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[内淋巴给药新方法的实验研究及其临床应用试验]

[Experimental study of a new method of endolymphatic antibiotic administration and a trial of its clinical use].

作者信息

Shcherbakova E G, Vyrenkov Iu E, Panchenkov R T, Iarema I V, Myl'nikov A V

出版信息

Antibiotiki. 1980 May;25(5):375-81.

PMID:6992708
Abstract

A new procedure for antibiotic administration via endolymphatic route was developed. Experiments performed on 34 dogs revealed differences in the pharmacokinetics of gentamicin in the central lymph after its administration in a dose of 4 mg/kg via endolymphatic and intramuscular routes: the maximum levels of 590 and 23 mg/kg were determined in 15 and 45 minutes respectively. In 1 hour the concentrations decreased to 17 and 10 mg/kg. When gentamicin was administered endolymphatically it remained in the lymph and blood in concentrations of 0.2 and 0.8 mg/kg respectively for 24 hours. The kinetics of gentamicin in the blood serum within the first 6 hours after its administration by both routes did not differ significantly. After endolymphatic administration high concentrations of gentamicin (56-36 mg/g) were determined in the paraaortal and retroperitoneal lymph nodes in 10-24 hours. Within the period of the 4th to the 13th day its concentrations of at least 5 mg/g were detected. The changes in the structure of the lymph nodes observed 18-48 hours after the antibiotic endolymphatic administration were reversible and returned to normal by the 96th hour. The first experience with the clinical use of the endolymphatic route of gentamicin administration showed its high efficacy in 84.8% of the patients with severe purulent inflammatory diseases of the organs of the abdominal cavity. The antibiotic was used in a dose of 80 mg once a day. The treatment course consisted of 5-6 infusions. Perspectives of the further experimental and clinical investigation of the procedure are indicated. Endolymphatic administration of antibiotics makes it possible to increase the efficacy of antibiotic therapy of a number of severe inflammatory infections.

摘要

开发了一种通过内淋巴途径给药抗生素的新方法。对34只狗进行的实验显示,庆大霉素以4mg/kg的剂量通过内淋巴和肌肉注射途径给药后,其在中枢淋巴中的药代动力学存在差异:分别在15分钟和45分钟时测定的最高水平为590mg/kg和23mg/kg。1小时后浓度降至17mg/kg和10mg/kg。当通过内淋巴给药庆大霉素时,它在淋巴和血液中的浓度分别为0.2mg/kg和0.8mg/kg,持续24小时。两种途径给药后最初6小时内血清中庆大霉素的动力学没有显著差异。内淋巴给药后,在10 - 24小时内,在主动脉旁和腹膜后淋巴结中测定到高浓度的庆大霉素(56 - 36mg/g)。在第4天至第13天期间,检测到其浓度至少为5mg/g。抗生素内淋巴给药后18 - 48小时观察到的淋巴结结构变化是可逆的,并在第96小时恢复正常。庆大霉素内淋巴给药临床应用的首次经验表明,其对84.8%的患有严重腹腔器官化脓性炎症疾病的患者具有高效。抗生素的使用剂量为每天80mg一次。治疗疗程包括5 - 6次输注。指出了该方法进一步实验和临床研究的前景。抗生素的内淋巴给药使得提高一些严重炎症感染的抗生素治疗效果成为可能。

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