Corneal Mucin‐Targeting Liposome Nanoplatforms Enable Effective Treatment of Dry Eye Diseases by Integrated Regulation of Ferroptosis and Inflammation DOI Creative Commons
Yin Zhang,

Tinglian Zhou,

Kai Wang

и другие.

Advanced Science, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 28, 2024

Abstract The incidence of dry eye disease (DED) has been increasing annually worldwide, creating an urgent need for new therapies. Due to the multifactorial mechanism underlying DED, traditional medications focused on decreasing ocular surface inflammation have unable address all harmful factors and fail achieve a complete clinical cure. Ferroptosis, form programmed cell death characterized by lipid peroxidation, become pivotal contributor oxidative stress‐driven pathology. Therefore, therapeutic targeting ferroptosis may be attractive option management. Herein, sialic acid‐targeting peptide‐modified liposome loaded with Cyclosporine A (CsA), typical anti‐inflammatory drug, Ferrostatin‐1 (Fer‐1), selective inhibitor, is developed termed as CF@SNPs, combing sustaining DED treatment. This multifunctional liposomal encapsulation demonstrates excellent aqueous solubility; moreover, peptide prolongs retention, further enhancing efficacy. CF@SNPs treatment comprehensively alleviates symptoms, including improving corneal defects, augmenting goblet count, restoring tear secretion. Specifically, attenuate pathology suppressing p53‐SLC7A11‐GSH‐dependent TNF‐α‐associated inflammatory cascades, accompanied favorable biocompatibility in vivo. These results underscore promising potential this superior nano‐formulation pharmacotherapy.

Язык: Английский

A look to the future: cyclodextrins and cyclodextrin-based drug delivery to the retina DOI
Phatsawee Jansook, Hákon Hrafn Sigurðsson, Þorsteinn Loftsson

и другие.

Expert Opinion on Drug Delivery, Год журнала: 2025, Номер unknown

Опубликована: Март 19, 2025

Retinal diseases are a leading cause of vision loss, affecting millions people worldwide. Current treatment options based on invasive methods such as intravitreal injections. Therefore, there is need for alternative therapeutic strategies that both effective and more patient-friendly. Topical drug delivery has gained attention preferred noninvasive approach, although it hindered by several ocular barriers. Cyclodextrin (CD)-based nanoparticles have emerged promising strategy to overcome these limitations enhancing permeability in the posterior segment eye. This review discusses potential CDs enabling pharmaceutical excipients, their role improving bioavailability, provides examples CD-based eye drop formulations currently under development or undergoing clinical trials. Also, active agents ophthalmology discussed. nanoparticle drops present solution shown success. approved excipients can act ingredients inherent retinal diseases. Future innovations hybrid systems integration novel compounds could provide efficient targeted

Язык: Английский

Процитировано

0

Topical Ocular Drug Delivery: The Impact of Permeation Enhancers DOI Creative Commons
Gonçalo Santos, Esmeralda Delgado, Beatriz Silva

и другие.

Pharmaceutics, Год журнала: 2025, Номер 17(4), С. 447 - 447

Опубликована: Март 31, 2025

Topical ophthalmic drug delivery targeting the posterior segment of eye has become a key area interest due to its non-invasive nature, safety, ease application, patient compliance, and cost-effectiveness. However, achievement effective bioavailability in ocular is significant challenge unique barriers, including precorneal factors anatomical like cornea, conjunctiva, sclera. Successful systems require increased residence time improved corneal penetration enhance intraocular bioavailability. A promising strategy overcome these barriers incorporating enhancers (DPEs) into formulations. These compounds facilitate by improving permeability across otherwise impermeable or poorly permeable membranes. At level, they act through three primary mechanisms: breaking tear film stability interfering with mucous layer; disrupting membrane components such as phospholipids proteins; loosening epithelial cellular junctions. DPEs offer potential improve therapeutic outcomes, particularly for drugs eye. This review focused on analyzing current literature regarding use topical delivery, highlighting their mechanisms action revolutionize treatments.

Язык: Английский

Процитировано

0

Areas for improvement in the current care and treatment of dry eye disease DOI

Nila Kirupaharan,

Matthew D Spangler,

John D. Sheppard

и другие.

Expert Review of Ophthalmology, Год журнала: 2025, Номер unknown

Опубликована: Апрель 14, 2025

Язык: Английский

Процитировано

0

Corneal Mucin‐Targeting Liposome Nanoplatforms Enable Effective Treatment of Dry Eye Diseases by Integrated Regulation of Ferroptosis and Inflammation DOI Creative Commons
Yin Zhang,

Tinglian Zhou,

Kai Wang

и другие.

Advanced Science, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 28, 2024

Abstract The incidence of dry eye disease (DED) has been increasing annually worldwide, creating an urgent need for new therapies. Due to the multifactorial mechanism underlying DED, traditional medications focused on decreasing ocular surface inflammation have unable address all harmful factors and fail achieve a complete clinical cure. Ferroptosis, form programmed cell death characterized by lipid peroxidation, become pivotal contributor oxidative stress‐driven pathology. Therefore, therapeutic targeting ferroptosis may be attractive option management. Herein, sialic acid‐targeting peptide‐modified liposome loaded with Cyclosporine A (CsA), typical anti‐inflammatory drug, Ferrostatin‐1 (Fer‐1), selective inhibitor, is developed termed as CF@SNPs, combing sustaining DED treatment. This multifunctional liposomal encapsulation demonstrates excellent aqueous solubility; moreover, peptide prolongs retention, further enhancing efficacy. CF@SNPs treatment comprehensively alleviates symptoms, including improving corneal defects, augmenting goblet count, restoring tear secretion. Specifically, attenuate pathology suppressing p53‐SLC7A11‐GSH‐dependent TNF‐α‐associated inflammatory cascades, accompanied favorable biocompatibility in vivo. These results underscore promising potential this superior nano‐formulation pharmacotherapy.

Язык: Английский

Процитировано

1