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Turbo Eye Drops to Treat Ocular Toxicity and Blindness from Sulfur Mustard

涡轮滴眼液治疗硫芥引起的眼部毒性和失明

基本信息

批准号：
10480748
负责人：
Rajiv Ravindra Mohan
金额：
$ 74.04万
依托单位：
UNIVERSITY OF MISSOURI-COLUMBIA
依托单位国家：
美国
项目类别：
财政年份：
2020
资助国家：
美国
起止时间：
2020-08-01 至 2025-07-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10480748
关键词：
Acute Adverse effects Affect Alkylating Agents Anatomy Angiogenic Factor Antidotes Basement membrane Biological Assay Blindness Cities Clinical Clinical Pathology Collagen Fibril Consult Cornea Corneal Injury Corneal Ulcer Data Development Diagnostic Imaging Dose Drops Electron Microscopy Enzyme-Linked Immunosorbent Assay Epithelial Euthanasia Extracellular Matrix Degradation Eye Eye Injuries Eyedrops FDA approved Fibrosis Fluorescein Formulation Frequencies Functional disorder Funding Generic Drugs Goals Grant Health Histologic Human Immunofluorescence Immunologic In Vitro Inflammation Inflammatory Inflammatory Response Intellectual Property Iran Iraq Joints Kansas Keratopathy Lead Letters Literature Magnetic Resonance Imaging Measures Mediating Methods Microscope Modeling Molecular Monitor Mustard Gas Ocular Pathology Ophthalmic Solutions Ophthalmic examination and evaluation Ophthalmologist Organ Culture Techniques Oryctolagus cuniculus Pain Pathology Pathway interactions Patients Persons Pharmaceutical Preparations Pilot Projects Process Production Property Rights Publications Publishing Recurrence Regimen Research Safety Schedule Scientist Secure Syria Techniques Technology Temperature Terrorism Testing Therapeutic Effect Time Tissues Toxic effect Transmission Electron Microscopy Treatment Protocols Vesicants Veterinarians Vision War Western Blotting World War I base bench to bedside corneal epithelium diagnostic tool drug development effective therapy efficacious treatment high risk in vivo in vivo evaluation limbal medical countermeasure meetings multimodality neovascularization novel side effect stem cells therapeutically effective tomography tonometry vapor

项目摘要

ABSTRACT Sulfur mustard gas (SM), a vesicating and warfare agent, has been used in many wars since World War I; most recently in Syria. SM rapidly penetrates the eye on contact and causes blindness by injuring corneal tissue- organization and function. Clinically, patients show a pathology termed as Mustard Gas Keratopathy that involves severe ocular inflammation, recurrent epithelial-erosions, epithelial-stromal separation limbal stem cell deficiency, corneal ulceration, haze and neovascularization. MGK pathophysiology is biphasic including acute and delayed-onset, and involves multiple mechanisms. We developed a novel, multimodal, non-steroidal topical ophthalmic drops, Turbo Eye Drop (TED), containing 4 FDA-approved generic drugs with differing mode of action, and stable at ambient temperature. Our pilot studies found that topical TED efficaciously treats acute and delayed-onset MGK in rabbits in vivo and human cornea ex vivo without significant side effects. Our central hypothesis is that topical TED treats acute and delayed-onset MGK in vivo by curbing SM-induced early inflammatory responses, extracellular matrix degradation, and production of excessive pro-fibrotic and pro- angiogenic factors without significant side effects. This project tests two novel hypotheses to establish an efficacious and safe topical therapy for acute and delayed-onset MGK in vivo, using four specific aims: Aim-1 defines TED treatment for acute MGK in vivo by testing the hypothesis that increasing frequency and duration of TED application will potently treat acute MGK and blindness without significant side effects. Aim-2 establishes TED treatment for delayed-onset MGK in vivo by testing the hypothesis that low TED topical dosing for longer duration will effectively cure delayed-onset MGK without issues in rabbits. Aim-3 uncovers mechanisms used by TED in mitigating acute and delayed-onset MGK in vivo and in vitro. Aim-4 secures intellectual property rights, develops regulatory strategies, and advances TED topical ophthalmic drops as an antidote for SM-induced ocular injury towards human application. This will be accomplished using an established SM-vapor rabbit in vivo and human cornea organ culture ex vivo models, GMP-grade TED eye drops, and monitoring eyes in live rabbits in a time-dependent manner with clinical eye exams and diagnostic imaging. The characterization of mechanisms used by TED in mitigating MGK will be studied using corneal tissues collected after euthanasia by measuring integrity of corneal epithelial basement membrane, epithelial-stromal organization, and collagen fibril arrangement using qPCR, ELISAs, immunofluorescence, H&E, and transmission electron microscopy techniques utilizing our published methods. Successful completion of the project will lead to the development of an effective and safe therapy for acute and delayed MGK and medical countermeasure to minimize ocular obliteration caused by the accidental or intentional use of SM in humans, and therefore will have very high impact in field and public safety.

摘要