Abstract
Purpose: The work was performed to investigate the feasibility of preparing ocular inserts loaded with Poly-ε-Caprolactone (PCL) nanoparticles as a sustained ocular delivery system.
Methods: First, Atorvastatin Calcium-Poly-ε-Caprolactone (ATC-PCL) nanoparticles were prepared and characterized. Then, the optimized nanoparticles were loaded within inserts formulated with Methylcellulose (MC) and Polyvinyl Alcohol (PVA) by a solvent casting technique and evaluated physically, for in-vitro drug release profile. Finally, an in-vivo study was performed on the selected formulation to prove non-irritability and sustained ocular anti-inflammatory efficacy compared with free drug-loaded ocuserts.
Results: The results revealed (ATC-PCL) nanoparticles prepared with 0.5% pluronic F127 were optimized with 181.72±3.6 nm particle size, 0.12±0.02 (PDI) analysis, -27.4± 0.69 mV zeta potential and 62.41%±4.7% entrapment efficiency. Nanoparticles loaded ocuserts manifested compatibility between drug and formulation polymers. Moreover, formulations complied with average weight 0.055±0.002 to 0.143±0.023 mg, and accepted pH. ATC-PCL nanoparticles loaded inserts prepared by 5% MC showed more sustained, prolonged in-vitro release over 24h. In-vivo study emphasized non-irritability, ocular anti-inflammatory effectiveness represented by smaller lid closure scores, and statistically significant lowering in PMN count after 3h.
Conclusion: These findings proposed a possibly simple, new and affordable price technique to prepare promising (ATC-PCL) nanoparticles loaded inserts to achieve sustained release with prolonged antiinflammatory efficacy.
Keywords: Atorvastatin calcium, Poly-ε-Caprolactone, nanoparticles, sustained release, ocular inserts, anti-inflammatory.
Graphical Abstract
[http://dx.doi.org/10.1016/j.ijpharm.2015.08.100 ] [PMID: 26341322]
[http://dx.doi.org/10.1016/j.jconrel.2008.12.018 ] [PMID: 19331856]
[http://dx.doi.org/10.1016/j.jddst.2018.12.005]
[http://dx.doi.org/10.3390/pharmaceutics11090460 ] [PMID: 31500106]
[http://dx.doi.org/10.1159/000367851] [PMID: 26068735]
[http://dx.doi.org/10.1039/C5RA26674B]
[http://dx.doi.org/10.9734/OR/2018/44459]
[http://dx.doi.org/10.1016/j.biomaterials.2012.06.019 ] [PMID: 22770799]
[http://dx.doi.org/10.1039/C5RA12732G]
[http://dx.doi.org/10.1016/j.jconrel.2009.08.012 ] [PMID: 19699771]
[http://dx.doi.org/10.3109/02713680903340738 ] [PMID: 19958126]
[http://dx.doi.org/10.3109/10837450903262017 ] [PMID: 19772377]
[http://dx.doi.org/10.1081/DDC-120016729 ] [PMID: 12648018]
[PMID: 18771005]
[PMID: 16375841]
[http://dx.doi.org/10.1016/S0928-0987(01)00095-1 ] [PMID: 11297896]
[http://dx.doi.org/10.1016/S0378-5173(00)00359-8 ] [PMID: 10802405]
[http://dx.doi.org/10.1002/jps.10227] [PMID: 12434408]
[http://dx.doi.org/10.1016/S0378-5173(00)00508-1 ] [PMID: 11084241]
[http://dx.doi.org/10.1208/pt070496] [PMID: 17285752]
[PMID: 7409999]
[http://dx.doi.org/10.1016/S0378-5173(99)00265-3 ] [PMID: 10528098]
[http://dx.doi.org/10.1016/S0168-3659(00)00364-3 ] [PMID: 11245908]
[http://dx.doi.org/10.5185/amlett.2012.icnano.153]
[http://dx.doi.org/10.1016/j.ijpharm.2004.11.010 ] [PMID: 15814246]
[http://dx.doi.org/10.1016/S0168-3659(98)00116-3 ] [PMID: 9971898]
[http://dx.doi.org/10.1007/s12272-013-0317-x] [PMID: 24395530]
[http://dx.doi.org/10.1016/j.polymer.2010.05.048]
[http://dx.doi.org/10.2147/IJN.S237314] [PMID: 32184589]
[http://dx.doi.org/10.1016/j.nano.2009.10.004 ] [PMID: 19857606]
[http://dx.doi.org/10.1023/A:1018936205485] [PMID: 8464811]