Öz
Herpes simpleks virüs tip-1 (HSV-1), ağız ve yüz lezyonlarından ölümcül ensefalite ve herpetik keratite kadar çeşitli sonuçlara neden olan yaygın bir patojendir. Asiklovir (ACV), HSV-1 enfeksiyonunun tedavisinde güncel bir seçenektir. Bununla birlikte, ACV-dirençli HSV-1’in ortaya çıkışı ve akut böbrek hasarı gibi uzun süreli ACV uygulamasının zararlı yan etkileri göz önüne alındığında, yeni antiviral terapötik ajanların ve yeni ilaç dağıtım sistemlerinin geliştirilmesi vazgeçilmez görünmektedir. Nanoteknolojinin gelişmesiyle birlikte nanopartiküller (NP), benzersiz fiziksel ve kimyasal özelliklerinden dolayı antimikrobiyal ajanlar ve ilaç taşıyıcıları olarak büyük ilgi görmüştür. Bu derlemede, NP’lerin HSV-1’e karşı antiviral aktivitesine ve bunların ACV dağıtımındaki uygulamalarına odaklandık.
Anahtar Kelimeler: Antiviral tedavi, HSV-1 enfeksiyonu, nanopartiküller, nanotaşıyıcılar, asiklovir
Kaynakça
Duarte LF, Farías MA, Álvarez DM, Bueno SM, Riedel CA, González PA. Herpes Simplex Virus Type 1 Infection of the Central Nervous System: Insights Into Proposed Interrelationships With Neurodegenerative Disorders. Front Cell Neurosci. 2019;13:46.
Reske A, Pollara G, Krummenacher C, Chain BM, Katz DR. Understanding HSV-1 entry glycoproteins. Rev Med Virol. 2007;17:205-15.
Baram-Pinto D, Shukla S, Gedanken A, Sarid R. Inhibition of HSV-1 attachment, entry, and cell-to-cell spread by functionalized multivalent gold nanoparticles. Small. 2010;6:1044-50.
Trigilio J, Antoine TE, Paulowicz I, Mishra YK, Adelung R, Shukla D. Tin Oxide Nanowires Suppress Herpes Simplex Virus-1 Entry and Cell-to-Cell Membrane Fusion. PLoS One. 2012;7:1-9.
Ohtsu Y, Susaki Y, Noguchi K. Absorption, Distribution, Metabolism, and Excretion of the Novel Helicase-Primase Inhibitor, Amenamevir (ASP2151), in Rodents. Eur J Drug Metab Pharmacokinet. 2018;43:693-706.
Pires de Mello CP, Bloom DC, Paixão IC. Herpes simplex virus type-1: replication, latency, reactivation and its antiviral targets. Antivir Ther. 2016;21:277-86.
Aridass D, Seetharaman S, Govindaraju K, Parija P, Sasikala S, Ramesh Kumar MR. Anti-herpes simplex virus (HSV-1 and HSV-2) activity of biogenic gold and silver nanoparticles using seaweed Sargassum wightii. Indian J Geo-Marine Sci. 2019;48:1252-7.
Hassan H, Bello RO, Adam SK, Alias E, Meor Mohd Affandi MMR, Shamsuddin AF, Basir R. Acyclovir-Loaded Solid Lipid Nanoparticles: Optimization, Characterization and Evaluation of Its Pharmacokinetic Profile. Nanomaterials (Basel). 2020;10:1785.
Rai M, Shegokar R. Metal nanoparticles in pharma. 1st ed. Chapter: 15. Springer International Publisher. 2017:337-63.
Rai M, Deshmukh SD, Ingle AP, Gupta IR, Galdiero M, Galdiero S. Metal nanoparticles: The protective nanoshield against virus infection. Crit Rev Microbiol. 2016;42:46-56.
Jeyaraj M, Gurunathan S, Qasim M, Kang MH, Kim JH. A Comprehensive Review on the Synthesis, Characterization, and Biomedical Application of Platinum Nanoparticles. Nanomaterials (Basel). 2019;9:1719.
Dhand C, Dwivedi N, Loh XJ, Ying ANJ, Verma NK, Beuerman RW, Lakshminarayanan R, Ramakrishna S. Methods and Strategies for the Synthesis of Diverse Nanoparticles and their Applications: A Comprehensive Overview RSC Adv. 2015;5:105003-37.
Maduray K, Parboosing R. Metal Nanoparticles: a Promising Treatment for Viral and Arboviral Infections. Biol Trace Elem Res. 2021;199:3159-76.
Mohammed Fayaz A, Ao Z, Girilal M, Chen L, Xiao X, Kalaichelvan P, Yao X. Inactivation of microbial infectiousness by silver nanoparticles-coated condom: a new approach to inhibit HIV- and HSV-transmitted infection. Int J Nanomedicine. 2012;7:5007-18.
Gaikwad S, Ingle A, Gade A, Rai M, Falanga A, Incoronato N, Russo L, Galdiero S, Galdiero M. Antiviral activity of mycosynthesized silver nanoparticles against herpes simplex virus and human parainfluenza virus type 3. Int J Nanomedicine. 2013;8:4303-14.
Kwon HJ, Jeong JH, Lee SW, Ryu YB, Jeong HJ, Jung K, Lim JS, Cho KO, Lee WS, Rho MC, Park SJ. In vitro anti-reovirus activity of kuraridin isolated from Sophora flavescens against viral replication and hemagglutination. J Pharmacol Sci. 2015;128:159-69.
Ramadan MA, Shawkey AE, Rabeh MA, Abdellatif AO. Promising antimicrobial activities of oil and silver nanoparticles obtained from Melaleuca alternifolia leaves against selected skin-infecting pathogens. J Herb Med. 2020;20:100289.
Szymańska E, Orłowski P, Winnicka K, Tomaszewska E, Bąska P, Celichowski G, Grobelny J, Basa A, Krzyżowska M. Multifunctional Tannic Acid/Silver Nanoparticle-Based Mucoadhesive Hydrogel for Improved Local Treatment of HSV Infection: In Vitro and In Vivo Studies. Int J Mol Sci. 2018;19:387.
Haggag EG, Elshamy AM, Rabeh MA, Gabr NM, Salem M, Youssif KA, Samir A, Bin Muhsinah A, Alsayari A, Abdelmohsen UR. Antiviral potential of green synthesized silver nanoparticles of Lampranthus coccineus and Malephora lutea. Int J Nanomedicine. 2019;14:6217-29.
El-Sheekh MM, Shabaan MT, Hassan L, Morsi HH. Antiviral activity of algae biosynthesized silver and gold nanoparticles against Herps Simplex (HSV-1) virus in vitro using cell-line culture technique. Int J Environ Health Res. 2020:1-12.
Halder A, Das S, Ojha D, Chattopadhyay D, Mukherjee A. Highly monodispersed gold nanoparticles synthesis and inhibition of herpes simplex virus infections. Mater Sci Eng C Mater Biol Appl. 2018;89:413-21.
I RI, Mj S, R G, Fj M, Mj B, Ma MF. Gold Nanoparticles Crossing Blood-Brain Barrier Prevent HSV-1 Infection and Reduce Herpes Associated Amyloid-βsecretion. J Clin Med. 2020;9:155.
Mishra YK, Adelung R, Röhl C, Shukla D, Spors F, Tiwari V. Virostatic potential of micro-nano filopodia-like ZnO structures against herpes simplex virus-1. Antiviral Res. 2011;92:305-12.
Farouk F, Shebl RI. Comparing Surface Chemical Modifications of Zinc Oxide Nanoparticles for Modulating their Antiviral Activity against Herpes Simplex Virus Type-1. Int J Nanoparticles Nanotech. 2018;4:1-14.
Tavakoli A, Ataei-Pirkooh A, Mm Sadeghi G, Bokharaei-Salim F, Sahrapour P, Kiani SJ, Moghoofei M, Farahmand M, Javanmard D, Monavari SH. Polyethylene glycol-coated zinc oxide nanoparticle: an efficient nanoweapon to fight against herpes simplex virus type 1. Nanomedicine (Lond). 2018;13:2675-90.
Tavakoli A, Hashemzadeh MS. Inhibition of herpes simplex virus type 1 by copper oxide nanoparticles. J Virol Methods. 2020;275:113688.
Liu ML, Bin Chen B, Li CM, Huang CZ. Carbon dots: Synthesis, formation mechanism, fluorescence origin and sensing applications. Green Chem. 2019;21:449-71.
Innocenzi P, Stagi L. Carbon-based antiviral nanomaterials: graphene, C-dots, and fullerenes. A perspective. Chem Sci. 2020;11:6606-22.
Bhartiya P, Singh A, Kumar H, Jain T, Singh BK, Dutta PK. Carbon dots: Chemistry, properties and applications. J Indian Chem. 2016;93:759-66.
Barras A, Pagneux Q, Sane F, Wang Q, Boukherroub R, Hober D, Szunerits S. High Efficiency of Functional Carbon Nanodots as Entry Inhibitors of Herpes Simplex Virus Type 1. ACS Appl Mater Interfaces. 2016;8:9004-13.
Thakral S, Mehta R. Fullerenes: An introduction and overview of their biological properties. Indian J Pharm Sci. 2006;68:13-9.
Klimova R, Andreev S, Momotyuk E, Demidova N, Fedorova N, Chernoryzh Y, Yurlov K, Turetskiy E, Baraboshkina E, Shershakova N, Simonov R, Kushch A, Khaitov M, Gintsburg A. Aqueous fullerene C60 solution suppresses herpes simplex virus and cytomegalovirus infections. Fullerenes Nanotub. Carbon Nanostructures. 2019;28:487-99.
Voynikov T, Nikolva I, Suzuki A, Higashino H, Petkova M, Mega N. A review on the properties and applications of perfluorocarbon emulsions. Acta medica Kinki University. 1990;15:1-20.
Sametband M, Kalt I, Gedanken A, Sarid R. Herpes simplex virus type-1 attachment inhibition by functionalized graphene oxide. ACS Appl Mater Interfaces. 2014;6:1228-35.
Donskyi IS, Azab W, Cuellar-Camacho JL, Guday G, Lippitz A, Unger WES, Osterrieder K, Adeli M, Haag R. Functionalized nanographene sheets with high antiviral activity through synergistic electrostatic and hydrophobic interactions. Nanoscale. 2019;11:15804-9.
Shen MX, Ma N, Li MK, Liu YY, Chen T, Wei F, Liu DY, Hou W, Xiong HR, Yang ZQ. Antiviral Properties of R. tanguticum Nanoparticles on Herpes Simplex Virus Type I In Vitro and In Vivo. Front Pharmacol. 2019;10:959.
Tahara K, Kobayashi M, Yoshida S, Onodera R, Inoue N, Takeuchi H. Effects of cationic liposomes with stearylamine against virus infection. Int J Pharm. 2018;543:311-7.
Grumezescu AM. Antimicrobial Nanoarchitectonics: From Synthesis to Applications. 11th ed. Chapter 14. Elsevier Science; 2017.
Luganini A, Nicoletto SF, Pizzuto L, Pirri G, Giuliani A, Landolfo S, Gribaudo G. Inhibition of herpes simplex virus type 1 and type 2 infections by peptide-derivatized dendrimers. Antimicrob. Agents Chemother. 2011;55:3231-9.
Tarallo R, Carberry TP, Falanga A, Vitiello M, Galdiero S, Galdiero M, Weck M. Dendrimers functionalized with membrane-interacting peptides for viral inhibition. Int J Nanomedicine. 2013;8:521-34.
Chamundeeswari M, J Jeslin J, Verma ML. Nanocarriers for drug delivery applications. Environ Chem Lett. 2019;17:849-65.
Kondel R, Shafiq N, Kaur IP, Singh MP, Pandey AK, Ratho RK, Malhotra S. Effect of Acyclovir Solid Lipid Nanoparticles for the Treatment of Herpes Simplex Virus (HSV) Infection in an Animal Model of HSV-1 Infection. Pharm Nanotechnol. 2019;7:389-403.
Muzzalupo R, Tavano L. Niosomal drug delivery for transdermal targeting: recent advances. Research and Reports in Transdermal Drug Delivery. 2015;4:23-33.
Akbarzadeh A, Rezaei-Sadabady R, Davaran S, Joo SW, Zarghami N, Hanifehpour Y, Samiei M, Kouhi M, Nejati-Koshki K. Liposome: classification, preparation, and applications. Nanoscale Res Lett. 2013;8:102.
Mukherjee B, Patra B, Layek B, Mukherjee A. Sustained release of acyclovir from nano-liposomes and nano-niosomes: an in vitro study. Int J Nanomedicine. 2007;2:213-25.
Mirzaei P, Monavari SH, Dadashzadeh S, Ebrahimi SA, Bolouri B, Haeri A. Preparation and Evaluation of the Antiviral Activity of Avyclovir Loaded Nano-Niosomes Against Herpes Simplex Virus Type 1. Pharmacophore. 2014;5:483-93.
Salem HF, Tamam SM, Lotayef SM. Biodegradable Liposomes for Acyclovir-Gold Nanoparticles As an Efficient Carrierfor Enhanced Topical Delivery. Int J Pharm Pharm Sci. 2017;9:60.
Rizwanullah ZS, Mir SZ, Amin S. Bilosomes nanocarriers for improved oral bioavailability of acyclovir: A complete characterization through in vitro, ex vivo and in vivo assessment. J Drug Deliv Sci Tec. 2020; 57:101634.
Donalisio M, Leone F, Civra A, Spagnolo R, Ozer O, Lembo D, Cavalli R. Acyclovir-Loaded Chitosan Nanospheres from Nano-Emulsion Templating for the Topical Treatment of Herpesviruses Infections. Pharmaceutics. 2018;10:46.
Foroozandeh P, Aziz AA. Insight into Cellular Uptake and Intracellular Trafficking of Nanoparticles. Nanoscale Res Lett. 2018;13:339.


