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. 2020 May 20;258(11):2563–2565. doi: 10.1007/s00417-020-04752-2

Possible prophylactic or preventive role of topical povidone iodine during accidental ocular exposure to 2019-nCoV

Phulen Sarma 1, Hardeep Kaur 1, Bikash Medhi 1, Anusuya Bhattacharyya 2,
PMCID: PMC7239348  PMID: 32436084

Dear Editor.

Ocular tropism of respiratory viruses is a well-known fact and is reported in cases of a wide range of viruses, e.g., adenovirus, respiratory syncytial virus, influenza virus, rhino virus, and corona viruses [1, 2]. Conjunctivitis is present in 3.175% of patients with COVID-19; however, only 0.703% of patients present with conjunctivitis as the first presenting feature [24] and 1.949% of patients demonstrate the virus in tear/conjunctival specimen [2]. These findings indicate ocular tropism of SARS-CoV-2. However, there is also a possibility of local replication of the virus followed by systemic involvement, especially in cases of droplet or aerosol transmission through the ocular route [47].

The anatomical and molecular link between the ocular system and the respiratory tract is already well-established [2]. The nasolacrimal duct (NLD) serves as an anatomical link between ocular system and respiratory tract [1]. Regarding molecular link, various cellular proteins such as α2-3-linked sialic acid (expressed in lower respiratory tract and ocular tissue) serves as an interaction site for diverse range of influenza viruses [2]. CD46, GD1a glycans act as cellular receptor for adeno virus, desmoglein-2/adenovirus receptor for adenovirus, or the coxsackievirus, ACE2 for SARS-CoV and ACE2 and CD147 for SARS-CoV-2 [1]. In case of SARS-CoV-2, initial interactions between the spike protein S1 domain and its host receptor (either ACE2 or CD147) are the initiating event in establishment of human host infection [8, 9].

Presence of an ocular renin angiotensin system (RAS) and ACE (angiotensin converting enzyme) activity is already demonstrated in retinal tissue, choroid, and sclera as early as 1988 [10, 11]. This was followed by the demonstration of ACE and Ang-II receptor expression in ciliary body (non-pigmented epithelium), cornea (epithelium and endothelium), conjunctiva (epithelium), trabecular meshwork cells, retinal ganglion cells, photoreceptor cells, nuclear layer of retina, and endothelial cell layer of chorioretinal vessels [12]. In vitro studies demonstrate corneal and conjunctival expression of ACE2, thus suggesting a link between the ocular system and respiratory system in case of COVID-19 [13]. Another route of entry of SARS-CoV-2 to human host is through its interactions with CD147 [14], which is present in tear and human ocular tissues, e.g., corneal epithelium, endothelium, keratocytes, conjunctiva, and retinal pigment epithelium [15]. Thus, the conjunctival route may play a major route in establishment of infection [5].

Accidental exposure to SARS-CoV-2 through ocular route

Though the face is covered with a mask by health care professionals, police, and frontline workers during their interaction with suspected or confirmed COVID-19 patients, the ocular route usually remain uncovered. Though protective goggles are available as a part of personal protection equipment (PPE) kits, however, their scarce availability is a concern even in the developed countries [16]. Thus, ocular route remains unprotected and unattended. Accidental ocular exposure to SARS-CoV-2 can occur in many conditions:

  1. Accidental hand-eye contact among persons working in COVID-19 environment.

  2. This issue becomes complicated when news of some incidences like intentional spitting on doctors [1719] and police personals [2022] by suspected or confirmed COVID-19 patients, which also can result in accidental ocular exposure.

However, until date, no post-exposure prophylaxis is available in case of accidental ocular exposure with SARS-CoV-2.

Povidone iodine 1% eye drop as post-exposure prophylaxis: can it have some role?

Povidone iodine is a broad spectrum antiviral agent covering both enveloped and non-enveloped viruses with established virucidal activity (adenovirus, mumps, rota virus, polio, coxsackie, rhino virus, herpes virus, rubella, measles, influenza, and human immunodeficiency virus) [23]. In rabbit model of adenoviral conjunctivitis, topical povidone iodine along with dexamethasone was found to be very effective [24]. In clinical settings, povidone iodine (5% and 1%) already showed clinical benefit in cases of adenoviral conjunctivitis [2527].

Now, coming to the efficacy of povidone iodine treatment in SARS-CoV, treatment with povidone iodine for 2 min reduces viral infectivity to below detectable level and the efficiency of povidone iodine was similar to 70% ethanol in terms of reducing viral infectivity [28]. There are reports citing efficacy of povidone iodine gurgle/mouth wash against SARS-CoV and MERS-CoV [29, 30], and on the basis of these findings, povidone iodine mouth wash/gurgle is being recommended in cases of SARS-CoV-2 also [31, 32] by various authors.

In in vitro studies, povidone iodine (1%) was successful in reducing the infectivity of the virus (both SARS-CoV and MARS-CoV, 1-min time contact period for SARS-CoV and 15-second contact time for MERS-CoV, were associated with significant loss of viral infectivity) [33]. Occurrence of resistance is not an issue with povidone iodine. So, here comes a theoretically potential role of using povidone iodine 1% locally (eye drop) in case of accidental ocular exposure or in case of 2019-nCoV-associated conjunctivitis. However, toxicity profile of povidone iodine is to be to be considered and we need more clinical data for further validation.

Acknowledgments

The authors acknowledge the contribution of Dr. Pramod Avti, Associate Prof, Department of Biophysics, PGIMER, Chandigarh; Manisha Prajapat, PhD scholar, Department of Pharmacology, PGIMER, Chandigarh; Dr. Mukundam Borah, Registrar, Department of Pharmacology, Guwahati Medical College and Hospital Guwahati Assam, India; Nishant Shekhar, Department of Pharmacology, PGIMER, Chandigarh; Dr. Subodh Kumar, NPDF, Department of Pharmacology, PGIMER, Chandigarh; Dr. Dipankar Das, HOD, Uvea, Neuro Ophthalmology and Ocular Pathology; Sri Sankaradeva Nethralaya, Guwahati, Assam; and Dr. Ajay Prakash, Asst. Professor, Department of Pharmacology, PGIMER, Chandigarh, towards the preparation of the manuscript.

Abbreviations

2019-nCoV

2019 novel corona virus

SARS-CoV

Severe acute respiratory syndrome coronavirus

MERS-CoV

Middle East respiratory Syndrome Coronavirus

ACE2

Angiotensin converting enzyme 2

COVID-19

Coronavirus disease 2019

PPE

Personal protective equipment

Author contributions

Concept: Phulen Sarma and Anusuya Bhattacharyya

Literature research and data extraction: Phulen Sarma, Hardeep Kaur, and Anusuya Bhattacharyya

Manuscript writing, revision of manuscript, and final approval: Phulen Sarma, Hardeep Kaur, Bikash Medhi, Anusuya Bhattacharyya

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Phulen Sarma, Email: phulen10@gmail.com.

Hardeep Kaur, Email: Aspireachieve.shine@gmail.com.

Bikash Medhi, Email: drbikashus@yahoo.com.

Anusuya Bhattacharyya, Email: anusuya.8k@gmail.com.

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