDepartment of Urology and Urological Surgery, University Medical Center Mannheim, Mannheim, Germany.
Walter MierDepartment of Nuclear Medicine, Heidelberg University Hospital, Heidelberg, Germany.
Gerd U AuffarthUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Victor A AugustinUniversity Clinic Heidelberg, Department of Ophthalmology, Heidelberg, Germany.
Philipp UhlInstitute of Pharmacy and Molecular Biotechnology, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Polyethylene glycol (PEG)ylation is an established, increasingly used method to prolong the half-lives of active compounds applied intravitreally. However, the biocompatibility of high doses of high molecular weight PEG has never been systematically assessed in a translational in vivo model. The aim of this study was to evaluate the intraocular inflammatory and pro-angiogenic response as well as structural and functional retinal alterations after the intravitreal injection of PEG of varying molecular weight injected intravitreally in a large animal in vivo pig model. Methods: This cohort study includes 12 pigs divided into 4 cohorts. Each cohort received an intravitreal injection of either 0.1 mL with 400 mg/mL of PEG-400, PEG-2000, PEG-40000 or an injection of balanced salt solution (BSS), respectively. Biocompatibility measurements including fundoscopy, optical coherence tomography (OCT) and electroretinography (ERG) were performed prior and 2, 4, and 6 weeks post-injection. Six weeks post-injection, the animals were euthanized, aqueous and vitreous taps were taken for cytokine and signal protein measurements, and immunostainings were performed. Results: All animals with intravitreal PEG-injections showed significant preretinal vitreous cells, most likely hyalocytes, as evidenced by OCT, but no signs of intraretinal inflammation were seen in the immunostainings conducted 6 weeks after injection. Untreated left control eyes and eyes injected with BSS showed no signs of inflammation throughout the whole study period. Functional and structural retinal parameters showed no significant alterations over the course of 6 weeks. Cytokine analyses showed no prolonged inflammatory reaction. Conclusions: The one-time intravitreal injection of PEG causes mild intravitreal inflammatory reactions, as evidenced in OCT by increased vitreous cells. However, retinal structure and function is not affected.

Indexed as

Biocompatible MaterialsPolyethylene GlycolsRetinaVitreous BodyAnimalsCytokinesDisease Models, AnimalElectroretinographyFemaleIntravitreal InjectionsMaterials TestingMolecular WeightSwineTomography, Optical CoherenceBiocompatible MaterialsCytokinesPolyethylene Glycols

Identifiers

PMID41711506
PMCPMC12924145

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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.