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Poly(Acrylic Acid)–Poly(Ethylene Glycol) Nanoparticles Designed for Ophthalmic Drug Delivery

Vasi, Ana-Maria; Popa, Marcel Ionel; Tanase, Edi Constantin; Butnaru, Maria; Verestiuc, Liliana

Authors

Ana-Maria Vasi

Marcel Ionel Popa

Edi Constantin Tanase

Maria Butnaru

Liliana Verestiuc



Abstract

Poly(acrylic acid) (PAA) and poly(ethylene glycol) (PEG), four-arm, amine-terminated particles with nanometer size and spherical shape were obtained by the polymers cross-linking, via activation with 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide hydrochloride, in a w/o emulsion. The morphology and surface charge of the final particles are strongly dependent on the molar ratio of PAA–PEG and the PAA concentration. The physicochemical characteristics correlated with the drug-loading capacity, in vitro and ex vivo release kinetics of pilocarpine hydrochloride and biocompatibility results indicate that these nanoparticles exhibit the prerequisite behavior for use as carriers of ophthalmic drugs.

Citation

Vasi, A.-M., Popa, M. I., Tanase, E. C., Butnaru, M., & Verestiuc, L. (2014). Poly(Acrylic Acid)–Poly(Ethylene Glycol) Nanoparticles Designed for Ophthalmic Drug Delivery. Journal of Pharmaceutical Sciences, 103(2), 676-686. https://doi.org/10.1002/jps.23793

Journal Article Type Article
Acceptance Date Oct 29, 2013
Online Publication Date Dec 19, 2013
Publication Date 2014-02
Deposit Date Apr 16, 2021
Journal Journal of Pharmaceutical Sciences
Print ISSN 0022-3549
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 103
Issue 2
Pages 676-686
DOI https://doi.org/10.1002/jps.23793
Keywords nanoparticlesophthalmic carrierspolymeric biomaterialspoly (acrylic acid)poly (ethylene glycol) four arms amine terminatedformulationw/o emulsionbiocompatibilitycontrolled release/delivery
Public URL https://nottingham-repository.worktribe.com/output/3961685
Publisher URL http://www.sciencedirect.com/science/article/pii/S0022354915306985


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