Food supplements

食品补充剂
  • 文章类型: Journal Article
    目的:放射性膀胱炎是盆腔癌治疗性放疗后常见的并发症。目前对这种病症的治疗是复杂的并且通常是无效的。
    方法:我们介绍了一例54岁的小细胞宫颈癌FIGOIIIC期患者的临床病例,该患者在术后放化疗后发展为2-3级放射性膀胱炎。患者表现出尿急和尿频增加,排尿困难,和下腹疼痛,对针灸和皮质类固醇治疗没有反应。一个疗程的IchNieuKhang植物疗法片剂,导致症状在开始后24小时内显着改善。症状在10天内完全缓解,超声检查显示膀胱壁增厚明显减少,膀胱排空功能改善。植物疗法耐受性良好,在60天的治疗期间没有观察到副作用。
    结论:这些研究结果表明,植物疗法治疗放射性膀胱炎可能是可行的。然而,需要进一步的临床对照试验来证实IchNieuKhang的疗效并促进其更广泛的临床应用。
    OBJECTIVE: Radiation cystitis is a frequent complication that can occur after therapeutic irradiation of pelvic cancers. The current treatment for this condition is complex and often ineffective.
    METHODS: We present a clinical case of a 54-year-old patient diagnosed with small cell cervical cancer FIGO stage IIIC who developed grade 2-3 radiation cystitis following post-operational chemoradiation therapy. The patient exhibited increased urinary urgency and frequency, dysuria, and low abdominal pain, which failed to respond to acupuncture and corticosteroid treatments. A course of Ich Nieu Khang phytotherapy tablets, resulted in significant improvement of symptoms within 24 hours of initiation. The symptoms resolved completely within 10 days, and ultrasonography documented a marked decrease in bladder wall thickening and improved bladder evacuation function. The phytotherapy was well-tolerated, and no side-effects were observed during the 60-day treatment period.
    CONCLUSIONS: These findings suggest that phytotherapy may be viable for managing radiation cystitis. However, further controlled clinical trials are needed to confirm the efficacy of Ich Nieu Khang and promote its broader clinical applications.
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  • 文章类型: Journal Article
    膳食补充剂是促进健康的产品。膳食补充剂作为食品的法律分类不会引起关注,但是对它们如何在人体中工作的一般理解似乎偏离了官方的定义。因此,有必要建立有效的膳食补充剂市场控制方法。这项研究旨在评估各种食品安全当局的建议对新注册产品中使用的成分的影响。它探讨了在欧洲食品安全局(EFSA)和波兰首席卫生检查员(GIS)发布建议后,如何修改所用产品成分的比例。关于产品成分的研究数据来自波兰国家膳食补充剂登记册,涵盖2012年至2021年11月28日。请注意,对103,102种产品进行了37种成分的分析,并应用连接点回归方法评估与成分使用相关的变化趋势。正如我们的研究指出的,大多数情况下,趋势的变化出现在产品成分中,欧洲食品安全局和波兰首席卫生检查员发布了具有最安全消费水平的建议。然而,这些变化似乎是随机出现的,不应毫无疑问地被认为是已发布建议的结果。
    Dietary supplements are health-promoting products. The legal categorization of dietary supplements as foods does not raise concerns, but a general understanding of how they work in the human body seems to deviate from the official definition. Thus, it is necessary to establish effective methods of market control related to dietary supplements. This research aims at assessing the impact of recommendations by various food safety authorities on ingredients used in newly registered products. It probes how the proportions of utilized product ingredients were modified after the European Food Safety Authority (EFSA) and Chief Sanitary Inspector in Poland (GIS) published their recommendations. Research data on the composition of products comes from the Polish national register of dietary supplements and covers the period from 2012 to 28 November 2021. Note that 103,102 products were analysed for the presence of thirty-seven ingredients, and the joinpoint regression method was applied to assess changing trends related to the use of ingredients. As our research points out, most often, changes in the trend appeared in product ingredients for which the European Food Safety Authority and Chief Sanitary Inspector in Poland issued the recommendation of having the safest level of consumption. However, these changes seem to emerge randomly and should not be unquestionably considered as the result of the published recommendations.
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  • 文章类型: Journal Article
    营养品的效率的倾向是产品含有足够量的维生素。一些研究强调了不同的质量问题。我们的目的是调查选定类型的食品补充剂中维生素的含量是否符合标签。我们专注于两种类型的食品补充剂,其中与内容相关的质量问题可能导致公共卫生风险:(a)怀孕时补充叶酸(作为5-甲基四氢叶酸(5-MTHF))和(b)普通人群中的维生素D。这项研究是针对斯洛文尼亚消费者通常使用的全球补充剂进行的。我们对一个生产批次的30种不同的食品补充剂进行了采样-6种和24种带有5-MTHF和胆钙化醇的样品,分别。我们发现两组样品的维生素含量都在80-150%的耐受区间之外。特别是,5-MTHF被发现更有问题,可能是由于其稳定性较低。这项研究表明需要更好的质量控制。在制造过程和产品保质期期间都需要质量控制。内容质量也应受到当局的外部控制。自愿的质量控制计划还将使消费者能够识别出足够质量的产品。
    A predisposition for the efficiency of nutraceuticals is that the product contains a sufficient quantity of a vitamin. Several studies have highlighted different quality issues. Our objective was to investigate whether the contents of the vitamins in selected types of food supplements were in accordance with labeling. We focused on two types of food supplements where content-related quality issues could result in public health risks: food supplements for supplementation with (a) folic acid (as 5-methyltetrahydrofolate (5-MTHF)) in pregnancy and (b) with vitamin D in the general population. The study was done on supplements from the global supply that are typically used by Slovenian consumers. We sampled one production batch of 30 different food supplements-six and 24 samples with 5-MTHF and cholecalciferol, respectively. We found samples with vitamin contents outside the 80-150% tolerance interval in both sets. Particularly, 5-MTHF was found to be more problematic, probably due to its lower stability. This study shows the need for better quality control. Quality control is needed during both the manufacturing process and product shelf lifetimes. Content quality should be also subject to external controls by authorities. Voluntarily quality control schemes would also enable consumers to identify products of sufficient quality.
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  • 文章类型: Journal Article
    Herbal tonic and adaptogens are often used to improve overall well-being. However, few clinical evidence supports their use and their safety is not known before marketing. In this context, the aim of our study was to analyze the spontaneous reports of suspected adverse reactions (ARs) to performance enhancing herbal dietary supplements collected by the Italian Phytovigilance System. Between March 2002 and September 2020, 110 spontaneous reports were collected, 58 of which related to products containing botanicals, alone or in association. Twenty-three serious reactions were reported, 21 of which required hospitalization, one was life-threatening and another caused disability. Dermatological and cardiovascular reactions were the most frequent. Hepatic ARs were the most serious (9 out of 10). A positive dechallenge was indicated in 69% of cases, while a positive rechallenge occurred in 15%. Concomitant use of other products was present in 18 reports (31%), while predisposing conditions were indicated in 17 (29%). Present data highlight safety concerns on herbal dietary supplements used as cognitive and physical performance enhancers, mainly due to their quality and use without expert supervision. Considering that postmarketing surveillance is not required for these products, spontaneous reports represent the only tool to point out risks related to food supplements.
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  • 文章类型: Journal Article
    The phenolic profiles of three typical Tuscan olive cultivars, Frantoio, Moraiolo, and Leccino, stored in different conditions (fresh, frozen, and whole lyophilized fruits), have been compared during the ripening period. Our main goals were to evaluate the phenolic content of whole freeze-dried fruits and to test the stability of the corresponding cake in oxidative-stress conditions. The comparison of fresh and whole freeze-dried fruits from the 2012 season gave unexpected results; e.g., oleuropein in lyophilized fruits was up to 20 times higher than in fresh olives with values up to 80.3 g/kg. Over time we noted that the olive pastes obtained from lyophilized olives contained highly stable phenolic compounds, even under strong oxidative stress conditions. Finally, it was also observed that the cake/powder obtained from unripe freeze-dried olives was very poor in oil content and therefore quite suitable for use in nutritional supplements rich in phenolic compounds, such as secoiridoids, which are not widely present in the human diet.
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