Advances in Drug Delivery Systems and Therapies for Ocular Disorders

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

Deadline for manuscript submissions: closed (31 May 2023) | Viewed by 3714

Special Issue Editor


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Guest Editor
Visual Quality Research Group, Maimonides Biomedical Research Institute of Cordoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba, 14004 Córdoba, Spain
Interests: nanotechnology; controlled drug delivery; magnetic nanoparticles; cancer therapy; biomaterials; tissue engineering
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Special Issue Information

Dear Colleagues,

In recent years, the number of patients with ocular diseases is increasing as a consequence of population aging. In 2020, 1 billion people suffered from vision impairment, and this figure is expected to increase to 1.8 billion people by 2050. The most common causes of ocular disorders are cataract, glaucoma, age-related macular degeneration, diabetic retinopathy, and presbyopia.

This Special Issue is focused on different disorders and pathogenesis occurring in the eye and their possible therapies for treatment. The main goal is to show the current status and future perspectives of different treatment approaches, from the use of artificial or natural biomaterials (ocular tissue engineering) to emerging ocular sustained drug delivery treatments (clinical trials).

Prof. Dr. Felisa Reyes-Ortega
Guest Editor

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Published Papers (2 papers)

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Research

21 pages, 5123 KiB  
Article
Phosphorylcholine and KR12-Containing Corneal Implants in HSV-1-Infected Rabbit Corneas
by Kamal Malhotra, Oleksiy Buznyk, Mohammad Mirazul Islam, Elle Edin, Sankar Basu, Marc Groleau, Delali Shana Dégué, Per Fagerholm, Adrien Fois, Sylvie Lesage, Jaganmohan R. Jangamreddy, Egidijus Šimoliūnas, Aneta Liszka, Hirak K. Patra and May Griffith
Pharmaceutics 2023, 15(6), 1658; https://doi.org/10.3390/pharmaceutics15061658 - 05 Jun 2023
Cited by 1 | Viewed by 1662
Abstract
Severe HSV-1 infection can cause blindness due to tissue damage from severe inflammation. Due to the high risk of graft failure in HSV-1-infected individuals, cornea transplantation to restore vision is often contraindicated. We tested the capacity for cell-free biosynthetic implants made from recombinant [...] Read more.
Severe HSV-1 infection can cause blindness due to tissue damage from severe inflammation. Due to the high risk of graft failure in HSV-1-infected individuals, cornea transplantation to restore vision is often contraindicated. We tested the capacity for cell-free biosynthetic implants made from recombinant human collagen type III and 2-methacryloyloxyethyl phosphorylcholine (RHCIII-MPC) to suppress inflammation and promote tissue regeneration in the damaged corneas. To block viral reactivation, we incorporated silica dioxide nanoparticles releasing KR12, the small bioactive core fragment of LL37, an innate cationic host defense peptide produced by corneal cells. KR12 is more reactive and smaller than LL37, so more KR12 molecules can be incorporated into nanoparticles for delivery. Unlike LL37, which was cytotoxic, KR12 was cell-friendly and showed little cytotoxicity at doses that blocked HSV-1 activity in vitro, instead enabling rapid wound closure in cultures of human epithelial cells. Composite implants released KR12 for up to 3 weeks in vitro. The implant was also tested in vivo on HSV-1-infected rabbit corneas where it was grafted by anterior lamellar keratoplasty. Adding KR12 to RHCIII-MPC did not reduce HSV-1 viral loads or the inflammation resulting in neovascularization. Nevertheless, the composite implants reduced viral spread sufficiently to allow stable corneal epithelium, stroma, and nerve regeneration over a 6-month observation period. Full article
(This article belongs to the Special Issue Advances in Drug Delivery Systems and Therapies for Ocular Disorders)
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12 pages, 2360 KiB  
Article
Evaluation of Conventional and Hyaluronic Acid-Coated Thymoquinone Liposomes in an In Vitro Model of Dry Eye
by Elisa Landucci, Costanza Mazzantini, Maura Calvani, Domenico E. Pellegrini-Giampietro and Maria Camilla Bergonzi
Pharmaceutics 2023, 15(2), 578; https://doi.org/10.3390/pharmaceutics15020578 - 08 Feb 2023
Cited by 10 | Viewed by 1689
Abstract
Dry eye disease (DED) is a common ocular disorder characterized by an inadequate lubrication of the eye by tears leading to inflammation and the alteration of the ocular surface. Current treatments are often limited due to their side effects and ineffectiveness. Thymoquinone (TQ) [...] Read more.
Dry eye disease (DED) is a common ocular disorder characterized by an inadequate lubrication of the eye by tears leading to inflammation and the alteration of the ocular surface. Current treatments are often limited due to their side effects and ineffectiveness. Thymoquinone (TQ) is a natural compound present in the essential oil of Nigella sativa L., with anti-inflammatory and antioxidant activities. In this study, conventional and hyaluronic acid-coated liposomes were developed to improve TQ activity at ocular level. In the present study, the cytoprotective effects of TQ or TQ liposomes were assessed against oxidative and inflammatory processes in human corneal epithelial cells (HCE-2). Hyperosmolarity conditions (450 mOsm) were used as a model of DED. Interleukin-1β (IL-1β), Interleukin-6 (IL-6) and tumor necrosis factor (TNFα) were quantified by quantitative real-time polymerase chain reaction (RT-qPCR); COX-2 and Phospho-NF-κB p65 (p-p65) by Western blotting (WB). Moreover, the mitochondrial reactive oxygen species (mtROS) levels were measured by MitoSOX assay. The hyperosmotic treatment induced a significant increase of the proinflammatory genes and proteins expression that were significantly decreased in the liposomes-treated cells. The coincubation with hyaluronic acid-coated liposomes significantly reverted the increase of mtROS production, evidently stimulated by the hyperosmotic stress. Our data suggest that TQ-loaded liposomes have potential as a therapeutic agent in dry eye disease, improving the TQ efficacy. Full article
(This article belongs to the Special Issue Advances in Drug Delivery Systems and Therapies for Ocular Disorders)
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