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阿法林:一种新型乳香抗炎产品的安全性和毒理学评价。

Safety and toxicological evaluation of Aflapin: a novel Boswellia-derived anti-inflammatory product.

机构信息

Laila Impex R&D Centre, Unit-I, Phase-III, Jawahar Autonagar, Vijayawada 520007, India.

出版信息

Toxicol Mech Methods. 2010 Nov;20(9):556-63. doi: 10.3109/15376516.2010.497978. Epub 2010 Sep 29.

Abstract

Boswellia serrata gum resin has been used for treatment of various ailments in different cultures for thousands of years. Aflapin(®) is a novel synergistic composition derived from B. serrata gum resin (Indian Patent Application No. 2229/CHE/2008). Aflapin is significantly better as an anti-inflammatory agent compared to the Boswellia extracts presently available in the market. To assess the safety of Aflapin, a battery of acute and sub-acute toxicity studies were conducted in various animal models according to the OECD test guidelines. The acute oral LD50 of Aflapin was greater than 5000 mg/kg in female Sprague Dawley (SD) rats. Acute dermal LD50 of Aflapin was greater than 2000 mg/kg in SD rats. A primary dermal irritation study conducted using New Zealand White rabbits indicated that Aflapin is non-irritating to skin. Aflapin caused minimal ocular irritation in a primary eye irritation test conducted on New Zealand Albino rabbits. A repeat dose 28-day sub-acute oral toxicity study in SD rats demonstrated no significant signs of toxicity. Various evaluations including hematology, clinical chemistry, gross necropsy, and histopathology did not show any significant adverse changes. The NOAEL of Aflapin was found to be greater than 2500 mg/kg body weight. These studies demonstrate broad spectrum safety of Aflapin in animal models.

摘要

乳香树胶树脂在不同文化中已经被用于治疗各种疾病数千年。Aflapin(®) 是一种新型协同组合物,源自乳香树胶树脂(印度专利申请号 2229/CHE/2008)。与目前市场上可用的乳香提取物相比,Aflapin 作为抗炎剂的效果显著更好。为评估 Aflapin 的安全性,根据 OECD 测试指南,在各种动物模型中进行了一系列急性和亚急性毒性研究。Aflapin 的急性经口 LD50 在雌性 Sprague Dawley (SD) 大鼠中大于 5000mg/kg。Aflapin 的急性经皮 LD50 在 SD 大鼠中大于 2000mg/kg。在新西兰白兔中进行的原发性皮肤刺激研究表明,Aflapin 对皮肤无刺激性。在新西兰白化兔中进行的原发性眼刺激试验中,Aflapin 引起的眼部刺激最小。在 SD 大鼠中进行的重复剂量 28 天亚急性口服毒性研究未显示出明显的毒性迹象。包括血液学、临床化学、大体剖检和组织病理学在内的各种评估均未显示出任何明显的不良变化。Aflapin 的无可见不良作用水平(NOAEL)大于 2500mg/kg 体重。这些研究表明 Aflapin 在动物模型中具有广泛的安全性。

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