» Articles » PMID: 32104452

Enhanced Drug Loading Efficiency of Contact Lenses Via Salt-induced Modulation

Overview
Date 2020 Feb 28
PMID 32104452
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Low drug loading efficiency is one of the main obstacles hindering the application of contact lenses (CLs) as the carrier for extended ocular drug delivery. Here in this study, a simple and effective drug loading method based on salt induced modulation was proposed and demonstrated with mechanism elucidation. First of all, using poly (2-hydroxyethyl methacrylate) (p-HEMA) as the contact lens material, betaxolol hydrochloride, Diclofenac Sodium and Betaxolol Base as the model drugs with different solubility, influence of salt concentration, salt type (sodium salts of sulfate, chloride, and sulfocyanate) and drug properties in the loading solution on drug loading efficiency was investigated. Mechanism of enhanced drug loading in contact lens was further explored via studying the influence of salt on the absorption isotherm, drug solubility and water content of CLs. Applicability of this method to other CLs materials was also investigated. It was demonstrated that adjusting the ionic strength of loading solutions resulted in significant increase of drug loading in CLs. Type and concentration of the salts and solubility of the drug were the main factors influencing enhancement ratio of drug loading. The mechanism for improved drug loading was related to the reduced drug solubility in loading solutions and the reduced bound water content in contact lenses. Modulation of drug loading by adjusting ionic strength was also applicable to other CLs and the light transmittance was not affected. This method was more suitable for salt-form drugs with high solubility. In summary, adjusting ionic strength of loading solution is an economical and effective way to improve drug loading in CLs, and this simple method may also find application in other hydrogel based drug delivery systems.

Citing Articles

Advances in chemistry and composition of soft materials for drug releasing contact lenses.

Chatterjee S, Upadhyay P, Mishra M, M S, Akshara M, N K RSC Adv. 2022; 10(60):36751-36777.

PMID: 35517957 PMC: 9057048. DOI: 10.1039/d0ra06681h.


Soft Contact Lenses as Drug Delivery Systems: A Review.

Rykowska I, Nowak I, Nowak R Molecules. 2021; 26(18).

PMID: 34577045 PMC: 8472272. DOI: 10.3390/molecules26185577.


Effect of Carbon Chain Length, Ionic Strength, and pH on the In Vitro Release Kinetics of Cationic Drugs from Fatty-Acid-Loaded Contact Lenses.

Torres-Luna C, Hu N, Domszy R, Fan X, Yang J, Briber R Pharmaceutics. 2021; 13(7).

PMID: 34371751 PMC: 8309118. DOI: 10.3390/pharmaceutics13071060.

References
1.
Yang H, Tyagi P, Kadam R, Holden C, Kompella U . Hybrid dendrimer hydrogel/PLGA nanoparticle platform sustains drug delivery for one week and antiglaucoma effects for four days following one-time topical administration. ACS Nano. 2012; 6(9):7595-606. DOI: 10.1021/nn301873v. View

2.
Urtti A . Challenges and obstacles of ocular pharmacokinetics and drug delivery. Adv Drug Deliv Rev. 2006; 58(11):1131-5. DOI: 10.1016/j.addr.2006.07.027. View

3.
Kim J, Chauhan A . Dexamethasone transport and ocular delivery from poly(hydroxyethyl methacrylate) gels. Int J Pharm. 2008; 353(1-2):205-22. DOI: 10.1016/j.ijpharm.2007.11.049. View

4.
Kirchhof S, Goepferich A, Brandl F . Hydrogels in ophthalmic applications. Eur J Pharm Biopharm. 2015; 95(Pt B):227-38. DOI: 10.1016/j.ejpb.2015.05.016. View

5.
Gonzalez-Chomon C, Concheiro A, Alvarez-Lorenzo C . Soft contact lenses for controlled ocular delivery: 50 years in the making. Ther Deliv. 2013; 4(9):1141-61. DOI: 10.4155/tde.13.81. View