壳聚糖-海藻酸盐包覆山竹提取物微粒的亚急性口服毒性试验

Gede Bagus Yoga Satriadinatha, Siti Farida, K. Mulia, D. Krisnamurti
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引用次数: 1

摘要

山竹果提取物壳聚糖-海藻酸盐包被微粒有望成为结肠癌患者的替代治疗方法,因为山竹果提取物的成分对结肠癌细胞系具有抗癌活性,壳聚糖-海藻酸盐可以更快地将化合物输送到结肠并加速其吸收。然而,目前还没有任何研究评估该化合物对肝脏(SGOT和SGPT)的亚急性毒性作用和临床毒性症状。本研究评价了壳聚糖海藻酸盐包被山竹果提取物微颗粒口服的亚急性毒性作用。50只BALB/c小鼠分为5组,剂量分别为0.5 g /kg、1.0 g /kg、2.0 g /kg、阴性对照和正常组。每只大鼠经灌胃管灌食提取物14天(亚急性期)。结果显示,治疗组与对照组SGOT水平(p = 0.061)、SGPT水平(p = 0.82)、体重增加(p = 0.076)差异均无统计学意义,且研究期间无临床体征。这些表明,亚急性给药壳聚糖海藻酸盐包覆的山竹果提取物微粒是安全的,直到剂量为2.0克/千公斤重。需要进一步的研究来评估这种提取物对其他参数和较长时间暴露的毒性作用。山竹果提取物壳聚糖-海藻酸盐包被微粒有望成为结肠癌患者的替代治疗方法,因为山竹果提取物的成分对结肠癌细胞系具有抗癌活性,壳聚糖-海藻酸盐可以更快地将化合物输送到结肠并加速其吸收。然而,目前还没有任何研究评估该化合物对肝脏(SGOT和SGPT)的亚急性毒性作用和临床毒性症状。本研究评价了壳聚糖海藻酸盐包被山竹果提取物微颗粒口服的亚急性毒性作用。50只BALB/c小鼠分为5组,剂量分别为0.5 g /kg、1.0 g /kg、2.0 g /kg、阴性对照和正常组。每只大鼠经灌胃管灌食提取物14天(亚急性期)。结果表明,两组间SGOT水平(p = 0.061)、SGPT水平(p = 0.82)和增重(p = 0.076)差异无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subacute oral toxicity test of chitosan-alginate coated microparticle of Garcinia mangostana Linn extract
Chitosan-alginate coated microparticle of Garcinia mangostana Linn extract promises an alternative treatment of colon cancer patients, as the component of Garcinia mangostana Linn extract has anticancer activity in colon cancer cell lines, and chitosan-alginate could deliver compound faster to colon and accelerate its absorption. However, there have not been any studies evaluating sub-acutely the toxicity effects of this compound on the liver (SGOT and SGPT) and clinical signs of toxicity. This study was conducted to evaluate the subacute toxicity effect of Chitosan-alginate coated microparticle of Garcinia mangostana Linn extract’s oral administration. Fifty BALB/c mice were divided into five groups, including doses of 0.5 gram/kg, 1.0 gram/kg, 2.0 gram/kg, negative control, and normal group. Each rat was given an extract by force-feeding via intragastric tube for 14 days (subacute). The results showed that differences in SGOT level (p = 0.061), SGPT level (p = 0.82), and weight gain (p = 0.076) were not significant between the treatment and control groups, accompanied by the absence of clinical signs during the study. These indicate that subacute administration of chitosan-alginate coated microparticle of Garcinia mangostana Linn extract is safe until a dose of 2.0 gram/kgBW. Further studies are needed to evaluate the toxicity effects of this extract on other parameters and in a longer duration of exposure.Chitosan-alginate coated microparticle of Garcinia mangostana Linn extract promises an alternative treatment of colon cancer patients, as the component of Garcinia mangostana Linn extract has anticancer activity in colon cancer cell lines, and chitosan-alginate could deliver compound faster to colon and accelerate its absorption. However, there have not been any studies evaluating sub-acutely the toxicity effects of this compound on the liver (SGOT and SGPT) and clinical signs of toxicity. This study was conducted to evaluate the subacute toxicity effect of Chitosan-alginate coated microparticle of Garcinia mangostana Linn extract’s oral administration. Fifty BALB/c mice were divided into five groups, including doses of 0.5 gram/kg, 1.0 gram/kg, 2.0 gram/kg, negative control, and normal group. Each rat was given an extract by force-feeding via intragastric tube for 14 days (subacute). The results showed that differences in SGOT level (p = 0.061), SGPT level (p = 0.82), and weight gain (p = 0.076) were not...
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