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Development and characterisation of electrospun timolol maleate-loaded polymeric contact lens coatings containing various permeation enhancers.
Mehta, Prina; Al-Kinani, Ali A; Arshad, Muhammad Sohail; Chang, Ming-Wei; Alany, Raid G; Ahmad, Zeeshan.
Affiliation
  • Mehta P; Leicester School of Pharmacy, De Montfort University, Leicester, LE1 9BH, UK.
  • Al-Kinani AA; Kingston University London, School of Life Sciences, Pharmacy and Chemistry, Kingston Upon Thames, Surrey, KT1 2EE, UK.
  • Arshad MS; Leicester School of Pharmacy, De Montfort University, Leicester, LE1 9BH, UK.
  • Chang MW; College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China; Zhejiang Provincial Key Laboratory of Cardio-Cerebral Vascular Detection Technology and Medicinal Effectiveness Appraisal, Zhejiang University, Hangzhou 310027, China.
  • Alany RG; Kingston University London, School of Life Sciences, Pharmacy and Chemistry, Kingston Upon Thames, Surrey, KT1 2EE, UK.
  • Ahmad Z; Leicester School of Pharmacy, De Montfort University, Leicester, LE1 9BH, UK. Electronic address: zahmad@dmu.ac.uk.
Int J Pharm ; 532(1): 408-420, 2017 Oct 30.
Article de En | MEDLINE | ID: mdl-28917987
ABSTRACT
Despite exponential growth in research relating to sustained and controlled ocular drug delivery, anatomical and chemical barriers of the eye still pose formulation challenges. Nanotechnology integration into the pharmaceutical industry has aided efforts in potential ocular drug device development. Here, the integration and in vitro effect of four different permeation enhancers (PEs) on the release of anti-glaucoma drug timolol maleate (TM) from polymeric nanofiber formulations is explored. Electrohydrodynamic (EHD) engineering, more specifically electrospinning, was used to engineer nanofibers (NFs) which coated the exterior of contact lenses. Parameters used for engineering included flow rates ranging from 8 to 15µL/min and a novel EHD deposition system was used; capable of hosting four lenses, masked template and a ground electrode to direct charged atomised structures. SEM analysis of the electrospun structures confirmed the presence of smooth nano-fibers; whilst thermal analysis confirmed the stability of all formulations. In vitro release studies demonstrated a triphasic release; initial burst release with two subsequent sustained release phases with most of the drug being released after 24h (86.7%) Biological evaluation studies confirmed the tolerability of all formulations tested with release kinetics modelling results showing drug release was via quasi-Fickian or Fickian diffusion. There were evident differences (p<0.05) in TM release dependant on permeation enhancer.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Timolol / Systèmes de délivrance de médicaments / Lentilles de contact Limites: Humans Langue: En Journal: Int J Pharm Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Timolol / Systèmes de délivrance de médicaments / Lentilles de contact Limites: Humans Langue: En Journal: Int J Pharm Année: 2017 Type de document: Article Pays d'affiliation: Royaume-Uni