Evidence map›Paper›PMID 41049113›Full record

ArticleOphthalmology science2026

In Vivo Comparison of Intracameral and Intravitreal Implantation of a Timolol Maleate Miniaturized Injectable Delivery System Device.

Chu Jian Ma, Youning Zhang, Daniel A Bernards, Michele Bloomer, John Dickson, Jayakumar Rajadas, Murty Vyakarnam, Tejal A Desai, Robert B Bhisitkul

Erratum issuedAbstract read
In one paragraph

Article in Ophthalmology science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Chu Jian MaUniversity of California San Francisco, School of Medicine, Department of Ophthalmology, San Francisco, California.
Youning ZhangUniversity of California San Francisco, School of Medicine, Department of Ophthalmology, San Francisco, California.
Daniel A BernardsUniversity of California San Francisco, Department of Bioengineering and Therapeutic Sciences, San Francisco, California.
Michele BloomerUniversity of California San Francisco, School of Medicine, Department of Ophthalmology, San Francisco, California.
John DicksonUniversity of California San Francisco, School of Medicine, Department of Ophthalmology, San Francisco, California.
Jayakumar RajadasStanford University School of Medicine, Stanford, California.
Murty VyakarnamOculinea, Inc., San Francisco, California.
Tejal A DesaiUniversity of California San Francisco, Department of Bioengineering and Therapeutic Sciences, San Francisco, California.
Robert B BhisitkulUniversity of California San Francisco, School of Medicine, Department of Ophthalmology, San Francisco, California.

Funding

Rapid-Prototyping and Design CoreP30EY002162 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ULLIAN, ERIK M · 1985 to 2024
$16.8M
Vision Bioinformatics and ComputationP30EY037668 · NEI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Yvonne Ou · 2025 to 2026
$2.0M
NEI NIH HHS P30 EY002162NEI NIH HHS P30 EY037668
6 · The paper itself

Abstract

Purpose: Miniaturized injectable delivery system (MIDS) devices engineered for zero-order release of timolol maleate are evaluated for intracameral (IC) or intravitreal (IVT) injection for ocular safety, effects on intraocular pressure (IOP) reduction, and target tissue drug concentrations. Design: Preclinical study with in vitro testing of MIDS drug delivery devices together with intraocular injection of the devices in normotensive rabbit eyes. Subjects: Twenty-four New Zealand rabbits received intraocular injections of MIDS devices. Methods: Timolol maleate MIDS devices were injected IC or IVT into normotensive New Zealand rabbit eyes (n = 24), with weekly ophthalmic examinations and IOP measurements for 8 or 16 weeks. Eight weeks postimplantation, eyes were enucleated for quantification of tissue drug concentrations by liquid chromatography with tandem mass spectrometry and histology on whole globes. Main Outcome Measures: Drug release pharmacokinetics; ocular safety and biocompatibility; IOP; and blood and target tissue drug concentrations. Results: At 8 weeks, IOP in experimental eyes was lowered by 11.1 ± 2.9% (n = 5, Conclusions: Intravitreal and IC devices showed similar IOP reductions; IVT injection led to a higher drug concentration in the target ciliary body tissue, and in normotensive rabbit eyes showed general reduction of IOP over 8 weeks, indicating the potential of MIDS technology to address issues of patient adherence with glaucoma eye drops. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

Drug deliveryGlaucomaMicrostructured biopolymersPharmacokineticsTimolol

Identifiers

PMID41049113
PMCPMC12494917

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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.