A sustained release formulation of novel quininib-hyaluronan microneedles inhibits angiogenesis and retinal vascular permeability in vivo

作者：Galvin Orla; Srivastava Akshay; Carroll Oliver; Kulkarni Rajiv; Dykes Steve; Vickers Steven; Dickinson Keith; Reynolds Alison L; Kilty Claire; Redmond Gareth; Jones Rob; Cheetham Sharon; Pandit Abhay; Kennedy Breandan N^*

来源：Journal of Controlled Release, 2016, 233: 198-207.

DOI：10.1016/j.jconrel.2016.04.004

• Blindness
• Angiogenesis
• Vascular permeability
• Novel drug therapy

Pathologic neovascularisation and ocular permeability are hallmarks of proliferative diabetic retinopathy and age-related macular degeneration. Current pharmacologic interventions targeting VEGF are effective in only 30-60% of patients and require multiple intraocular injections associated with iatrogenic infection. Thus, our goal is to develop novel small molecule drugs that are VEGF-independent are amenable to sustained ocular-release, and which reduce retinal angiogenesis and retinal vascular permeability. Here, the anti-angiogenic drug quininib was formulated into hyaluronan (HA) microneedles whose safety and efficacy was evaluated in vivo. Quininib-HA microneedles were formulated via desolvation from quininib-HA solution and subsequent cross-linking with 4-arm-PEG-amine prior to freeze-drying. Scanning electron microscopy revealed hollow needle-shaped particle ultrastructure, with a zeta potential of -35.5 mV determined by electrophoretic light scattering. The incorporation efficiency and pharmacokinetic profile of quininib released in vitro from the microneedles was quantified by HPLC. Quininib incorporation into these microneedles was 90%. In vitro, 20% quininib was released over 4 months; or in the presence of increasing concentrations of hyaluronidase, 60% incorporated quininib was released over 4 months. Zebrafish hyaloid vasculature assays demonstrated quininib released from these microneedles significantly (p < 0.0001) inhibited ocular developmental angiogenesis compared to control. Sustained amelioration of retinal vascular permeability (RVP) was demonstrated using a bespoke cysteinyl leukotriene induced rodent model. Quininib-HA microparticles significantly inhibited RVP in Brown Norway rats one month after administration compared to neat quininib control (p = 0.0071). In summary, quininib-HA microneedles allow for sustained release of quininib; are safe in vivo and quininib released from these microneedles effectively inhibits angiogenesis and RVP in vivo.

• 出版日期2016-7-10