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螺旋霉素在犊牛呼吸道的分布及生物利用度

Respiratory tract distribution and bioavailability of spiramycin in calves.

作者信息

Friis C, Erhardsen E, Madsen E B, Nielsen P, Raun K

机构信息

Department of Pharmacology and Toxicology, Royal Veterinary and Agricultural University, Copenhagen, Denmark.

出版信息

Am J Vet Res. 1991 Aug;52(8):1269-73.

PMID:1928908
Abstract

Pharmacokinetic determinants of spiramycin and its distribution into the respiratory tract were studied in 2 groups of calves, 4 to 10 weeks old. Group-A calves (n = 4) were used to determine pharmacokinetic variables of spiramycin after IV (15 and 30 mg/kg of body weight) and oral administrations of the drug (30 mg/kg) and to measure distribution of spiramycin into nasal and bronchial secretions. Group-B calves (n = 4) were used to determine distribution of spiramycin into lung tissue and bronchial mucosa. Spiramycin disposition was best described by use of an open 3-compartment model. Mean (+/- SD) elimination half-life was 28.7 +/- 12.3 hours, and steady-state volume of distribution was 23.5 +/- 6.0 L/kg. Bio-availability after oral administration was 4 +/- 3%. High and persistent concentrations of spiramycin were achieved in the respiratory tract tissues and fluids. Tissue-to-plasma concentration ratio was 58 for lung tissue and 18 for bronchial mucosa at 3 hours after spiramycin administration and 137 and 49, respectively at 24 hours. Secretion-to-plasma concentration ratio was 4 for nasal secretions and 7 for bronchial secretions, and remained almost constant with time. Thus, spiramycin penetrates well into the respiratory tract, although the value in bronchial secretions is lower than that in lung tissues and bronchial mucosa. Calculations indicate that a loading dose of 45 mg/kg, administered IV, followed by a maintenance dose of 20 mg/kg, IV, once daily is required to maintain active concentrations of spiramycin against bovine pathogens in bronchial secretions.

摘要

在两组4至10周龄的犊牛中研究了螺旋霉素的药代动力学决定因素及其在呼吸道中的分布。A组犊牛(n = 4)用于确定静脉注射(15和30mg/kg体重)和口服给药(30mg/kg)后螺旋霉素的药代动力学变量,并测量螺旋霉素在鼻腔和支气管分泌物中的分布。B组犊牛(n = 4)用于确定螺旋霉素在肺组织和支气管黏膜中的分布。使用开放的三室模型能最好地描述螺旋霉素的处置情况。平均(±标准差)消除半衰期为28.7±12.3小时,稳态分布容积为23.5±6.0L/kg。口服给药后的生物利用度为4±3%。在呼吸道组织和体液中可达到高且持久的螺旋霉素浓度。给药后3小时,肺组织的组织与血浆浓度比为58,支气管黏膜为18;24小时时分别为137和49。鼻腔分泌物与血浆浓度比为4,支气管分泌物为7,且随时间几乎保持恒定。因此,尽管支气管分泌物中的值低于肺组织和支气管黏膜中的值,但螺旋霉素能很好地渗透到呼吸道中。计算表明,需要静脉注射45mg/kg的负荷剂量,随后每天静脉注射20mg/kg的维持剂量,以维持支气管分泌物中针对牛病原体的螺旋霉素活性浓度。

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