Electrospun formulations of acyclovir, ciprofloxacin and cyanocobalamin for ocular drug delivery

被引:39
作者
Baskakova, Alexandra [1 ,2 ]
Awwad, Sahar [2 ]
Jimenez, Jennifer Quiros [2 ,3 ]
Gill, Hardyal [2 ]
Novikov, Oleg [1 ]
Khaw, Peng T. [4 ,5 ]
Brocchini, Steve [2 ]
Zhilyakova, Elena [1 ]
Williams, Gareth R. [2 ]
机构
[1] Belgorod State Univ, Dept Pharmaceut Technol, 85 Pobeda St, Belgorod 308001, Russia
[2] UCL, Sch Pharm, 29-39 Brunswick Sq, London WC1N 1AX, England
[3] Univ Alcala de Henares, Dept Chem Engn, E-28871 Madrid, Spain
[4] Moorfields Eye Hosp, NIHR Biomed Res Ctr, London EC1V 9EL, England
[5] UCL, Inst Ophthalmol, London EC1V 9EL, England
基金
英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
Electrospinning; Ocular drug delivery; In vitro; Half-life; Antivirals; Posterior segment; Fibers; Sustained release; CMV RETINITIS; IN-VITRO; PHARMACOKINETICS; COMPATIBILITY; NANOFIBERS; MANAGEMENT;
D O I
10.1016/j.ijpharm.2016.02.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Two series of fibers containing the active ingredients acyclovir, ciprofloxacin and cyanocobalamin, and combinations of these drugs, were prepared by electrospinning. One set used the hydrophilic poly (vinylpyrrolidone) (PVP) as the filament-forming polymer, while the other used the slow-dissolving poly (e-caprolactone) (PCL). The fibers were found to have cylindrical morphologies, although there was evidence for solvent occlusion with the PVP systems and for some drug particles in the PCL materials. The active ingredients were generally present in the amorphous physical form in the case of PVP, but evidence of crystallinity was observed with PCL. The existence of intermolecular interactions between the drugs and polymers was proven using simple molecular modeling calculations. Drug release from the various fibers was tested in a validated in vitro outflow model of the eye, and the fiber formulations found to be capable of extending drug release. We thus conclude that electrospun matrices such as those prepared in this work have potential for use as intravitreal implants. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 218
页数:11
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