TY - JOUR
T1 - NAD+-associated-hyaluronic acid and poly(L-lysine) polyelectrolyte complexes
T2 - An evaluation of their potential for ocular drug delivery
AU - Casey-Power, Saoirse
AU - Vardar, Camila
AU - Ryan, Richie
AU - Behl, Gautam
AU - McLoughlin, Peter
AU - Byrne, Mark E.
AU - Fitzhenry, Laurence
N1 - Funding Information:
This work was supported by the South East Technological University (SETU) PhD Scholarship Programme (Formerly WIT Co-fund PhD Scholarship Programme 2019 - WIT 2019 Call 1 CoFund).
Publisher Copyright:
© 2023 The Authors
Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - This study details the formation and characterisation of a novel nicotinamide adenine dinucleotide (NAD+)-associated polymeric nanoparticle system. The development of a polyelectrolyte complex (PEC) composed of two natural polyelectrolytes, hyaluronic acid and poly(L-lysine), and an evaluation of its suitability for NAD+ ocular delivery, primarily based on its physicochemical properties and in vitro release profile under physiological ocular flow rates, were of key focus. Following optimisation of formulation method conditions such as complexation pH, mode of addition, and charge ratio, the PEC was successfully formulated under mild formulation conditions via polyelectrolyte complexation. With a size of 235.1 ± 19.0 nm, a PDI value of 0.214 ± 0.140, and a zeta potential value of – 38.0 ± 1.1 mV, the chosen PEC, loaded with 430 µg of NAD+ per mg of PEC, exhibited non-Fickian, sustained release at physiological flowrates of 10.9 ± 0.2 mg of NAD+ over 14 h. PECs containing up to 200 µM of NAD+ did not induce any significant cytotoxic effects on an immortalised human corneal epithelial cell line. Using fluorescent labeling, the NAD+-associated PECs demonstrated retention within the corneal epithelium layer of a porcine model up to 6 h post incubation under physiological conditions. A study of the physicochemical behaviour of the PECs, in terms of size, zeta potential and NAD+ complexation in response to environmental stimuli,highlighted the dynamic nature of the PEC matrix and its dependence on both pH and ionic condition. Considering the successful formation of reproducible NAD+-associated PECs with suitable characteristics for ocular drug delivery via an inexpensive formulation method, they provide a promising platform for NAD+ ocular delivery with a strong potential to improve ocular health.
AB - This study details the formation and characterisation of a novel nicotinamide adenine dinucleotide (NAD+)-associated polymeric nanoparticle system. The development of a polyelectrolyte complex (PEC) composed of two natural polyelectrolytes, hyaluronic acid and poly(L-lysine), and an evaluation of its suitability for NAD+ ocular delivery, primarily based on its physicochemical properties and in vitro release profile under physiological ocular flow rates, were of key focus. Following optimisation of formulation method conditions such as complexation pH, mode of addition, and charge ratio, the PEC was successfully formulated under mild formulation conditions via polyelectrolyte complexation. With a size of 235.1 ± 19.0 nm, a PDI value of 0.214 ± 0.140, and a zeta potential value of – 38.0 ± 1.1 mV, the chosen PEC, loaded with 430 µg of NAD+ per mg of PEC, exhibited non-Fickian, sustained release at physiological flowrates of 10.9 ± 0.2 mg of NAD+ over 14 h. PECs containing up to 200 µM of NAD+ did not induce any significant cytotoxic effects on an immortalised human corneal epithelial cell line. Using fluorescent labeling, the NAD+-associated PECs demonstrated retention within the corneal epithelium layer of a porcine model up to 6 h post incubation under physiological conditions. A study of the physicochemical behaviour of the PECs, in terms of size, zeta potential and NAD+ complexation in response to environmental stimuli,highlighted the dynamic nature of the PEC matrix and its dependence on both pH and ionic condition. Considering the successful formation of reproducible NAD+-associated PECs with suitable characteristics for ocular drug delivery via an inexpensive formulation method, they provide a promising platform for NAD+ ocular delivery with a strong potential to improve ocular health.
KW - Nanoparticles
KW - Polyelectrolyte complexes
KW - Polyelectrolyte complexation
KW - Ocular drug delivery
KW - NAD+
KW - Hyaluronic acid
KW - Physicochemical characterisation
KW - Microfluidic release
KW - Ex vivo permeation
KW - Hyaluronic Acid
KW - Humans
KW - Drug Delivery Systems
KW - NAD
KW - Animals
KW - Swine
KW - Polyelectrolytes/chemistry
KW - Polylysine
UR - https://doi.org/10.1016/j.ejpb.2023.10.004
UR - http://www.scopus.com/inward/record.url?scp=85173263234&partnerID=8YFLogxK
U2 - 10.1016/j.ejpb.2023.10.004
DO - 10.1016/j.ejpb.2023.10.004
M3 - Article
C2 - 37797681
SN - 0939-6411
VL - 192
SP - 62
EP - 78
JO - European Journal of Pharmaceutics and Biopharmaceutics
JF - European Journal of Pharmaceutics and Biopharmaceutics
IS - November 2023
ER -