All Stories

  1. A Cationic Block Co‐Polymer for Gene Delivery in the Posterior Segment of the Eye
  2. Microsphere-loaded dual-response in situ gel for enhanced ocular drug delivery
  3. Inhibiting the NLRP3 inflammasome pathway: An effective way to treat chronic inflammation in experimental autoimmune uveitis
  4. Small Extracellular Vesicles Released from ARPE-19 Cells Grown under Diabetic Retinopathy Conditions Promote NLRP3 Inflammasome Activation
  5. Characterisation of vitreous derived small extracellular vesicles in diabetic retinopathy
  6. Design and delivery effect of prolonged-retention dexamethasone and tacrolimus microcrystals eye drops
  7. The NLRP3 inflammasome pathway contributes to chronic inflammation in experimental autoimmune uveitis
  8. Serum Albumin and Glycemic Variability Could Contribute to Diabetic Retinopathy Progression by Regulating Chronic Inflammatory Pathways
  9. Utilizing an Ex Vivo Skin Penetration Analysis Model for Predicting Ocular Drug Penetration: A Feasibility Study with Curcumin Formulations
  10. Development of transferosomes for topical ocular drug delivery of curcumin
  11. Mechanism of Ocular Penetration of Lipophilic Drugs from Lipophilic Vehicles
  12. Future Therapeutics: Targeting the NLRP3 Inflammasome Pathway to Manage Diabetic Retinopathy Development and Progression
  13. Tissue-based models for ocular permeability studies
  14. Systemic Inflammasome Biomarkers as Predictors of Diabetic Retinopathy Progression: Evidence from a Pilot Study
  15. Comprehensive Grading System for Experimental Autoimmune Uveitis in Mice
  16. Non-aqueous formulations in topical ocular drug delivery – A paradigm shift?
  17. Preclinical characterization of water-free cyclosporine eye drops – Factors impacting ocular penetration ex vivo and in vivo
  18. NLRP3 Inflammasome as a Potential Therapeutic Target in Dry Eye Disease
  19. Orally Delivered Connexin43 Hemichannel Blocker, Tonabersat, Inhibits Vascular Breakdown and Inflammasome Activation in a Mouse Model of Diabetic Retinopathy
  20. Characterization of NLRP3 Inflammasome Activation in the Onset of Diabetic Retinopathy
  21. Extracellular Vesicles as Biomarkers and Therapeutics for Inflammatory Eye Diseases
  22. Preparation and Characterisation of a Cyclodextrin-Complexed Mānuka Honey Microemulsion for Eyelid Application
  23. Preclinical confirmation of UVC efficacy in treating infectious keratitis
  24. Blocking connexin43 hemichannels prevents TGF‐β2 upregulation and epithelial–mesenchymal transition in retinal pigment epithelial cells
  25. Ocular Distribution of Papaverine Using Non-aqueous Vehicles
  26. Ex vivo evaluation of the influence of pH on the ophthalmic safety, antibacterial efficacy and storage stability of povidone‐iodine
  27. Differential Action of Connexin Hemichannel and Pannexin Channel Therapeutics for Potential Treatment of Retinal Diseases
  28. Formulation Considerations for the Management of Dry Eye Disease
  29. The influence of hyperglycemia on the safety of ultrasound in retinal pigment epithelial cells
  30. Connexin43 hemichannel block inhibits NLRP3 inflammasome activation in a human retinal explant model of diabetic retinopathy
  31. Tonabersat Inhibits Connexin43 Hemichannel Opening and Inflammasome Activation in an In Vitro Retinal Epithelial Cell Model of Diabetic Retinopathy
  32. Targeting connexin hemichannels to control the inflammasome: the correlation between connexin43 and NLRP3 expression in chronic eye disease
  33. Connexin43 hemichannels: A potential drug target for the treatment of diabetic retinopathy
  34. Depot formulations to sustain periocular drug delivery to the posterior eye segment
  35. Preclinical studies evaluating the effect of semifluorinated alkanes on ocular surface and tear fluid dynamics
  36. Ultrasound-responsive nanobubbles for enhanced intravitreal drug migration: An ex vivo evaluation
  37. Connexin43 hemichannel block protects against the development of diabetic retinopathy signs in a mouse model of the disease
  38. Brinzolamide–loaded nanoemulsions: ex vivo transcorneal permeation, cell viability and ocular irritation tests
  39. Intravitreal pro-inflammatory cytokines in non-obese diabetic mice: Modelling signs of diabetic retinopathy
  40. Intracellular oligonucleotide delivery using the cell penetrating peptide Xentry
  41. Hyaluronic acid coated albumin nanoparticles for targeted peptide delivery in the treatment of retinal ischaemia
  42. Effects of enzymatic degradation on dynamic mechanical properties of the vitreous and intravitreal nanoparticle mobility
  43. Micelle directed chemical polymerization of polypyrrole particles for the electrically triggered release of dexamethasone base and dexamethasone phosphate
  44. 3-Dimensionally ordered macroporous PEDOT ion-exchange resins prepared by vapor phase polymerization for triggered drug delivery: Fabrication and characterization
  45. Semifluorinated alkane based systems for enhanced corneal penetration of poorly soluble drugs
  46. Drug delivery to the lens for the management of cataracts
  47. The inflammasome pathway is amplified and perpetuated in an autocrine manner through connexin43 hemichannel mediated ATP release
  48. Erratum to “Ultrasound-mediated nanoparticle delivery across ex vivo bovine retina after intravitreal injection” [Eur. J. Pharm. Biopharm. 119 (2017) 125–136]
  49. Development of a novel stability indicating RP-HPLC method for quantification of Connexin43 mimetic peptide and determination of its degradation kinetics in biological fluids
  50. Immunohistochemical Characterization of Connexin43 Expression in a Mouse Model of Diabetic Retinopathy and in Human Donor Retinas
  51. Drug-device combination approaches for delivery to the eye
  52. Ultrasound-mediated nanoparticle delivery across ex vivo bovine retina after intravitreal injection
  53. Medicated ocular bandages and corneal health: potential excipients and active pharmaceutical ingredients
  54. Phase transition of a microemulsion upon addition of cyclodextrin – applications in drug delivery
  55. Overcoming ocular drug delivery barriers through the use of physical forces
  56. Preparation and evaluation of PLGA nanoparticle-loaded biodegradable light-responsive injectable implants as a promising platform for intravitreal drug delivery
  57. Randomised masked trial of the clinical safety and tolerability of MGO Manuka Honey eye cream for the management of blepharitis
  58. Preclinical development of MGO Manuka Honey microemulsion for blepharitis management
  59. Nanoparticle-loaded biodegradable light-responsive in situ forming injectable implants for effective peptide delivery to the posterior segment of the eye
  60. Tonabersat Prevents Inflammatory Damage in the Central Nervous System by Blocking Connexin43 Hemichannels
  61. Nanocarrier mediated retinal drug delivery: overcoming ocular barriers to treat posterior eye diseases
  62. Polymeric micelles for ocular drug delivery: From structural frameworks to recent preclinical studies
  63. Hyaluronic Acid Coated Albumin Nanoparticles for Targeted Peptide Delivery to the Retina
  64. PLGA nanoparticles for intravitreal peptide delivery: statistical optimization, characterization and toxicity evaluation
  65. Ocular drug delivery—eye on innovation
  66. Azithromycin and Dexamethasone Loaded β-Glucan Films for the Treatment of Blepharitis
  67. Semi-fluorinated alkanes for topical delivery of Cyclosporine
  68. Stimuli-responsive systems for tuneable ocular drug delivery
  69. NLCs for Ocular Drug Delivery
  70. Ex vivo investigation of ocular tissue distribution following intravitreal administration of connexin43 mimetic peptide using the microdialysis technique and LC-MS/MS
  71. Modern approaches to the ocular delivery of cyclosporine A
  72. Light-responsivein situforming injectable implants for effective drug delivery to the posterior segment of the eye
  73. Nanoparticle cross-linked collagen shields for sustained delivery of pilocarpine hydrochloride
  74. Connexin43 in retinal injury and disease
  75. Cytotoxicity considerations and electrically tunable release of dexamethasone from polypyrrole for the treatment of back-of-the-eye conditions
  76. ZnO/PVP nanoparticles induce gelation in type I collagen
  77. In vitro and ex vivo corneal penetration and absorption models
  78. Highly porous Poly(3,4-ethylenedioxythiophene) prepared by vapor phase polymerization for biomedical applications
  79. Electrically-responsive implants for drug delivery to the posterior segment of the eye
  80. Development of gatifloxacin-loaded cationic polymeric nanoparticles for ocular drug delivery
  81. Neuroprotection in the treatment of glaucoma – A focus on connexin43 gap junction channel blockers
  82. Sustained intravitreal delivery of connexin43 mimetic peptide by poly(d,l-lactide-co-glycolide) acid micro- and nanoparticles – Closing the gap in retinal ischaemia
  83. Ocular delivery systems for topical application of anti-infective agents
  84. Intravitreal injection of lipoamino acid-modified connexin43 mimetic peptide enhances neuroprotection after retinal ischemia
  85. Electro-responsive macroporous polypyrrole scaffolds for triggered dexamethasone delivery
  86. Implants for drug delivery to the posterior segment of the eye: A focus on stimuli-responsive and tunable release systems
  87. Dendrimers for gene delivery - a potential approach for ocular therapy?
  88. Cytotoxicity and Vitreous Stability of Chemically Modified Connexin43 Mimetic Peptides for the Treatment of Optic Neuropathy
  89. Injectable implants for the sustained release of protein and peptide drugs
  90. Synergistic effect of chemical penetration enhancer and iontophoresis on transappendageal transport of oligodeoxynucleotides
  91. Improved Corneal Wound Healing through Modulation of Gap Junction Communication Using Connexin43-Specific Antisense Oligodeoxynucleotides
  92. Characterization and evaluation of β-glucan formulations as injectable implants for protein and peptide delivery
  93. Evaluation of Fluorescence Resonance Energy Transfer Approaches as a Tool to Quantify the Stability of Antisense Oligodeoxynucleotides
  94. Environment-sensitive polymers for ophthalmic drug delivery
  95. Ion-ActivatedIn SituGelling Systems for Antisense Oligodeoxynucleotide Delivery to the Ocular Surface
  96. Role of gap junctions in chronic pain
  97. In vitro release characteristics and cellular uptake of poly(D,L-lactic-co-glycolic acid) nanoparticles for topical delivery of antisense oligodeoxynucleotides
  98. Comparison of ion-activated in situ gelling systems for ocular drug delivery. Part 2: Precorneal retention and in vivo pharmacodynamic study
  99. Comparison of ion-activated in situ gelling systems for ocular drug delivery. Part 1: Physicochemical characterisation and in vitro release
  100. Ocular Drug Delivery
  101. Imaging Techniques and their Role in Dosage form Design and Drug Delivery Research
  102. Ocular Drug Delivery