首页> 外文期刊>Aquaculture >Bioaccumulation of trimethoprim, sulfamethoxazole and N-acetyl-sulfamethoxazole in Artemia nauplii and residual kinetics in seabass larvae after repeated oral dosing of medicated nauplii.
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Bioaccumulation of trimethoprim, sulfamethoxazole and N-acetyl-sulfamethoxazole in Artemia nauplii and residual kinetics in seabass larvae after repeated oral dosing of medicated nauplii.

机译:反复口服加药无节幼体后,节肢动物无节幼体中甲氧苄啶,磺胺甲恶唑和N-乙酰基-磺基甲恶唑的生物蓄积和鲈鱼幼虫的残留动力学。

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The pharmacokinetics of trimethoprim (TMP), sulfamethoxazole (SMX) and its metabolite N-acetyl-sulfamethoxazole (N-acetyl-SMX), were studied in Artemia nauplii as a function of the duration and temperature of their storage, following their enrichment with the therapeutics using the bioencapsulation technique. A decrease in the therapeutic content of the nauplii was observed upon storage at 18deg C and 25deg C and it is suggested that medicated nauplii should either be administered fresh to fish larvae orafter storage for 8 h at 5deg C, at the most. Under the latter conditions, satisfactory levels of TMP and SMX were achieved, high survival rates and dry weight contents of the nauplii were preserved and minimal leakage of the therapeutics to the environment was secured. Treatment of sea bass larvae with 1, 3, 6 or 10 doses of medicated Artemia nauplii, showed that maximum levels of the therapeutics are achieved in fish larvae when 10 doses are used. Following the treatment scheme of oral administration of10 doses of medicated Artemia nauplii to fish larvae, the residual kinetics of TMP, SMX and N-acetyl-SMX were studied in sea bass larvae. TMP and SMX showed different kinetic characteristics. A steady state of SMX concentration was achieved in fish bodytissue during the 5-day medication period. TMP, SMX and N-acetyl-SMX were detectable in small amounts in fish body tissue even 100 h after treatment. It is concluded that oral medication of fish larvae through the use of Artemia nauplii as a carrier oftherapeutics, appears to be a promising approach to be used as an alternative method of treatment.
机译:在卤虫无节幼体中研究了甲氧苄氨嘧啶(TMP),磺胺甲恶唑(SMX)及其代谢产物N-乙酰基-磺胺甲恶唑(N-乙酰基-SMX)的药代动力学,作为其储存时间和温度的函数,并对其进行了富集。使用生物封装技术的药物。当在18°C和25°C下储存时,观察到无节幼体的治疗含量降低,因此建议将加药的无节幼体新鲜施用于鱼幼体,或至多在5°C下储存8小时。在后一种条件下,达到了令人满意的TMP和SMX水平,保留了无节幼体的高存活率和干重含量,并确保了治疗剂向环境的最小泄漏。用1、3、6或10剂量的加药无节幼体对海鲈幼虫的治疗表明,当使用10剂量的鱼幼虫时,可以达到最大的治疗水平。遵循对鱼幼虫口服给药10剂药用无节幼体的治疗方案,研究了鲈鱼幼虫中TMP,SMX和N-乙酰基-SMX的残留动力学。 TMP和SMX表现出不同的动力学特性。在5天的服药期间,鱼体内的SMX浓度达到稳定状态。即使在治疗后100小时,在鱼体组织中仍可少量检测到TMP,SMX和N-乙酰-SMX。结论是,通过使用无节幼体作为治疗药物的载体对鱼幼虫进行口服药物治疗似乎是一种有前途的方法,可以用作替代治疗方法。

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