In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine

Purpose: Acanthamoeba keratitis often is refractory to medical and surgical therapy, primarily because of the remarkable resilience of Acanthamoeba cysts. In this study, we directly compared the cysticidal activity and potency of several candidate medical therapies in vitro. Design: Experimental stu...

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Main Authors: Travis K. Redd, MD, MPH, Maya Talbott, MHS, Vicky Cevallos, MT, Prajna Lalitha, MD, Gerami D. Seitzman, MD, Thomas M. Lietman, MD, Jeremy D. Keenan, MD, MPH
Format: Article
Language:English
Published: Elsevier 2021-06-01
Series:Ophthalmology Science
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666914521000233
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spelling doaj-c52fe4e8729f43c79aa3c87613b51a812021-07-29T04:24:05ZengElsevierOphthalmology Science2666-91452021-06-0112100025In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and ChlorhexidineTravis K. Redd, MD, MPH0Maya Talbott, MHS1Vicky Cevallos, MT2Prajna Lalitha, MD3Gerami D. Seitzman, MD4Thomas M. Lietman, MD5Jeremy D. Keenan, MD, MPH6Francis I. Proctor Foundation, University of California, San Francisco; Casey Eye Institute, Oregon Health &amp; Science University, Portland, OregonFrancis I. Proctor Foundation, University of California, San FranciscoFrancis I. Proctor Foundation, University of California, San FranciscoAravind Eye Hospital, Madurai, IndiaFrancis I. Proctor Foundation, University of California, San Francisco; Department of Ophthalmology, University of California, San FranciscoFrancis I. Proctor Foundation, University of California, San Francisco; Department of Ophthalmology, University of California, San FranciscoFrancis I. Proctor Foundation, University of California, San Francisco; Department of Ophthalmology, University of California, San Francisco; Correspondence: Jeremy D. Keenan, MD, MPH, Francis I. Proctor Foundation, University of California, San Francisco, 490 Illinois Street, San Francisco, CA 94107.Purpose: Acanthamoeba keratitis often is refractory to medical and surgical therapy, primarily because of the remarkable resilience of Acanthamoeba cysts. In this study, we directly compared the cysticidal activity and potency of several candidate medical therapies in vitro. Design: Experimental study. Participants: In vitro Acanthamoeba specimens obtained from 9 patients with keratitis seen at the Francis I. Proctor Foundation from 2008 through 2012. Methods: The minimum cysticidal concentration (MCC) of povidone iodine, natamycin, and chlorhexidine was investigated using an established assay technique. The relative potency of each agent was estimated starting with concentrations commonly used in clinical practice and determining the number of two-fold dilutions required to reach the MCC. Statistical comparisons of relative potency were performed using bootstrap simulations and permutation tests. Main Outcome Measures: Minimum cysticidal concentration and the number of two-fold dilutions required to reach the MCC. Results: The MCC for chlorhexidine ranged from 3.1 to 25 μg/ml (median, 12.5 μg/ml; interquartile range [IQR], 6.25–12.5 μg/ml), the MCC for natamycin ranged from 390.6 to 3125 μg/ml (median, 390.6 μg/ml; IQR, 390.6–781.2 μg/ml), and the MCC for povidone iodine ranged from 0.3 to 78.1 μg/ml (median, 2.4 μg/ml; IQR, 0.6–9.8 μg/ml). Doses commonly used in clinical practice (povidone iodine 1%, natamycin 5%, and chlorhexidine 0.04%) were approximately 12, 7, and 5 two-fold dilutions higher than the drug’s corresponding median MCC, respectively (P < 0.001, comparing 3 drugs). Povidone iodine 1% had the highest potency of the 3 medications tested, requiring more dilutions than natamycin 5% (P < 0.001) and chlorhexidine 0.04% (P < 0.001) to reach the MCC. Conclusions: All 3 medications demonstrated in vitro cysticidal activity in each of the 9 isolates. The potency of 1% povidone iodine was greater than standard formulations of natamycin or chlorhexidine. Although its clinical efficacy is yet to be determined, povidone iodine may be considered as a potential adjuvant treatment in cases of recalcitrant Acanthamoeba keratitis.http://www.sciencedirect.com/science/article/pii/S2666914521000233AcanthamoebaChlorhexidineIodineNatamycin
collection DOAJ
language English
format Article
sources DOAJ
author Travis K. Redd, MD, MPH
Maya Talbott, MHS
Vicky Cevallos, MT
Prajna Lalitha, MD
Gerami D. Seitzman, MD
Thomas M. Lietman, MD
Jeremy D. Keenan, MD, MPH
spellingShingle Travis K. Redd, MD, MPH
Maya Talbott, MHS
Vicky Cevallos, MT
Prajna Lalitha, MD
Gerami D. Seitzman, MD
Thomas M. Lietman, MD
Jeremy D. Keenan, MD, MPH
In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
Ophthalmology Science
Acanthamoeba
Chlorhexidine
Iodine
Natamycin
author_facet Travis K. Redd, MD, MPH
Maya Talbott, MHS
Vicky Cevallos, MT
Prajna Lalitha, MD
Gerami D. Seitzman, MD
Thomas M. Lietman, MD
Jeremy D. Keenan, MD, MPH
author_sort Travis K. Redd, MD, MPH
title In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
title_short In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
title_full In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
title_fullStr In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
title_full_unstemmed In Vitro Comparison of the Acanthamoeba Cysticidal Activity of Povidone Iodine, Natamycin, and Chlorhexidine
title_sort in vitro comparison of the acanthamoeba cysticidal activity of povidone iodine, natamycin, and chlorhexidine
publisher Elsevier
series Ophthalmology Science
issn 2666-9145
publishDate 2021-06-01
description Purpose: Acanthamoeba keratitis often is refractory to medical and surgical therapy, primarily because of the remarkable resilience of Acanthamoeba cysts. In this study, we directly compared the cysticidal activity and potency of several candidate medical therapies in vitro. Design: Experimental study. Participants: In vitro Acanthamoeba specimens obtained from 9 patients with keratitis seen at the Francis I. Proctor Foundation from 2008 through 2012. Methods: The minimum cysticidal concentration (MCC) of povidone iodine, natamycin, and chlorhexidine was investigated using an established assay technique. The relative potency of each agent was estimated starting with concentrations commonly used in clinical practice and determining the number of two-fold dilutions required to reach the MCC. Statistical comparisons of relative potency were performed using bootstrap simulations and permutation tests. Main Outcome Measures: Minimum cysticidal concentration and the number of two-fold dilutions required to reach the MCC. Results: The MCC for chlorhexidine ranged from 3.1 to 25 μg/ml (median, 12.5 μg/ml; interquartile range [IQR], 6.25–12.5 μg/ml), the MCC for natamycin ranged from 390.6 to 3125 μg/ml (median, 390.6 μg/ml; IQR, 390.6–781.2 μg/ml), and the MCC for povidone iodine ranged from 0.3 to 78.1 μg/ml (median, 2.4 μg/ml; IQR, 0.6–9.8 μg/ml). Doses commonly used in clinical practice (povidone iodine 1%, natamycin 5%, and chlorhexidine 0.04%) were approximately 12, 7, and 5 two-fold dilutions higher than the drug’s corresponding median MCC, respectively (P < 0.001, comparing 3 drugs). Povidone iodine 1% had the highest potency of the 3 medications tested, requiring more dilutions than natamycin 5% (P < 0.001) and chlorhexidine 0.04% (P < 0.001) to reach the MCC. Conclusions: All 3 medications demonstrated in vitro cysticidal activity in each of the 9 isolates. The potency of 1% povidone iodine was greater than standard formulations of natamycin or chlorhexidine. Although its clinical efficacy is yet to be determined, povidone iodine may be considered as a potential adjuvant treatment in cases of recalcitrant Acanthamoeba keratitis.
topic Acanthamoeba
Chlorhexidine
Iodine
Natamycin
url http://www.sciencedirect.com/science/article/pii/S2666914521000233
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