NAD plus -associated-hyaluronic acid and poly(L-lysine) polyelectrolyte complexes: An evaluation of their potential for ocular drug delivery

被引:3
作者
Casey-Power, Saoirse [1 ]
Vardar, Camila [2 ]
Ryan, Richie [1 ]
Behl, Gautam [3 ]
McLoughlin, Peter [1 ]
Byrne, Mark E. [2 ,4 ]
Fitzhenry, Laurence [1 ]
机构
[1] South East Technol Univ, Pharmaceut & Mol Biotechnol Res Ctr, Ocular Therapeut Res Grp, Waterford Campus, Waterford X91 K0EK, Ireland
[2] Rowan Univ, Rowan Virtua Sch Translat Biomed Engn & Sci, Dept Biomed Engn, 201 Mull Hill Rd, Glassboro, NJ 08028 USA
[3] EirGen Pharm, UNIT 64-64A,Westside Business Pk,Old Kilmeaden Rd, Co Waterford X91 YV67, Ireland
[4] Rowan Univ, Dept Chem Engn, 201 Mull Hill Rd, Glassboro, NJ 08028 USA
关键词
Nanoparticles; Polyelectrolyte complexes; Polyelectrolyte complexation; Ocular drug delivery; NAD plus; Hyaluronic acid; Physicochemical characterisation; Microfluidic release; Ex vivo permeation; HYDROGEL CONTACT-LENSES; POLY-L-LYSINE; CHITOSAN NANOPARTICLES; RELEASE KINETICS; IONIC-STRENGTH; CHAIN-LENGTH; STABILITY; CHARGE; BIOAVAILABILITY; MECHANISMS;
D O I
10.1016/j.ejpb.2023.10.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 mu g 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 mu M 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.
引用
收藏
页码:62 / 78
页数:17
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