毒性试验在臭氧治疗应用及安全性中的重要性

Silvia Menéndez-Cepero, Z. Zamora, F. Hernández
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引用次数: 3

摘要

直到今天,还没有任何关于系统臭氧治疗的不同途径的官方登记。为了证明这种疗法的安全性,我们评估了几种臭氧(O3)的应用方式,如直肠注入(RI)、自体血液治疗(M-AHT)和腹腔注射(IP)。对于RI,进行了一些毒理学试验,如:急性、亚慢性、诱变(骨髓染色体畸变和微核)、致畸和刺激研究(在15天内分别使用40 mg/L和10 mL)。对于M-AHT,进行了急性毒理学(在大鼠中分别给予21,47和64mg /L,体积为2ml,每天评估15天)和诱变(染色体畸变分析,微核试验和姐妹染色单体交换试验)研究。对于IP应用,亚慢性(O3在15天内以11,29和35mg /L的浓度和80ml /kg的体积给予小鼠)和基因毒性(细胞毒性和致裂活性)研究进行了评估。对O3 RI进行的所有毒理学研究均符合官方登记的要求(未观察到有害影响)。然而,为了证明这些方法的完全安全性,必须对M-AHT和IP O3应用进行更多的毒理学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Importance of the Toxicological Tests in the Application and Safety of Ozone Therapy
Until today, there is not any official registry of the different routes of systemic ozone therapy. With the aim to prove the safety of this therapy, several ways of ozone (O3) applications were evaluated, such as rectal insufflation (RI), major autohemotherapy (M-AHT) and intraperitoneal application (IP). For RI, some toxicological tests were performed such as: acute, sub-chronic, mutagenic (bone marrow chromosomic aberrations and micronucleus), teratogenic  and irritation studies (at 40 mg/L and 10 mL during 15 days). For M-AHT, acute toxicological (in rats with 21, 47 and 64 mg/L and a volume of 2 mL with daily evaluation up to 15 days) and mutagenic (chromosomal aberration analysis, micronucleus assay and sister chromatid exchange test) studies were performed. For IP application, subchronic (O3 was administered during 15 days in mice at concentrations of 11, 29 and 35 mg/L and volumes of 80 mL/kg) and genotoxic (cytotoxic and clastogenic activity) studies were evaluated. All the toxicological studies performed for the O3 RI fulfilled the requirements established for an official registry (no deleterious effects were observed). However, more toxicological studies must be done with respect to M-AHT and IP O3 applications in order to prove the complete safety of these ways.
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