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Prevention of Cardiovascular Diseases with Anti-Inflammatory and Anti- Oxidant Nutraceuticals and Herbal Products: An Overview of Pre-Clinical and Clinical Studies. 抗炎和抗氧化营养药品和草药产品预防心血管疾病:临床前和临床研究综述。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180815144803
Sajal Jain, Harpal S Buttar, Meena Chintameneni, Ginpreet Kaur

Background: Inflammation-induced endothelial abnormalities, dietary habits, and tobacco smoking are considered to be the primary risk factors for causing atherosclerosis and Cardiovascular Diseases (CVDs), including Coronary Heart Disease (CHD), cerebrovascular disorders, peripheral arterial disease, rheumatic heart disease, congenital heart defects, deep vein thrombosis and pulmonary embolism. Prevention of CVDs with anti-inflammatory and anti-oxidant agents has been a challenging task for decades. Currently, CVDs have taken a top position among the health-related issues and are considered the foremost cause of mortality and morbidity around the globe.

Objective: Emerging evidence from several sources indicates that nutraceuticals and plant products may be a cost-effective approach for the prevention of CVDs. A limited number of clinical studies done with nutraceuticals have shown positive effects for promoting health and well-being as well as reduction of CVDs in humans. Some plants from which nutraceutical ingredients are isolated and will be discussed in this review are: Murraya koenigii, Curcuma longa, Beta vulgaris, Allium sativum, Allium cepa, Lagenaria siceraria Stand, Trigonella foenum-graecum.

Methods: Literature searches were done using keywords for plants, nutraceuticals, and plant products that have revealed beneficial effects in the prevention of CVDs. The anti-oxidant and anti-inflammatory actions of nutraceuticeuticals and plant ingredients play a significant role in capturing free radicals and reducing endothelial risk factors associated with the occurrence CVDs.

Results: This review has explored the usefulness of animal studies performed with nutraceuticals and herbal products and to understand their mode of action in the prevention of CVDs. Also, we have referred to patents for different nutraceuticals for better understanding their quantitative effects and dosage forms.

Conclusion: It is concluded that nutraceuticals possess enormous health benefits and their interventions can be highly beneficial in the prevention/reduction of CVDs and related disorders such as atherosclerosis, hypertension, heart attack and stroke. The findings of this review provide an update on the emerging uses of nutraceuticals, functional foods, and herbal remedies in humans. Nevertheless, large-scale randomized, placebo-controlled, double-blind clinical trials are needed to confirm the health benefit claims about nutraceuticals and herbal products to establish their long-term safety and to resolve the controversy about the role of clinical nutrition in curing lifestyle diseases.

背景:炎症诱导的内皮异常、饮食习惯和吸烟被认为是导致动脉粥样硬化和心血管疾病(cvd)的主要危险因素,包括冠心病(CHD)、脑血管疾病、外周动脉疾病、风湿性心脏病、先天性心脏缺陷、深静脉血栓形成和肺栓塞。几十年来,用抗炎和抗氧化剂预防心血管疾病一直是一项具有挑战性的任务。目前,心血管疾病已在健康相关问题中占据首要地位,并被认为是全球死亡和发病的首要原因。目的:来自多个来源的新证据表明,营养药品和植物产品可能是预防心血管疾病的一种具有成本效益的方法。对营养保健品进行的数量有限的临床研究表明,营养保健品对促进人类健康和福祉以及减少心血管疾病有积极作用。从植物中分离出的营养成分主要有:金银花、姜黄、甜菜、葱、韭菜、Lagenaria siceraria Stand、Trigonella foenum-graecum。方法:以植物、营养药品和植物产品为关键词进行文献检索,发现它们对预防心血管疾病有有益作用。营养保健品和植物成分的抗氧化和抗炎作用在捕获自由基和降低心血管疾病发生的内皮危险因素方面起着重要作用。结果:本综述探讨了用营养品和草药产品进行的动物研究的有用性,并了解了它们在预防心血管疾病中的作用模式。此外,我们还参考了不同营养保健品的专利,以便更好地了解它们的定量效果和剂型。结论:营养保健品具有巨大的健康效益,其干预措施在预防/减少心血管疾病及相关疾病(如动脉粥样硬化、高血压、心脏病发作和中风)方面非常有益。本综述的发现提供了营养保健品、功能性食品和草药在人类中的新用途的最新情况。然而,需要大规模的随机、安慰剂对照、双盲临床试验来证实营养保健品和草药产品的健康益处,以确定其长期安全性,并解决关于临床营养在治疗生活方式疾病中的作用的争议。
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引用次数: 36
Advances in Developing Prophylactics and Therapeutics to Counter Inflammatory, Allergic and Infectious Diseases. 抗炎症、过敏性和感染性疾病的预防和治疗研究进展。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X1201180821095512
Ashok Munjal, Hafiz M N Iqbal, Kuldeep Dhama
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引用次数: 0
Community-Acquired Pneumonia in Children. 儿童社区获得性肺炎。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180621163821
Alexander K C Leung, Alex H C Wong, Kam L Hon

Background: Community-acquired pneumonia is an important cause of morbidity in developed countries and an important cause of morbidity and mortality in developing countries. Prompt diagnosis and appropriate treatment are very important.

Objective: To provide an update on the evaluation, diagnosis, and treatment of community-acquired pneumonia in children.

Methods: A PubMed search was completed in Clinical Queries using the key term "communityacquired pneumonia". The search strategy included meta-analyses, randomized controlled trials, clinical trials, observational studies, and reviews. Patents were searched using the key term "community-acquired pneumonia" from www.google.com/patents, http://espacenet.com, and www. freepatentsonline.com.

Results: Generally, viruses, notably respiratory syncytial virus, are the most common cause of community- acquired pneumonia in children younger than 5 years. Streptococcus pneumoniae is the most common bacterial cause across all age groups. Other important bacterial causes in children younger than 5 years include Haemophilus influenzae, Streptococcus pyogenes, Staphylococcus aureus, and Moraxella catarrhalis. In children 5 years or older, in addition to S. pneumoniae, other important bacterial causes include Mycoplasma pneumoniae and Chlamydophila pneumonia. In the majority of cases, bacterial and viral pneumonia cannot be reliably distinguished from each other on clinical grounds. In practice, most children with pneumonia are treated empirically with antibiotics; the choice of which depends on the patient's age and most likely pathogen. Recent patents related to the management of community-acquired pneumonia are discussed.

Conclusion: In previously healthy children under the age of 5 years, high dose amoxicillin is the treatment of choice. For those with type 1 hypersensitivity to penicillin, clindamycin, azithromycin, clarithromycin, and levofloxacin are reasonable alternatives. For children with a non-type 1 hypersensitivity to penicillin, cephalosporins such as cefixime, cefprozil, cefdinir, cefpodoxime, and cefuroxime should be considered. In previously healthy children over the age of 5 years, macrolides such as azithromycin and clarithromycin are the drugs of choice.

背景:社区获得性肺炎是发达国家发病的重要原因,也是发展中国家发病和死亡的重要原因。及时诊断和适当治疗非常重要。目的:提供儿童社区获得性肺炎的评估、诊断和治疗的最新进展。方法:在临床查询中使用关键词“社区获得性肺炎”完成PubMed检索。检索策略包括荟萃分析、随机对照试验、临床试验、观察性研究和综述。使用关键词“社区获得性肺炎”从www.google.com/patents, http://espacenet.com和www上搜索专利。结果:一般来说,病毒,特别是呼吸道合胞病毒,是5岁以下儿童社区获得性肺炎的最常见原因。肺炎链球菌是所有年龄组中最常见的细菌病因。5岁以下儿童的其他重要细菌病因包括流感嗜血杆菌、化脓性链球菌、金黄色葡萄球菌和卡他莫拉菌。在5岁或以上的儿童中,除了肺炎链球菌外,其他重要的细菌病因包括肺炎支原体和嗜衣原体肺炎。在大多数情况下,细菌性和病毒性肺炎不能根据临床理由可靠地相互区分。在实践中,大多数肺炎儿童都是经验性地使用抗生素治疗;选择哪种取决于病人的年龄和最可能的病原体。讨论了最近与社区获得性肺炎管理相关的专利。结论:在既往健康的5岁以下儿童中,大剂量阿莫西林是首选的治疗方法。对于1型青霉素过敏患者,克林霉素、阿奇霉素、克拉霉素和左氧氟沙星是合理的选择。对于对青霉素非1型过敏的儿童,应考虑使用头孢克肟、头孢丙嗪、头孢地尼、头孢多肟和头孢呋辛等头孢菌素。在以前健康的5岁以上儿童中,阿奇霉素和克拉霉素等大环内酯类药物是首选药物。
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引用次数: 22
Febrile Infection-Related Epilepsy Syndrome (FIRES): An Overview of Treatment and Recent Patents. 发热性感染相关癫痫综合征(FIRES):治疗综述及近期专利
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180508122450
Kam L Hon, Alexander K C Leung, Alcy R Torres

Background: New-Onset Refractory Status Epilepticus (NORSE) refers to a clinical presentation in a patient without active epilepsy or other existing relevant neurological disorder, with new onset of refractory status epilepticus in the absence of a clear acute or active structural, metabolic, or toxic cause. Febrile Infection-Related Epilepsy Syndrome (FIRES) is a subset of NORSE that requires a febrile infection between 24 hours and 2 weeks prior to the onset of refractory status epilepticus, with or without fever at the onset of status epilepticus, and with no restriction to the age of the patient. The literature on FIRES is scarce.

Objective: This article reviews the pathophysiology, clinical features, and various treatment modalities in the treatment of FIRES.

Methods: A Medline/Pubmed search was conducted using Clinical Queries with the key terms "Febrile Infection-Related Epilepsy Syndrome", "FIRES", "New-Onset Refractory Status Epilepticus" and "NORSE". The search strategy included meta-analyses, randomized controlled trials, clinical trials, reviews and pertinent references. Patents were searched using the key term "FIRES", "NORSE" and "Febrile Epilepsy Syndrome" from www.google.com/patents, www.uspto.gov, and www.freepatentsonline.com.

Results: FIRES almost invariably begins with a mild nonspecific febrile illness in an otherwise healthy individual. Twenty-four hours to two weeks later, seizures begin and quickly become very frequent and worsen, becoming status epilepticus. Seizures can be simple motor, complex partial or secondary generalized. The exact etiology is not known. It is possible that the syndrome is caused by an inflammatory or autoimmune mechanism. Seizures in FIRES are notoriously very difficult to treat. Treatment modalities include, among others, various antiepileptic drugs, ketogenic diet, intravenous corticosteroids, intravenous immunoglobulin, and burst-suppression coma. The outcome is poor; most children are left with significant cognitive disability and refractory epilepsy. Recent patents for the management of FIRES are discussed.

Conclusion: FIRES is a rare epilepsy syndrome of unclear etiology in which children, usually of school age, suddenly develop very frequent seizures after a mild febrile illness. Seizures in FIRES are typically difficult to treat. The prognosis is poor.

背景:新发难治性癫痫持续状态(NORSE)是指没有活动性癫痫或其他相关神经系统疾病的患者,在没有明确的急性或活动性结构、代谢或毒性原因的情况下,出现新发难治性癫痫持续状态的临床表现。发热性感染相关癫痫综合征(FIRES)是NORSE的一个子集,要求在难耐癫痫持续状态发作前24小时至2周发生发热性感染,癫痫持续状态发作时伴有或不伴有发热,且患者年龄不受限制。关于火灾的文献很少。目的:综述火灾的病理生理、临床特点及各种治疗方法。方法:以“发热性感染相关癫痫综合征”、“FIRES”、“新发难固性癫痫持续状态”和“NORSE”为关键词,通过Medline/Pubmed进行检索。检索策略包括荟萃分析、随机对照试验、临床试验、综述和相关参考文献。使用关键词“FIRES”、“NORSE”和“发热性癫痫综合征”从www.google.com/patents、www.uspto.gov和www.freepatentsonline.com.Results检索专利:FIRES几乎总是以健康个体的轻度非特异性发热性疾病开始。24小时至两周后,癫痫发作开始并迅速变得非常频繁和恶化,成为癫痫持续状态。癫痫发作可为简单的运动性,复杂的局部或继发性全身性。确切的病因尚不清楚。该综合征可能是由炎症或自身免疫机制引起的。众所周知,火灾的发作很难治疗。治疗方式包括,除其他外,各种抗癫痫药物,生酮饮食,静脉注射皮质类固醇,静脉注射免疫球蛋白和突发抑制昏迷。结果很糟糕;大多数儿童留下了严重的认知障碍和顽固性癫痫。本文还讨论了用于管理FIRES的最新专利。结论:FIRES是一种病因不明的罕见癫痫综合征,通常为学龄儿童,在轻度发热性疾病后突然频繁发作。火灾的发作通常难以治疗。预后很差。
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引用次数: 33
Impact of Ocular Compatible Lipoids and Castor Oil in Fabrication of Brimonidine Tartrate Nanoemulsions by 33 Full Factorial Design. 采用 33 全因子设计,研究眼部兼容脂质和蓖麻油对酒石酸溴莫尼定纳米乳液制备的影响。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180730115225
Rimple, Maria J Newton

Background: Brimonidine Tartrate (BRT) is used in the treatment of glaucoma. Brimonidine tartrate nanoemulsion was fabricated in this research work to enhance the permeability through barriers and faster onset of action and therapeutic effect.

Objective: To fabricate an ocular compatible nanoemulsion of brimonidine tartrate by using surfactant and co-surfactants.

Methods: The experimental work involved compatibility studies by using FTIR, DSC and crystallinity study by XRD. The prepared nanoemulsion was studied by photon correlation spectroscopy by Malvern S90 for the particle size analysis and characterized for Z average value (d.nm.) and PDI. Further studies were conducted by laser light scattering technique by delsanano common and TEM.

Results: The study demonstrated that the formulations BN2, BN3, BN10 demonstrated the z average value of 19.48, 22.14,26.50 d.nm. With 0.337, 0.270, 0.289 PDI respectively, the formulae BN2, BN3, BN10 demonstrated the distribution average diameter (nm) of 376.8 + 258.4, 542.8 + 494.4, 398.8 + 263.9 with the diameter of 267.5, 298.5, 272.7, respectively. The zeta potential of BN10 was -21.26 mV and other parameters such as TEM and drug release studies were also reported.

Conclusion: The nanoemulsion of brimonidine tartrate was prepared successfully by using castor oil, Lipoid S75 (Fat free soybean phospholipids with 70% phosphatidylcholine), Lipoid E80 (Egg phospholipids with 80% phosphatidylcholine) and PF- 68. The optimised formula demonstrated the lower droplet size, satisfactory zeta potential, and high drug loading and reproducible drug release profile. Brimonididne taratarate is reported in various recent patents for various applications and is the potential candidate for future therapy. Nanoemulsion is widely explored as potential alternatives for conventional ophthalmic formulation based approaches. It enhances the ocular bioavailability by reducing the drug protein binding, increasing the corneal resident time, enhancing the drug permeability and providing a sustained drug release.It reported a significant increase in therapeutic efficacy for various chronic ocular disease states of both the anterior and posterior ocular segments.

背景:酒石酸溴莫尼定(BRT酒石酸溴莫尼定(BRT)用于治疗青光眼。本研究工作制备了酒石酸溴莫尼定纳米乳液,以提高其通过屏障的渗透性,加快起效和治疗效果:通过使用表面活性剂和辅助表面活性剂,制备眼部兼容的酒石酸溴莫尼定纳米乳液:方法:实验工作包括利用傅立叶变换红外光谱(FTIR)、电化学稳定性分析(DSC)和X射线衍射(XRD)进行相容性研究和结晶度研究。用马尔文 S90 光子相关光谱仪对制备的纳米乳液进行粒度分析,并对 Z 平均值(d.nm.)和 PDI 进行表征。此外,还利用激光光散射技术和 TEM 进行了进一步研究:研究表明,制剂 BN2、BN3 和 BN10 的 Z 平均值分别为 19.48、22.14 和 26.50 d.nm。在 PDI 分别为 0.337、0.270、0.289 的情况下,配方 BN2、BN3、BN10 的分布平均直径(nm)分别为 376.8 + 258.4、542.8 + 494.4、398.8 + 263.9,直径分别为 267.5、298.5、272.7。BN10 的 zeta 电位为 -21.26 mV,其他参数如 TEM 和药物释放研究也有报道:结论:使用蓖麻油、Lipoid S75(含 70% 磷脂酰胆碱的无脂大豆磷脂)、Lipoid E80(含 80% 磷脂酰胆碱的鸡蛋磷脂)和 PF- 68 成功制备了酒石酸溴莫尼定纳米乳剂。优化配方显示出较低的液滴尺寸、令人满意的 zeta 电位、较高的药物载量和可重复的药物释放曲线。Brimonidne taratarate 在最近的多项专利中都有不同的应用,是未来治疗的潜在候选药物。纳米乳液作为传统眼科制剂的潜在替代品,受到了广泛的关注。它通过减少药物蛋白结合、增加角膜驻留时间、提高药物渗透性和提供持续的药物释放来提高眼部生物利用度。
{"title":"Impact of Ocular Compatible Lipoids and Castor Oil in Fabrication of Brimonidine Tartrate Nanoemulsions by 3<sup>3</sup> Full Factorial Design.","authors":"Rimple, Maria J Newton","doi":"10.2174/1872213X12666180730115225","DOIUrl":"10.2174/1872213X12666180730115225","url":null,"abstract":"<p><strong>Background: </strong>Brimonidine Tartrate (BRT) is used in the treatment of glaucoma. Brimonidine tartrate nanoemulsion was fabricated in this research work to enhance the permeability through barriers and faster onset of action and therapeutic effect.</p><p><strong>Objective: </strong>To fabricate an ocular compatible nanoemulsion of brimonidine tartrate by using surfactant and co-surfactants.</p><p><strong>Methods: </strong>The experimental work involved compatibility studies by using FTIR, DSC and crystallinity study by XRD. The prepared nanoemulsion was studied by photon correlation spectroscopy by Malvern S90 for the particle size analysis and characterized for Z average value (d.nm.) and PDI. Further studies were conducted by laser light scattering technique by delsanano common and TEM.</p><p><strong>Results: </strong>The study demonstrated that the formulations BN2, BN3, BN10 demonstrated the z average value of 19.48, 22.14,26.50 d.nm. With 0.337, 0.270, 0.289 PDI respectively, the formulae BN2, BN3, BN10 demonstrated the distribution average diameter (nm) of 376.8 + 258.4, 542.8 + 494.4, 398.8 + 263.9 with the diameter of 267.5, 298.5, 272.7, respectively. The zeta potential of BN10 was -21.26 mV and other parameters such as TEM and drug release studies were also reported.</p><p><strong>Conclusion: </strong>The nanoemulsion of brimonidine tartrate was prepared successfully by using castor oil, Lipoid S75 (Fat free soybean phospholipids with 70% phosphatidylcholine), Lipoid E80 (Egg phospholipids with 80% phosphatidylcholine) and PF- 68. The optimised formula demonstrated the lower droplet size, satisfactory zeta potential, and high drug loading and reproducible drug release profile. Brimonididne taratarate is reported in various recent patents for various applications and is the potential candidate for future therapy. Nanoemulsion is widely explored as potential alternatives for conventional ophthalmic formulation based approaches. It enhances the ocular bioavailability by reducing the drug protein binding, increasing the corneal resident time, enhancing the drug permeability and providing a sustained drug release.It reported a significant increase in therapeutic efficacy for various chronic ocular disease states of both the anterior and posterior ocular segments.</p>","PeriodicalId":20960,"journal":{"name":"Recent patents on inflammation & allergy drug discovery","volume":"12 2","pages":"169-183"},"PeriodicalIF":4.2,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2174/1872213X12666180730115225","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36355380","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: 10
The Promising Pharmacological Effects and Therapeutic/Medicinal Applications of Punica Granatum L. (Pomegranate) as a Functional Food in Humans and Animals. 石榴(Punica Granatum L.,石榴)作为一种功能食品在人与动物中的药理作用和治疗/药物应用前景
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180221154713
Muhammad Saeed, Muhammad Naveed, Jannat BiBi, Asghar A Kamboh, Muhammad A Arain, Qurban A Shah, Mahmoud Alagawany, Mohamed E A El-Hack, Mervat A Abdel-Latif, Mohd I Yatoo, Ruchi Tiwari, Sandip Chakraborty, Kuldeep Dhama

Background: Punica granatum L. (pomegranate), is a shrub mostly available in the Mediterranean Sea region. The fruits have gained the substantial attention among researchers due to their promising biological activities including anti-inflammatory, antibacterial, antidiarrheal, immune modulatory, antitumor, wound healing and antifungal that have been attributed to various constituents of seeds, bark, juice, pericarp, and leaf of this tree across the globe. The phenolic compounds of pomegranate have been documented to possess numbers of prophylactic and therapeutic utilities against various pathological infections as well as non-infectious disorders.

Objective: The current review expedites the pharmacological role of Punica granatum L. in curing elements related to infectious and non-infectious disorders.

Methods: The current review is based on literature and patents already available on various scientific databases highlighting the role of Punica granatum along with its therapeutic potentials against infectious and non-infectious disorders. The databases included under study were PubMed, Med line, PubMed Central, Science Direct and few other scientific databases. The information obtained through these diverse databases is compiled, critically interpreted and presented in the current study.

Results: Multi-dimensional beneficial application of pomegranate plant is recorded. The pomegranate seed oil has phytoestrogenic compounds and the fruit is rich in phenolic compounds with strong antioxidant activity. The fruit and bark of pomegranate are used against intestinal parasites, dysentery, and diarrhea in different animals and human models. Since the ancient time the juice and seeds had considered the best therapy for throat and heart disorders. Ellagic acid is one of the main components of pomegranate with potent antioxidant activity. Results from different studies reported that Punica granatum L or its byproducts can be used as natural food additives in human and animal nutrition in order to boost immunity, microbial safety and provide the housing environment without affecting body weight gain. In addition, Punica granatum L. byproducts can modulate immune function and gut microbiota of broiler chickens as well as reduce the odorous gas emissions from excreta. Naturally occurring polyphenols in a pomegranate can be a potential alternative medicine for the prevention of avian Colibacillosis diseases and can also be used as an intestine astringent to relieve diarrhea and enteritis in chickens.

Conclusion: The present review gives the insight towards major components of pomegranate as well as their pharmacological activities against pathological disorders. In spite of many beneficial properties of Punica granatum L., more research evidence on a molecular basis is needed to find out the molecular mechanism of action in various animals and human

背景:石榴是一种灌木,主要分布在地中海地区。由于其具有抗炎、抗菌、止泻、免疫调节、抗肿瘤、伤口愈合和抗真菌等生物活性,其果实受到了研究人员的广泛关注,这些活性被认为是来自于全球各地的这种树的种子、树皮、果汁、果皮和叶子的各种成分。石榴的酚类化合物已被证明对各种病理性感染和非感染性疾病具有预防和治疗作用。目的:综述石榴在感染性和非感染性疾病相关因素中的药理作用。方法:目前的综述是基于各种科学数据库中已有的文献和专利,强调了石榴的作用以及它对传染性和非传染性疾病的治疗潜力。纳入研究的数据库包括PubMed、Med line、PubMed Central、Science Direct和其他一些科学数据库。通过这些不同的数据库获得的信息被编译,批判性地解释并呈现在当前的研究中。结果:记录了石榴植物的多维有益应用。石榴籽油含有植物雌激素化合物,石榴果实含有丰富的酚类化合物,具有很强的抗氧化活性。石榴的果实和树皮在不同的动物和人类模型中被用来治疗肠道寄生虫、痢疾和腹泻。自古以来,果汁和种子就被认为是治疗咽喉和心脏疾病的最佳方法。鞣花酸是石榴的主要成分之一,具有很强的抗氧化活性。不同的研究结果表明,石榴或其副产品可以作为人类和动物营养的天然食品添加剂,以提高免疫力,微生物安全性和提供居住环境,而不影响体重增加。此外,石榴副产物还能调节肉鸡的免疫功能和肠道菌群,减少粪便中恶臭气体的排放。石榴中天然存在的多酚可以作为预防禽大肠杆菌病的潜在替代药物,也可以作为肠道收敛剂来缓解鸡的腹泻和肠炎。结论:本文综述了石榴的主要成分及其抗病理疾病的药理作用。尽管石榴有许多有益的特性,但需要更多的分子基础研究证据来发现各种动物和人体模型的分子作用机制,以验证石榴作为一种有效的治疗剂的有效性。
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引用次数: 67
Anti-Inflammatory Drugs and Herbs with Special Emphasis on Herbal Medicines for Countering Inflammatory Diseases and Disorders - A Review. 抗炎药物和草药,特别强调抗炎症疾病和失调的草药-综述。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180115153635
Mohd I Yatoo, Arumugam Gopalakrishnan, Archana Saxena, Oveas R Parray, Noore A Tufani, Sandip Chakraborty, Ruchi Tiwari, Kuldeep Dhama, Hafiz M N Iqbal

Background: Diseases with inflammatory etiopathology have increased in incidence in recent times. Drugs used for therapeutic management of such inflammatory diseases are relieving the ailment but at the same time also countering serious life threatening consequences. Moreover, they are costly and rarely available at all places. In this context, research and development on medicinal herbs have opened a new era in the prophylactic and therapeutic management of inflammatory diseases.

Objective: To highlight the importance of anti-inflammatory medicine-synthetic drugs and natural herbs, their constituents, mechanism of action, benefits, side effects and future prospects. The overall aim is to provide better health services to patients regardless of their background on equality basis.

Results: Anti-inflammatory herbs have proven beneficial by combating inflammatory responses that lead to severe abnormality in body systems. Inflammation though a protective response to infection or injury and may result in pathological outcome when aggravated or of severe degree thus needs an early intervention for proper resolution. Medicinal plants or their constituents are considered beneficial due to the properties i.e., satisfactory potency, ease of availability, cheapness, less or no side effects, safer and efficient as compared to the synthetic counterparts. These medicinal herbs contain phytoconstituents that can prevent undesirable inflammatory processes and also posses anti-inflammatory activity. Steroids, glycosides, phenolics, flavonoids, alkaloids, polysaccharides, terpenoids, cannabinoids, fatty acids are common phytoconstituents present in these plants. Different mechanisms have been explored for the anti-inflammatory action of these active ingredients. They may synergize the anti-inflammatory pathway enzymes, factors, proteins or interfere with these in the inflammatory pathway like lipooxygenases, cyclooxygenases, tumor necrosis factors, interleukins, prostaglandin, nitric oxide, mitogenactivated protein, nuclear factor, etc. Considering all the above-mentioned factors, further research from molecular to cellular level will enable a better understanding of the mechanisms. Common antiinflammatory herbal plants are Curcuma longa, Zingiber officinale, Rosmarinus officinalis, Borago officinalis, Urtica dioica, Uncaria tomentosa, Vaccinium myrtillus, Olea europaea and much more. They are believed to be without side effects unlike the chemical counterparts or synthetic anti-inflammatory agents e.g. steroids, nonsteroid anti-inflammatory drugs, and immunosuppresants used for controlling and suppressing inflammatory crisis. A proper phytochemical, pharmacological and physiological evaluation will enable their safe and effective use in inflammatory conditions. Many of these anti-inflammatory drugs and herbal preparations have been patented with some under consideration.

Conclusion: <

背景:近年来,炎症性疾病的发病率有所增加。用于治疗这些炎症性疾病的药物在缓解疾病的同时,也在对抗严重的危及生命的后果。此外,它们价格昂贵,而且很少在所有地方都能买到。在此背景下,草药的研究和开发为炎症性疾病的预防和治疗管理开辟了一个新的时代。目的:介绍抗炎药物——合成药物和天然草药的重要性、成分、作用机制、益处、毒副作用及发展前景。总的目标是在平等的基础上向病人提供更好的保健服务,不论其背景如何。结果:抗炎草药已被证明对对抗导致身体系统严重异常的炎症反应有益。炎症虽然是对感染或损伤的一种保护性反应,但当炎症加重或严重时可能导致病理结果,因此需要早期干预以适当解决。药用植物或其成分被认为是有益的,因为其特性,即令人满意的效力,易于获得,便宜,较少或没有副作用,与合成对应物相比更安全和有效。这些草药含有植物成分,可以防止不良的炎症过程,也具有抗炎活性。类固醇、糖苷、酚类、黄酮类、生物碱、多糖、萜类、大麻素、脂肪酸是这些植物中常见的植物成分。这些活性成分的抗炎作用机制已被探索。它们可以协同抗炎途径中的酶、因子、蛋白或干扰这些炎症途径中的酶、因子、蛋白,如脂氧化酶、环氧化酶、肿瘤坏死因子、白细胞介素、前列腺素、一氧化氮、有丝分裂原活化蛋白、核因子等。考虑到上述因素,进一步从分子水平到细胞水平的研究将有助于更好地了解其机制。常见的抗炎草本植物有姜黄、生姜、迷迭香、蒲公英、荨麻、钩藤、桃金娘、油橄榄等等。它们被认为没有副作用,不像化学对应物或合成抗炎剂,如类固醇、非类固醇抗炎药和用于控制和抑制炎症危机的免疫抑制剂。适当的植物化学、药理学和生理学评估将使其在炎症条件下安全有效地使用。许多这些抗炎药物和草药制剂已经获得专利,有些正在考虑中。结论:天然草药作为抗炎药安全、有效,是一种较好的选择。植物成分的作用机制与合成分子一样有效。今后的研究应着眼于这些植物在不同疾病中的不同有益应用的分子机制。本文介绍了近年来抗炎药物和草药类专利的研究进展,并对该领域的发展现状和前景进行了展望。
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引用次数: 85
Role of Curcumin in Regulation of TNF-α Mediated Brain Inflammatory Responses. 姜黄素在调节TNF-α介导的脑炎症反应中的作用。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2018-01-01 DOI: 10.2174/1872213X12666180703163824
Tirthraj Baj, Rohit Seth

Background: Inflammation is a protective response of the body system that protects the body from the various kinds of external and internal insults; however, it has been found that most chronic illnesses are caused by dysregulated and excessive inflammation. Inflammation plays a major role in developing neurological diseases. In the brain cytokines, TNF-α and TNF-β are known to mediate inflammation in many diseases. Functions of these cytokines are regulated by the activation of transcription factor NF-κb. Recent evidence suggest that curcumin has an immense therapeutic potential because of its anti-inflammatory and anti-oxidant properties. It has been tested for treating various chronic illnesses associated with the brain.

Objective: The study aims to elucidate the role of curcumin in alleviating the inflammatory reactions initiated by TNF-α and NF-κb signaling.

Methods: This study is a survey of literature from sources like PubMed central, science direct, medline and available scientific databases to determine how inflammation plays an important role in the development of neurodegenerative diseases and the role of curcumin as an anti-inflammatory agent. Looking into the importance of curcumin in alleviating inflammatory responses, several patents are filed and accepted which are referenced in this article.

Results: Neuro-inflammation mediated by TNF-α plays a major role in the development of pathologies like Alzheimer's disease, Parkinson's disease, multiple sclerosis, amyotrophic lateral sclerosis etc. Curcumin appears to subside or reduce the inflammatory responses. Thus, it appears to have therapeutic potential for treating various neuroinflammatory diseases.

Conclusion: Cytokines get upregulated during neurodegenerative diseases as a result of which inflammatory responses are initiated in the brain. Curcumin is reported to have anti-inflammatory properties and thereby its supplementation may help in reducing the inflammation. Future research on this area will further explain the mode of action of curcumin in alleviating neuroinflammation.

背景:炎症是身体系统的一种保护性反应,保护身体免受各种外部和内部的伤害;然而,已经发现大多数慢性疾病是由失调和过度炎症引起的。炎症在神经系统疾病中起着重要作用。在脑细胞因子中,TNF-α和TNF-β在许多疾病中介导炎症。这些细胞因子的功能受转录因子NF-κb的激活调控。最近的证据表明,姜黄素具有巨大的治疗潜力,因为它具有抗炎和抗氧化的特性。它已经被测试用于治疗各种与大脑有关的慢性疾病。目的:研究姜黄素在缓解TNF-α和NF-κb信号引发的炎症反应中的作用。方法:本研究是对PubMed central、science direct、medline和现有科学数据库等来源的文献进行调查,以确定炎症在神经退行性疾病的发展中如何发挥重要作用以及姜黄素作为抗炎剂的作用。研究姜黄素在减轻炎症反应中的重要性,本文引用了一些专利申请和接受。结果:TNF-α介导的神经炎症在阿尔茨海默病、帕金森病、多发性硬化症、肌萎缩侧索硬化症等疾病的发生发展中起重要作用。姜黄素似乎可以平息或减少炎症反应。因此,它似乎具有治疗各种神经炎症性疾病的治疗潜力。结论:细胞因子在神经退行性疾病中上调,导致大脑炎症反应的启动。据报道,姜黄素具有抗炎特性,因此补充姜黄素可能有助于减轻炎症。未来在这方面的研究将进一步阐明姜黄素减轻神经炎症的作用机制。
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引用次数: 29
Cutaneous Larva Migrans. 皮肤幼虫迁移。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2017-05-01 DOI: 10.2174/1872213X11666170110162344
A. Leung, B. Barankin, K. Hon
BACKGROUNDCutaneous larva migrans is one of the most common skin diseases reported in travelers returning from tropical regions. Western physicians, however, are often not familiar of this condition.OBJECTIVETo review in depth the epidemiology, pathophysiology, clinical manifestations, complications, and treatment of cutaneous larva migrans.METHODSA PubMed search was completed in Clinical Queries using the key term "cutaneous larva migrans". The search included meta-analyses, randomized controlled trials, clinical trials, and reviews. Patents were searched using the key term "cutaneous larva migrans" from www.google.com/patents, www.uspto.gov, and www.freepatentsonline.com.RESULTSCutaneous larva migrans is a zoonotic infestation caused by penetration and migration in the epidermis of filariform larva of different kinds of animal hookworms through contact with feces of infected animals. Cutaneous larva migrans is endemic in tropical and subtropical regions. Clinically, cutaneous larva migrans is characterized by an intensely pruritic erythematous migrating tortuous or serpiginous, slightly raised track. The diagnosis is mainly clinical, based on the history of travel to an endemic area and exposure to contaminated soil/sand and the characteristic serpiginous track. Treatment options as well as recent patents related to the management of cutaneous larva migrans are also discussed. Compared with oral antihelminthics, topical treatment over the affected area is less effective. Oral ivermectin is the treatment of choice.CONCLUSIONThe pruritic serpiginous track is pathognomonic. Oral ivermectin is the treatment of choice.
背景:皮肤迁徙幼虫是热带旅行者中最常见的皮肤病之一。然而,西方医生往往不熟悉这种情况。目的综述皮肤迁徙幼虫的流行病学、病理生理、临床表现、并发症及治疗方法。方法在“临床查询”中使用关键词“皮肤迁移幼虫”完成PubMed检索。研究包括荟萃分析、随机对照试验、临床试验和综述。在www.google.com/patents、www.uspto.gov和www.freepatentsonline.com.RESULTSCutaneous中搜索关键词“皮肤幼虫迁移”进行专利检索,幼虫迁移是不同种类的动物钩虫丝状幼虫通过接触被感染动物的粪便,在表皮渗透迁移而引起的人畜共患疾病。皮肤幼虫迁徙是热带和亚热带地区的地方病。临床上,皮肤幼虫迁移的特征是强烈瘙痒的红斑性迁移,弯曲或蛇形,轻度凸起。诊断主要是临床诊断,根据流行地区旅行史和接触污染的土壤/沙子以及特有的蛇形足迹。治疗方案以及最近的专利有关的管理皮肤幼虫迁移也进行了讨论。与口服抗虫剂相比,局部治疗患处效果较差。口服伊维菌素是治疗的首选。结论瘙痒性蛇形道是典型的。口服伊维菌素是治疗的首选。
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引用次数: 7
Rifaximin - Chitosan Nanoparticles for Inflammatory Bowel Disease (IBD). 利福昔明-壳聚糖纳米颗粒治疗炎性肠病(IBD)。
IF 4.2 Q3 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2017-05-01 DOI: 10.2174/1872213X10666161230111226
J. Kumar, A. Newton
BACKGROUNDInflammatory Bowel Disease (IBD) cannot be controlled easily and the recurrence is the most challenging issue for the physicians. There are various controlled and colon targeted drug delivery systems available for the treatment with limited success rate. Nanoparticles prepared by using the colon targeted polymers such as chitosan may improve the IBD due to their smaller size, unique physico chemical properties and targeting potential.OBJECTIVEThe aim of this investigation was designed to formulate and develop a colon targeted polysaccharide nanoparticles of rifaximin (RFX) by using linear polysaccharide chitosan, for the improvement of rifaximin solubility, overall therapeutic efficacy and colon targeting.METHODSThe research was focused on developing RFX nanoparticles for the treatment of Inflammatory Bowel Disease (IBD) by ionic gelation method. Nanoparticles were subjected to various characterization techniques such as XRD, FTIR and mean particle size (MPS) by Master Sizer and Zeta Sizer. Transmission Electron Microscopy (TEM), drug entrapment efficiency and zeta potential are also determined for the developed formulations. The efficiency of drug release from prepared formulation was studied in vitro by using a dialysis bag diffusion technique in the buffer condition mimicking stomach, intestine and colonic pH conditions.RESULTSThe prepared nanoparticles demonstrated the size in the nano range. The drug release profile was controlled in the upper GI tract and the maximum amount of drug was released in the colonic conditions. The prepared nanoparticles significantly improved the solubility of rifaximin. The zeta potential of the best chitosan preparation was found to be 37.79, which confirms the stability of prepared nanosuspension.CONCLUSIONNanoparticles with small particle size found to have high encapsulation efficiency and relatively high loading capacity and predetermined in vitro release profile.
背景炎症性肠病(IBD)不易控制,复发对医生来说是最具挑战性的问题。有各种可控和结肠靶向药物递送系统可用于治疗,但成功率有限。使用结肠靶向聚合物(如壳聚糖)制备的纳米粒子由于其较小的尺寸、独特的物理化学性质和靶向潜力,可以改善IBD。目的利用线性多糖壳聚糖制备利福昔明结肠靶向多糖纳米颗粒(RFX),以提高利福昔敏的溶解度、整体疗效和结肠靶向性。方法采用离子凝胶法研制用于治疗炎症性肠病(IBD)的RFX纳米粒子。通过Master Sizer和Zeta Sizer对纳米颗粒进行了各种表征技术,如XRD、FTIR和平均粒径(MPS)。还测定了所开发制剂的透射电子显微镜(TEM)、药物包封效率和ζ电位。在模拟胃、肠和结肠pH条件的缓冲条件下,使用透析袋扩散技术在体外研究了制剂的药物释放效率。结果所制备的纳米颗粒的尺寸在纳米范围内。药物释放曲线在上消化道中得到控制,并且在结肠条件下释放最大量的药物。制备的纳米颗粒显著提高了利福昔明的溶解度。最佳壳聚糖制剂的ζ电位为37.79,这证实了所制备的纳米悬浮液的稳定性。结论小颗粒纳米颗粒具有较高的包封效率和相对较高的负载能力,并具有预定的体外释放特性。
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引用次数: 19
期刊
Recent patents on inflammation & allergy drug discovery
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