Evidence map›Paper›PMID 40430889›Full record

ReviewPharmaceutics2025

Ocular Drug Delivery: Emerging Approaches and Advances.

Shilpkala Gade, Yin So, Deepakkumar Mishra, Shubhamkumar M Baviskar, Ahmad A Assiri, Katie Glover, Ravi Sheshala, Lalitkumar K Vora, Raghu Raj Singh Thakur

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Topical pyridostigmine for ocular myasthenia gravis: a translational hypothesis.Medical hypothesis, discovery & innovation ophthalmology journal · 2026
    Article
  13. Review
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.

Shilpkala GadeSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.
Yin SoSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0009-0004-5952-8835
Deepakkumar MishraSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0000-0002-5021-6825
Shubhamkumar M BaviskarSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0000-0001-6979-2454
Ahmad A AssiriSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0009-0006-1081-1394
Katie GloverSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.
Ravi SheshalaDepartment of Pharmaceutics, School of Pharmacy, Anurag University, Hyderabad 500088, Telangana, India.
Lalitkumar K VoraSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0000-0001-8106-9066
Raghu Raj Singh ThakurSchool of Pharmacy, Queen's University Belfast, Medical Biology Centre, Belfast BT9 7BL, UK.ORCID 0000-0001-7582-2082

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex anatomical and physiological barriers make the eye a challenging organ to treat from a drug delivery perspective. Currently available treatment methods (topical eyedrops) for anterior segment diseases pose several limitations in terms of bioavailability and patient compliance. Conventional drug delivery methods to treat posterior segment ocular diseases are primarily intravitreal injection (IVT) of solutions. IVT is highly invasive and leads to retinal toxicity, endophthalmitis, and intraocular inflammation, frequently requiring professional administration and frequent clinical visits. Advanced drug delivery treatment strategies could improve patient compliance and convenience. Long-acting drug delivery platforms (biodegradable or nonbiodegradable) provide sustained/controlled release of drugs for at least four to six months. Smart drug delivery alternatives, for instance, in situ forming implants, are injectable formulations that form semisolid-to-solid implants in response to the various stimuli of pH, light, osmolarity, and temperature. Additionally, nanoparticulate drug delivery systems, contact lenses, electrospun patches, and microneedle-based drug delivery systems provide minimally invasive treatment options for ocular disorders. This comprehensive review focuses on advanced drug delivery options for the management of ocular disorders.

Indexed as

advanced drug delivery systemsocular disorderspharmacodynamicspharmacokineticssustained drug release

Identifiers

PMID40430889
PMCPMC12115122

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.