Drug Delivery Systems for Ocular Diseases

A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Drug Delivery and Controlled Release".

Deadline for manuscript submissions: 31 December 2025 | Viewed by 734

Special Issue Editors


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Guest Editor
Ocupharm Research Group, Department of Optometry and Vision, Faculty of Optics and Optometry, Complutense University of Madrid, C/Arcos de Jalón 118, 28037 Madrid, Spain
Interests: dry eye; myopia; contact lenses; ocular biochemistry; glaucoma
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Guest Editor
Advanced Materials and Healthcare Technologies Division, School of Pharmacy, University of Nottingham, University Park, Nottingham NG7 2RD, UK
Interests: biomaterials characterization; hydrogels; polymeric micelles; drug delivery systems; controlled release; ocular delivery; drug-loaded contact lenses; antibiofilm medical devices
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

We are pleased to invite you to contribute to our Special Issue on drug delivery systems for ocular diseases. It is known that topical instillation for the treatment of ocular diseases has important deficiencies, mainly due to the permeability barrier of the ocular surface. To improve the drug efficacy with low concentrations, new drug release systems have been developed in recent years. These systems allow for an increase in the release time and in drug penetration, enhancing the drug efficacy and tolerance.

In this Special Issue, original research articles and reviews are welcome. Research areas may include (but are not limited to) the following: drug delivery systems, contact lens delivery, nanoparticles, liposomes, microneedles, and nanocarriers.

We look forward to receiving your contributions.

Prof. Dr. Gonzalo Carracedo
Dr. Maria Vivero-Lopez
Guest Editors

Manuscript Submission Information

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Keywords

  • ocular diseases
  • contact lens delivery
  • drug delivery systems
  • nanotechnology

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Published Papers (1 paper)

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Review

14 pages, 250 KiB  
Review
Unraveling the Mechanisms, Clinical Impact, Comparisons, and Safety Profiles of Slow-Release Therapies in Glaucoma
by Marco Zeppieri, Caterina Gagliano, Daniele Tognetto, Mutali Musa, Federico Bernardo Rossi, Angelo Greggio, Giuliano Gualandi, Alessandro Galan and Silvia Babighian
Pharmaceutics 2025, 17(5), 580; https://doi.org/10.3390/pharmaceutics17050580 - 28 Apr 2025
Viewed by 293
Abstract
Glaucoma, a primary cause of irreversible blindness, is most effectively managed by reducing intraocular pressure (IOP). Topical eye drops, which are conventional treatments, frequently encounter constraints regarding patient compliance, inconsistent dosage, and tolerability. Slow-release drug delivery systems have emerged as a promising innovation [...] Read more.
Glaucoma, a primary cause of irreversible blindness, is most effectively managed by reducing intraocular pressure (IOP). Topical eye drops, which are conventional treatments, frequently encounter constraints regarding patient compliance, inconsistent dosage, and tolerability. Slow-release drug delivery systems have emerged as a promising innovation in response to these challenges. The objective of these systems is to enhance the efficacy of treatment and patient compliance by ensuring the consistent and sustained delivery of therapeutic agents over extended periods. Implantable devices, injectable formulations, and external applications are all categorized as slow-release therapies. By delivering medication directly to the target tissues in a controlled manner, these technologies have the potential to circumvent common issues associated with traditional regimens, such as forgotten doses or improper administration. These systems have been shown to obtain clinically meaningful reductions in IOP in studies, with some demonstrating efficacy that is comparable to that of established daily topical treatments. Despite their potential, slow-release therapies encounter obstacles that necessitate resolution. Potential complications during implantation or removal, long-term biocompatibility, and the cost of treatment are all areas of concern. Furthermore, further investigation is required to comprehensively assess their relative economic feasibility, patient acceptability, and long-term safety profiles in comparison to conventional treatments. This review summarizes the most recent findings in the scientific literature, underlining the role and possible limits of slow-release therapies in glaucoma with the aim of offering a comprehensive understanding of their potential clinical applications and challenges. This emphasizes the potential for these innovations to revolutionize care by addressing current knowledge gaps, while also emphasizing the areas in which further development and research are required. Full article
(This article belongs to the Special Issue Drug Delivery Systems for Ocular Diseases)
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