July 2019
Volume 60, Issue 9
Open Access
ARVO Annual Meeting Abstract  |   July 2019
Therapeutic Effect of Topical Apatinib in a Murine Model of Corneal Neovascularization
Author Affiliations & Notes
  • HYEON JEONG YOON
    Chonnam National University Hospital, Gwangju, Korea (the Democratic People's Republic of)
  • Ying Li
    Chonnam National University Hospital, Gwangju, Korea (the Democratic People's Republic of)
  • Lan Li
    Chonnam National University Hospital, Gwangju, Korea (the Democratic People's Republic of)
  • Ru Jun Jin
    Chonnam National University Hospital, Gwangju, Korea (the Democratic People's Republic of)
  • Je Moon Woo
    University of Ulsan College of Medicine, Korea (the Republic of)
  • Kyung Chul Yoon
    Chonnam National University Hospital, Gwangju, Korea (the Democratic People's Republic of)
  • Footnotes
    Commercial Relationships   HYEON JEONG YOON, None; Ying Li, None; Lan Li, None; Ru Jun Jin, None; Je Moon Woo, None; Kyung Chul Yoon, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science July 2019, Vol.60, 943. doi:
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      HYEON JEONG YOON, Ying Li, Lan Li, Ru Jun Jin, Je Moon Woo, Kyung Chul Yoon; Therapeutic Effect of Topical Apatinib in a Murine Model of Corneal Neovascularization. Invest. Ophthalmol. Vis. Sci. 2019;60(9):943.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To investigate the efficacy of topical apatinib compared with 0.5% bevacizumab in a murine model of corneal neovascularization (CNV).

Methods : Murine CNV was induced by means of total disepithelization and alkali burn. The mice were divided into five groups: control, PBS, 0.1% and 0.5% of apatinib, and 0.5% of bevacizumab. CNV area and index were measured 7 and 14 days after treatment. After corneal tissues were excised at day 14, CNV (blood and lymphatic) and leukocyte infiltration were quantified by CD31, LYVE1, and CD45 immunofluorescence, respectively. Hematoxylin-eosin corneal cross sections and whole mounted toludine blue staining were used to compare anatomy and vessel density of each groups.

Results : After 14 days, treatment groups with 0.1% and 0.5% apatinib, and 0.5% bevacizumab decreased CNV area and index compared with control group. A significant decreased in blood and lymphatic vascularization by CD31, LYVE1, and CD45 immunofluorescence was observed in the 0.5% apatinib and 0.5% bevacizumab groups. Number of inflammatory cells and vessel density increased in both 0.5% apatinib and 0.5% bevacizumab groups.

Conclusions : Instillation of topical application of apatinib could improve CNV area and index, status of inflammation, and blood and lymphatic vascularization equivalent to 0.5% bevacizumab.

This abstract was presented at the 2019 ARVO Annual Meeting, held in Vancouver, Canada, April 28 - May 2, 2019.

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