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Current Pharmaceutical Analysis

Editor-in-Chief

ISSN (Print): 1573-4129
ISSN (Online): 1875-676X

Review Article

Analytical Methodologies for the Estimation of Acyclovir as Key Members of Anti-viral Agent: Two Decades in Review

Author(s): Akhil Gupta and Shilpi Pathak*

Volume 19, Issue 8, 2023

Published on: 15 September, 2023

Page: [597 - 609] Pages: 13

DOI: 10.2174/1573412919666230908161943

Price: $65

Abstract

Herpes simplex virus (HSV) is a viral infection that primarily targets oral and genital organs in humans. Acyclovir is a widely prescribed anti-viral agent used in the infection caused by herpes simplex virus (HSV). This article emphasizes several analytical techniques, including spectrophotometry, High-performance liquid chromatography, High-performance thin-layer liquid chromatography, Ultra performance liquid chromatography, and Liquid chromatography/ Mass detection for the quantification of acyclovir in different matrices like biological fluids and Pharmaceutical formulation. In the proposed work, numerous methods for different techniques were extracted from various databases such as Science Direct, Springer, PubMed, SCOPUS, Web of Science, etc. According to the recommendation from the internal conference on harmonization, this review describes how to determine the presence of utilizing acyclovir in different analytical techniques alone or in combination with another drug.

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Graphical Abstract

[1]
James, S.H.; Kimberlin, D.W.; Whitley, R.J. Antiviral therapy for herpesvirus central nervous system infections: Neonatal herpes simplex virus infection, herpes simplex encephalitis, and congenital cytomegalovirus infection. Antiviral Res., 2009, 83(3), 207-213.
[http://dx.doi.org/10.1016/j.antiviral.2009.04.010] [PMID: 19414035]
[2]
Brady, R.C.; Bernstein, D.I. Treatment of herpes simplex virus infections. Antiviral Res., 2004, 61(2), 73-81.
[http://dx.doi.org/10.1016/j.antiviral.2003.09.006] [PMID: 14670580]
[3]
Kaufman, B.; Gandhi, S.A.; Louie, E.; Rizzi, R.; Illei, P. Herpes simplex virus hepatitis: Case report and review. Clin. Infect. Dis., 1997, 24(3), 334-338.
[http://dx.doi.org/10.1093/clinids/24.3.334] [PMID: 9114181]
[4]
Clercq, E.D. Antivirals for the treatment of herpesvirus infections. J. Antimicrob. Chemother., 1993, 32, 121-132.
[http://dx.doi.org/10.1093/jac/32.suppl_A.121] [PMID: 8407694]
[5]
Muralidharan, S.; Kalaimani, J.; Parasuraman, S.; Dhanaraj, S.A. Development and validation of acyclovir HPLC external standard method in human plasma: Application to pharmacokinetic studies. Adv. Pharm., 2014, 2014, 1-5.
[http://dx.doi.org/10.1155/2014/284652]
[6]
Kim, J.M.; Nishi, C.; Grant, J.M. A retrospective review of empiric acyclovir prescribing practices for suspected viral central nervous system infections: A single-centre study. J. Assoc. Med. Microbiol.Infect. Dis. Canada,, 2023, 2023
[7]
Schuierer, L.; Gebhard, M.; Ruf, H.G.; Jaschinski, U.; Berghaus, T.M.; Wittmann, M.; Braun, G.; Busch, D.H.; Hoffmann, R. Impact of acyclovir use on survival of patients with ventilator-associated pneumonia and high load herpes simplex virus replication. Crit. Care, 2020, 24(1), 12.
[http://dx.doi.org/10.1186/s13054-019-2701-5] [PMID: 31924246]
[8]
Szczubiałka, K.; Pyrć K.; Nowakowska, M. In search for effective and definitive treatment of herpes simplex virus type 1 (HSV-1) infections. RSC Advances, 2016, 6(2), 1058-1075.
[http://dx.doi.org/10.1039/C5RA22896D]
[9]
Wei, Y.P.; Yao, L.Y.; Wu, Y.Y.; Liu, X.; Peng, L.H.; Tian, Y.L.; Ding, J.H.; Li, K.H.; He, Q.G. Critical review of synthesis, toxicology and detection of acyclovir. Molecules, 2021, 26(21), 6566-6591.
[http://dx.doi.org/10.3390/molecules26216566] [PMID: 34770975]
[10]
de Miranda, P.; Blum, M.R. Pharmacokinetics of acyclovir after intravenous and oral administration. J. Antimicrob. Chemother., 1983, 12, 29-37.
[http://dx.doi.org/10.1093/jac/12.suppl_B.29] [PMID: 6355048]
[11]
Robert Blum, M.; Liaq, S.H.T.; De Miranda, P. Overview of acyclovir pharmacokinetic disposition in adults and children. Am. J. Med., 1982, 73(1), 186-192.
[http://dx.doi.org/10.1016/0002-9343(82)90088-2] [PMID: 7048911]
[12]
Kuchekar, B.S.; Gandhi, P.; Momin, N.; Kharade, S.; Konapure, N.P. Spectrophotometric estimation of acyclovir in pharmaceutical dosage forms. Indian J. Pharm. Sci., 2006, 68(4), 516-517.
[http://dx.doi.org/10.4103/0250-474X.27833]
[13]
Akshata, L.; Afaque, A.; Mallinath, K. Uv spectrophotometric analysis and validation of acyclovir in solid dosage form. Int. J. Curr. Pharm. Res., 2020, 12, 100-103.
[14]
Dongare, U.S.; Chemate, S.Z.; Jadhav, S.A.; Pawar, V.R. Spectrophotometric determination and validation of acyclovir in tablet dosage form. Int. J. Pharm. Tech. Res., 2012, 4, 1840-1845.
[15]
Dessai, P.; Fatrekar, N. Stability indicating method development and validation of UV method for the determination of acyclovir in tablet dosage form. INDO Am. J. Pharm. Sci., 2018, 05, 8955-8960.
[16]
Padala, N.R.; Baishakhi, D.; Assaleh, F.H.; Katakam, P.; Chandu, B.R. UV-spectrophotometric estimation of acyclovir in bulk and pharmaceutical dosage forms. J. Pharm. Innov., 2013, 2(4), 40-43.
[http://dx.doi.org/10.7897/2277-4572.02451]
[17]
Zendelovska, D.; Simeska, S.; Atanasovska, E.; Georgievska, K.; Kikerkov, I.; Labachevski, N.; Jakovski, K.; Balkanov, T. Determination of acyclovir in human plasma samples by HPLC method with UV detection: Application to single-dose pharmacokinetic study. Open Access Maced. J. Med. Sci., 2015, 3(1), 32-36.
[http://dx.doi.org/10.3889/oamjms.2015.011] [PMID: 27275193]
[18]
Chaudhari, S.; Mannan, A.; Daswadkar, S. Development and validation of UV spectrophotometric method for simultaneous estimation of acyclovir and silymarin in niosome formulation. Pharm. Lett., 2016, 8, 128-133.
[19]
Hamdi, A.; Fegas, R.; Berka, B.; Clarck, B. Development of an assay for acyclovir in pharmaceutical preparation and human by HPLC. Asian J. Chem., 2005, 17, 1264-1270.
[20]
Ghumre, S.V.; Jadhav, V.M.; Bharati, V.J.K. High pressure liquid chromatographic method development and validation for estimation of acyclovir in bulk and marketed formulation. Int. J. Pharm. Sci. Res., 2016, 7, 2194-2200.
[21]
Mule, G The estimation of acyclovir in bulk and tablet dosage form by using specificity and analytical method development., Acta Sci. Pharm. Sci., 2022, 6, 09-12.
[22]
Lotfy, H.M. Stability indicating methods for the determination of acyclovir in the presence of its degradation product. Anal. Chem.an indian J, 2010, 9, 398-407.
[23]
Al Quadeib, B.T. A simple RP-HPLC method for acyclovir determination in tablet and cream dosage forms. DRUG Discov., 2019, 13, 107-114.
[24]
Ravisankar, P.; Niharika, A.; Sireesha, S.; Sai Koushik, O.; Himaja, V. Development and validation of rp-hplc method for quantitative estimation of acyclovir in bulk drug and tablets. J. Chem. Pharm. Sci., 2015, 8, 73-80.
[25]
Radha, R.; Nettem, H.B. Method development and validation of acyclovir by RP-HPLC. Int. J. All Res. Educ. Sci. Methods, 2022, 10, 301-307.
[26]
Musmade, A.; Jain, H.; Prajapati, R. Development and validation of stability indicating rp-hplc method for analysis of acyclovir in API and pharmaceutical dosage form. World J. Pharm. Res., 2015, 4, 1043-1052.
[27]
Sreedhar, Y.P.K.C. New analytical method development and validation of aclcovir by Rp-Hplc method. UNIQUE J. Pharm. Biol. Sci., 2016, 04, 20-26.
[28]
Kasu, P.K. Stability indicating RP-HPLC method development and validation for the estimation of acyclovir in bulk and pharmaceutical dosage form under stress degradation conditions. J. Crit. Rev., 2023, 10, 160-169.
[29]
Manoharan, G.; Mohamed, R.A.W. Development and validation of a stability-indicating RP-HPLC method for the estimation of aciclovir in bulk and ointment dosage form. Int. J. Pharm. Phytopharm. Res., 2019, 9, 11-18.
[30]
Panchal, S.G.; Birajdar, A.S.; Pawar, S.S.; Joshi, A.A. RP-HPLC and UV method development and validation of acyclovir in bulk and ointment formulation. Acta Pharm. Sci., 2022, 6, 14-24.
[31]
Emami, J.; Bazargan, N. HPLC determination of acyclovir in human serum and its application in bioavailability studies. Res. Pharm. Sci., 2009, 4, 47-54.
[32]
Yu, L.; Xiang, B.; Zhan, Y. A simple high-performance liquid chromatographic method for the determination of acyclovir in human plasma and application to a pharmacokinetic study. Arzneimittelforschung, 2008, 58(4), 199-202.
[PMID: 18540483]
[33]
Testireci, H.; Dulger, H.; Ertekin, A.; Kahraman, T. The determination of acyclovir in sheep serum, human serum, saliva and urine by HPLC. East. J. Med., 1998, 3, 62-66.
[34]
Kharia, A.; Singhai, A. Reverse phase high performance liquid chromatography method for quantification of acyclovir in rat plasma. Drug Deliv. Lett., 2013, 3(3), 233-238.
[http://dx.doi.org/10.2174/22103031113039990009]
[35]
Sharma, M.; Nautiyal, P.; Jain, S.; Jain, D. Simple and rapid RP-HPLC method for simultaneous determination of acyclovir and zidovudine in human plasma. J. AOAC Int., 2010, 93(5), 1462-1467.
[http://dx.doi.org/10.1093/jaoac/93.5.1462] [PMID: 21140658]
[36]
Weller, D.R.; Balfour, H.H., Jr; Vezina, H.E. Simultaneous determination of acyclovir, ganciclovir, and (R)-9-[4-hydroxy-2-(hydroxymethyl)butyl]guanine in human plasma using high-performance liquid chromatography. Biomed. Chromatogr., 2009, 23(8), 822-827.
[http://dx.doi.org/10.1002/bmc.1192] [PMID: 19358150]
[37]
Alqahtani, S.M.; Altharawi, A.; Altamimi, M.A.; Alossaimi, M.A.; Mahdi, W.A.; Ramzan, M.; Hussain, A. Method development, stability, and pharmacokinetic studies of acyclovir-loaded topical formulation in spiked rat plasma. Processes , 2022, 10(10), 2079.
[http://dx.doi.org/10.3390/pr10102079]
[38]
de Jalón, E.G.; Campanero, M.A.; Ygartua, P.; Santoyo, S. HPLC determination of acyclovir in skin layers and percutaneous penetration samples. J. Liq. Chromatogr. Relat. Technol., 2002, 25(20), 3187-3197.
[http://dx.doi.org/10.1081/JLC-120016218]
[39]
Silva, G.R.; Caldeira, A.S.P.; Damico, F.M.; Takahashi, B.S.; Silva-Cunha, A.; Fialho, S.L. Analysis of acyclovir in vitreous humor by a validated HPLC method. Pharmazie, 2013, 68(4), 235-239.
[PMID: 23700787]
[40]
Stulzer, H.K.; Tagliari, M.P.; Murakami, F.S.; Silva, M.A.S.; Laranjeira, M.C.M. Development and validation of an RP-HPLC method to quantitate acyclovir in cross-linked chitosan microspheres produced by spray drying. J. Chromatogr. Sci., 2008, 46(6), 496-500.
[http://dx.doi.org/10.1093/chromsci/46.6.496] [PMID: 18647469]
[41]
Reolon, J.B.; Brustolin, M.; Haas, S.E.; Bender, E.A.; Malesuik, M.D.; Colomé, L.M. Development and validation of high-performance liquid chromatography method for simultaneous determination of acyclovir and curcumin in polymeric microparticles. J. Appl. Pharm. Sci., 2018, 8, 136-141.
[42]
Mulabagal, V.; Annaji, M.; Kurapati, S.; Dash, R.P.; Srinivas, N.R.; Tiwari, A.K.; Babu, R.J. Stability‐indicating HPLC method for acyclovir and lidocaine in topical formulations. Biomed. Chromatogr., 2020, 34(3), e4751-e4760.
[http://dx.doi.org/10.1002/bmc.4751] [PMID: 31756271]
[43]
Ateş M.; Kaynak, M.S.; Şahin, S. Simultaneous determination of acyclovir, metoprolol and phenol red by a RP-HPLC method for intestinal perfusion studies. Hacettepe Univ. J. Fac. Pharm., 2015, 35, 146-161.
[44]
Dasari, G.S.S.; Nagesh, B.A.; Rajeshwari, A.; Marothu, V.K. Development and validation of RP-HPLC method for estimation of zolmitriptan in tablet dosage form. Asian J. Chem., 2009, 21, 5019-5022.
[45]
Dubhashi, S.S.; Vavia, P.R. HPTLC method to study skin permeation of acylovir. J. Pharm. Biomed. Anal., 2000, 23(6), 1017-1022.
[http://dx.doi.org/10.1016/S0731-7085(00)00369-1] [PMID: 11095303]
[46]
Patil, P.M.; Wankhede, S.B.; Chaudhari, P.D. A validated stability indicating HPTLC method for estimation of acyclovir in tablets in presence of its alkaline hydrolysis degradation product. Bull. Fac. Pharm. Cairo Univ., 2014, 52(2), 245-257.
[http://dx.doi.org/10.1016/j.bfopcu.2014.09.002]
[47]
Chopra, P.R.; Rao, J.R.; Dhale, C. Stability indicating HPTLC method development for simultaneous estimation of acyclovir and hydrocortisone in API and pharmaceutical dosage form. Int. Res. J. Pharm., 2019, 10(10), 70-76.
[http://dx.doi.org/10.7897/2230-8407.1010301]
[48]
Huidobro, A.L.; Rupérez, F.J.; Barbas, C. LC methods for acyclovir and related impurities determination. J. Pharm. Biomed. Anal., 2005, 37(4), 687-694.
[http://dx.doi.org/10.1016/j.jpba.2004.11.039] [PMID: 15797789]
[49]
Susantakumar, P.; Gaur, A.; Sharma, P. Development and validation of lc-ms/ms method for the estimation of acyclovir in pharmaceutical dosage form. Pharmacophore, 2011, 2, 173-187.
[50]
Dayananda, R.N.S.K. Development and validation of LC-MS/MS method for the analysis of p-toluenesulfonicacid, in antiviral drug acyclovir. Int. J. Innov. Res. Sci. Eng. Technol., 2015, 4(3), 839-847.
[http://dx.doi.org/10.15680/IJIRSET.2015.0403005]
[51]
Shao, C. Quantification of acyclovir in human plasma by ultra-high-performance liquid chromatography - heated electrospray ionization - tandem mass spectrometry for bioequivalence evaluation. J. Anal. Bioanal. Tech., 2012, 3(4), 1-6.
[http://dx.doi.org/10.4172/2155-9872.1000139]

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