4.7 Article

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

期刊

INTERNATIONAL JOURNAL OF PHARMACEUTICS
卷 502, 期 1-2, 页码 208-218

出版社

ELSEVIER
DOI: 10.1016/j.ijpharm.2016.02.015

关键词

Electrospinning; Ocular drug delivery; In vitro; Half-life; Antivirals; Posterior segment; Fibers; Sustained release

资金

  1. Russian Government
  2. University of Alcala
  3. UCL Overseas Research Student Fund
  4. National Institute of Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust
  5. UCL Institute of Ophthalmology
  6. Moorfields Special Trustees
  7. Helen Hamlyn Trust
  8. Medical Research Council
  9. Fight for Sight
  10. Freemasons Grand Charity
  11. UK Engineering & Physical Sciences Research Council (EPSRC) [EP/I033270/1]
  12. EPSRC Centre
  13. Engineering and Physical Sciences Research Council [EP/I033270/1] Funding Source: researchfish
  14. National Institute for Health Research [NF-SI-0512-10101] Funding Source: researchfish
  15. EPSRC [EP/I033270/1] Funding Source: UKRI

向作者/读者索取更多资源

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.

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