The efficacy of ascorbate treatment after severe experimental alkali burns depends upon the route of administration.
نویسندگان
چکیده
Rabbit eyes were subjected to severe alkali burns (35 sec, 12 mm, 1N sodium hydroxide). In one experiment, rabbits in the treated group received a daily subcutaneous injection of neutralized ascorbic acid solution (0.5 gm/kg body weight), while control animals received no treatment. At the termination of the experiment (30 days), 11 of 16 eyes (68.8%) in the control group had ulcerated or formed descemetoceles, and in the experimental (treated) group, 15 of 20 eyes (75%) had ulcerated, formed descemetoceles, or perforated. In a second experiment, burned rabbits received topical 10% ascorbic acid while control eyes were given the vehicle only. At the termination of the experiment (34 days), 16 of 20 eyes (80%) in the control group had ulcerated or perforated, compared to five of 18 eyes (27.8%) in the ascorbate treated groups. The failure of systemic administration of ascorbic acid to prevent corneal ulceration could be explained on the basis of inadequate penetration of ascorbic acid into the anterior segment of severely burned rabbit eyes. On the other hand, immediate topical treatment of identically burned rabbit eyes achieved greatly elevated aqueous humor ascorbate levels and provided substantial protection from corneal ulceration and perforation.
منابع مشابه
Topical ascorbate decreases the incidence of corneal ulceration after experimental alkali burns.
A double-masked study of the effects of topical ascorbate on alkali burns utilized 37 rabbit eyes subjected to 20 sec, 12 mm, IN sodium hydroxide burns. Preliminary studies established the ocular acceptability, penetrability, and stability of the solutions used. Eighteen eyes in the experimental group were given two drops of10% ascorbate in Adsorbotear vehicle hourly for 14 hr of each day. Nine...
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When established corneal ulcers induced by alkali burning were treated with 10% ascorbate drops, no perforation occurred, in contrast to a 25% incidence in the control group. If perforations and descemetoceles were grouped together, these difference became insignificant (i.e., 14.2% ascorbate-treated vs. 25% control). Prolongation of descemetocele presence without perforation in the ascorbate-t...
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عنوان ژورنال:
- Investigative ophthalmology & visual science
دوره 19 12 شماره
صفحات -
تاریخ انتشار 1980