Future medicine

  • 文章类型: Review
    据估计,全世界每年有数百万人经历各种类型的组织损伤。再生医学的诞生和发展是为了理解和应用,目的是替换受影响的器官或某些细胞。这项研究,制造,生产,RNA在细胞中的分布已成为开发和测试广泛应用于不同医学领域的疗法和治疗的基础。针对COVID-19的疫苗被认为是RNA治疗研究的辉煌和杰出成就之一。具有生物衍生RNA疗法的特点,快速执行的机制,安全生产,以及根据实际需求创建蛋白质的灵活性。基于这篇综述中的上述优点,我们讨论了用于再生医学的RNA疗法,以及目前用于再生医学的RNA疗法的类型。目前正在RNA疗法中研究或测试疾病与再生医学之间的关系。我们还涵盖了RNA疗法对再生医学的作用机制,以及我们目前对RNA疗法在该领域的影响的理解中的一些局限性。此外,我们还涵盖了为再生医学开发RNA疗法,专注于再生医学的RNA疗法。作为最后一点,我们讨论了未来再生医学治疗的潜在应用,以及它们的机制。
    It is estimated that millions of people around the world experience various types of tissue injuries every year. Regenerative medicine was born and developed for understanding and application with the aim of replacing affected organs or some cells. The research, manufacture, production, and distribution of RNA in cells have acted as a basic foundation for the development and testing of therapies and treatments that are widely applied in different fields of medicine. Vaccines against COVID-19 are considered one of the brilliant and outstanding successes of RNA therapeutics research. With the characteristics of bio-derived RNA therapeutics, the mechanism of rapid implementation, safe production, and flexibility to create proteins depending on actual requirements. Based on the advantages above in this review, we discuss RNA therapeutics for regenerative medicine, and the types of RNA therapies currently being used for regenerative medicine. The relationship between disease and regenerative medicine is currently being studied or tested in RNA therapeutics. We have also covered the mechanisms of action of RNA therapy for regenerative medicine and some of the limitations in our current understanding of the effects of RNA therapy in this area. Additionally, we have also covered developing RNA therapeutics for regenerative medicine, focusing on RNA therapeutics for regenerative medicine. As a final point, we discuss potential applications for therapeutics for regenerative medicine in the future, as well as their mechanisms.
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  • 文章类型: Journal Article
    这项研究严格评估了四种人工智能(AI)语言模型的性能-ChatGPT,克劳德·艾伊,谷歌吟游诗人,和困惑AI-跨越四个关键指标:准确性、相关性,清晰度,和完整性。我们使用了多种研究方法,从14种场景中获取意见。这有助于我们确保我们的发现是准确和可靠的。研究表明,克劳德AI比其他人表现更好,因为它给出了完整的响应。与其他AI工具相比,其相关性平均得分为3.64,完整性平均得分为3.43。ChatGPT总是做得很好,谷歌巴德的反应不清楚,变化很大,很难理解它,所以谷歌吟游诗人没有一致性。这些结果提供了有关AI语言模型在医学建议方面做得好或不好的重要信息。它们帮助我们更好地使用它们,告诉我们如何改善使用AI的未来技术变革。研究表明,AI能力与复杂的医疗场景相匹配。
    This study rigorously evaluates the performance of four artificial intelligence (AI) language models - ChatGPT, Claude AI, Google Bard, and Perplexity AI - across four key metrics: accuracy, relevance, clarity, and completeness. We used a strong mix of research methods, getting opinions from 14 scenarios. This helped us make sure our findings were accurate and dependable. The study showed that Claude AI performs better than others because it gives complete responses. Its average score was 3.64 for relevance and 3.43 for completeness compared to other AI tools. ChatGPT always did well, and Google Bard had unclear responses, which varied greatly, making it difficult to understand it, so there was no consistency in Google Bard. These results give important information about what AI language models are doing well or not for medical suggestions. They help us use them better, telling us how to improve future tech changes that use AI. The study shows that AI abilities match complex medical scenarios.
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  • 文章类型: Review
    RNA治疗涉及利用天然和人工RNA分子来控制细胞基因和蛋白质的表达和功能。从1990年代开始初始化,RNA疗法现在显示出用于治疗各种疾病的RNA疗法的开发和应用的快速增长。尤其是对无法用药的疾病.最近针对COVID-19感染的mRNA疫苗的巨大成功再次凸显了RNA疗法在未来医学中的重要作用。在这次审查中,我们将首先简要介绍RNA治疗的关键研究,从RNA分子的第一个发现到RNA疗法的临床应用。然后,我们将从疾病治疗中的各种类别中对RNA疗法的机制进行分类。为了强调RNA疗法的巨大潜力,我们还提供已经进行临床试验或已经获得FDA批准的关键RNA产品。具有全面的RNA生物学知识,以及分析的进展,技术和计算机辅助科学,RNA疗法可以带来未来进一步扩大市场的希望。
    RNA therapies involve the utilization of natural and artificial RNA molecules to control the expression and function of cellular genes and proteins. Initializing from 1990s, RNA therapies now show the rapid growth in the development and application of RNA therapeutics for treating various conditions, especially for undruggable diseases. The outstanding success of recent mRNA vaccines against COVID-19 infection again highlighted the important role of RNA therapies in future medicine. In this review, we will first briefly provide the crucial investigations on RNA therapy, from the first pieces of discovery on RNA molecules to clinical applications of RNA therapeutics. We will then classify the mechanisms of RNA therapeutics from various classes in the treatment of diseases. To emphasize the huge potential of RNA therapies, we also provide the key RNA products that have been on clinical trials or already FDA-approved. With comprehensive knowledge on RNA biology, and the advances in analysis, technology and computer-aid science, RNA therapies can bring a promise to be more expanding to the market in the future.
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  • 文章类型: Systematic Review
    背景:癌症是导致死亡的主要原因,癌细胞由于长期暴露于补充化疗治疗而产生耐药性的易感性被称为多药耐药癌细胞(MDRC),这是恶性肿瘤治疗的一个重要障碍。由于补充药物失去了效力,近年来,开发潜在的替代和新颖的治疗方法已被提升为重中之重。在这种情况下,来自植物和动物来源的生物活性蛋白凝集素显示出具有巨大治疗潜力的抗癌药物的宝贵来源。
    目的:本手稿的主要目的是启发基于证据的(从1986年到2022年)使用凝集素替代治疗方法的可能分子机制,而不是用于癌症治疗的补充药物。
    方法:已适当遵循PRISMA规则,并系统地综合了定性和定量数据。文章是基于临床和临床前报告发表的凝集素,研究了深入的细胞机制,逆转药物综合肿瘤学,作为纳米携带的靶向递送。1986年至2022年对文章进行了系统筛选,并根据电子数据库搜索进行了筛选,Medline(PubMed),谷歌学者,WebofScience,百科全书,Scopus,和ClinicalTrials.gov数据库。
    结果:搜索发现了来自38个不同国家的4,212种出版物,其中170篇参考文章被用于我们的分析,在16种联合疗法及其作用方式中,包括剂量和作用机制的27项临床试验研究。纳入了属于28个不同家庭的30种凝集素的报告。根据一些临床和临床前报告,对凝集素的逆转机制和针对MDRC的替代疗法进行了严格的筛选,凝集素可以抑制过表达的基因,如P-53,EGFR,还有P-GP,MRP,和ABC转运蛋白与药物的细胞内运输有关。因为,药物外排机制导致MDRC,在这种现象中,凝集素在逆转外排机制中起关键作用。很少有临床前报道提到,凝集素与补充药物结合显示出协同作用,并且作为纳米药物载体有助于递送到靶向部位。
    结论:我们已经讨论了使用凝集素的替代疗法,并深入了解了对抗MDRC癌症的逆转耐药机制,增强功效,减少毒性和不良事件,并确保有针对性的交付,并对其在癌症诊断和预后方面的应用进行了讨论。然而,在药物开发和临床试验中需要进一步的研究,这可能有助于阐述MDRC癌症的逆转机制和开启新的治疗模式.
    BACKGROUND: Cancer is characterized as the leading cause of death, and the susceptibility of cancer cells to develop resistance due to long-term exposure to complementary chemotherapeutic treatment is referred to as multidrug resistance cancer cells (MDRC), which is a significant obstacle in the treatment of malignancies. Since complementary medicine lost its effectiveness, the development of potential alternative and novel therapeutic approaches has been elevated to a top priority in recent years. In this context, a bioactive protein lectin from plant and animal sources exhibits an invaluable source of anticancer agents with vast therapeutic potential.
    OBJECTIVE: This manuscript\'s primary purpose is to enlighten the evidence-based (from 1986 to 2022) possible molecular mechanism of alternative treatment approaches using lectins over the complementary medicines used for cancer treatment.
    METHODS: The PRISMA rules have been followed properly and qualitative and quantitative data are synthesized systematically. Articles were identified based on Clinical and preclinical reports published on lectin that investigated the in-depth cellular mechanisms, of reverse drug integrative oncology, as a nano-carried targeted delivery. Articles were systematically screened from 1986 to 2022 and selected based on electronic database searches, Medline (PubMed), Google Scholar, Web of Science, Encyclopaedias, Scopus, and ClinicalTrials.gov database.
    RESULTS: The search turned up 4,212 publications from 38 different nations, of which 170 reference articles were used in our analysis, in 16 combination therapy and their mode of action, and 27 clinical trial studies including dosage and mechanism of action were included. Reports from the 30 lectins belonging to 28 different families have been included. The reversal mechanism of lectin and alternative therapy against MDRC is critically screened and according to a few clinical and preclinical reports, lectin can suppress the overexpressing genes like P-53, EGFR, and P-gp, MRP, and ABC transporter proteins associated with intracellular transportation of drugs. Since, the drug efflux mechanism leads to MDRC, in this phenomenon, lectin plays a key role in reversing the efflux mechanism. Few preclinical reports have mentioned that lectin shows synergism in combination with complementary medicine and as a nano drug carrier helps to deliver to the targeted site.
    CONCLUSIONS: We have discussed the alternative therapy using lectin and an in-depth insight into the reversal drug resistance mechanisms to combat MDRC cancer, enhance the efficacy, reduce toxicity and adverse events, and ensure targeted delivery, and their application in the field of cancer diagnosis and prognosis has been discussed. However, further investigation is necessary in drug development and clinical trials which could be helpful to elaborate the reversal mechanism and unlock newer treatment modalities in MDRC cancer.
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  • 文章类型: Journal Article
    背景:病原菌中的抗生素耐药性已引起全球紧急情况,促使人们寻找另一种治疗方法。噬菌体是一个多世纪前发现的,并已被证明是抗生素治疗失败期间的成功替代品。本文综述了噬菌体治疗革兰氏阳性病原体的科学研究以及噬菌体治疗临床试验和商业化的总体前景。
    这篇综述旨在强调革兰氏阳性细菌中的噬菌体疗法以及将来对噬菌体疗法的需求。用于治疗革兰氏阳性细菌感染的噬菌体疗法使用了很长时间。然而,对革兰氏阳性细菌中噬菌体功效的评价有限。噬菌体对细菌菌株的天然效率和效力与其他非抗生素试剂相比是有利的。使用噬菌体治疗口腔生物膜,皮肤感染,近年来,由革兰氏阳性细菌引起的复发性感染已成为主要的研究领域。此外,噬菌体疗法领域的研究热潮为噬菌体疗法增加了大量的信息。
    结论:我们得出结论,噬菌体作为替代治疗的需求在未来是显而易见的。然而,噬菌体疗法可用作储备治疗。这篇综述着重于噬菌体疗法在治疗革兰氏阳性细菌感染中的潜在用途。以及他们的治疗方面。此外,我们讨论了噬菌体药物商业化的困难及其作为突破性药物的问题。
    BACKGROUND: Antibiotic resistance among pathogenic bacteria has created a global emergency, prompting the hunt for an alternative cure. Bacteriophages were discovered over a century ago and have proven to be a successful replacement during antibiotic treatment failure. This review discusses on the scientific investigation of phage therapy for Gram-positive pathogens and general outlook of phage therapy clinical trials and commercialization.
    UNASSIGNED: This review aimed to highlight the phage therapy in Gram-positive bacteria and the need for phage therapy in the future. Phage therapy to treat Gram-positive bacterial infections is in use for a very long time. However, limited review on the phage efficacy in Gram-positive bacteria exists. The natural efficiency and potency of bacteriophages against bacterial strains have been advantageous amidst the other non-antibiotic agents. The use of phages to treat oral biofilm, skin infection, and recurrent infections caused by Gram-positive bacteria has emerged as a predominant research area in recent years. In addition, the upsurge in research in the area of phage therapy for spore-forming Gram-positive bacteria has added a wealth of information to phage therapy.
    CONCLUSIONS: We conclude that the need of phage as an alternative treatment is obvious in future. However, phage therapy can be used as reserve treatment. This review focuses on the potential use of phage therapy in treating Gram-positive bacterial infections, as well as their therapeutic aspects. Furthermore, we discussed the difficulties in commercializing phage drugs and their problems as a breakthrough medicine.
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  • 文章类型: Journal Article
    背景:抗生素抗性细菌构成全球健康威胁。传统抗生素会失去效力,近年来,开发新型有效的抗菌药物已成为当务之急。在这个领域,植物代表了具有巨大治疗潜力的抗菌化合物的宝贵来源。
    目的:回顾植物抗菌药物的全部可能范围(植物化合物,提取物和精油)从2016年到2021年发现,以及它们降低细菌耐药性的潜力。他们对抗细菌的活动,特别强调多重耐药细菌,行动机制,与传统抗生素的可能组合,讨论了在当前医学中的作用和未来的前景。
    方法:对植物源化合物的抗菌活性及其对细菌作用机理的研究进行了鉴定和总结,包括2016年1月至2021年1月的捐款。使用PubMed搜索引擎以及相关关键字和运算符从Medline数据库中提取文章。
    结果:搜索产生了来自149个国家的11,689篇文章,其中101篇文章被纳入这篇综述。包括来自20个家庭的41种植物化学物质的报告。还包括来自17个科的39种植物的植物提取物和精油的报告。多酚和萜烯是研究的最活跃的植物化学物质,单独或作为植物提取物或精油的一部分。质膜破坏是最常见的抗菌作用机制。酚羟基的数量和位置,双键,在类黄酮的情况下,离域电子和与糖的共轭似乎对抗菌能力至关重要。植物化学物质与β-内酰胺抗生素的组合是研究最多的,外排泵的抑制是最常见的协同机制。
    结论:近年来,萜烯,黄酮,黄酮醇和一些生物碱和苯丙素,分离或作为提取物的一部分,已经显示出有希望的抗菌活性,被膜破坏它们最常见的机制。然而,需要通过新的组学技术和网络药理学来提高它们作为适当抗微生物药物的利用率,以找到其中最有效的组合或与抗生素的组合。
    BACKGROUND: Antibiotic-resistant bacteria pose a global health threat. Traditional antibiotics can lose their effectiveness, and the development of novel effective antimicrobials has become a priority in recent years. In this area, plants represent an invaluable source of antimicrobial compounds with vast therapeutic potential.
    OBJECTIVE: To review the full possible spectrum of plant antimicrobial agents (plant compounds, extracts and essential oils) discovered from 2016 to 2021 and their potential to decrease bacterial resistance. Their activities against bacteria, with special emphasis on multidrug resistant bacteria, mechanisms of action, possible combinations with traditional antibiotics, roles in current medicine and future perspectives are discussed.
    METHODS: Studies focusing on the antimicrobial activity of compounds of plant origin and their mechanism of action against bacteria were identified and summarized, including contributions from January 2016 until January 2021. Articles were extracted from the Medline database using PubMed search engine with relevant keywords and operators.
    RESULTS: The search yielded 11,689 articles from 149 countries, of which 101 articles were included in this review. Reports from 41 phytochemicals belonging to 20 families were included. Reports from plant extracts and essential oils from 39 plant species belonging to 17 families were also included. Polyphenols and terpenes were the most active phytochemicals studied, either alone or as a part of plant extracts or essential oils. Plasma membrane disruption was the most common mechanism of antimicrobial action. Number and position of phenolic hydroxyl groups, double bonds, delocalized electrons and conjugation with sugars in the case of flavonoids seemed to be crucial for antimicrobial capacity. Combinations of phytochemicals with beta-lactam antibiotics were the most studied, and the inhibition of efflux pumps was the most common synergistic mechanism.
    CONCLUSIONS: In recent years, terpenes, flavones, flavonols and some alkaloids and phenylpropanoids, either isolated or as a part of extracts, have shown promising antimicrobial activity, being membrane disruption their most common mechanism. However, their utilization as appropriate antimicrobials need to be boosted by means of new omics technologies and network pharmacology to find the most effective combinations among them or in combination with antibiotics.
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  • 文章类型: Journal Article
    印度尼西亚的心态一直专注于使用天然药物,食物,和治愈的做法被国家的文化广泛认可。传统医学中使用的传统药物和草药通常会导致发现针对某些疾病的药物。这篇综述的目的是研究关于Sembung植物重要性的循证数据,Blumeabalsamifera,作为一种潜在的传统医学。分布,民族药理学,次生代谢产物,和对几种疾病的生物活性是本综述的重点。使用术语“B.”搜索与Sembung工厂相关的信息和研究。balsamifera,\"\"植物化学物质,“和”药理活性“关于研究之门,谷歌学者,科学直接,PubMed,和2020年之前基于科学信息的数据库。一些民族医学文章推荐B.balsamifera治疗鼻窦炎,绞痛,咳嗽,肾结石,流感,或者作为利尿剂.这些知识已经在东南亚的几个国家得到了应用。B.balsamifera已被报道含有几种植物化学物质挥发性(萜类,脂肪酸,酚类物质,酒精,醛类,醚,酮,吡啶,呋喃,和烷烃)和非挥发性(类黄酮,黄烷酮,和查尔酮)。B.balsamifera的提取物和植物化学物质含有几种生物能力,如抗氧化剂,抗菌,抗真菌药,抗炎,降血脂,抗不孕,肝保护活性,抗糖尿病药,胃保护,抗肿瘤,抗癌,和针对冠状病毒病-19感染的免疫调节剂。这篇综述为balsamifica作为营养食品或未来药物制剂的潜在应用提供了必要的数据。
    Indonesia\'s mindset has been focusing on the use of natural medicines, food, and healing practices widely recognized by the nation\'s culture. Traditional medicines and herbs used in traditional medicine can often lead to the discovery of drugs against certain diseases. The aim of this review was to study evidence-based data on the importance of Sembung plant, Blumea balsamifera, as a potential traditional medicine. The distribution, ethnopharmacology, secondary metabolites, and bioactivity against several diseases are focused in this review. Information and research related to Sembung plant were searched using the terms \"B. balsamifera,\" \"phytochemicals,\" and \"pharmacological activity\" on ResearchGate, Google Scholar, Science Direct, PubMed, and scientific information-based databases up to 2020. Several ethnomedical articles recommend B. balsamifera for the treatment of sinusitis, colic pain, cough, kidney stones, flu, or as a diuretic. This knowledge has already been applied in several countries in Southeast Asia. B. balsamifera has been reported to contain several phytochemicals both volatile (terpenoids, fatty acids, phenols, alcohol, aldehydes, ethers, ketones, pyridines, furans, and alkanes) and non-volatile (flavonoids, flavanones, and chalcones). Extracts and phytochemicals of B. balsamifera contain several biological capacities such as antioxidant, antimicrobial, antifungal, anti-inflammatory, hypolipidemic, anti-infertility, hepatoprotective activity, antidiabetic, gastroprotective, antitumor, anticancer, and immunomodulatory agent against Coronavirus disease-19 infection. This review provides essential data for the potential application of B. balsamifera as a nutraceutical or in future medicinal preparations.
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  • 文章类型: Journal Article
    噬菌体是有前途的抗菌剂。尽管它们已被认为是细菌病毒,并且被认为与真核细胞不相互作用,越来越多的证据表明,噬菌体可能通过与巨噬细胞的相互作用对免疫系统产生重大影响,中性粒细胞,和T细胞极化。在这项研究中,podovirus噬菌体的影响,siphovirus,研究了肌病毒形态对CD-1小鼠体液免疫的影响。此外,在这些小鼠中测试了噬菌体的组织分布。在小鼠噬菌体的分布或注射噬菌体后小鼠血清中细胞因子水平的变化中都没有发现共同的模式。重要的是,免疫前在小鼠中鉴定出预先存在的IgM类抗体,该抗体针对具有肌病毒和syphovirus形态型的噬菌体的衣壳蛋白.用无任何佐剂的噬菌体对CD1小鼠进行三重免疫后,抗噬菌体血清多克隆IgG抗体水平升高。使用蛋白质印迹分析和质谱鉴定由IgM和/或IgG抗体识别的免疫原性噬菌体蛋白。此外,免疫后收集的小鼠血清证明了中和特性,导致所研究的噬菌体的传染性大幅下降。此外,在施用这些噬菌体之前收集的血清样品显示出降低噬菌体感染性的一些能力。此外,具有podovirus形态型的变形杆菌噬菌体PM16在免疫小鼠中没有引起IgM或IgG抗体,免疫前后,小鼠血清样品中均未发现对PM16的中和活性。
    Bacteriophages are promising antibacterial agents. Although they have been recognized as bacterial viruses and are considered to be non-interacting with eukaryotic cells, there is growing evidence that phages may have a significant impact on the immune system via interactions with macrophages, neutrophils, and T-cell polarization. In this study, the influence of phages of podovirus, siphovirus, and myovirus morphotypes on humoral immunity of CD-1 mice was investigated. In addition, tissue distribution of the phages was tested in these mice. No common patterns were found either in the distribution of phages in mice or in changes in the levels of cytokines in the sera of mice once injected with phages. Importantly, pre-existing IgM-class antibodies directed against capsid proteins of phages with myovirus and siphovirus morphotypes were identified in mice before immunization. After triple immunization of CD1-mice with phages without any adjuvant, levels of anti-phage serum polyclonal IgG antibodies increased. Immunogenic phage proteins recognized by IgM and/or IgG antibodies were identified using Western blot analysis and mass spectrometry. In addition, mice serum collected after immunization demonstrated neutralizing properties, leading to a substantial decrease in infectivity of investigated phages with myovirus and siphovirus morphotypes. Moreover, serum samples collected before administration of these phages exhibited some ability to reduce the phage infectivity. Furthermore, Proteus phage PM16 with podovirus morphotype did not elicit IgM or IgG antibodies in immunized mice, and no neutralizing activities against PM16 were revealed in mouse serum samples before and after immunization.
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  • 文章类型: Journal Article
    耐药菌对全球人类健康构成严重威胁。目前的抗生素正在失去功效,迫切需要新的抗微生物剂。活生物体是抗菌化合物的宝贵来源。最具代表性的动物天然产物的抗菌活性,细菌,本文对真菌和植物起源进行了综述。他们对耐药细菌的活性,他们的行动机制,抵抗他们的可能发展,讨论了他们在当前医学中的作用和未来的前景。电子数据库,如PubMed,Scopus和ScienceDirect用于搜索科学贡献,直到2020年9月,使用相关关键字。异质来源的天然化合物已被证明具有抗菌能力,包括对抗抗生素抗性细菌.最常见的抗微生物作用机制与蛋白质生物合成和细胞壁和膜的改变有关。各种天然化合物,尤其是植物化学物质,已显示出与抗生素的协同能力。关于开发针对天然抗微生物化合物的特异性抗性机制的文献很少。新技术,如组学,网络药理学和信息学有可能在未来鉴定和表征新的天然抗菌化合物。这些知识可能有助于制定未来的治疗策略。
    Drug-resistant bacteria pose a serious threat to human health worldwide. Current antibiotics are losing efficacy and new antimicrobial agents are urgently needed. Living organisms are an invaluable source of antimicrobial compounds. The antimicrobial activity of the most representative natural products of animal, bacterial, fungal and plant origin are reviewed in this paper. Their activity against drug-resistant bacteria, their mechanisms of action, the possible development of resistance against them, their role in current medicine and their future perspectives are discussed. Electronic databases such as PubMed, Scopus and ScienceDirect were used to search scientific contributions until September 2020, using relevant keywords. Natural compounds of heterogeneous origins have been shown to possess antimicrobial capabilities, including against antibiotic-resistant bacteria. The most commonly found mechanisms of antimicrobial action are related to protein biosynthesis and alteration of cell walls and membranes. Various natural compounds, especially phytochemicals, have shown synergistic capacity with antibiotics. There is little literature on the development of specific resistance mechanisms against natural antimicrobial compounds. New technologies such as -omics, network pharmacology and informatics have the potential to identify and characterize new natural antimicrobial compounds in the future. This knowledge may be useful for the development of future therapeutic strategies.
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  • 文章类型: Journal Article
    由于纳米材料对诊断和治疗的潜在益处,它们广泛用于医疗应用和个人护理产品。纳米材料的相互作用,尺寸非常小,用组织,细胞和微环境,可以揭示在生物有机体中化学上相同和更大的对应物无法产生的有害影响。在这次审查中,对未来医学的挑战,讨论了纳米材料的纳米毒性。
    对相关文献进行了详细的综述,并根据纳米材料的医学应用对其毒性进行了评估。
    大多数作者说“在下一个时代,唯一有效的技术将是纳米技术”;然而,关于这项技术对人类的影响没有共识,环境与生态平衡。关于纳米材料对人类健康的毒性作用的研究也随着技术的发展而变化。纳米毒理学研究,如在3D人体器官的体内,细胞,先进的基因研究,和-组学方法开始取代传统方法。纳米材料在暴露生产者中的纳米毒性和不利影响,行业工人,患者将纳米材料变成未来医学的双刃剑。为了控制和应对相关风险,应该实施法规和立法,研究人员必须在医学的各个领域进行联合多学科研究,纳米技术,纳米医学,和生物医学工程。
    Due to nanomaterials’ potential benefits for diagnosis and treatment, they are widely used in medical applications and personal care products. Interaction of nanomaterials, which are very small in size, with tissue, cell and microenvironment, can reveal harmful effects that cannot be created with chemically identical and larger counterparts in biological organisms. In this review, a challenge for future medicine, nanotoxicity of nanomaterials is discussed.
    A detailed review of related literature was performed and evaluated as per medical applications of nanomaterials their toxicity.
    Most authors state “the only valid technology will be nanotechnology in the next era”; however, there is no consensus on the impact of this technology on humankind, environment and ecological balance. Studies dealing with the toxic effect of nanomaterials on human health have also varied with developing technology. Nanotoxicology studies such as in vivo-like on 3D human organs, cells, advanced genetic studies, and -omic approaches begin to replace conventional methods. Nanotoxicity and adverse effects of nanomaterials in exposed producers, industry workers, and patients make nanomaterials a double-edged sword for future medicine. In order to control and tackle related risks, regulation and legislations should be implemented, and researchers have to conduct joint multidisciplinary studies in various fields of medical sciences, nanotechnology, nanomedicine, and biomedical engineering.
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