4.7 Article

Melatonin loaded hybrid nanomedicine: DoE approach, optimization and in vitro study on diabetic retinopathy model

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 627, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2022.122195

Keywords

PLGA-PEG; Ocular topical delivery; Mucoadhesion; Controlled release; In vivo ocular tolerability

Funding

  1. University of Catania (Programma Ricerca di Ateneo 2020-2022, Linea 2
  2. Project NanoRET and (partially) project [3]
  3. Italian Minister of University [PRIN 2020FR7TCL]
  4. International Ph.D. program in Neurosciences, University of Catania, Italy

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This study designed and optimized melatonin-loaded lipid-polymer hybrid nanoparticles (mel-LPHNs) for the topical management of retinal diseases. The optimized nanomedicine showed suitable characteristics for ophthalmic administration, including good mucoadhesive properties, controlled release profile, and increased neuroprotective and antioxidant activities compared to melatonin aqueous solution. The development of mel-LPHNs provides a novel and safe hybrid platform for the localized treatment of retinal diseases.
Melatonin (MEL) is a pleiotropic neurohormone of increasing interest as a neuroprotective agent in ocular dis-eases. Improving the mucoadhesiveness is a proposed strategy to increase the bioavailability of topical formu-lations. Herein, the design and optimization of MEL-loaded lipid-polymer hybrid nanoparticles (mel-LPHNs) using Design of Experiment (DoE) was performed. LPHNs consisted of PLGA-PEG polymer nanoparticles coated with a cationic lipid-shell. The optimized nanomedicine showed suitable size for ophthalmic administration (189.4 nm; PDI 0.260) with a positive surface charge (+39.8 mV), high encapsulation efficiency (79.8 %), suitable pH and osmolarity values, good mucoadhesive properties and a controlled release profile. Differential Scanning Calorimetry and Fourier-Transform Infrared Spectroscopy confirmed the encapsulation of melatonin in the systems and the interaction between lipids and polymer matrix. Biological evaluation in an in vitro model of diabetic retinopathy demonstrated enhanced neuroprotective and antioxidant activities of mel-LPHNs, compared to melatonin aqueous solution at the same concentration (0.1 and 1 mu M). A modified Draize test was performed to assess the ocular tolerability of the formulation showing no signs of irritation. To the best our knowledge, this study reported for the first time the development of mel-LPHNs, a novel and safe hybrid platform suitable for the topical management of retinal diseases.

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