首页 > 最新文献

Current Drug Therapy最新文献

英文 中文
Nanosphere Precision: Emulsomes Revolutionizing Cancer Targeted Therapy 纳米球精度:乳状液为癌症靶向治疗带来革命性变革
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-06-07 DOI: 10.2174/0115748855299918240529063242
Meghna Dheek, Shikha Baghel Chauhan, Indu Singh
Emulsomes have gained attention because they are a novel lipoidal vesicular system thathas an internal solid fat core surrounded by a phospholipid bilayer. Cancer is a complex and broadterm that refers to a group of diseases characterized by the uncontrolled growth and spread of abnormalcells in the body. In the context of cancer targeting, emulsomes have shown promising potentialdue to their ability to improve the solubility, stability, and bioavailability of anticancer drugs, leadingto enhanced therapeutic efficacy and reduced systemic toxicity.This article addresses emulsomal composition, preparation techniques, and different kinds of emulsomesloaded with drugs like fluvastatin and raloxifene hydrochloride to target cancer cells. The useof emulsomes in cancer targeting holds great promise for improving the precision, efficacy, and safetyof cancer treatments.A comprehensive search of relevant scientific literature was performed. This involved searching databasessuch as PubMed, Scopus, Web of Science, and others to identify relevant studies, articles,and reviews related to the topic.Emulsomes loaded with specific drugs show promising results in cancer treatment. Examples includepiceatannol-loaded emulsomes for colon cancer, raloxifene hydrochloride-loaded emulsomes forbreast cancer, and fluvastatin-loaded emulsomes for prostate cancer.Emulsomes represent a cutting-edge approach to cancer drug delivery, offering a versatile and effectivesolution to address challenges associated with traditional anticancer formulations. Ongoing researchholds promise for the continued development of personalized cancer therapy.
乳状液体是一种新型的类脂囊泡系统,内部有一个由磷脂双分子层包围的固体脂肪核心,因此备受关注。癌症是一个复杂而宽泛的术语,指的是一组以异常细胞在体内不受控制地生长和扩散为特征的疾病。在癌症靶向治疗方面,乳状液因其能够提高抗癌药物的溶解度、稳定性和生物利用度,从而提高疗效并降低全身毒性,已显示出广阔的应用前景。本文介绍了乳状液的组成、制备技术,以及不同类型的乳状液载药(如氟伐他汀和盐酸雷洛昔芬)靶向治疗癌细胞的情况。乳状液在癌症靶向治疗中的应用为提高癌症治疗的精确性、有效性和安全性带来了巨大希望。我们对相关科学文献进行了全面搜索,包括搜索 PubMed、Scopus、Web of Science 等数据库,以确定与该主题相关的研究、文章和综述。乳状液是治疗癌症药物递送的前沿方法,为解决传统抗癌制剂所面临的挑战提供了一种多用途的有效解决方案。正在进行的研究为继续开发个性化癌症疗法带来了希望。
{"title":"Nanosphere Precision: Emulsomes Revolutionizing Cancer Targeted Therapy","authors":"Meghna Dheek, Shikha Baghel Chauhan, Indu Singh","doi":"10.2174/0115748855299918240529063242","DOIUrl":"https://doi.org/10.2174/0115748855299918240529063242","url":null,"abstract":"\u0000\u0000Emulsomes have gained attention because they are a novel lipoidal vesicular system that\u0000has an internal solid fat core surrounded by a phospholipid bilayer. Cancer is a complex and broad\u0000term that refers to a group of diseases characterized by the uncontrolled growth and spread of abnormal\u0000cells in the body. In the context of cancer targeting, emulsomes have shown promising potential\u0000due to their ability to improve the solubility, stability, and bioavailability of anticancer drugs, leading\u0000to enhanced therapeutic efficacy and reduced systemic toxicity.\u0000This article addresses emulsomal composition, preparation techniques, and different kinds of emulsomes\u0000loaded with drugs like fluvastatin and raloxifene hydrochloride to target cancer cells. The use\u0000of emulsomes in cancer targeting holds great promise for improving the precision, efficacy, and safety\u0000of cancer treatments.\u0000A comprehensive search of relevant scientific literature was performed. This involved searching databases\u0000such as PubMed, Scopus, Web of Science, and others to identify relevant studies, articles,\u0000and reviews related to the topic.\u0000Emulsomes loaded with specific drugs show promising results in cancer treatment. Examples include\u0000piceatannol-loaded emulsomes for colon cancer, raloxifene hydrochloride-loaded emulsomes for\u0000breast cancer, and fluvastatin-loaded emulsomes for prostate cancer.\u0000Emulsomes represent a cutting-edge approach to cancer drug delivery, offering a versatile and effective\u0000solution to address challenges associated with traditional anticancer formulations. Ongoing research\u0000holds promise for the continued development of personalized cancer therapy.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141373225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exploring the Synergistic Antimicrobial Potential of Garlic and Honey: AComprehensive Review 探索大蒜和蜂蜜的协同抗菌潜力:综合评述
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-06-06 DOI: 10.2174/0115748855287440240529080448
Priti Yadav, Surendra Lalwani, D. Chanchal, Nidhi Mittal, Jitendra Singh Chaudhary
This article explores the well-established therapeutic attributes of honey and garlic,renowned for their potent antibacterial effects. This investigation aims to elucidate the synergisticantibacterial potential resulting from the combined use of these two natural substances.A comprehensive examination of honey's antibacterial and antifungal characteristics is conducted, delineating its intricate mechanism of action with a focus on hydrogen peroxide and otherphytochemicals. Simultaneously, various processes underpinning the antibacterial properties of garlicare discussed, with particular emphasis on its key bioactive component, allicin.This research unveils a novel perspective on the interaction between honey and garlic. It isintricately analyzed how garlic's bioactive components disrupt microbial cell membranes, whilehoney employs diverse tactics to combat illnesses. This interaction opens new possibilities for modernantibacterial approaches.Quantitative findings and the significance of the study are discussed in detail. The practical applications of the synergistic antibacterial potential are underscored, emphasizing its relevancein food preservation and medicinal contexts. The research accentuates the promising use of garlic andhoney blends as natural alternatives to artificial preservatives, with implications for wound care andinfection prevention.Emphasizing the valuable applications of synergistic antibacterial potential across diverse industries, including food preservation and medicine, this study underscores the importance ofharnessing the combined antibacterial qualities of garlic and honey as a sustainable solution to emerging challenges in food safety and health.
本文探讨了蜂蜜和大蒜久负盛名的治疗特性,这两种天然物质具有强大的抗菌功效。文章对蜂蜜的抗菌和抗真菌特性进行了全面的研究,并以过氧化氢和其他植物化学物质为重点,描述了其复杂的作用机制。同时,还讨论了大蒜抗菌特性的各种基本过程,特别强调了大蒜的关键生物活性成分大蒜素。该研究揭示了大蒜与蜂蜜相互作用的新视角,深入分析了大蒜的生物活性成分如何破坏微生物细胞膜,而蜂蜜又如何采用多种策略来抗击疾病。详细讨论了研究的定量结果和意义。详细讨论了研究的定量发现和意义,强调了协同抗菌潜力的实际应用,并强调了其在食品保鲜和医药方面的相关性。该研究强调了大蒜和蜂蜜混合物作为人工防腐剂天然替代品的应用前景,对伤口护理和感染预防具有重要意义。该研究强调了协同抗菌潜力在食品保鲜和医药等不同行业中的宝贵应用,强调了利用大蒜和蜂蜜的综合抗菌特性作为应对食品安全和健康领域新挑战的可持续解决方案的重要性。
{"title":"Exploring the Synergistic Antimicrobial Potential of Garlic and Honey: A\u0000Comprehensive Review","authors":"Priti Yadav, Surendra Lalwani, D. Chanchal, Nidhi Mittal, Jitendra Singh Chaudhary","doi":"10.2174/0115748855287440240529080448","DOIUrl":"https://doi.org/10.2174/0115748855287440240529080448","url":null,"abstract":"\u0000\u0000This article explores the well-established therapeutic attributes of honey and garlic,\u0000renowned for their potent antibacterial effects. This investigation aims to elucidate the synergistic\u0000antibacterial potential resulting from the combined use of these two natural substances.\u0000\u0000\u0000\u0000A comprehensive examination of honey's antibacterial and antifungal characteristics is conducted, delineating its intricate mechanism of action with a focus on hydrogen peroxide and other\u0000phytochemicals. Simultaneously, various processes underpinning the antibacterial properties of garlic\u0000are discussed, with particular emphasis on its key bioactive component, allicin.\u0000\u0000\u0000\u0000This research unveils a novel perspective on the interaction between honey and garlic. It is\u0000intricately analyzed how garlic's bioactive components disrupt microbial cell membranes, while\u0000honey employs diverse tactics to combat illnesses. This interaction opens new possibilities for modern\u0000antibacterial approaches.\u0000\u0000\u0000\u0000Quantitative findings and the significance of the study are discussed in detail. The practical applications of the synergistic antibacterial potential are underscored, emphasizing its relevance\u0000in food preservation and medicinal contexts. The research accentuates the promising use of garlic and\u0000honey blends as natural alternatives to artificial preservatives, with implications for wound care and\u0000infection prevention.\u0000\u0000\u0000\u0000Emphasizing the valuable applications of synergistic antibacterial potential across diverse industries, including food preservation and medicine, this study underscores the importance of\u0000harnessing the combined antibacterial qualities of garlic and honey as a sustainable solution to emerging challenges in food safety and health.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141377251","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Current Treatment Approaches for Alzheimer’s Disease and Possible Drug Targets 阿尔茨海默病的现有治疗方法和可能的药物靶点
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-06-04 DOI: 10.2174/0115748855307998240529063710
Ashutosh Ranjan, Shashikesh Shukla, Shamsher Singh
Alzheimer's disease is a neurological condition that is becoming increasingly common andis typified by dementia. Drug development for AD is a major issue with a startlingly high failure ratedespite a marked increase in the frequency of the disease linked to genetic factors. As AD is the mostcommon neurological illness and contributes to both the high patient burden and the cost ofhealthcare, this issue must be addressed.The current manuscript aims to focus on the current treatment approaches of newer drugs under clinicaltrials of Alzheimer’s disease by targeting the various pathological pathways that are involved inAD.Data provided in this review are from literature surveys and ongoing clinical trials from reputedsearch engines like PubMed, ResearchGate, Science Direct, and Google Scholar, as well as fromvarious respected authors and—registered websites such as memory.ucsf.edu/genetics/familial-Alzheimer’s-disease and https://www.clinicaltrials.gov.There are diverse forms of drugs and multiple pathways on which many advancements and clinicaltrials have been conductedand are undergoing. Various investigations and studies are going on.There are different pathogenesis of AD, such as Tau, vascular, Amyloid β, estrogen deficiency, andthe role of gut microbiota in AD. Donepezil, Rivastigmine, etc., are currently used for treatment, andcertain drugs are in different stages of clinical trials, such as ANI792, ACC-001, CAD106 &ABvac40,and it is concluded that after successful trials of the new drugs, they can be used for the treatmentof AD with maximum benefits and less side effect.
阿尔茨海默病是一种日益常见的神经系统疾病,以痴呆症为典型特征。阿兹海默症的药物研发是一个重大问题,尽管该病的发病率与遗传因素有关,但失败率却高得惊人。本手稿旨在针对阿尔茨海默病的各种病理途径,重点介绍目前正在进行临床试验的新型药物的治疗方法。本综述提供的数据来自文献调查和正在进行的临床试验,这些数据来自PubMed、ResearchGate、Science Direct和Google Scholar等知名搜索引擎,以及各种受人尊敬的作者和注册网站,如memory.ucsf.edu/genetics/familial-Alzheimer's-disease和https://www.clinicaltrials.gov.There,这些药物和途径形式多样,已经取得了许多进展,并正在进行临床试验。AD 的发病机制多种多样,如 Tau、血管、淀粉样蛋白 β、雌激素缺乏以及肠道微生物群在 AD 中的作用。多奈哌齐(Donepezil)、利伐斯的明(Rivastigmine)等药物目前已被用于治疗,某些药物正处于不同的临床试验阶段,如 ANI792、ACC-001、CAD106 和ABvac40,这些新药试验成功后,可用于治疗 AD,且疗效显著,副作用较小。
{"title":"Current Treatment Approaches for Alzheimer’s Disease and Possible Drug Targets","authors":"Ashutosh Ranjan, Shashikesh Shukla, Shamsher Singh","doi":"10.2174/0115748855307998240529063710","DOIUrl":"https://doi.org/10.2174/0115748855307998240529063710","url":null,"abstract":"\u0000\u0000Alzheimer's disease is a neurological condition that is becoming increasingly common and\u0000is typified by dementia. Drug development for AD is a major issue with a startlingly high failure rate\u0000despite a marked increase in the frequency of the disease linked to genetic factors. As AD is the most\u0000common neurological illness and contributes to both the high patient burden and the cost of\u0000healthcare, this issue must be addressed.\u0000The current manuscript aims to focus on the current treatment approaches of newer drugs under clinical\u0000trials of Alzheimer’s disease by targeting the various pathological pathways that are involved in\u0000AD.\u0000Data provided in this review are from literature surveys and ongoing clinical trials from reputed\u0000search engines like PubMed, ResearchGate, Science Direct, and Google Scholar, as well as from\u0000various respected authors and—registered websites such as memory.ucsf.edu/genetics/familial-Alzheimer’s-\u0000disease and https://www.clinicaltrials.gov.\u0000There are diverse forms of drugs and multiple pathways on which many advancements and clinical\u0000trials have been conductedand are undergoing. Various investigations and studies are going on.\u0000There are different pathogenesis of AD, such as Tau, vascular, Amyloid β, estrogen deficiency, and\u0000the role of gut microbiota in AD. Donepezil, Rivastigmine, etc., are currently used for treatment, and\u0000certain drugs are in different stages of clinical trials, such as ANI792, ACC-001, CAD106 &ABvac40,\u0000and it is concluded that after successful trials of the new drugs, they can be used for the treatment\u0000of AD with maximum benefits and less side effect.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141386881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fabrication and Characterization of Sustained-Release Eudragit RSPOMicrosphere of Lornoxicam by Spray Drying Technique 利用喷雾干燥技术制备缓释洛诺昔康的 Eudragit RSPOMicrosphere 并确定其特性
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-05-10 DOI: 10.2174/0115748855294736240502073344
Hiren V. Patel, Nayankumar C. Ratnakar, Himanshu Paliwal, B. Prajapati
Lornoxicam is a potent non-steroidal anti-inflammatory drug (NSAID) withstrong analgesic properties; however, its short half-life necessitates frequent administration for sustained efficacy.The objective of the present study was to identify critical formulation parameters affectingsustained release Eudragit RSPO microsphere of lornoxicam employing the concept of design of experimentsThe lornoxicam-loaded microspheres were prepared using a spray drying technique by optimizing the drug:polymer ratio(X1) and inlet air temperature (X2) using a 32 full factorial design.The percentage drug entrapment (Y1), percentage yield (Y2) and cumulative percentage of the drugdissolved at 18 hr (Y3) were selected as dependent variables. Microspheres were evaluated for percentage drug entrapment, mean particle size, percentage yield, in vitro drug release study and scanning electron microscopy (SEM).The optimized batch showed 84.51% drug release after 18 h with significantly higher drugentrapment and percentage yield. The optimization was further verified using overlay and desirabilityplots. The sustained release behavior of the drug from microspheres in GIT was displayed. The predicted and observed responses for the optimized formulation were in close agreement with the releaseprofile of the drug.The sustained release microspheres of lornoxicam may prove to be an effective analgesicwith excellent anti-inflammatory potential.
洛诺昔康是一种强效非甾体抗炎药(NSAID),具有很强的镇痛特性;然而,它的半衰期很短,需要频繁给药才能保持药效。本研究的目的是利用实验设计的概念,确定影响洛诺昔康 Eudragit RSPO 微球持续释放的关键配方参数。本研究采用喷雾干燥技术,通过优化药物:聚合物比例(X1)和进气温度(X2),采用 32 全因子设计法制备了负载洛诺昔康的微球。对微球进行了药物夹带率、平均粒径、产率、体外药物释放研究和扫描电子显微镜(SEM)评估。使用叠加图和可取图进一步验证了优化结果。显示了微球在胃肠道中的药物持续释放行为。洛诺昔康的缓释微球可能被证明是一种有效的镇痛药,具有很好的抗炎潜力。
{"title":"Fabrication and Characterization of Sustained-Release Eudragit RSPO\u0000Microsphere of Lornoxicam by Spray Drying Technique","authors":"Hiren V. Patel, Nayankumar C. Ratnakar, Himanshu Paliwal, B. Prajapati","doi":"10.2174/0115748855294736240502073344","DOIUrl":"https://doi.org/10.2174/0115748855294736240502073344","url":null,"abstract":"\u0000\u0000Lornoxicam is a potent non-steroidal anti-inflammatory drug (NSAID) with\u0000strong analgesic properties; however, its short half-life necessitates frequent administration for sustained efficacy.\u0000\u0000\u0000\u0000The objective of the present study was to identify critical formulation parameters affecting\u0000sustained release Eudragit RSPO microsphere of lornoxicam employing the concept of design of experiments\u0000\u0000\u0000\u0000The lornoxicam-loaded microspheres were prepared using a spray drying technique by optimizing the drug:polymer ratio(X1) and inlet air temperature (X2) using a 32 full factorial design.\u0000The percentage drug entrapment (Y1), percentage yield (Y2) and cumulative percentage of the drug\u0000dissolved at 18 hr (Y3) were selected as dependent variables. Microspheres were evaluated for percentage drug entrapment, mean particle size, percentage yield, in vitro drug release study and scanning electron microscopy (SEM).\u0000\u0000\u0000\u0000The optimized batch showed 84.51% drug release after 18 h with significantly higher drug\u0000entrapment and percentage yield. The optimization was further verified using overlay and desirability\u0000plots. The sustained release behavior of the drug from microspheres in GIT was displayed. The predicted and observed responses for the optimized formulation were in close agreement with the release\u0000profile of the drug.\u0000\u0000\u0000\u0000The sustained release microspheres of lornoxicam may prove to be an effective analgesic\u0000with excellent anti-inflammatory potential.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140994097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oligohydramnios and Intrauterine Premature Closure of Ductus Arteriosus Associated with the Use of NSAIDs During Pregnancy – An Overview of Clinical Evidence 与孕期使用非甾体抗炎药有关的少子畸形和宫内动脉导管早闭--临床证据综述
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-24 DOI: 10.2174/0115748855308697240409035903
Naina Mohamed Pakkir Maideen, Sultan Al Rashid, M. Gobinath, Mohamed Harshath Jahir Hussain
Pregnant women may experience low back pain and other pain symptoms,fever, and inflammatory conditions that may harm the fetus and mother if left untreated. The mostcommon uses of non-steroidal anti-inflammatory drugs (NSAIDs) are the treatment of inflammation,pain and pyrexia. However, after 20-30 weeks of gestation, using NSAIDs during pregnancy maycause oligohydramnios and premature ductus arteriosus closure, which could harm the developingfetus.The purpose of this review article is to critically examine the clinical evidence that iscurrently available for oligohydramnios and premature ductus arteriosus closure linked to NSAIDs.Online databases such as Medline/Pubmed/PMC, EBSCOhost, Scopus, Web of science,Embase, Science Direct, Google Scholar, and reference lists were searched to identify articles whichdealt with NSAIDs-associated oligohydramnios and premature closure of ductus arteriosus.Numerous regulatory agencies released warnings about oligohydramnios and premature closureof ductus arteriosus linked to NSAIDs. Furthermore, a number of case reports, case series, andsome observational studies have also been published about the possibility of oligohydramnios andpremature closure of ductus arteriosus linked to NSAIDs use.Women who are pregnant for 20 weeks or more should refrain from self-medicatingwith NSAIDs without consulting a pharmacist or a physician. The use of NSAIDs during pregnancyshould carefully be considered due to potential risks to the mother and developing fetus, especiallyafter 20-30 weeks of gestation. To guarantee the best possible health for the expectant mother and theunborn child, healthcare professionals should weigh the benefits and risks and look into alternateoptions. Pregnant women may opt for acetaminophen (paracetamol) to relieve pain and fever duringpregnancy. Pregnant women should seek medical attention if there is persisting pain for more thanthree days.
孕妇可能会出现腰痛和其他疼痛症状、发烧和炎症,如果不及时治疗,可能会对胎儿和母亲造成伤害。非甾体抗炎药(NSAIDs)最常见的用途是治疗炎症、疼痛和热病。然而,在妊娠 20-30 周后,在孕期使用非甾体抗炎药可能会导致少尿症和动脉导管早闭,这可能会对发育中的胎儿造成伤害。我们检索了 Medline/Pubmed/PMC、EBSCOhost、Scopus、Web of science、Embase、Science Direct、Google Scholar 等在线数据库和参考文献列表,以确定与非甾体抗炎药相关的少尿症和动脉导管过早闭合的文章。此外,一些病例报告、系列病例和一些观察性研究也已发表,说明使用非甾体抗炎药可能会导致少子畸形和动脉导管早闭。怀孕 20 周或更长时间的妇女应避免在未咨询药剂师或医生的情况下自行服用非甾体抗炎药。由于非甾体抗炎药对母亲和发育中的胎儿(尤其是妊娠 20-30 周后的胎儿)有潜在风险,因此在怀孕期间使用非甾体抗炎药应慎重考虑。为了保证孕妇和胎儿的最佳健康状况,医护人员应权衡其益处和风险,并考虑其他选择。孕妇可以选择对乙酰氨基酚(扑热息痛)来缓解孕期疼痛和发烧。如果疼痛持续超过三天,孕妇应及时就医。
{"title":"Oligohydramnios and Intrauterine Premature Closure of Ductus Arteriosus Associated with the Use of NSAIDs During Pregnancy – An Overview of Clinical Evidence","authors":"Naina Mohamed Pakkir Maideen, Sultan Al Rashid, M. Gobinath, Mohamed Harshath Jahir Hussain","doi":"10.2174/0115748855308697240409035903","DOIUrl":"https://doi.org/10.2174/0115748855308697240409035903","url":null,"abstract":"\u0000\u0000Pregnant women may experience low back pain and other pain symptoms,\u0000fever, and inflammatory conditions that may harm the fetus and mother if left untreated. The most\u0000common uses of non-steroidal anti-inflammatory drugs (NSAIDs) are the treatment of inflammation,\u0000pain and pyrexia. However, after 20-30 weeks of gestation, using NSAIDs during pregnancy may\u0000cause oligohydramnios and premature ductus arteriosus closure, which could harm the developing\u0000fetus.\u0000\u0000\u0000\u0000The purpose of this review article is to critically examine the clinical evidence that is\u0000currently available for oligohydramnios and premature ductus arteriosus closure linked to NSAIDs.\u0000\u0000\u0000\u0000Online databases such as Medline/Pubmed/PMC, EBSCOhost, Scopus, Web of science,\u0000Embase, Science Direct, Google Scholar, and reference lists were searched to identify articles which\u0000dealt with NSAIDs-associated oligohydramnios and premature closure of ductus arteriosus.\u0000\u0000\u0000\u0000Numerous regulatory agencies released warnings about oligohydramnios and premature closure\u0000of ductus arteriosus linked to NSAIDs. Furthermore, a number of case reports, case series, and\u0000some observational studies have also been published about the possibility of oligohydramnios and\u0000premature closure of ductus arteriosus linked to NSAIDs use.\u0000\u0000\u0000\u0000Women who are pregnant for 20 weeks or more should refrain from self-medicating\u0000with NSAIDs without consulting a pharmacist or a physician. The use of NSAIDs during pregnancy\u0000should carefully be considered due to potential risks to the mother and developing fetus, especially\u0000after 20-30 weeks of gestation. To guarantee the best possible health for the expectant mother and the\u0000unborn child, healthcare professionals should weigh the benefits and risks and look into alternate\u0000options. Pregnant women may opt for acetaminophen (paracetamol) to relieve pain and fever during\u0000pregnancy. Pregnant women should seek medical attention if there is persisting pain for more than\u0000three days.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140661726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A State-of-the-art Review on Artificial Intelligence and Machine Learning Applications 人工智能和机器学习应用现状综述
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-24 DOI: 10.2174/0115748855297767240408053500
Rishav Sharma, R. Malviya, Prerna Uniyal, Bhupendra Prajapati
The integration of artificial intelligence and machine learning holds greatpromise for enhancing healthcare institutions and providing fresh perspectives on the origins andadvancement of long-term illnesses. In the healthcare sector, artificial intelligence and machine learningare used to address supply and demand concerns, genomic applications, and new advancementsin drug development, cancer, and heart disease.The article explores the ways that machine learning, AI, precision medicine, and genomicsare changing healthcare. The essay also discusses how AI's examination of various patient data couldenhance healthcare institutions, provide fresh insights into chronic conditions, and advance precisionmedicine. The potential uses of machine learning for genome analysis are also examined in the paper,particularly about genetic biomarker-based disease risk and symptom prediction.The challenges posed by the phenotype-genotype relationship are examined, as well asthe significance of comprehending disease pathways in order to create tailored treatments. Moreover,it offers a streamlined and modularized method that predicts how genotypes affect cell propertiesusing machine-learning models, enabling the development of personalized drugs. The collective feedbackhighlights the rapid interdisciplinary growth of medical genomics following the completion ofthe Human Genome Project. It also emphasizes how important genomic data is for improvinghealthcare outcomes and facilitating personalized medicine.The study's conclusions point to a revolutionary shift in healthcare: the application ofAI/ML to illness control. Even though these innovations have a lot of potential benefits, problemslike algorithm interpretability and ethical issues need to be worked out before they can be successfullyincorporated into routine medical practice. Using machine learning in medicine has enormous potentialbenefits for the biotech industry. Further research, ongoing regulatory frameworks, and collaborationbetween medical professionals and data analysts are necessary to fully utilize machine learningas well as artificial intelligence in disease management.
人工智能与机器学习的结合为加强医疗保健机构以及为长期疾病的起源和发展提供新的视角带来了巨大的前景。文章探讨了机器学习、人工智能、精准医疗和基因组学改变医疗保健的方式。文章还讨论了人工智能对各种患者数据的检查如何能够增强医疗机构的实力,为慢性病提供新的见解,并推动精准医疗的发展。文章还探讨了机器学习在基因组分析中的潜在用途,特别是基于基因生物标记的疾病风险和症状预测。文章还探讨了表型-基因型关系带来的挑战,以及理解疾病路径对创造定制化治疗方法的意义。此外,它还提供了一种简化的模块化方法,利用机器学习模型预测基因型如何影响细胞特性,从而实现个性化药物的开发。集体反馈凸显了人类基因组计划完成后医学基因组学的快速跨学科发展。研究结论指出了医疗保健领域的革命性转变:将人工智能/移动医疗应用于疾病控制。尽管这些创新有很多潜在的好处,但在将其成功纳入常规医疗实践之前,还需要解决算法可解释性和伦理等问题。在医学中使用机器学习对生物技术行业有巨大的潜在好处。要在疾病管理中充分利用机器学习和人工智能,还需要进一步的研究、持续的监管框架以及医疗专业人员和数据分析师之间的合作。
{"title":"A State-of-the-art Review on Artificial Intelligence and Machine Learning Applications","authors":"Rishav Sharma, R. Malviya, Prerna Uniyal, Bhupendra Prajapati","doi":"10.2174/0115748855297767240408053500","DOIUrl":"https://doi.org/10.2174/0115748855297767240408053500","url":null,"abstract":"\u0000\u0000The integration of artificial intelligence and machine learning holds great\u0000promise for enhancing healthcare institutions and providing fresh perspectives on the origins and\u0000advancement of long-term illnesses. In the healthcare sector, artificial intelligence and machine learning\u0000are used to address supply and demand concerns, genomic applications, and new advancements\u0000in drug development, cancer, and heart disease.\u0000\u0000\u0000\u0000The article explores the ways that machine learning, AI, precision medicine, and genomics\u0000are changing healthcare. The essay also discusses how AI's examination of various patient data could\u0000enhance healthcare institutions, provide fresh insights into chronic conditions, and advance precision\u0000medicine. The potential uses of machine learning for genome analysis are also examined in the paper,\u0000particularly about genetic biomarker-based disease risk and symptom prediction.\u0000\u0000\u0000\u0000The challenges posed by the phenotype-genotype relationship are examined, as well as\u0000the significance of comprehending disease pathways in order to create tailored treatments. Moreover,\u0000it offers a streamlined and modularized method that predicts how genotypes affect cell properties\u0000using machine-learning models, enabling the development of personalized drugs. The collective feedback\u0000highlights the rapid interdisciplinary growth of medical genomics following the completion of\u0000the Human Genome Project. It also emphasizes how important genomic data is for improving\u0000healthcare outcomes and facilitating personalized medicine.\u0000\u0000\u0000\u0000The study's conclusions point to a revolutionary shift in healthcare: the application of\u0000AI/ML to illness control. Even though these innovations have a lot of potential benefits, problems\u0000like algorithm interpretability and ethical issues need to be worked out before they can be successfully\u0000incorporated into routine medical practice. Using machine learning in medicine has enormous potential\u0000benefits for the biotech industry. Further research, ongoing regulatory frameworks, and collaboration\u0000between medical professionals and data analysts are necessary to fully utilize machine learning\u0000as well as artificial intelligence in disease management.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140661923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
COVID-19 Study: A New Principle Discovery COVID-19 研究:新原理发现
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-19 DOI: 10.2174/0115748855287311240416050237
D. Lu, Ting-Ren Lu
The impact and burden of coronavirus outbreak (COVID-19, SARS-CoV-2) still existsworldwide. Different knowledge, opinions, and techniques determine the various outcomes and potencyof preventive and therapeutic strategies. COVID-19 infections, long COVID, and the complexityof treatment variability are challenging issues for therapeutic promotion and cost-effective consideration.To speed up global efforts against COVID-19, clinical diagnosis, therapeutic selections,and drug combination studies should be optimized in different ways. The epidemic condition, vaccination,techniques, and therapeutic options are open to new expeditions. To target infectious andtherapeutic variability, biomedical mechanisms and pathways should be understood. Facilitating andenhancing new global machinery and roadmap against viral-induced social damages and potentialepidemics should be established for biological and pharmaceutical purposes. Thus, in this study, theways of medical translation for COVID-19 treatment are discussed.
冠状病毒(COVID-19、SARS-CoV-2)疫情的影响和负担在全球范围内依然存在。不同的知识、观点和技术决定了预防和治疗策略的不同结果和效力。COVID-19 感染、COVID 时间长、治疗方法复杂多变是治疗推广和成本效益考虑的挑战性问题。疫情、疫苗接种、技术和治疗方案都有待新的探索。针对传染和治疗的变异性,应了解生物医学机制和途径。应为生物和制药目的建立新的全球机制和路线图,促进和加强应对病毒引起的社会破坏和潜在流行。因此,本研究讨论了 COVID-19 治疗的医学转化途径。
{"title":"COVID-19 Study: A New Principle Discovery","authors":"D. Lu, Ting-Ren Lu","doi":"10.2174/0115748855287311240416050237","DOIUrl":"https://doi.org/10.2174/0115748855287311240416050237","url":null,"abstract":"\u0000\u0000The impact and burden of coronavirus outbreak (COVID-19, SARS-CoV-2) still exists\u0000worldwide. Different knowledge, opinions, and techniques determine the various outcomes and potency\u0000of preventive and therapeutic strategies. COVID-19 infections, long COVID, and the complexity\u0000of treatment variability are challenging issues for therapeutic promotion and cost-effective consideration.\u0000To speed up global efforts against COVID-19, clinical diagnosis, therapeutic selections,\u0000and drug combination studies should be optimized in different ways. The epidemic condition, vaccination,\u0000techniques, and therapeutic options are open to new expeditions. To target infectious and\u0000therapeutic variability, biomedical mechanisms and pathways should be understood. Facilitating and\u0000enhancing new global machinery and roadmap against viral-induced social damages and potential\u0000epidemics should be established for biological and pharmaceutical purposes. Thus, in this study, the\u0000ways of medical translation for COVID-19 treatment are discussed.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140684793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigating the Mechanism of Banxia Xiexin Decoction in Treating Gastritis and Diabetes Mellitus through Network Pharmacology andMolecular Docking Analysis 通过网络药理学和分子对接分析研究半夏泻心汤治疗胃炎和糖尿病的机制
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-18 DOI: 10.2174/0115748855287070240409061220
Yikuan Du, Xianhong Chi, Qianwen Chen, Yue Xiao, Zhendong Ma, Zhenjie Wang, Zhuoming Guo, Peng Chen, Zilin Chen, Mengting Zhang, Jinyan Guo, YuQi Zhou, Chun Yang
Banxia Xiexin decoration (BXD), a complex prescription in Traditional ChineseMedicine (TCM), clinically acts as a treatment for gastritis and diabetes while its mechanism oftreatment remains unknown.This study aimed to explore the common mechanism of BXD in treating gastritis anddiabetes based on network pharmacology and molecular docking technology.The seven Chinese herbal components and drug targets were collected from the TraditionalChinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) for gastritis anddiabetes using GeneCards, DisGeNET, Comparative Toxicogenomics Database (CTD), and OnlineMendelian Inheritance in Man (OMIM) databases. Common drug and disease targets were importedinto the STRING data platform for protein-protein interaction (PPI) analysis, and Cytoscape 3.7.2software for network topology analysis, and core targets were filtered.There were 124 components, 249 targets, 449 targets for gastritis, and 4005 targets for diabetes.After mapping, 83 BXD targets for gastritis and diabetes were obtained, and the targets withhigh correlation were STAT 3, JUN, TNF, IL-6, etc. More relevant targets were involved in the cancerpathway, AGE-RAGE signaling pathway of diabetic complications, fluid shear stress, and atherosclerosispathway.This study preliminarily reveals that BXD may play a role in the treatment of gastritisand diabetes mellitus through multi-components, multi-targets, and multi-pathways, and proposessome potential "component-target-pathway" hypotheses in light of previous reports.
半夏泻心汤(BXD)是一种中药复方制剂,临床上主要用于治疗胃炎和糖尿病,但其治疗机制尚不清楚。本研究利用GeneCards、DisGeNET、比较毒物基因组学数据库(CTD)和OnlineMendelian Inheritance in Man(OMIM)数据库,从中药系统药理学数据库和分析平台(TCMSP)中收集了七种中药成分和药物靶点,并将其导入到中药系统药理学数据库和分析平台。经图谱分析,胃炎和糖尿病共有83个BXD靶点,相关性较高的靶点有STAT 3、JUN、TNF、IL-6等。本研究初步揭示了BXD可能通过多成分、多靶点、多通路在胃炎和糖尿病的治疗中发挥作用,并结合之前的报道提出了一些潜在的 "成分-靶点-通路 "假说。
{"title":"Investigating the Mechanism of Banxia Xiexin Decoction in Treating Gastritis and Diabetes Mellitus through Network Pharmacology and\u0000Molecular Docking Analysis","authors":"Yikuan Du, Xianhong Chi, Qianwen Chen, Yue Xiao, Zhendong Ma, Zhenjie Wang, Zhuoming Guo, Peng Chen, Zilin Chen, Mengting Zhang, Jinyan Guo, YuQi Zhou, Chun Yang","doi":"10.2174/0115748855287070240409061220","DOIUrl":"https://doi.org/10.2174/0115748855287070240409061220","url":null,"abstract":"\u0000\u0000Banxia Xiexin decoration (BXD), a complex prescription in Traditional Chinese\u0000Medicine (TCM), clinically acts as a treatment for gastritis and diabetes while its mechanism of\u0000treatment remains unknown.\u0000\u0000\u0000\u0000This study aimed to explore the common mechanism of BXD in treating gastritis and\u0000diabetes based on network pharmacology and molecular docking technology.\u0000\u0000\u0000\u0000The seven Chinese herbal components and drug targets were collected from the Traditional\u0000Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) for gastritis and\u0000diabetes using GeneCards, DisGeNET, Comparative Toxicogenomics Database (CTD), and Online\u0000Mendelian Inheritance in Man (OMIM) databases. Common drug and disease targets were imported\u0000into the STRING data platform for protein-protein interaction (PPI) analysis, and Cytoscape 3.7.2\u0000software for network topology analysis, and core targets were filtered.\u0000\u0000\u0000\u0000There were 124 components, 249 targets, 449 targets for gastritis, and 4005 targets for diabetes.\u0000After mapping, 83 BXD targets for gastritis and diabetes were obtained, and the targets with\u0000high correlation were STAT 3, JUN, TNF, IL-6, etc. More relevant targets were involved in the cancer\u0000pathway, AGE-RAGE signaling pathway of diabetic complications, fluid shear stress, and atherosclerosis\u0000pathway.\u0000\u0000\u0000\u0000This study preliminarily reveals that BXD may play a role in the treatment of gastritis\u0000and diabetes mellitus through multi-components, multi-targets, and multi-pathways, and proposes\u0000some potential \"component-target-pathway\" hypotheses in light of previous reports.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140687384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Omentin 1: A Promising Regulator and Therapeutic Target in the Battle against Obesity, Diabetes, and Alzheimer’s Disease 网织蛋白 1:抗击肥胖症、糖尿病和阿尔茨海默病的有望调节器和治疗靶点
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-16 DOI: 10.2174/0115748855296758240408040336
Shiv Kumar Kushawaha, Radhika Sharma, Mahendra Singh Ashawat
Mechanistic investigations in both animal models and human subjects have consistently elucidated a causal relationship between obesity, diabetes, and Alzheimer's disease (AD). Alzheimer's disease is the predominant etiology of dementia, marked by progressive cerebral degeneration char-acterized by the formation of intracellular neurofibrillary tangles and extracellular amyloid beta (Aβ) plaques. Adipose tissue secretes bioactive signaling molecules known as adipokines. Interactions be-tween adipose tissue and the central nervous system serve as the foundational mechanism contrib-uting to the elevated susceptibility of individuals with obesity to the onset of neurologic disorders, including cognitive and mood-related disturbances. Omentin is a recently discovered adipokine that has gained attention for study because of its pleiotropic effects on several disorders. The specific receptor responsible for binding with Omentin remains unidentified thus far. This investigation elu-cidates the variability in Omentin levels observed in multiple pathological conditions. Therapeutic methods to raise omentin-1 levels may be helpful for the treatment or prevention of several illnesses. Increases in circulating omentin-1 levels can be achieved with weight loss, an olive oil-rich diet, aerobic exercise, atorvastatin therapy, and the use of diabetes medications. It is also possible to use circulating omentin-1 as a biomarker of obesity, diabetes, metabolic syndrome, atherosclerosis, is-chemic heart disease, inflammatory disease, cancer, and neurological diseases via AMP-activated protein kinase/Akt/nuclear factor-κB/mitogen-activated protein kinase (ERK, JNK, and p38) signal-ing. This review provides insights into the potential use of omentin-1 as a biomarker for Obesity, Diabetes, and associated metabolic and neurological disorders.
对动物模型和人体进行的机理研究不断阐明肥胖、糖尿病和阿尔茨海默病(AD)之间的因果关系。阿尔茨海默病是痴呆症的主要病因,其特征是细胞内神经纤维缠结和细胞外淀粉样β(Aβ)斑块形成的渐进性脑退化。脂肪组织会分泌被称为脂肪因子的生物活性信号分子。脂肪组织与中枢神经系统之间的相互作用是导致肥胖者更易患神经系统疾病(包括认知和情绪相关障碍)的基本机制。奥门冬酰胺是最近发现的一种脂肪因子,因其对多种疾病的多效应而备受关注。迄今为止,负责与奥门汀结合的特定受体仍未确定。这项研究阐明了在多种病理情况下观察到的奥门冬酰胺水平的变化。提高网织蛋白-1水平的治疗方法可能有助于治疗或预防多种疾病。通过减肥、富含橄榄油的饮食、有氧运动、阿托伐他汀治疗和使用糖尿病药物,可以提高循环中网织蛋白-1的水平。通过 AMP 激活蛋白激酶/Akt/核因子-κB/介原激活蛋白激酶(ERK、JNK 和 p38)信号转导,还可将循环网织蛋白-1 用作肥胖、糖尿病、代谢综合征、动脉粥样硬化、缺血性心脏病、炎症性疾病、癌症和神经系统疾病的生物标志物。本综述深入探讨了网蛋白-1 作为肥胖症、糖尿病以及相关代谢和神经疾病生物标记物的潜在用途。
{"title":"Omentin 1: A Promising Regulator and Therapeutic Target in the Battle against Obesity, Diabetes, and Alzheimer’s Disease","authors":"Shiv Kumar Kushawaha, Radhika Sharma, Mahendra Singh Ashawat","doi":"10.2174/0115748855296758240408040336","DOIUrl":"https://doi.org/10.2174/0115748855296758240408040336","url":null,"abstract":"\u0000\u0000Mechanistic investigations in both animal models and human subjects have consistently elucidated a causal relationship between obesity, diabetes, and Alzheimer's disease (AD). Alzheimer's disease is the predominant etiology of dementia, marked by progressive cerebral degeneration char-acterized by the formation of intracellular neurofibrillary tangles and extracellular amyloid beta (Aβ) plaques. Adipose tissue secretes bioactive signaling molecules known as adipokines. Interactions be-tween adipose tissue and the central nervous system serve as the foundational mechanism contrib-uting to the elevated susceptibility of individuals with obesity to the onset of neurologic disorders, including cognitive and mood-related disturbances. Omentin is a recently discovered adipokine that has gained attention for study because of its pleiotropic effects on several disorders. The specific receptor responsible for binding with Omentin remains unidentified thus far. This investigation elu-cidates the variability in Omentin levels observed in multiple pathological conditions. Therapeutic methods to raise omentin-1 levels may be helpful for the treatment or prevention of several illnesses. Increases in circulating omentin-1 levels can be achieved with weight loss, an olive oil-rich diet, aerobic exercise, atorvastatin therapy, and the use of diabetes medications. It is also possible to use circulating omentin-1 as a biomarker of obesity, diabetes, metabolic syndrome, atherosclerosis, is-chemic heart disease, inflammatory disease, cancer, and neurological diseases via AMP-activated protein kinase/Akt/nuclear factor-κB/mitogen-activated protein kinase (ERK, JNK, and p38) signal-ing. This review provides insights into the potential use of omentin-1 as a biomarker for Obesity, Diabetes, and associated metabolic and neurological disorders.\u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140698831","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Selenium Supplementation on Thyroid Nodule Volume in Euthyroid Patients: A Randomized Clinical Trial 补充硒对甲状腺功能正常患者甲状腺结节体积的影响:随机临床试验
IF 0.6 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2024-04-16 DOI: 10.2174/0115748855283065240403073316
Zeid Zerehsaz, M. Yaghoubi, Ali Teimouri, Zohreh Mousavi, Mona Najaf Najafi, Ali Moradi, Masoud Mohebbi, A. Sahebkar
Evaluating the Effect of Selenium Supplementation on Thyroid Nodule Volume in Euthyroid PatientsSelenium is an essential trace element, which plays a role in regulation of the metabolism of thyroid hormones.This study was designed to evaluate the effect of selenium on the volume of thyroid nodules in euthyroid patients.In this triple-blinded clinical trial, a total of 60 euthyroid patients with benign thyroid nodules (solitary or multinodular goiter) and normal serum selenium were randomly divided into the case and control (n=30 each) groups. The case group received selenium 200 μg/day while the control group received placebo for 3 months. Thyroid ultrasound was used to measure thyroid nodule volume.Selenium supplementation (200 µg/day) retained the serum selenium levels of participants in the case group (P=0.251), while, the control group showed a significant drop in serum selenium levels (P=0.007). Moreover, the thyroid volume in case group showed a significant decrease after selenium supplementation (P=0.012); however, a nonsignificant increase was seen in thyroid volume in control group (P=0.832).Selenium supplementation can reduce thyroid nodule volume in euthyroid patients.Selenium; supplementation; thyroid; thyroid volume; thyroid nodule; euthyroid  
评估补硒对甲状腺功能正常患者甲状腺结节体积的影响硒是人体必需的微量元素,在甲状腺激素代谢中起着调节作用。本研究旨在评估补硒对甲状腺功能正常患者甲状腺结节体积的影响。在这项三盲临床试验中,60 名甲状腺良性结节(单发或多发结节性甲状腺肿)且血清硒含量正常的甲状腺功能正常患者被随机分为病例组和对照组(各 30 人)。病例组每天服用硒200微克,对照组服用安慰剂3个月。硒补充剂(200 微克/天)保持了病例组参与者的血清硒水平(P=0.251),而对照组的血清硒水平显著下降(P=0.007)。此外,病例组的甲状腺体积在补硒后出现了显著下降(P=0.012);而对照组的甲状腺体积则出现了非显著性增加(P=0.832)。
{"title":"Effects of Selenium Supplementation on Thyroid Nodule Volume in Euthyroid Patients: A Randomized Clinical Trial","authors":"Zeid Zerehsaz, M. Yaghoubi, Ali Teimouri, Zohreh Mousavi, Mona Najaf Najafi, Ali Moradi, Masoud Mohebbi, A. Sahebkar","doi":"10.2174/0115748855283065240403073316","DOIUrl":"https://doi.org/10.2174/0115748855283065240403073316","url":null,"abstract":"\u0000\u0000Evaluating the Effect of Selenium Supplementation on Thyroid Nodule Volume in Euthyroid Patients\u0000\u0000\u0000\u0000Selenium is an essential trace element, which plays a role in regulation of the metabolism of thyroid hormones.\u0000\u0000\u0000\u0000This study was designed to evaluate the effect of selenium on the volume of thyroid nodules in euthyroid patients.\u0000\u0000\u0000\u0000In this triple-blinded clinical trial, a total of 60 euthyroid patients with benign thyroid nodules (solitary or multinodular goiter) and normal serum selenium were randomly divided into the case and control (n=30 each) groups. The case group received selenium 200 μg/day while the control group received placebo for 3 months. Thyroid ultrasound was used to measure thyroid nodule volume.\u0000\u0000\u0000\u0000Selenium supplementation (200 µg/day) retained the serum selenium levels of participants in the case group (P=0.251), while, the control group showed a significant drop in serum selenium levels (P=0.007). Moreover, the thyroid volume in case group showed a significant decrease after selenium supplementation (P=0.012); however, a nonsignificant increase was seen in thyroid volume in control group (P=0.832).\u0000\u0000\u0000\u0000Selenium supplementation can reduce thyroid nodule volume in euthyroid patients.\u0000\u0000\u0000\u0000Selenium; supplementation; thyroid; thyroid volume; thyroid nodule; euthyroid  \u0000","PeriodicalId":11004,"journal":{"name":"Current Drug Therapy","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140697311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Current Drug Therapy
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1