Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses
Abstract
1. Introduction
1.1. Acanthamoeba Cultivation
1.2. Nanoparticles
1.3. Contact Lens Solutions
1.4. Cytotoxicity
- EV—Experimental value
- ECSC—Effector cells spontaneous control
- TCSC—Target cells spontaneous control
- TCMC—Target cell maximum control
1.5. Adhesion to Contact Lenses
1.6. Amoebae Adhesion—Control
1.7. Amoebae Adhesion—Contact Lens Solutions Only
1.8. Amoebae Adhesion—Contact Lens Solutions + AgTANPs
2. Conclusions and Perspectives
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Somani, S.N.; Ronquillo, Y.; Moshirfar, M. Acanthamoeba keratitis. In StatPearls; StatPearls Publishing LLC: Treasure Island, FL, USA, 2020. [Google Scholar]
- Szentmary, N.; Daas, L.; Shi, L.; Laurik, K.L.; Lepper, S.; Milioti, G.; Seitz, B. Acanthamoeba keratitis—Clinical signs, differential diagnosis and treatment. J. Curr. Ophthalmol. 2018, 31, 16–23. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Lorenzo-Morales, J.; Martin-Navarro, C.M.; Lopez-Arencibia, A.; Arnalich-Montiel, F.; Pinero, J.E.; Valladares, B. Acanthamoeba keratitis: An emerging disease gathering importance worldwide? Trends Parasitol. 2013, 29, 181–187. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Wu, Y.T.-Y.; Willcox, M.; Zhu, H.; Stapleton, F. Contact lens hygiene compliance and lens case contamination: A review. Cont. Lens Anterior Eye 2015, 38, 307–316. [Google Scholar] [CrossRef] [Scilit]
- Radford, C.F.; Minassian, D.C.; Dart, J.K. Acanthamoeba keratitis in England and Wales: Incidence, outcome, and risk factors. Br. J. Ophthalmol. 2002, 86, 536–542. [Google Scholar] [CrossRef] [Scilit]
- Li, W.; Wang, Z.; Qu, J.; Zhang, Y.; Sun, X. Acanthamoeba keratitis related to contact lens use in a tertiary hospital in China. BMC Ophthalmol. 2019, 19, 202. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Lee, S.M.; Lee, J.E.; Lee, D.I.; Yu, H.S. Adhesion of Acanthamoeba on Cosmetic Contact Lenses. J. Korean Med. Sci. 2018, 33, e26. [Google Scholar] [CrossRef] [Scilit]
- Bunsuwansakul, C.; Mahboob, T.; Hounkong, K.; Laohaprapanon, S.; Chitapornpan, S.; Jawjit, S.; Yasiri, A.; Barusrux, S.; Bunluepuech, K.; Sawangjaroen, N.; et al. Acanthamoeba in Southeast Asia—Overview and Challenges. Korean J. Parasitol. 2019, 57, 341–357. [Google Scholar] [CrossRef] [Scilit]
- Niederkorn, J.Y. The biology of Acanthamoeba keratitis. Exp. Eye Res. 2021, 202, 108365. [Google Scholar] [CrossRef] [Scilit]
- Maycock, N.J.; Jayaswal, R. Update on Acanthamoeba keratitis: Diagnosis, Treatment, and Outcomes. Cornea 2016, 35, 713–720. [Google Scholar] [CrossRef] [Scilit]
- Panjwani, N. Pathogenesis of Acanthamoeba keratitis. Ocul. Surf. 2010, 8, 70–79. [Google Scholar] [CrossRef] [Scilit]
- Kot, K.; Lanocha-Arendarczyk, N.A.; Kosik-Bogacka, D.I. Amoebas from the genus Acanthamoeba and their pathogenic properties. Ann. Parasitol. 2018, 64, 299–308. [Google Scholar] [CrossRef] [PubMed]
- Bonini, S.; Di Zazzo, A.; Varacalli, G.; Coassin, M. Acanthamoeba keratitis: Perspectives for Patients. Curr. Eye Res. 2021, 46, 771–776. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Kumar, R.; Lloyd, D. Recent advances in the treatment of Acanthamoeba keratitis. Clin. Infect. Dis. 2002, 35, 434–441. [Google Scholar] [CrossRef] [Scilit]
- Clarke, B.; Sinha, A.; Parmar, D.N.; Sykakis, E. Advances in the diagnosis and treatment of Acanthamoeba keratitis. J. Ophthalmol. 2012, 2012, 484892. [Google Scholar] [CrossRef] [Scilit]
- Kokot, J.; Dobrowolski, D.; Lyssek-Boron, A.; Milka, M.; Smedowski, A.; Wojcik, L.; Wowra, B.; Wyligala, E. New approach to diagnosis and treatment of Acanthamoeba keratitis-systematic review of literature. Klin. Oczna. 2012, 114, 311–316. [Google Scholar]
- Padzik, M.; Hendiger, E.; Szaflik, J.; Chomicz, L. Amoebae of the genus Acanthamoeba—Pathological agents in humans. Postep. Mikrobiol. 2017, 56, 429–439. [Google Scholar] [CrossRef] [Scilit]
- Siddiqui, R.; Khan, N.A. Biology and pathogenesis of Acanthamoeba. Parasit. Vectors 2012, 5, 6. [Google Scholar] [CrossRef] [Scilit]
- de Lacerda, A.G.; Lira, M. Acanthamoeba keratitis: A review of biology, pathophysiology and epidemiology. Ophthalmic Physiol. Opt. 2021, 41, 116–135. [Google Scholar] [CrossRef] [Scilit]
- Hussain, R.H.; Afiqah, W.N.; Ghani, M.K.; Khan, N.A.; Siddiqui, R.; Anuar, T.S. In vitro effects of multi-purpose contact lens disinfecting solutions towards survivability of Acanthamoeba genotype T4 in Malaysia. Saudi J. Biol. Sci. 2021, 28, 2352–2359. [Google Scholar] [CrossRef] [Scilit]
- Moon, E.K.; Park, H.R.; Quan, F.S.; Kong, H.H. Efficacy of Korean Multipurpose Contact Lens Disinfecting Solutions against Acanthamoeba castellanii. Korean J. Parasitol. 2016, 54, 697–702. [Google Scholar] [CrossRef] [Scilit]
- Lakhundi, S.; Khan, N.A.; Siddiqui, R. Inefficacy of marketed contact lens disinfection solutions against keratitis-causing Acanthamoeba castellanii belonging to the T4 genotype. Exp. Parasitol. 2014, 141, 122–128. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Fears, A.C.; Metzinger, R.C.; Killeen, S.Z.; Reimers, R.S.; Roy, C.J. Comparative in vitro effectiveness of a novel contact lens multipurpose solution on Acanthamoeba castellanii. J. Ophthalmic Inflamm. Infect. 2018, 8, 19. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Lorenzo-Morales, J.; Khan, N.A.; Walochnik, J. An update on Acanthamoeba keratitis: Diagnosis, pathogenesis and treatment. Parasite 2015, 22, 10. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Padzik, M.; Chomicz, L.; Szaflik, J.P.; Chruscikowska, A.; Perkowski, K.; Szaflik, J.P. In vitro effects of selected contact lens care solutions on Acanthamoeba castellanii strains in Poland. Exp. Parasitol. 2014, 145, S98–S101. [Google Scholar] [CrossRef] [Scilit]
- Hendiger, E.B.; Padzik, M.; Zochowska, A.; Baltaza, W.; Oledzka, G.; Zyskowska, D.; Bluszcz, J.; Jarzynka, S.; Chomicz, L.; Grodzik, M.; et al. Tannic acid-modified silver nanoparticles enhance the anti-Acanthamoeba activity of three multipurpose contact lens solutions without increasing their cytotoxicity. Parasit. Vectors 2020, 13, 624. [Google Scholar] [CrossRef] [Scilit]
- Hendiger, E.B.; Padzik, M.; Sifaoui, I.; Reyes-Batlle, M.; López-Arencibia, A.; Zyskowska, D.; Grodzik, M.; Pietruczuk-Padzik, A.; Hendiger, J.; Olędzka, G.; et al. Silver Nanoparticles Conjugated with Contact Lens Solutions May Reduce the Risk of Acanthamoeba Keratitis. Pathogens 2021, 10, 583. [Google Scholar] [CrossRef] [Scilit]
- Anwar, A.; Soomaroo, A.; Anwar, A.; Siddiqui, R.; Khan, N.A. Metformin-coated silver nanoparticles exhibit anti-acanthamoebic activities against both trophozoite and cyst stages. Exp. Parasitol. 2020, 215, 107915. [Google Scholar] [CrossRef] [Scilit]
- Anwar, A.; Siddiqui, R.; Shah, M.R.; Khan, N.A. Gold Nanoparticle-Conjugated Cinnamic Acid Exhibits Antiacanthamoebic and Antibacterial Properties. Antimicrob. Agents Chemother. 2018, 62, 10. [Google Scholar] [CrossRef] [Scilit]
- Anwar, A.; Siddiqui, R.; Raza Shah, M.; Ahmed Khan, N. Gold Nanoparticles Conjugation Enhances Antiacanthamoebic Properties of Nystatin, Fluconazole and Amphotericin B. J. Microbiol. Biotechnol. 2019, 29, 171–177. [Google Scholar] [CrossRef] [Scilit]
- Sharma, G.; Kalra, S.K.; Tejan, N.; Ghoshal, U. Nanoparticles based therapeutic efficacy against Acanthamoeba: Updates and future prospect. Exp. Parasitol. 2020, 218, 108008. [Google Scholar] [CrossRef] [Scilit]
- Machado, L.F.; Sanfelice, R.A.; Bosqui, L.R.; Assolini, J.P.; Scandorieiro, S.; Navarro, I.T.; Depieri Cataneo, A.H.; Wowk, P.F.; Nakazato, G.; Bordignon, J.; et al. Biogenic silver nanoparticles reduce adherence, infection, and proliferation of Toxoplasma gondii RH strain in HeLa cells without inflammatory mediators induction. Exp. Parasitol. 2020, 211, 107853. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Said, D.E.; Elsamad, L.M.; Gohar, Y.M. Validity of silver, chitosan, and curcumin nanoparticles as anti-Giardia agents. Parasitol. Res. 2012, 111, 545–554. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Hendiger, E.B.; Padzik, M.; Sifaoui, I.; Reyes-Batlle, M.; Lopez-Arencibia, A.; Rizo-Liendo, A.; Bethencourt-Estrella, C.J.; Nicolas-Hernandez, D.S.; Chiboub, O.; Rodriguez-Exposito, R.L.; et al. Silver Nanoparticles as a Novel Potential Preventive Agent against Acanthamoeba keratitis. Pathogens 2020, 9, 350. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Anwar, A.; Numan, A.; Siddiqui, R.; Khalid, M.; Khan, N.A. Cobalt nanoparticles as novel nanotherapeutics against Acanthamoeba castellanii. Parasit. Vectors 2019, 12, 280–282. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Borase, H.P.; Patil, C.D.; Sauter, I.P.; Rott, M.B.; Patil, S.V. Amoebicidal activity of phytosynthesized silver nanoparticles and their in vitro cytotoxicity to human cells. FEMS Microbiol. Lett. 2013, 345, 127–131. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Sieniawska, E. Activities of Tannins--From In Vitro Studies to Clinical Trials. Nat. Prod. Commun. 2015, 10, 1877–1884. [Google Scholar] [CrossRef] [Scilit]
- Athar, M.; Khan, W.A.; Mukhtar, H. Effect of dietary tannic acid on epidermal, lung, and forestomach polycyclic aromatic hydrocarbon metabolism and tumorigenicity in Sencar mice. Cancer Res. 1989, 49, 5784–5788. [Google Scholar]
- Scalbert, A.; Monties, B.; Janin, G. Tannins in wood: Comparison of different estimation methods. J. Agric. Food Chem. 1989, 37, 1324–1329. [Google Scholar] [CrossRef] [Scilit]
- Haslam, E. Vegetable tannins—Lessons of a phytochemical lifetime. Phytochemistry 2007, 68, 2713–2721. [Google Scholar] [CrossRef] [Scilit]
- Khan, N.S.; Ahmad, A.; Hadi, S.M. Anti-oxidant, pro-oxidant properties of tannic acid and its binding to DNA. Chem. Biol. Interact. 2000, 125, 177–189. [Google Scholar] [CrossRef] [Scilit]
- Padzik, M.; Hendiger, E.B.; Chomicz, L.; Grodzik, M.; Szmidt, M.; Grobelny, J.; Lorenzo-Morales, J. Tannic acid-modified silver nanoparticles as a novel therapeutic agent against Acanthamoeba. Parasitol. Res. 2018, 117, 3519–3525. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Bakay, B.B.; Polat, Z.A. In vitro evaluation of adhesion of two acanthamoeba strains to cosmetic contact lenses. Eye Contact Lens 2018, 44, S241–S246. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Kobayashi, T.; Gibbon, L.; Mito, T.; Shiraishi, A.; Uno, T.; Ohashi, Y. Efficacy of commercial soft contact lens disinfectant solutions against Acanthamoeba. Jpn. J. Ophthalmol. 2011, 55, 547–557. [Google Scholar] [CrossRef] [Scilit] [PubMed]
- Niyyati, M.; Sasani, R.; Mohebali, M.; Ghazikhansari, M.; Kargar, F.; Hajialilo, E.; Rezaeian, M. Anti-Acanthamoeba effects of silver and gold nanoparticles and contact lenses disinfection solutions. Iran. J. Parasitol. 2018, 13, 180. [Google Scholar]
- Hamouda, R.A.; Hussein, M.H.; Abo-Elmagd, R.A.; Bawazir, S.S. Synthesis and biological characterization of silver nanoparticles derived from the cyanobacterium Oscillatoria limnetica. Sci. Rep. 2019, 1, 13071. [Google Scholar] [CrossRef] [Scilit]
- Alomari, A.A.; Kloub Fares, K.E.; Moustafa, N.E. Green synthesis of assembled silver nanoparticles in nano capsules of Peganum harmala L. leaf extract. Antibacterial activity and conjugate investigation. Cogent Chem. 2018, 4, 1532374. [Google Scholar] [CrossRef] [Scilit]
- Orlowski, P.; Tomaszewska, E.; Gniadek, M.; Baska, P.; Nowakowska, J.; Sokolowska, J.; Nowak, Z.; Donten, M.; Celichowski, G.; Grobelny, J.; et al. Tannic acid modified silver nanoparticles show antiviral activity in herpes simplex virus type 2 infection. PLoS ONE 2014, 9, e104113. [Google Scholar] [CrossRef] [Scilit]
- Available online: https://www.fortunebusinessinsights.com/industry-reports/contact-lenses-market-101775 (accessed on 18 May 2022).


| Manufacturer | Solution | Ingredients | Minimum Disinfection Time (h) |
|---|---|---|---|
| Menicon | Solo Care Aqua (SCA) | Polyhexanide (0.0001%), Hydrolock (dexpanthenol, sorbitol), sodium phosphate, tromethamine, poloxamer 407, disodium edetate | 4 |
| Alcon | Opti-Free (O-F) | TearGlyde (Tetronic 1304, nonanoyl ethylenediaminetriacetic acid), Polyquad (polyquaternium-1; 0.001%), Aldox (myristamidopropyl dimethylamine; 0.0005%) | 6 |
| Bausch + Lomb | ReNu MultiPlus (ReNu) | Hydranate (hydroxyalkylphosphonate; 0.03%), boric acid, edetate disodium, poloxamine (1%), sodium borate, sodium chloride, preserved with Dymed (polyaminopropyl biguanide; 0.0001%) | 4 |
| FDA Group | Manufacturer | Polymer | Water Content | Ionic |
|---|---|---|---|---|
| 1 | Acuvue Oasys 1-Day with Hydraluxe | Senofilcon A | 38% | No |
| 2 | Focus Dailes All Day Comfort | Nelfilcon A | 69% | No |
| 3 | Bausch + Lomb PureVision | Balafilcon A | 36% | Yes |
| 4 | Daily FitViev | Methafilcon A | 56% | Yes |
| FDA 1 | FDA 2 | FDA 3 | FDA 4 | |
|---|---|---|---|---|
| SCA | 17.61 ± 3.69 | no activity | 21.47 ± 16.83 | 23.47 ± 41.59 |
| SCA + 1.25 ppm AgTANPs | 46.31 ± 1.55 | 26.58 ± 41.44 | 26.79 ± 26.79 | 17.33 ± 1.47 |
| SCA + 2.5 ppm AgTANPs | 76.61 ± 11.99 | 69.64 ± 20.95 | 26.12 ± 53.77 | 39.52 ± 12.25 |
| SCA + 5 ppm AgTANPs | 93.25 ± 5.51 | 70.22 ± 23.66 | 30.21 ± 30.65 | 91.88 ± 4.68 |
| SCA + 10 ppm AgTANPs | 96.86 ± 0.47 | 70.51 ± 8.57 | 89.24 ± 6.75 | 86.60 ± 14.37 |
| O-F | no activity | 4.28 ± 20.95 | no activity | 36.52 ± 27 |
| O-F + 1.25 ppm AgTANPs | no activity | 60.86 ± 31.18 | no activity | 33.56 ± 35.88 |
| O-F + 2.5 ppm AgTANPs | 88.46 ± 10.27 | 88.28 ± 9.49 | no activity | 88.66 ± 3.55 |
| O-F + 5 ppm AgTANPs | 83.16 ± 4.94 | 99.79 ± 0.19 | 49.16 ± 16.42 | 97.15 ± 0.39 |
| O-F + 10 ppm AgTANPs | 89.24 ± 7.57 | 100 | 80.93 ± 4.96 | 98.83 ± 0.49 |
| ReNu | no activity | 14.99 ± 10.53 | 22.46 ± 4.27 | no activity |
| RenNu + 1.25 ppm AgTANPs | 27.82 ± 46.06 | 34.03 ± 15.06 | 42.64 ± 15.32 | no activity |
| ReNu + 2.5 ppm AgTANPs | 48.99 ± 34.85 | 38.09 ± 9.06 | 42.64 ± 5.74 | no activity |
| ReNu + 5 ppm AgTANPs | 89.85 ± 0.86 | 65.58 ± 19.18 | 48.08 ± 26.44 | 50.21 ± 7.87 |
| ReNu + 10 ppm AgTANPs | 92.99 ± 3.43 | 82.16 ± 3.06 | 78.96 ± 7.51 | 69.77 ± 17.01 |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Padzik, M.; Chomicz, L.; Bluszcz, J.; Maleszewska, K.; Grobelny, J.; Conn, D.B.; Hendiger, E.B. Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses. Microorganisms 2022, 10, 1076. https://doi.org/10.3390/microorganisms10061076
Padzik M, Chomicz L, Bluszcz J, Maleszewska K, Grobelny J, Conn DB, Hendiger EB. Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses. Microorganisms. 2022; 10(6):1076. https://doi.org/10.3390/microorganisms10061076
Chicago/Turabian StylePadzik, Marcin, Lidia Chomicz, Julita Bluszcz, Karolina Maleszewska, Jaroslaw Grobelny, David Bruce Conn, and Edyta B. Hendiger. 2022. "Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses" Microorganisms 10, no. 6: 1076. https://doi.org/10.3390/microorganisms10061076
APA StylePadzik, M., Chomicz, L., Bluszcz, J., Maleszewska, K., Grobelny, J., Conn, D. B., & Hendiger, E. B. (2022). Tannic Acid-Modified Silver Nanoparticles in Conjunction with Contact Lens Solutions Are Useful for Progress against the Adhesion of Acanthamoeba spp. to Contact Lenses. Microorganisms, 10(6), 1076. https://doi.org/10.3390/microorganisms10061076

