Comparative evaluation of effect of phlebotropic agents on vascular wall permeability in preclinical studies

A. V. Buzlama, A. A. Verlina, A. Y. Kuznetsov, E. A. Aleksenko
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Abstract

Introduction. As there is insufficient evidence to date to determine phlebotropic drug preferences, further research in this area is warranted. Aim. To evaluate the effect of topical and oral phlebotropic agents on vascular wall permeability in preclinical studies. Materials and methods. The objects of the study were 6 phlebotropic agents for external and oral use, which were administered according to the recommendations specified in the instructions for use, 2 hours before the trypan blue. The model for preclinical studies: the xylene petechiae test with trypan blue staining. The evaluation criterion was the intensity of staining, which was expressed semiquantitatively (points). The test system was 100 white male outbred conventional mice. Results and discussion. Heparin + EPL + escin (Detragel) significantly reduces the intensity of staining in the xylene petechiae test. It was found that with a single external application reduces the intensity of staining by 25.0% compared to the control, which significantly by 60.0% exceeded the effectiveness of the drug heparin 1000 IU; with a course application of 15 days in 2 times, which significantly, least by 50%, exceeded the effect of the drug heparin 1000 IU and cosmetic product containing troxerutin. MPFF 1000 mg (Detralex) at a single oral administration significantly reduced the intensity of staining by 35.0% compared to the control group, which significantly by 69.2% exceeded the effectiveness of the reproduced preparations of MPFF and diosmin 600 mg. The indicated results are explained by differences in production technology, composition of components and are consistent with the known data on clinical efficacy of different groups of venotonics. Conclusion. In preclinical studies on the model of xylene petechiae with trypan blue staining, high efficacy of the original drug MPFF 1 (Detralex) at a single oral application and the drug heparin + EPL + escin (Detragel) at external single and course application for 15 days was established, which showed a significant difference with the control group, not less than 50% exceeded the efficacy of analogues and may indicate the effect on the permeability of the vascular wall.
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临床前研究中促排卵药剂对血管壁通透性影响的比较评估
导言。由于迄今为止还没有足够的证据来确定静脉注射药物的偏好,因此有必要在这一领域开展进一步的研究。研究目的在临床前研究中评估局部和口服促排卵药物对血管壁通透性的影响。材料和方法。研究对象是 6 种外用和口服促血细胞生成剂,按照使用说明中的建议,在胰蓝注射前 2 小时给药。临床前研究的模型:二甲苯瘀斑试验和胰蓝染色。评价标准是染色强度,以半定量(点数)表示。试验系统为 100 只白色雄性近交常规小鼠。结果与讨论在二甲苯瘀斑试验中,肝素 + EPL + escin(Detragel)可显著降低染色强度。研究发现,与对照组相比,单次外用可使染色强度降低 25.0%,比肝素 1000 IU 的疗效高出 60.0%;15 天为一个疗程,分 2 次使用,比肝素 1000 IU 和含有曲克芦丁的化妆品的疗效高出至少 50%。与对照组相比,单次口服 MPFF 1000 毫克(Detralex)可显著降低染色强度 35.0%,比 MPFF 和地奥司明 600 毫克复方制剂的效果高出 69.2%。上述结果可以用生产技术和成分组成的差异来解释,并且与不同组别静脉注射剂临床疗效的已知数据一致。结论在二甲苯瘀斑(胰盘蓝染色)模型的临床前研究中,确定了原研药 MPFF 1(Detralex)单次口服和肝素 + EPL + escin(Detragel)药物外用单次和疗程 15 天的高疗效,与对照组有显著差异,比类似物的疗效高出不少于 50%,这可能表明了对血管壁通透性的影响。
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