Employing a PLGA-TPGS based nanoparticle to improve the ocular delivery of Acyclovir.

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作者： Musaed,Alkholief ^[1] ; Hammam,Albasit ^[1] ; Adel,Alhowyan ^[1] ; Sultan,Alshehri ^[2] ; Mohammad,Raish ^[2] ; Mohd,Abul Kalam ^[1] ; Aws,Alshamsan ^[1]

作者单位： Nanobiotechnology Unit, Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia. ^[1] Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box: 2457, Riyadh 11451, Saudi Arabia. ^[2]

关键词 Acyclovir Corneal permeation DLS, Dynamic Light Scattering Ocular pharmacokinetics PDI, polydispersity index PLGA PLGA, Poly-(d,l-lactic-co-glycolic acid)STF, simulated tear fluid TPGS TPGS, D-α-Tocopherol polyethylene glycol succinate UPLC, ultra-performance liquid chromatography

DOI 10.1016/j.jsps.2018.11.011

PMID 30766442

发布时间 2020-09-29

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Saudi pharmaceutical journal

2019年27卷2期

293-302页

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Employing a PLGA-TPGS based nanoparticle to improve the ocular delivery of Acyclovir.

Saudi pharmaceutical journal

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Saudi pharmaceutical journal

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Employing a PLGA-TPGS based nanoparticle to improve the ocular delivery of Acyclovir.

Saudi pharmaceutical journal

相似文献

Saudi pharmaceutical journal

相关期刊

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