patent

专利
  • 文章类型: Journal Article
    背景:糖尿病性周围神经病变(DPN)是糖尿病的并发症,在全世界范围内发生在40-60百万个体中,并与其他慢性疾病相关。然而,目前还没有审查研究提出国家的最先进的技术和技术,以避免这一重要的健康问题。
    方法:本综述是根据科学论文和专利进行的。这些文件是从丁香花中取回的,PubMed,和WebofScience数据库,和INPI的专利,ESPACENET,WIPO,和GOOGLE专利。因此,分析了由14篇科学论文和667项专利组成的样本。
    结果:从数据分析来看,我们概述了DPN生物医学技术的发展,并发现了中国的开拓精神,美国,和日本在该地区,重点关注DPN的治疗。基于此,我们进行了SWOT分析,以帮助指导该地区未来的努力,应主要侧重于开发预防技术,早期诊断,and,最重要的是,医治本病对减轻本病在社会各界的重要影响。
    结论:这项研究发现糖尿病周围神经病变产物的浓度,尤其是治疗药物,在高收入国家。它强调了全球合作的必要性,并将战略重点放在治疗依从性和预防策略上,以有效管理DPN。
    BACKGROUND: Diabetic peripheral neuropathy (DPN) is a complication of diabetes that occurs in 40 - 60 million individuals worldwide and is associated with other chronic diseases. However, there are no review studies that present the state-of- the- art and technologies developed to circumvent this important health problem.
    METHODS: This review was conducted based on scientific papers and patents. The papers were retrieved from Lilacs, PubMed, and Web of Science databases, and the patents from INPI, ESPACENET, WIPO, and GOOGLE PATENTS. Thus, a sample consisting of 14 scientific articles and 667 patents was analyzed.
    RESULTS: From the analysis of the data, we drew an overview of the development of biomedical technologies for DPN and detected the pioneering spirit of China, the USA, and Japan in the area, with a focus on the treatment of DPN. Based on this, we carried out a SWOT analysis to help direct future efforts in the area, which should focus primarily on developing technologies for prevention, early diagnosis, and, above all, cure of the disease to reduce the important impact of this disease in various sectors of society.
    CONCLUSIONS: This study finds a concentration of diabetic peripheral neuropathy products, especially therapeutic drugs, in high-income countries. It highlights the need for global collaboration and strategic focus on therapeutic adherence and preventive strategies to effectively manage DPN.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    植物蛋白越来越被视为业余和专业运动员的关键营养来源。本研究的目的是回顾涉及植物基蛋白质应用的发明和实验文章,专用于运动员的食品中的肽和氨基酸,于2014-2023年期间发布。文献检索是根据PRISMA声明在几个关键数据库中进行的,包括Scopus和ISIWebofScience.总之,发现了106项专利和35篇原创文章。文章中描述的专利和发明调查显示,使用了52个类群(主要是一年生草本植物),创造可食用的种子,主要代表豆科和禾本科。大多数发明是由两到五名科学家的研究团队开发的,隶属于中国,美利坚合众国和日本。最大量的发明应用了基于植物的蛋白质(尤其是蛋白质分离物),宣布营养活性,并以液体或固体稠度制备。根据审查的研究,大豆和马铃薯蛋白质的摄入可能比动物蛋白质(不包括阻力训练)提供更好的结果,而豌豆和大米蛋白的消费不具有任何独特的合成代谢特性超过乳清蛋白。对其他调查的分析表明,食品的可接受性和消费量各不相同,虽然四篇文章中对经过测试的食品的高度评价似乎是其感官价值的影响,以及其他元素,如生产方法,健康效益和成本效益。考虑到有用植物物种的巨大潜力,可以得出结论,未来的研究重点是寻找新的植物蛋白来源,适合为业余和专业运动员准备食品,保持兴趣。
    Plant proteins are increasingly seen as critical nutrient sources for both amateur and professional athletes. The aim of the presented study was to review the inventions and experimental articles referring to the application of plant-based proteins, peptides and amino acids in food products dedicated to sportspeople and published in the period 2014-2023. The literature search was conducted according to PRISMA statementsacross several key databases, including Scopus and ISI Web of Science. Altogether, 106 patents and 35 original articles were found. The survey of patents and inventions described in the articles showed the use of 52 taxa (mainly annual herbaceous plants), creating edible seeds and representing mainly the families Fabaceae and Poaceae. The majority of inventions were developed by research teams numbering from two to five scientists, affiliated in China, The United States of America and Japan. The greatest number of inventions applied plant-based proteins (especially protein isolates), declared the nutritional activity and were prepared in liquid or solid consistency. According to the reviewed studies, the intake of soybean and potato proteins might provide better results than animal-based protein (excluding resistance training), whereas the consumption of pea and rice protein does not possess any unique anabolic properties over whey protein. The analysis of other investigations demonstrated the varied acceptability and consumption of food products, while the high rating of the tested food products presented in four articles seems to be an effect of their sensual values, as well as other elements, such as production method, health benefits and cost-effectiveness. Considering the great potential of useful plant species, it might be concluded that future investigations focusing on searching for novel plant protein sources, suitable for the preparation of food products dedicated to amateur and professional sportspeople, remain of interest.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    绿色蜂胶是一种由麦草芽孢杆菌生产的树脂,它的主要化合物是类黄酮,肉桂酸衍生物,例如ArtepillinC和百家乐。这种树脂有抗菌作用,抗真菌药,抗炎,抗氧化剂,和抗癌活动。这篇综述旨在分析各种配方中含有绿色蜂胶的药物专利。搜索是在国家工业产权研究所(INPI)进行的,西班牙和拉丁美洲专利检索(Latipat-Espacenet),世界知识产权组织(WIPO),和谷歌专利,结合了绿色蜂胶的关键字,绿色蜂胶提取物,药理学,和医药产品。初步研究确定了60项专利,在应用纳入标准后从中选出22人.选定的专利涉及具有药理活性的产品,从癌症治疗到食品补充剂,包括改善绿色蜂胶化合物控释的创新。大多数文件涉及绿色蜂胶提取物的制备和/或配方,其次是创新的提取方法,治疗和全身使用,最后通过局部使用和质量控制技术和程序。因此,审查的绿色蜂胶专利为绿色蜂胶的制药应用提供了宝贵的见解,显示其在不同的配方和治疗的潜力。
    Green propolis is a resin produced from Baccharis dracunculifolia, which has as its main compounds flavonoids, derivatives of cinnamic acids, such as artepillin C and baccarin. This resin has antibacterial, antifungal, anti-inflammatory, antioxidant, and anticancer activities. This review aimed to analyze pharmaceutical patents containing green propolis in various formulations. The search was conducted in the National Institute of Industrial Property (INPI), the Patent Search of Spain and Latin America (Latipat-Espacenet), the World Intellectual Property Organization (WIPO), and Google Patents, with a combination of the keywords green propolis, green propolis extract, pharmacology, and pharmaceutical product. Primary research identified 60 patents, from which 22 were selected after applying the inclusion criteria. The selected patents referred to products with pharmacological activities, from cancer treatment to food supplements and included innovations for improved controlled release of the green propolis compounds. Most of the documents concerned the preparation and/or formulation of the green propolis extract, followed by innovative extraction methods, treatment and systemic use, and finally by topical use and quality control techniques and procedures. Thus, the reviewed patents of green propolis provided valuable insights into the pharmaceutical applications of green propolis, showing its potential in diverse formulations and treatments.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    干扰素基因刺激因子(STING)是一种先天性免疫传感器。STING的激活引发下游反应,导致促炎细胞因子(TNF-α,IL-1β)通过核因子κB(NF-κB)或通过干扰素调节因子3(IRF3)表达I型干扰素(IFN)。IFN最终可以导致适应性免疫应答的促进,包括激活肿瘤特异性CD8+T细胞以消除肿瘤。因此,STING的激活已被认为是癌症治疗的潜在策略。
    本文从药物化学角度概述了充当抗癌剂的CDN样和非核苷酸STING激动剂(2021年1月至2023年10月)的结构和药理数据。本评论中的数据来自EPO,WIPO,RCSBPDB,CDDI。
    近年来,已经鉴定了几种结构不同的STING激动剂。作为免疫增强剂,它们用于治疗肿瘤,受到科学界和制药公司的广泛关注。尽管出现了多重挑战,STING激动剂可能为免疫治疗提供机会。
    UNASSIGNED: Stimulator of Interferon Genes (STING) is an innate immune sensor. Activation of STING triggers a downstream response that results in the expression of proinflammatory cytokines (TNF-α, IL-1β) via nuclear factor kappa-B (NF-κB) or the expression of type I interferons (IFNs) via an interferon regulatory factor 3 (IRF3). IFNs can eventually result in promotion of the adaptive immune response including activation of tumor-specific CD8+ T cells to abolish the tumor. Consequently, activation of STING has been considered as a potential strategy for cancer treatment.
    UNASSIGNED: This article provides an overview on structures and pharmacological data of CDN-like and non-nucleotide STING agonists acting as anticancer agents (January 2021 to October 2023) from a medicinal chemistry perspective. The data in this review come from EPO, WIPO, RCSB PDB, CDDI.
    UNASSIGNED: In recent years, several structurally diverse STING agonists have been identified. As an immune enhancer, they are used in the treatment of tumors, which has received extensive attention from scientific community and pharmaceutical companies. Despite the multiple challenges that have appeared, STING agonists may offer opportunities for immunotherapy.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    据报道,PIM激酶(PIM-1,PIM-2和PIM-3)在控制细胞存活的信号级联中起关键作用,扩散,和差异化。这些激酶的过度表达导致血液恶性肿瘤,如弥漫性大B细胞淋巴瘤(DLBCL),多发性骨髓瘤,白血病,淋巴瘤和前列腺癌等.PIM激酶作为生物标志物和潜在的治疗靶标已显示出对精确癌症治疗的希望。选择性PIM-1、PIM-2和/或PIM-3同种型抑制剂已经在患有晚期癌症(包括复发性/难治性癌症)的患者中显示出显著结果。
    关于PIM激酶(PIM-1,PIM-2和PIM-3)在肿瘤发生中的综合文献综述,获得专利的PIM激酶抑制剂(2016年至今),和他们的药理学和结构见解已被强调。
    最近,PIM激酶即.作为治疗靶标的PIM-1、PIM-2和PIM-3(丝氨酸/苏氨酸蛋白激酶家族的成员)已经在肿瘤学特别是血液恶性肿瘤中引起了相当大的兴趣。专利的PIM激酶抑制剂由杂环(稠合)环结构(如吲哚)组成,吡啶,吡嗪,吡唑,吖嗪,哌嗪,噻唑,恶二唑,喹啉,三唑并吡啶,吡唑并吡啶,咪唑并吡啶嗪,恶二唑-硫酮,吡唑并嘧啶,三唑并吡啶嗪,咪唑并吡啶嗪,吡唑并喹唑啉和吡唑并吡啶等。在癌症化疗中显示出有希望的结果。
    UNASSIGNED: PIM Kinases (PIM-1, PIM-2, and PIM-3) have been reported to play crucial role in signaling cascades that govern cell survival, proliferation, and differentiation. Over-expression of these kinases leads to hematological malignancies such as diffuse large B cell lymphomas (DLBCL), multiple myeloma, leukemia, lymphoma and prostate cancer etc. PIM kinases as biomarkers and potential therapeutic targets have shown promise toward precision cancer therapy. The selective PIM-1, PIM-2, and/or PIM-3 isoform inhibitors have shown significant results in patients with advanced stages of cancer including relapsed/refractory cancer.
    UNASSIGNED: A comprehensive literature review of PIM Kinases (PIM-1, PIM-2, and PIM-3) in oncogenesis, the patented PIM kinase inhibitors (2016-Present), and their pharmacological and structural insights have been highlighted.
    UNASSIGNED: Recently, PIM kinases viz. PIM-1, PIM-2, and PIM-3 (members of the serine/threonine protein kinase family) as therapeutic targets have attracted considerable interest in oncology especially in hematological malignancies. The patented PIM kinase inhibitors comprised of heterocyclic (fused)ring structure(s) like indole, pyridine, pyrazine, pyrazole, pyridazine, piperazine, thiazole, oxadiazole, quinoline, triazolo-pyridine, pyrazolo-pyridine, imidazo-pyridazine, oxadiazole-thione, pyrazolo-pyrimidine, triazolo-pyridazine, imidazo-pyridazine, pyrazolo-quinazoline and pyrazolo-pyridine etc. showed promising results in cancer chemotherapy.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    VEGFR,受体酪氨酸激酶抑制剂(TKI),是促进血管生成和血管通透性的重要调节因子。它在肿瘤血管生成等过程中起着重要作用,肿瘤细胞侵袭,和转移。VEGFR主要由三种亚型组成:VEGFR-1、VEGFR-2和VEGFR-3。其中,VEGFR-2是VEGF的关键信号受体,参与各种病理和生理功能。目前,VEGFR-2与多种癌症密切相关,如非小细胞肺癌(NSCLC),肝细胞癌,肾细胞癌,乳腺癌,胃癌,神经胶质瘤,等。因此,VEGFR-2是各种癌症治疗的关键靶标。越来越多的VEGFR抑制剂被发现用于治疗癌症。他们在临床上取得了巨大的成功。然而,VEGFR抑制剂通常表现出严重的细胞毒性,阻力,和适应症的局限性,从而削弱了临床治疗效果。近年来,许多靶向VEGFR的小分子抑制剂已被鉴定具有抗耐药性,较低的细胞毒性,和更好的亲和力。这里,我们概述了VEGFR的结构和生理功能,以及目前在临床使用的一些VEGFR抑制剂。此外,我们总结了体内和体外活动,选择性,构效关系,以及过去三年(2021-2023年)专利中报道的VEGFR小分子抑制剂的治疗或预防性使用,从而提出了靶向VEGFR抑制剂未来发展的前景和见解。
    VEGFR, a receptor tyrosine kinase inhibitor (TKI), is an important regulatory factor that promotes angiogenesis and vascular permeability. It plays a significant role in processes such as tumor angiogenesis, tumor cell invasion, and metastasis. VEGFR is mainly composed of three subtypes: VEGFR-1, VEGFR-2, and VEGFR-3. Among them, VEGFR-2 is the crucial signaling receptor for VEGF, which is involved in various pathological and physiological functions. At present, VEGFR-2 is closely related to a variety of cancers, such as non-small cell lung cancer (NSCLC), Hepatocellular carcinoma, Renal cell carcinoma, breast cancer, gastric cancer, glioma, etc. Consequently, VEGFR-2 serves as a crucial target for various cancer treatments. An increasing number of VEGFR inhibitors have been discovered to treat cancer, and they have achieved tremendous success in the clinic. Nevertheless, VEGFR inhibitors often exhibit severe cytotoxicity, resistance, and limitations in indications, which weaken the clinical therapeutic effect. In recent years, many small molecule inhibitors targeting VEGFR have been identified with anti-drug resistance, lower cytotoxicity, and better affinity. Here, we provide an overview of the structure and physiological functions of VEGFR, as well as some VEGFR inhibitors currently in clinical use. Also, we summarize the in vivo and in vitro activities, selectivity, structure-activity relationship, and therapeutic or preventive use of VEGFR small molecule inhibitors reported in patents in the past three years (2021-2023), thereby presenting the prospects and insights for the future development of targeted VEGFR inhibitors.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    慢性炎症是由与所有神经系统疾病相关的激活的小胶质细胞状态定义的。包括老年痴呆症,帕金森病,和肌萎缩侧索硬化症(一种影响大脑和脊髓的运动神经元疾病)。P2X7受体(P2X7R)是存在于小胶质细胞表面上的ATP激活的离子门控通道。在病理设置下延长ATP释放导致持续的P2X7R激活,这导致炎症小体的发育和细胞因子的释放。P2X7R及其促成作用最近与神经退行性疾病有关,使其成为一个潜在的研究课题。这项研究概述了当前的化学品专利,生物制剂,和医药应用。世界知识产权组织(WIPO)欧洲专利局(EPO,Espacenet),和美国专利商标局(USPTO)数据库使用关键字“P2X7R和神经炎症”搜索专利。“在2015年至2021年的研究期间,共审查了103项专利。保护这些创新的国家是美国,PCT(专利合作条约)欧洲,加拿大,澳大利亚,和印度。JanssenPharmaceuticaNV的应用最多,其次是Acetelion制药有限公司。,RenovisInc.,KellyMichaelG,KincaidJhon,默克公司专利GMBH,H伦德贝克A/S,还有更多。P2X7R可能是癌症的诊断和治疗靶点,疼痛紊乱,和炎症。对于P2X7R,已经发现了几种化合物,目前是临床试验研究的主题。这项研究以P2X7R拮抗剂的专利为特色,有助于治疗包括神经炎症在内的疾病。
    Chronic inflammation is defined by an activated microglial state linked to all neurological disorders, including Alzheimer\'s disease, Parkinson\'s disease, and amyotrophic lateral sclerosis (a motor neuron disease that affects the brain and spinal cord). P2X7 receptors (P2X7R) are ATP-activated ion-gated channels present on microglial surfaces. Prolonged ATP release under pathological settings results in sustained P2X7R activation, which leads to inflammasome development and cytokine release. P2X7R and its enabling roles have recently been linked to neurodegenerative diseases, making it a potential research subject. This research provides an overview of current patents for chemicals, biologics, and medicinal applications. The World Intellectual Property Organization (WIPO), European Patent Office (EPO, Espacenet), and the United States Patent and Trademark Office (USPTO) databases were searched for patents using the keywords \"P2X7R and Neuroinflammation.\" During the study period from 2015 to 2021, 103 patents were examined. The countries that protected these innovations were the United States, PCT (Patent Cooperation Treaty states), Europe, Canada, Australia, and India. Janssen Pharmaceutica NV had the most applications, followed by Acetelion Pharmaceuticals LTD., Renovis Inc., Kelly Michael G, Kincaid Jhon, Merck Patent GMBH, H Lundbeck A/S, and many more. The P2X7R is a possible diagnostic and therapeutic target for cancer, pain disorders, and inflammation. For P2X7 R, several compounds have been discovered and are presently the subject of clinical trial investigations. This study featured patents for P2X7R antagonists, which help treat conditions including neuroinflammation.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    与满足维持整个人口生命所必需的营养需求的一般营养范围不同,个性化营养的特点是通过根据个人的生活方式或遗传特征提供定制营养来保持健康。个性化营养技术和服务的发展日益增多,由于根据个体的多样性和健康兴趣的增加,获得了关于营养需求差异的知识。关于遗传学,正在开发技术来区分个人的各种特征并提供定制营养。因此,为了了解个性化营养技术的现状,了解基因组学是获取基于基因组学的营养研究信息的必要条件。我们审查了与个性化营养靶向基因组学相关的专利,并研究了它们的作用机制。利用专利数据库,我们检索了694项营养基因组学专利,并提取了561个高度相关的有效数据点.此外,通过选择与基于基因组的个性化营养技术相关的核心专利进行了深入审查。使用遗传评分和疾病特异性饮食建议等方法的个性化营养技术显着增加。
    Unlike general nutritional ranges that meet the nutritional needs essential for maintaining the life of an entire population, personalized nutrition is characterised by maintaining health through providing customized nutrition according to individuals\' lifestyles or genetic characteristics. The development of technology and services for personalized nutrition is increasing, owing to the acquisition of knowledge about the differences in nutritional requirements according to the diversity of individuals and an increase in health interest. Regarding genetics, technology is being developed to distinguish the various characteristics of individuals and provide customized nutrition. Therefore, to understand the current state of personalized nutrition technology, understanding genomics is necessary to acquire information on nutrition research based on genomics. We reviewed patents related to personalized nutrition-targeting genomics and examined their mechanisms of action. Using the patent database, we searched 694 patents on nutritional genomics and extracted 561 highly relevant valid data points. Furthermore, an in-depth review was conducted by selecting core patents related to genome-based personalized nutrition technology. A marked increase was observed in personalized nutrition technologies using methods such as genetic scoring and disease-specific dietary recommendations.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Meta-Analysis
    食源性疾病是全球公共卫生问题,每年有十分之一的人在食用受污染的食物后患病。作为回应,食品工业已经实施了几种新的病原体控制策略,例如使用直接应用噬菌体进行生物防治的生物技术工具。我们进行了系统的审查和荟萃分析,评估了专利噬菌体作为食源性病原体生物防治的效率,并确定了抗菌作用的物理化学特征。制定了纳入和排除标准。包括的标准:噬菌体专利文件,用于食品和科学文章的生物防治,以及使用噬菌体专利用于食品生物防治的书籍章节。排除标准:专利文件,科学文章,和书籍章节,包括人类的噬菌体疗法,动物,在我们的研究中没有考虑对植物的生物防治,但没有对食物的应用。系统分析确定了77份文件,46篇科学论文,31篇专利文献和23篇文章被纳入荟萃分析。单核细胞增生李斯特菌和沙门氏菌。包括筛查中确定的大部分目标,所以我们专注于这些菌株进行荟萃分析。对李斯特菌和沙门氏菌噬菌体共进行了383和192次实验,用于定量数据分析。用于书目搜索的索引数据库(Scopus,WebofScience(WoS)和PubMed(Medline)由Python3PythonCoreTeam(2015)编写的自动脚本解决,并保存在GitHub(https://github.com/glenjasper)上。随机效应荟萃分析显示(i)苹果中李斯特菌噬菌体的显着抗菌作用,苹果汁,梨,梨汁,(ii)鸡蛋中沙门氏菌噬菌体的显着抗菌作用,苹果,和即食鸡肉,(iii)在两项荟萃分析中均未发现异质性,(iv)检测到李斯特菌噬菌体的发表偏倚,但未检测到沙门氏菌噬菌体的发表偏倚。(v)ListShield和Felix01噬菌体对李斯特菌和沙门氏菌的生物防治效果最好,分别,(vi)噬菌体和细菌的浓度,时间和食物在李斯特菌的生物防治中有显著的效果,(vii)温度和时间对沙门氏菌噬菌体的抗菌活性有显著影响。系统审查和荟萃分析,以确定以前获得专利的噬菌体对乳制品上致病菌的效率,肉,水果和蔬菜。此外,发现疗效的关键因素,以便未来噬菌体生物技术在食品中的应用可以得到最佳部署。
    Food-borne diseases are a global public health issue with 1 in 10 people falling ill after eating contaminated food every year. In response, the food industry has implemented several new pathogen control strategies, such as biotechnological tools using the direct application of bacteriophages for biological control. We have undertaken a systematic review and meta-analysis that evaluated the efficiency of patented phages as a biological control for food-borne pathogens and determined the physical-chemical characteristics of the antimicrobial effect. Included and excluded criteria was developed. Included criteria: Phage patent files with an application in biological control on food and scientific articles and book chapters that used phages patented for food biological control. Excluded criteria: Patent documents, scientific articles, and book chapters that included phage therapy in humans, animals, and biological control on plants but did not have an application on food were not considered in our study. The systematic analysis identified 77 documents, 46 scientific articles, and 31 documents of patents and 23 articles was included in the meta-analysis. Listeria monocytogenes and Salmonella sp. comprised most of the targets identified in the screening, so that we focused on these strains to do the meta-analysis. There are a total of 383 and 192 experiments for Listeria and Salmonella phages for quantitative data analysis.Indexing databases for the bibliographic search (Scopus, Web of Science (WoS) and PubMed (Medline) were addressed by an automated script written in Python 3 Python Core Team (2015) and deposited on GitHub ( https://github.com/glenjasper ).A random-effects meta-analysis revealed (i) significant antimicrobial effect of Listeria phages in apple, apple juice, pear, and pear juice, (ii) significant antimicrobial effect of Salmonella phages in eggs, apple, and ready-to-eat chicken, (iii) no heterogeneity was identified in either meta-analysis, (iv) publication bias was detected for Listeria phages but not for Salmonella phages. (v) ListShield and Felix01 phages showed the best result for Listeria and Salmonella biological control, respectively, (vi) concentration of phage and bacteria, time and food had significant effect in the biological control of Listeria, (vii) temperature and time had a significant effect on the antimicrobial activity of Salmonella phages. The systematic review and meta-analyses to determine the efficiency of bacteriophages previously patented against pathogenic bacteria on dairy products, meat, fruits and vegetables. Besides, the discovering of key factors for efficacy, so that future applications of phage biotechnology in foods can be optimally deployed.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    Safranal(一种单萜醛)是藏红花的主要挥发性成分,是藏红花独特气味的原因。一些研究表明,藏药的药理活性包括抗氧化剂,抗炎,心脏保护,神经保护,肾保护,胃肠保护,等。这项研究旨在回顾安全和最新的先前知识的药理和医学作用。此外,收集了一些与safranal药理作用有关的专利。因此,电子数据库,包括WebofSciences,Scopus,并因药理作用和美国专利而出版,专利范围,从2010年到2022年6月,通过相关英文关键词对Google专利进行了全面搜索。根据我们的审查,大多数研究都与中枢神经系统的安全性作用有关,例如抗焦虑,镇痛药,抗惊厥药,抗缺血,抗震颤,记忆增强及其对神经退行性疾病如阿尔茨海默氏症的保护作用,帕金森病和亨廷顿病。安全的其他作用是平喘,抗高血压药,抗衰老,anticataract,等。此外,该药物对代谢综合征和糖尿病肾病具有保护作用。不同的机制,包括抗氧化剂,抗炎,肌肉放松,抗凋亡,以及对与氧化应激信号通路相关的基因和蛋白质表达的调节作用,炎症,凋亡,扩散,等。参与藏药药理作用。一些用于预防和/或治疗不同疾病如肝癌的专利,睡眠障碍,抑郁症,认知障碍,肥胖和PMS也包括在内.根据文件,尽管需要更多的临床研究来验证Safranal对人类的有益作用,但Safranal被认为是有前途的治疗剂。
    Safranal (a monoterpene aldehyde) is the major volatile component of saffron which is responsible for the saffron unique odor. Several studies have shown the pharmacological activities of safranal including anti-oxidant, anti-inflammatory, cardioprotective, neuroprotective, nephroprotective, gastrointestinal protective, etc. This study was designed to review the pharmacological and medical effects of safranal and up-to-date previous knowledge. Moreover, some patents related to the pharmacological effects of safranal were gathered. Therefore, electronic databases including Web of Sciences, Scopus, and Pubmed for pharmacological effects and US patent, Patentscope, and Google Patent for patents were comprehensively searched by related English keywords from 2010 to June 2022. According to our review, most of the studies are related to the safranal effects on CNS such as antianxiety, analgesic, anticonvulsant, antiischemic, anti-tremor, memory enhancement and its protective effects on neurodegenerative disorders such as Alzheimer\'s, Parkinson and Huntington diseases. Other effects of safranal are antiasthmatic, antihypertensive, antiaging, anticataract, etc. Moreover, the protective effects of this agent on metabolic syndrome and diabetic nephropathy have been shown. Different mechanisms including anti-oxidant, anti-inflammatory, muscle relaxation, antiapoptotic, and regulatory effects on the genes and proteins expression related to signaling pathways of oxidative stress, inflammation, apoptosis, proliferation, etc. are involved in safranal pharmacological effects. Some patents for the prevention and/or treatment of different diseases such as liver cancer, sleep disorder, depression, cognitive disorder, obesity and PMS were also included. Based on the documents, safranal is considered a promising therapeutic agent although more clinical studies are needed to verify the beneficial effects of safranal in humans.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号