Literature DB >> 21628988

[In vitro evaluation for corneal damages by anti-glaucoma combination eye drops using human corneal epithelial cell (HCE-T)].

Noriaki Nagai1, Takatoshi Murao, Kyouhei Oe, Yoshimasa Ito, Norio Okamoto, Yoshikazu Shimomura.   

Abstract

The combination of anti-glaucoma eye drops is frequently used in clinical treatment, and it is known that the combination can cause corneal damage. Recently, an anti-glaucoma combination eye drops is developed, and the treatment by the combination eye drops is expected to enhance quality of life. However, effects of the combination eye drops on corneal epithelial cell damage have not been clarified. In this study, we investigated the corneal epithelial cell damage of commercially available anti-glaucoma combination eye drops, such as Xalacom® (latanoprost/timolol maleate combination eye drops), Duotrav® (travoprost/timolol maleate combination eye drops) and Cosopt® (dorzolamide hydrochloride/timolol maleate combination eye drops) using the human corneal epithelial cell (HCE-T). The cytotoxicity in Xalacom® was higher than that in Xalatan® (eye drops containing latanoprost) and Timoptol® (eye drops containing timolol maleate), and the benzalkonium chloride (BAC) and timolol maleate were related to cytotoxicity in Xalacom®. The cytotoxicity in Duotrav® and Cosopt® was lower than that in Timoptol®. The Duotrav® is preserved with a non-BAC system (POLYQUAD, polidronium chloride). Therefore, it was suggested that the POLYQUAD related to the low cytotoxicity in Duotrav®. On the other hand, the D-mannitol reduced the cytotoxicity by BAC in this study. This result suggested that the cytotoxicity in Cosopt® was reduced by D-mannitol. The Duotrav® and Cosopt® may be less damaging to the ocular surface of glaucoma patients receiving long-term eye drop therapy in compared with the combination of anti-glaucoma eye drops.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21628988     DOI: 10.1248/yakushi.131.985

Source DB:  PubMed          Journal:  Yakugaku Zasshi        ISSN: 0031-6903            Impact factor:   0.302


  6 in total

1.  Evaluation of corneal damage caused by iodine preparations using human corneal epithelial cells.

Authors:  Yuuka Shibata; Yuta Tanaka; Takashi Tomita; Takanori Taogoshi; Yasuhiro Kimura; Taiichiro Chikama; Kenji Kihira
Journal:  Jpn J Ophthalmol       Date:  2014-09-18       Impact factor: 2.447

2.  Prospective unmasked randomized evaluation of the iStent inject (®) versus two ocular hypotensive agents in patients with primary open-angle glaucoma.

Authors:  Antonio M Fea; Jose I Belda; Marek Rękas; Anselm Jünemann; Lydia Chang; Luis Pablo; Lilit Voskanyan; L Jay Katz
Journal:  Clin Ophthalmol       Date:  2014-05-07

3.  Efficiency, safety, and patient preference of switching from dorzolamide 1%/timolol 0.5% to brinzolamide 1%/timolol 0.5% while maintaining the prostaglandin F2α analog.

Authors:  Yoshie Shimizu; Shunsuke Nakakura; Makiko Nishiyama; Hitoshi Tabuchi; Yoshiaki Kiuchi
Journal:  Clin Ophthalmol       Date:  2015-03-11

4.  The signs of ocular-surface disorders after switching from latanoprost to tafluprost/timolol fixed combination: a prospective study.

Authors:  Hideaki Okumichi; Yoshiaki Kiuchi; Tetsuya Baba; Takashi Kanamoto; Tomoko Naito; Shunsuke Nakakura; Hitoshi Tabuchi; Hiroki Nii; Chie Sueoka; Yosuke Sugimoto
Journal:  Clin Ophthalmol       Date:  2017-06-21

5.  Energy-dependent endocytosis is responsible for drug transcorneal penetration following the instillation of ophthalmic formulations containing indomethacin nanoparticles.

Authors:  Noriaki Nagai; Fumihiko Ogata; Hiroko Otake; Yosuke Nakazawa; Naohito Kawasaki
Journal:  Int J Nanomedicine       Date:  2019-02-18

6.  In Vitro Toxicity Evaluation of New Generic Latanost® and Latacom® as an Ophthalmic Formulation.

Authors:  Jessica Sze Chia Ng; Yi Xin Tan; Nor Amalina Ahmad Alwi; Kar Ming Yee; Ahmad Hazri Abdul Rashid; Ka-Liong Tan; Chuei Wuei Leong
Journal:  J Curr Glaucoma Pract       Date:  2021 Sep-Dec
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.