Validation of the method for determining lincomycin levels and calculating lincomycin levels in broiler chicken plasma using high-performance liquid chromatography.

IF 0.9 Q3 VETERINARY SCIENCES Open Veterinary Journal Pub Date : 2024-06-01 Epub Date: 2024-06-30 DOI:10.5455/OVJ.2024.v14.i6.13
Cahyo Wibisono, Agustina Dwi Wijayanti, Alfian Yusak Muzaki, Dyah Ayu Widiasih, Aldila Noviatri
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Abstract

Background: Antibiotic residues that come from food of animal origin, such as broiler chicken, have a variety of consequences on human health and increase the likelihood of antibiotic resistance. Lincomycin residue investigations in broiler chicken especially in plasma broiler chicken should be undertaken utilizing the validation method analysis.

Aim: The purpose of this study is to determine the high-performance liquid chromatography (HPLC) as a validation method for calculating the residual concentration of lincomycin in broiler chicken blood plasma and compare it with the minimum Inhibitor Concentration (MIC) and Maximum Residue Limits (MRLs) standards for lincomycin.

Methods: Thirty-five-day-old broiler chickens cobb 700 were weighed and randomly allocated to and separated into control (placebo) and six treatment groups of varying doses and duration. The treatment group's suggested dosage of lincomycin was 50, 100, or 150 mg/kg/day given to 18-day-old chicken, along with drinking water for a week (A group) and 2 weeks (P group). Lincomycin levels in blood plasma were validated using HPLC. The residual lincomycin concentrations 24 hours and 1 week after injection were compared to the lincomycin MIC and the Indonesian National Standard of MRL.

Result: The validation of linscomycin reveals a linear value in blood plasma with an R2 of 0.9983. Precision and accuracy levels indicate promising results for detecting lincomycin. The retention duration for 100 µg/ml lincomycin was 10.0-10.5 minutes. Lincomycin had LOD and LOQ values of 13.98 and 4.86 µg/ml, respectively. After 1 week of dosing at 50 and 100 mg/kg dosages, lincomycin residue detection was 0.00, which was below the MRL criterion of <0.1 ppm. The study found that the residual concentration of 150 mg/kg dosages for a week and 100/150 mg/kg doses for 2 weeks above the lincomycin MIC limits against Mycoplasma synoviae, Staphylococcus aureus, and Salmonella enteritidis.

Conclusion: Lincomycin detection by HPLC in chicken blood plasma showed promising results in terms of linearity, accuracy, precision, specificity, and sensitivity. Lincomycin administration for 1 week at doses of 50 and 100 mg/kg resulted in the lowest residual concentration below the lincomycin MIC and MRL standards.

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利用高效液相色谱法验证测定肉鸡血浆中林可霉素含量和计算林可霉素含量的方法。
背景:肉鸡等动物源性食品中的抗生素残留会对人类健康造成各种影响,并增加产生抗生素耐药性的可能性。本研究旨在确定高效液相色谱法(HPLC)作为计算肉鸡血浆中林可霉素残留浓度的验证方法,并将其与林可霉素的最低抑制浓度(MIC)和最高残留限量(MRLs)标准进行比较:称重 35 日龄的科布 700 肉鸡,将其随机分配到对照组(安慰剂)和六个不同剂量和持续时间的治疗组。治疗组的林可霉素建议剂量为 50、100 或 150 毫克/千克/天,给 18 日龄的鸡饮用,持续一周(A 组)和两周(P 组)。使用高效液相色谱法验证血浆中的林可霉素水平。将注射后 24 小时和 1 周的林可霉素残留浓度与林可霉素 MIC 和印度尼西亚国家标准 MRL 进行比较:结果:林可霉素在血浆中的线性值为 0.9983。精密度和准确度水平表明林可霉素的检测结果良好。100 µg/ml 林可霉素的保留时间为 10.0-10.5 分钟。林可霉素的 LOD 值和 LOQ 值分别为 13.98 微克/毫升和 4.86 微克/毫升。按 50 毫克/千克和 100 毫克/千克的剂量给药 1 周后,林可霉素的残留检测值为 0.00,低于滑膜支原体、金黄色葡萄球菌和肠炎沙门氏菌的最大残留限量标准:结论:采用高效液相色谱法检测鸡血浆中的林可霉素,在线性、准确度、精密度、特异性和灵敏度方面均有良好的结果。以 50 和 100 毫克/千克的剂量服用林可霉素 1 周后,最低残留浓度低于林可霉素 MIC 和 MRL 标准。
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来源期刊
Open Veterinary Journal
Open Veterinary Journal VETERINARY SCIENCES-
CiteScore
1.40
自引率
0.00%
发文量
112
审稿时长
12 weeks
期刊介绍: Open Veterinary Journal is a peer-reviewed international open access online and printed journal that publishes high-quality original research articles. reviews, short communications and case reports dedicated to all aspects of veterinary sciences and its related subjects. Research areas include the following: Infectious diseases of zoonotic/food-borne importance, applied biochemistry, parasitology, endocrinology, microbiology, immunology, pathology, pharmacology, physiology, epidemiology, molecular biology, immunogenetics, surgery, ophthalmology, dermatology, oncology and animal reproduction. All papers are peer-reviewed. Moreover, with the presence of well-qualified group of international referees, the process of publication will be done meticulously and to the highest standards.
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