Pharmacokinetics, Pharmacodynamics and Depletion of Florfenicol Applied in White Leg Shrimp (Litopenaeus vannamei) Aquaculture and Impact on Shrimp Hepatopancreas Histology
Huynh, Thi Kim Duyen; Nguyen, Quoc Thinh; Scippo, Marie-Louiseet al.
[en] Florfenicol (FF) is one of the common antimicrobials used to control bacterial disease in shrimp aquaculture. This study aimed to determine the pharmacokinetics (PK) parameters of FF in white leg shrimp plasma, hepatopancreas and muscle as well as its residue depletion in shrimp muscle and the impact on shrimp hepatopancreas histology during and after FF medication. In the PK experiment, shrimp were fed once at 10 mg FF/kg body weight (bw) via oral in-feed administration to determine PK parameters in plasma, hepatopancreas and muscle. The maximum concentration (Cmax) of 60.56 μg/L in plasma was observed after 1.77 h (Tmax). In muscle, a Cmax of 11.76 μg/kg was attained after 0.20 h, while in hepatopancreas, the Cmax was higher (386.92 μg/kg) and was rapidly obtained (Tmax = 0.19 h). The Cmax values in shrimp plasma were below the minimum inhibitory concentration (MIC) against Vibrio parahaemolyticus, known to cause acute hepatopancreatic necrosis disease (AHPND) in shrimp. Therefore, it can be concluded that to ensure the effectiveness of this treatment, the dose should be higher than 10 mg FF/kg bw. FF depletion in white leg shrimp muscle and its histological impact on hepatopancreas were determined after feeding FF-medicated feed once-a-day or twice-a-day for 3 consecutive days with a dose of 10 mg FF/kg bw. The residues in shrimp muscle were rapidly eliminated and fell below the limit of quantification at 24 h after stopping medication. The withdrawal time of FF in shrimp muscle was 27.9 degree-days (2 days at 26.5 °C) according to the maximum residue limit (MRL) of 100 µg/kg set by the European Commission and Korean Ministry and when feeding FF twice-a-day for 3 days. The results from histological analysis showed that there was no negative effect on shrimp hepatopancreas after stopping medication in both once- and twice-a-day treatments.
Disciplines :
Food science
Author, co-author :
Huynh, Thi Kim Duyen ; Faculty of Science and Seafood Processing Technology, College of Aquaculture and Fisheries, Can Tho University, Can Tho 94000, Vietnam
Nguyen, Quoc Thinh ; Faculty of Science and Seafood Processing Technology, College of Aquaculture and Fisheries, Can Tho University, Can Tho 94000, Vietnam
Scippo, Marie-Louise ; Université de Liège - ULiège > Département de sciences des denrées alimentaires (DDA) > Analyse des denrées alimentaires
Dang, Thi Hoang Oanh; Faculty of Science and Seafood Processing Technology, College of Aquaculture and Fisheries, Can Tho University, Can Tho 94000, Vietnam
Devreese, Mathias ; Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium
Douny, Caroline ; Université de Liège - ULiège > Département de sciences des denrées alimentaires (DDA) > Analyse des denrées alimentaires
Croubels, Siska ; Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium
Le, Quoc Viet; Faculty of Science and Seafood Processing Technology, College of Aquaculture and Fisheries, Can Tho University, Can Tho 94000, Vietnam
Tran, Minh Phu ; Faculty of Science and Seafood Processing Technology, College of Aquaculture and Fisheries, Can Tho University, Can Tho 94000, Vietnam
Language :
English
Title :
Pharmacokinetics, Pharmacodynamics and Depletion of Florfenicol Applied in White Leg Shrimp (Litopenaeus vannamei) Aquaculture and Impact on Shrimp Hepatopancreas Histology
Vietnam Association of Seafood Exporters and Producers (VASEP) Vietnam Aquaculture and Fisheries Overview 2024 Available online: https://vasep.com.vn/san-pham-xuat-khau/tom/tong-quan-nganh-tom (accessed on 20 November 2024)
Nguyen K.A.T. Nguyen T.A.T. Jolly C. Nguelifack B.M. Economic efficiency of extensive and intensive shrimp production under conditions of disease and natural disaster risks in Khánh Hòa and Trà Vinh Provinces, Vietnam Sustainability 2020 12 2140 10.3390/su12052140
Tran L. Nunan L. Redman R.M. Mohney L.L. Pantoja C.R. Fitzsimmons K. Lightner D.V. Determination of the infectious nature of the agent of acute hepatopancreatic necrosis syndrome affecting penaeid shrimp Dis. Aquat. Org. 2013 105 45 55 10.3354/dao02621 23836769
Flegel T.W. Sritunyaluucksana K. Recent research on acute hepatopancreatic necrosis disease (AHPND) and Enterocytozoon hepatopenaei in Thailand Asian Fish. Sci. 2018 31 257 269 10.33997/j.afs.2018.31.S1.018
Thinh N.Q. Maita M. Phu T.M. Chemical use in intensive white-leg shrimp aquaculture in Tra Vinh province, Vietnam Int. J. Sci. Res. Publ. 2020 56 70 77 10.22144/ctu.jsi.2020.040
Chanratchakool P. Phillips M.J. Social and economic impacts and management of shrimp disease among small-scale farmers in Thailand and Viet Nam FAO Fish. Tech. Paper 2002 406 177 189
Zhou J. Fang W. Yang X. Zhou S. Hu L. Li X. Qi X. Su H. Xie L. A nonluminescent and highly virulent Vibrio harveyi strain is associated with “bacterial white tail disease” of Litopenaeus vannamei shrimp PLoS ONE 2012 7 e29961 10.1371/journal.pone.0029961
Rico A. Oliveira R. McDonough S. Matser A. Khatikarn J. Satapornvanit K. Nogueira A.J.A. Soares A.M.V.M. Domingues I. Van den Brink P.J. Use, fate and ecological risks of antibiotics applied in tilapia cage farming in Thailand Environ. Pollut. 2014 191 8 16 10.1016/j.envpol.2014.04.002
Phu T.M. Phuong N.T. Dung T.T. Hai D.M. Son V.N. Rico A. Clausen J.H. Madsen H. Murray F. Dalsgaard A. An evaluation of fish health-management practices and occupational health hazards associated with P angasius catfish (P angasianodon hypophthalmus) aquaculture in the M ekong D elta, V ietnam Aquac. Res. 2016 47 2778 2794 10.1111/are.12728
Chi T.T.K. Clausen J.H. Van P.T. Tersbøl B. Dalsgaard A. Use practices of antimicrobials and other compounds by shrimp and fish farmers in Northern Vietnam Aquac. Rep. 2017 7 40 47 10.1016/j.aqrep.2017.05.003
Ren X. Pan L. Wang L. Tissue distribution, elimination of florfenicol and its effect on metabolic enzymes and related genes expression in the white shrimp Litopenaeus vannamei following oral administration Aquac. Res. 2016 47 1584 1595 10.1111/are.12619
Phu T.M. Vinh P.Q. Dao N.L.A. Viet L.Q. Thinh N.Q. Chemical use in intensive white-leg shrimp aquaculture in Ben Tre province, Vietnam Training 2019 73 46 47 10.29322/IJSRP.9.08.2019.p92112
Lillehaug A. Børnes C. Grave K. A pharmaco-epidemiological study of antibacterial treatments and bacterial diseases in Norwegian aquaculture from 2011 to 2016 Dis. Aquat. Org. 2018 128 117 125 10.3354/dao03219
Wang W. Dai X. Li Z. Meng Q. Tissue distribution and elimination of florfenicol in topmouth culter (Culter alburnus) after oral administration Czech J. Food Sci. 2009 27 214 221 10.17221/183/2008-CJFS
Lambert T. Antibiotics that affect the ribosome Rev. Sci. Tech. (Int. Off. Epizoot.) 2012 31 57 64 10.20506/rst.31.1.2095 22849268
Nejad A.J. Peyghan R. Varzi H.N. Shahriyari A. Florfenicol pharmacokinetics following intravenous and oral administrations and its elimination after oral and bath administrations in common carp (Cyprinus carpio) Vet. Res. Forum 2017 8 327 331
Dowling P.M. Chloramphenicol, thiamphenicol and florfenicol Antimicrobial Therapy in Veterinary Medicine 4th ed. Gigu S. Prescott J.F. Baggot J.D. Walker R.D. Dowling P.M. Blackwell Scientific Publications Ames, Iowa 2006 241 248 10.1002/9781119654629
Samuelsen O.B. Bergh Ø. Efficacy of orally administered florfenicol and oxolinic acid for the treatment of vibriosis in cod (Gadus morhua) Aquaculture 2004 235 27 35 10.1016/S0044-8486(03)00446-0
Caipang C.M.A. Lazado C.C. Brinchmann M.F. Berg I. Kiron V. In vivo modulation of immune response and antioxidant defense in Atlantic cod, Gadus morhua following oral administration of oxolinic acid and florfenicol Comp. Biochem. Physiol. Part C Toxicol. Pharmacol. 2009 150 459 464 10.1016/j.cbpc.2009.07.001 19596082
Huang K. Chen S.J. Huang J. Yang L. Ju Y. Zhu X.R. Peng D.X. Analysis of antibiotic resistance of Salmonella isolated from animals and identification of its florfenicol resistant gene China Anim. Husb. Vet. Med. 2015 42 459 466
Park B.K. Lim J.H. Kim M.S. Yun H.I. Pharmacokinetics of florfenicol and its metabolite, florfenicol amine, in the Korean catfish (Silurus asotus) J. Vet. Pharmacol. Ther. 2006 29 37 40 10.1111/j.1365-2885.2006.00709.x
Gaunt P.S. Langston C. Wrzesinski C. Gao D. Adams P. Crouch L. Sweeney D. Endris R. Single intravenous and oral dose pharmacokinetics of florfenicol in the channel catfish (Ictalurus punctatus) J. Vet. Pharmacol. Ther. 2012 35 503 507 10.1111/j.1365-2885.2011.01340.x
Yang Q. Xie L. Wu Z. Chen X. Yang Y. Liu J. Zhang Q. Pharmacokinetics of florfenicol after oral administration in yellow catfish, Pelteobagrus fulvidraco J. World Aquac. Soc. 2013 44 586 592 10.1111/jwas.12055
Pham Q.V. Nguyen Q.T. Devreese M. Croubels S. Dang T.H.O. Dalsgaard A. Maita M. Tran M.P. Pharmacokinetics and depletion of florfenicol in striped catfish Pangasianodon hypophthalmus after oral administration Fish. Sci. 2023 89 357 365 10.1007/s12562-023-01682-w
Martinsen B. Horsberg T.E. Varma K.J. Sams R. Single dose pharmacokinetic study of florfenicol in Atlantic salmon (Salmo salar) in seawater at 11 C Aquaculture 1993 112 1 11 10.1016/0044-8486(93)90153-P
Horsberg T.E. Hoff K.A. Nordmo R. Pharmacokinetics of florfenicol and its metabolite florfenicol amine in Atlantic salmon J. Aquat. Anim. Health 1996 8 292 301 10.1577/1548-8667(1996)008<0292:POFAIM>2.3.CO;2
Kverme K.O. Haugland G.T. Hannisdal R. Kallekleiv M. Colquhoun D.J. Lunestad B.T. Wergeland H.I. Samuelsen O.B. Pharmacokinetics of florfenicol in lumpfish (Cyclopterus lumpus L.) after a single oral administration Aquaculture 2019 512 734279 10.1016/j.aquaculture.2019.734279
Feng J.B. Huang D.R. Zhong M. Liu P. Dong J.D. Pharmacokinetics of florfenicol and behaviour of its metabolite florfenicol amine in orange-spotted grouper (Epinephelus coioides) after oral administration J. Fish Dis. 2016 39 833 843 10.1111/jfd.12416
Samuelsen O.B. Bergh Ø. Ervik A. Pharmacokinetics of florfenicol in cod Gadus morhua and in vitro antibacterial activity against Vibrio anguillarum Dis. Aquat. Org. 2003 56 127 133 10.3354/dao056127
Yang F. Yang F. Wang G. Kong T. Liu B. Pharmacokinetics of florfenicol and its metabolite florfenicol amine in crucian carp (Carassius auratus) at three temperatures after single oral administration Aquaculture 2019 503 446 451 10.1016/j.aquaculture.2019.01.037
Lim J.H. Kim M.S. Hwang Y.H. Song I.B. Park B.K. Yun H.I. Pharmacokinetics of florfenicol following intramuscular and intravenous administration in olive flounder (Paralichthys olivaceus) J. Vet. Pharmacol. Ther. 2011 34 206 208 10.1111/j.1365-2885.2010.01231.x
Pourmolaie B. Eshraghi H.R. Haghighi M. Mortazavi S.A. Rohani M.S. Pharmacokinetics of florfenicol administrated to rainbow trout (Oncorhynchus mykiss) by oral gavages and medicated feed routes Bull. Environ. Pharmacol. Life Sci. 2015 4 14 17
Mallik S.K. Shahi N. Pathak R. Kala K. Patil P.K. Singh B. Ravindran R. Krishna N. Pandey P.K. Pharmacokinetics and biosafety evaluation of a veterinary drug florfenicol in rainbow trout, Oncorhynchus mykiss (Walbaum 1792) as a model cultivable fish species in temperate water Front. Pharmacol. 2023 14 1033170 10.3389/fphar.2023.1033170 36755946
Feng J.B. Jia X.P. Single dose pharmacokinetic study of flofenicol in tilapia (Oreochromis niloticus× O. aureus) held in freshwater at 22 C Aquaculture 2009 289 129 133 10.1016/j.aquaculture.2008.12.023
Rairat T. Hsieh C.Y. Thongpiam W. Sung C.H. Chou C.C. Temperature-dependent pharmacokinetics of florfenicol in Nile tilapia (Oreochromis niloticus) following single oral and intravenous administration Aquaculture 2019 503 483 488 10.1016/j.aquaculture.2018.12.081
Fang W. Li G. Zhou S. Li X. Hu L. Zhou J. Pharmacokinetics and tissue distribution of thiamphenicol and florfenicol in Pacific white shrimp Litopenaeus vannamei in freshwater following oral administration J. Aquat. Anim. Health 2013 25 83 89 10.1080/08997659.2012.754799 23480025
Tipmongkolsilp N. Limpanon Y. Patamalai B. Lusanandana P. Wongtavatchai J. Oral medication with florfenicol for black tiger shrimps Penaeus monodon Thai J. Vet. Med. 2006 36 39 47 10.56808/2985-1130.2043
Feng Y. Zhai Q. Wang J. Li J. Li J. Comparison of florfenicol pharmacokinetics in Exopalaemon carinicauda at different temperatures and administration routes J. Vet. Pharmacol. Ther. 2019 42 230 238 10.1111/jvp.12734
Toutain P.L. Ferran A. Bousquet-Mélou A. Species differences in pharmacokinetics and pharmacodynamics Comp. Vet. Pharmacol. 2010 199 19 48 10.1007/978-3-642-10324-7_2
Manan H. Zhong J.M.H. Othman F. Ikhwanuddin M.H.D. Histopathology of the hepatopancreas of pacific white shrimp, Penaeus vannamei from none early mortality syndrome (EMS) shrimp ponds J. Fish. Aquat. Sci. 2015 10 562 568 10.3923/jfas.2015.562.568
Bray W.A. Williams R.R. Lightner D.V. Lawrence A.L. Growth, survival and histological responses of the marine shrimp, Litopenaeus vannamei, to three dosage levels of oxytetracycline Aquaculture 2006 258 97 108 10.1016/j.aquaculture.2006.04.018
Romano N. Koh C.B. Ng W.K. Dietary microencapsulated organic acids blend enhances growth, phosphorus utilization, immune response, hepatopancreatic integrity and resistance against Vibrio harveyi in white shrimp, Litopenaeus vannamei Aquaculture 2015 435 228 236 10.1016/j.aquaculture.2014.09.037
Maftuch K.A. Eslfitri D. Sanoesi E. Prihanto A.A. Enrofloxacin stimulates cell death in several tissues of vannamei shrimp (Litopenaeus vannamei) Comp. Clin. Pathol. 2017 26 249 254 10.1007/s00580-016-2384-0
Avunje S. Patil P.K. Ezaz W. Praveena E. Ray A. Viswanathan B. Alavandi S.V. Puthiyedathu S.K. Vijayan K.K. Effect of oxytetracycline on the biosafety, gut microbial diversity, immune gene expression and withdrawal period in Pacific whiteleg shrimp, Penaeus vannamei Aquaculture 2021 543 736957 10.1016/j.aquaculture.2021.736957
Sotomayor M.A. Reyes J.K. Restrepo L. Domínguez-Borbor C. Maldonado M. Bayot B. Efficacy assessment of commercially available natural products and antibiotics, commonly used for mitigation of pathogenic Vibrio outbreaks in Ecuadorian Penaeus (Litopenaeus) vannamei hatcheries PLoS ONE 2019 14 e0210478 10.1371/journal.pone.0210478
Balouiri M. Sadiki M. Ibnsouda S.K. Methods for in vitro evaluating antimicrobial activity: A review J. Pharm. Anal. 2016 6 71 79 10.1016/j.jpha.2015.11.005
Jiang H. Yu T. Yang Y. Yu S. Wu J. Lin R. Li Y. Fang J. Zhu C. Co-occurrence of antibiotic and heavy metal resistance and sequence type diversity of Vibrio parahaemolyticus isolated from Penaeus vannamei at freshwater farms, seawater farms, and markets in Zhejiang province, China Front. Microbiol. 2020 11 1294 10.3389/fmicb.2020.01294 32676056
Clinical and Laboratory Standards Institute (CLSI) Performance Standards for Antimicrobial Susceptibility Testing 27th ed. Clinical and Laboratory Standards Institute Wayne, PA, USA 2017 36
Ali N.G. Aboyadak I.M. El-Sayed H.S. Chemotherapeutic control of Gram-positive infection in white sea bream (Diplodus sargus, Linnaeus 1758) broodstock Vet. World 2019 12 316 10.14202/vetworld.2019.316-324
Huynh T.K.D. Scippo M.L. Devreese M. Croubels S. Nguyen Q.T. Douny C. Dang T.H.O. Le Q.V. Tran M.P. Pharmacokinetics and Withdrawal Times of Cefotaxime in White Leg Shrimp (Litopenaeus vannamei) After Oral Administration Fishes 2024 9 232 10.3390/fishes9060232
Nima N. Duangsuwan P. Pongtippatee P. Kanjanasopa D. Withyachumnarnkul B. Types of cells in the hepatopancreas of the Pacific whiteleg shrimp Litopenaeus vannamei being infected by Enterocytozoon hepatopenaei Songklanakarin J. Sci. Technol. 2022 44 97 102 10.14456/sjst-psu.2022.15
United States Department of Agriculture Food Safety and Inspection Service (USDA) Office of Public Health Science Determination and Confirmation of Florfenicol CLG-FLOR1.04 USDA Washington, DC, USA 2010 1 27
Association of Official Analytical Chemists (AOAC) AOAC Guidelines for Single Laboratory Validation of Chemical Methods for Dietary Supplements and Botanicals 2002 26 Available online: https://s27415.pcdn.co/wp-content/uploads/2020/01/64ER20-7/Validation_Methods/d-AOAC_Guidelines_For_Single_Laboratory_Validation_Dietary_Supplements_and_Botanicals.pdf (accessed on 12 January 2025)
European Commission (EC) Commission Decision 2002/657/EC of 12 August 2002 Implementing Council Directive 96/23/EC Concerning the Performance of Analytical Methods and the Interpretation of Results OJEU Luxembourg, Luxembourg 2002 Volume 221 8 36
Hekman P. Withdrawal-Time Calculation Program WT1. 4 BRD Agency for the Registration of Veterinary Medicinal Products Wageningen, The Netherlands 2004 1 8
European Medicine Agency (EMA) Guideline on Determination of Withdrawal Periods for Edible Tissues 2022 Available online: https://www.ema.europa.eu/en/documents/scientific-guideline/adopted-guideline-determination-withdrawal-periods-edible-tissues-revision-2_en.pdf (accessed on 10 June 2024)
Mohney L.L. Bell T.A. Lightner D.V. Shrimp Antimicrobial Testing. I. In Vitro Susceptibility of Thirteen Gram-Negative Bacteria to Twelve Antimicrobials J. Aquat. Anim. Health 1992 4 257 261 10.1577/1548-8667(1992)004<0257:SATIIV>2.3.CO;2
Roque A. Molina-Aja A. Bolán-Mejıa C. Gomez-Gil B. In vitro susceptibility to 15 antibiotics of vibrios isolated from penaeid shrimps in Northwestern Mexico Int. J. Antimicrob. Agents 2001 17 383 387 10.1016/S0924-8579(01)00308-9
Vaseeharan B. Ramasamy P. Murugan T. Chen J.C. In vitro susceptibility of antibiotics against Vibrio spp. and Aeromonas spp. isolated from Penaeus monodon hatcheries and ponds Int. J. Antimicrob. Agents 2005 26 285 291 10.1016/j.ijantimicag.2005.07.005 16139992
Rebouças R.H. de Sousa O.V. Lima A.S. Vasconcelos F.R. de Carvalho P.B. dos Fernandes Vieira R.H.S. Antimicrobial resistance profile of Vibrio species isolated from marine shrimp farming environments (Litopenaeus vannamei) at Ceará, Brazil Environ. Res. 2011 111 21 24 10.1016/j.envres.2010.09.012 20970784
Al-Othrubi S.M.Y. Kqueen C.Y. Mirhosseini H. Hadi Y.A. Radu S. Antibiotic resistance of Vibrio parahaemolyticus isolated from cockles and shrimp sea food marketed in Selangor, Malaysia Clin. Microbiol. 2014 3 148 10.4172/2327-5073.1000148
Melo L.M.R.D. Almeida D. Hofer E. Reis C.M.F.D. Theophilo G.N.D. Santos A.F.D.M. Vieira R.H.S.D.F. Antibiotic resistance of Vibrio parahaemolyticus isolated from pond-reared Litopenaeus vannamei marketed in Natal, Brazil Braz. J. Microbiol. 2011 42 1463 1469 10.1590/S1517-83822011000400032
Yano Y. Hamano K. Satomi M. Tsutsui I. Aue-umneoy D. Diversity and characterization of oxytetracycline-resistant bacteria associated with non-native species, white-leg shrimp (Litopenaeus vannamei), and native species, black tiger shrimp (Penaeus monodon), intensively cultured in Thailand J. Appl. Microbiol. 2011 110 713 722 10.1111/j.1365-2672.2010.04926.x
Zanetti S. Spanu T. Deriu A. Romano L. Sechi L.A. Fadda G. In vitro susceptibility of Vibrio spp. isolated from the environment Int. J. Antimicrob. Agents 2001 17 407 409 10.1016/S0924-8579(01)00307-7 11337229
Tran T.H.T. Yanagawa H. Nguyen K.T. Hara-Kudo Y. Taniguchi T. Hayashidani H. Prevalence of Vibrio parahaemolyticus in seafood and water environment in the Mekong Delta, Vietnam J. Vet. Med. Sci. 2018 80 1737 1742 10.1292/jvms.18-0241
Rocha R.d.S. de Sousa O.V. dos Fernandes Vieira R.H.S. Multidrug-resistant Vibrio associated with an estuary affected by shrimp farming in Northeastern Brazil Mar. Pollut. Bull. 2016 105 337 340 10.1016/j.marpolbul.2016.02.001 26876560
Saifedden G. Farinazleen G. Nor-Khaizura A. Kayali A.Y. Nakaguchi Y. Nishibuchi M. Son R. Antibiotic Susceptibility profile of Vibrio parahaemolyticus isolated from shrimp in Selangor, Malaysia Int. Food Res. J. 2016 23 2732 2736
Morales-Covarrubias M.S. Tlahuel-Vargas L. Martínez-Rodríguez I.E. Lozano-Olvera R. Palacios-Arriaga J.M. Necrotising hepatobacterium (NHPB) infection in Penaeus vannamei with florfenicol and oxytetracycline: A comparative experimental study Rev. Cient. 2012 22 72 80
Ferri G. Lauteri C. Vergara A. Antibiotic resistance in the finfish aquaculture industry: A review Antibiotics 2022 11 1574 10.3390/antibiotics11111574
Tu H.T. Silvestre F. Phuong N.T. Kestemont P. Effects of pesticides and antibiotics on penaeid shrimp with special emphases on behavioral and biomarker responses Environ. Toxicol. Chem. 2010 29 929 938 10.1002/etc.99
Verri T. Mandal A. Zilli L. Bossa D. Mandal P.K. Ingrosso L. Zonno V. Vilella S. Ahearn G.A. Storelli C. D-glucose transport in decapod crustacean hepatopancreas Comp. Biochem. Physiol. A Mol. Integr. Physiol. 2001 130 585 606 10.1016/S1095-6433(01)00434-2
Faroongsarng D. Chandumpai A. Chiayvareesajja S. Theapparat Y. Bioavailability and absorption analysis of oxytetracycline orally administered to the standardized moulting farmed Pacific white shrimps (Penaeus vannamei) Aquaculture 2007 269 89 97 10.1016/j.aquaculture.2007.04.019
Ma R. Wang Y. Zou X. Fu G. Li C. Fan P. Fang W. Pharmacokinetics of oxytetracycline in Pacific white shrimp, Penaeus vannamei, after oral administration of a single-dose and multiple-doses Aquaculture 2019 512 734348 10.1016/j.aquaculture.2019.734348
Chiayvareesajja S. Chandumpai A. Theapparat Y. Faroongsarng D. The complete analysis of oxytetracycline pharmacokinetics in farmed Pacific white shrimp (Litopenaeus vannamei) J. Vet. Pharmacol. Ther. 2006 29 409 414 10.1111/j.1365-2885.2006.00785.x
Ma R. Wang Y. Zou X. Hu K. Sun B. Fang W. Fu G. Yang X. Pharmacokinetics of sulfamethoxazole and trimethoprim in Pacific white shrimp, Litopenaeus vannamei, after oral administration of single-dose and multiple-dose Environ. Toxicol. Pharmacol. 2017 52 90 98 10.1016/j.etap.2017.03.019
Fang X. Zhou J. Liu X. Pharmacokinetics and tissue distribution of enrofloxacin after single intramuscular injection in Pacific white shrimp J. Vet. Pharmacol. Ther. 2018 41 148 154 10.1111/jvp.12431
Ma R. Huang L. Wei W. Wang Y. Zou X. Zhou J. Li X. Fang W. Pharmacokinetics of enrofloxacin and its metabolite ciprofloxacin in Pacific white shrimp Litopenaeus vannamei after multiple-dose oral administration Fish. Sci. 2018 84 869 876 10.1007/s12562-018-1229-y
Dowling P.M. Chloramphenicol, thiamphenicol, and florfenicol Antimicrobial Therapy in Veterinary Medicine Wiley Hoboken, NJ, USA 2013 269 277
AliAbadi F.S. Lees P. Antibiotic treatment for animals: Effect on bacterial population and dosage regimen optimisation Int. J. Antimicrob. Agents 2000 14 307 313 10.1016/S0924-8579(00)00142-4
European Commission (EC) Commission Regulation (EU) No 37/2010 of 22 December 2009 on Pharmacologically Active Substances and Their Classification Regarding Maximum Residue Limits in Foodstuffs of Animal Origin OJEU Luxembourg 2010 1 72
Korean Ministry of Food and Drug Safety, MRLs Vet Drugs, Republic of Korea 2019 Available online: https://apps.fas.usda.gov/newgainapi/api/Report/DownloadReportByFileName?fileName=Korea%27s+Veterinary+Drug+MRL+Situation_Seoul_Korea+-+Republic+of_11-16-2011.pdf (accessed on 20 May 2024)
Rairat T. Hsieh M.K. Ho W.C. Lu Y.P. Fu Z.Y. Chuchird N. Chou C.C. Effects of temperature on the pharmacokinetics, optimal dosage, tissue residue, and withdrawal time of florfenicol in asian seabass (Lates calcarifer) Food Addit. Contam. Part A 2023 40 235 246 10.1080/19440049.2022.2155710
Lin H.C. Chen W.Y. Bayesian population physiologically-based pharmacokinetic model for robustness evaluation of withdrawal time in tilapia aquaculture administrated to florfenicol Ecotoxicol. Environ. Saf. 2021 210 111867 10.1016/j.ecoenv.2020.111867
Wang W. Lin H. Xue C. Khalid J. Elimination of chloramphenicol, sulphamethoxazole and oxytetracycline in shrimp, Penaeus chinensis following medicated-feed treatment Environ. Int. 2004 30 367 373 10.1016/j.envint.2003.08.006
Caceci T. Neck K.F. Lewis D.D.H. Sis R.F. Ultrastructure of the hepatopancreas of the pacific white shrimp, Penaeus vannamei (Crustacea: Decapoda) J. Mar. Biol. Assoc. UK 1988 68 323 337 10.1017/S002531540005222X
Pathak M.S. Reddy A.K. Kulkarni M.V. Harikrishna V. Srivastava P.P. Chadha N.K. Lakra W.S. Histological alterations in the hepatopancreas and growth performance of Pacific white shrimp (Litopenaeus vannamei, Boone 1931) reared in potassium fortified inland saline ground water Int. J. Curr. Microbiol. Appl. Sci. 2018 7 3531 3542 10.20546/ijcmas.2018.704.398
Hu K.J. Leung P.C. Food digestion by cathepsin L and digestion-related rapid cell differentiation in shrimp hepatopancreas Comp. Biochem. Physiol. Part B Biochem. Mol. Biol. 2007 146 69 80 10.1016/j.cbpb.2006.09.010
Nunes E.T. Braga A.A. Camargo-Mathias M.I. Histochemical study of the hepatopancreas in adult females of the pink-shrimp Farfantepenaeus brasiliensis Latreille, 1817 Acta Histochem. 2014 116 243 251 10.1016/j.acthis.2013.07.011