All Stories

  1. Targeting connexin hemichannels to control the inflammasome: the correlation between connexin43 and NLRP3 expression in chronic eye disease
  2. Brinzolamide–loaded nanoemulsions: ex vivo transcorneal permeation, cell viability and ocular irritation tests
  3. Hyaluronic acid coated albumin nanoparticles for targeted peptide delivery in the treatment of retinal ischaemia
  4. Effects of enzymatic degradation on dynamic mechanical properties of the vitreous and intravitreal nanoparticle mobility
  5. Micelle directed chemical polymerization of polypyrrole particles for the electrically triggered release of dexamethasone base and dexamethasone phosphate
  6. 3-Dimensionally ordered macroporous PEDOT ion-exchange resins prepared by vapor phase polymerization for triggered drug delivery: Fabrication and characterization
  7. Semifluorinated alkane based systems for enhanced corneal penetration of poorly soluble drugs
  8. Drug delivery to the lens for the management of cataracts
  9. The inflammasome pathway is amplified and perpetuated in an autocrine manner through connexin43 hemichannel mediated ATP release
  10. Erratum to “Ultrasound-mediated nanoparticle delivery across ex vivo bovine retina after intravitreal injection” [Eur. J. Pharm. Biopharm. 119 (2017) 125–136]
  11. Development of a novel stability indicating RP-HPLC method for quantification of Connexin43 mimetic peptide and determination of its degradation kinetics in biological fluids
  12. Immunohistochemical Characterization of Connexin43 Expression in a Mouse Model of Diabetic Retinopathy and in Human Donor Retinas
  13. Drug-device combination approaches for delivery to the eye
  14. Ultrasound-mediated nanoparticle delivery across ex vivo bovine retina after intravitreal injection
  15. Medicated ocular bandages and corneal health: potential excipients and active pharmaceutical ingredients
  16. Phase transition of a microemulsion upon addition of cyclodextrin – applications in drug delivery
  17. Overcoming ocular drug delivery barriers through the use of physical forces
  18. Preparation and evaluation of PLGA nanoparticle-loaded biodegradable light-responsive injectable implants as a promising platform for intravitreal drug delivery
  19. Randomised masked trial of the clinical safety and tolerability of MGO Manuka Honey eye cream for the management of blepharitis
  20. Preclinical development of MGO Manuka Honey microemulsion for blepharitis management
  21. Nanoparticle-loaded biodegradable light-responsive in situ forming injectable implants for effective peptide delivery to the posterior segment of the eye
  22. Tonabersat Prevents Inflammatory Damage in the Central Nervous System by Blocking Connexin43 Hemichannels
  23. Nanocarrier mediated retinal drug delivery: overcoming ocular barriers to treat posterior eye diseases
  24. Polymeric micelles for ocular drug delivery: From structural frameworks to recent preclinical studies
  25. Hyaluronic Acid Coated Albumin Nanoparticles for Targeted Peptide Delivery to the Retina
  26. PLGA nanoparticles for intravitreal peptide delivery: statistical optimization, characterization and toxicity evaluation
  27. Ocular drug delivery—eye on innovation
  28. Azithromycin and Dexamethasone Loaded β-Glucan Films for the Treatment of Blepharitis
  29. Semi-fluorinated alkanes for topical delivery of Cyclosporine
  30. Stimuli-responsive systems for tuneable ocular drug delivery
  31. NLCs for Ocular Drug Delivery
  32. Ex vivo investigation of ocular tissue distribution following intravitreal administration of connexin43 mimetic peptide using the microdialysis technique and LC-MS/MS
  33. Modern approaches to the ocular delivery of cyclosporine A
  34. Light-responsivein situforming injectable implants for effective drug delivery to the posterior segment of the eye
  35. Nanoparticle cross-linked collagen shields for sustained delivery of pilocarpine hydrochloride
  36. Connexin43 in retinal injury and disease
  37. ZnO/PVP nanoparticles induce gelation in type I collagen
  38. In vitro and ex vivo corneal penetration and absorption models
  39. Highly porous Poly(3,4-ethylenedioxythiophene) prepared by vapor phase polymerization for biomedical applications
  40. Electrically-responsive implants for drug delivery to the posterior segment of the eye
  41. Development of gatifloxacin-loaded cationic polymeric nanoparticles for ocular drug delivery
  42. Neuroprotection in the treatment of glaucoma – A focus on connexin43 gap junction channel blockers
  43. Sustained intravitreal delivery of connexin43 mimetic peptide by poly(d,l-lactide-co-glycolide) acid micro- and nanoparticles – Closing the gap in retinal ischaemia
  44. Ocular delivery systems for topical application of anti-infective agents
  45. Intravitreal injection of lipoamino acid-modified connexin43 mimetic peptide enhances neuroprotection after retinal ischemia
  46. Implants for drug delivery to the posterior segment of the eye: A focus on stimuli-responsive and tunable release systems
  47. Dendrimers for gene delivery - a potential approach for ocular therapy?
  48. Cytotoxicity and Vitreous Stability of Chemically Modified Connexin43 Mimetic Peptides for the Treatment of Optic Neuropathy
  49. Injectable implants for the sustained release of protein and peptide drugs
  50. Synergistic effect of chemical penetration enhancer and iontophoresis on transappendageal transport of oligodeoxynucleotides
  51. Improved Corneal Wound Healing through Modulation of Gap Junction Communication Using Connexin43-Specific Antisense Oligodeoxynucleotides
  52. Characterization and evaluation of β-glucan formulations as injectable implants for protein and peptide delivery
  53. Evaluation of Fluorescence Resonance Energy Transfer Approaches as a Tool to Quantify the Stability of Antisense Oligodeoxynucleotides
  54. Environment-sensitive polymers for ophthalmic drug delivery
  55. Ion-ActivatedIn SituGelling Systems for Antisense Oligodeoxynucleotide Delivery to the Ocular Surface
  56. Role of gap junctions in chronic pain
  57. In vitro release characteristics and cellular uptake of poly(D,L-lactic-co-glycolic acid) nanoparticles for topical delivery of antisense oligodeoxynucleotides
  58. Comparison of ion-activated in situ gelling systems for ocular drug delivery. Part 2: Precorneal retention and in vivo pharmacodynamic study
  59. Comparison of ion-activated in situ gelling systems for ocular drug delivery. Part 1: Physicochemical characterisation and in vitro release
  60. Ocular Drug Delivery
  61. Imaging Techniques and their Role in Dosage form Design and Drug Delivery Research
  62. Ocular Drug Delivery