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“Modifiable Hyperkalemia with Timely Recognition”- Beta Blocker (Metoprolol succinate) induced “及时识别可改变的高钾血症”-受体阻滞剂(琥珀酸美托洛尔)诱导
Pub Date : 2022-07-15 DOI: 10.9734/ajrimps/2022/v11i330190
P. Prasad, S. Raj
This case report describes the very rarest possibility of drug induced hyperkalemia with beta blockers. In literature search only 2 cases were reported as metoprolol succinate induced hyperkalemia in diabetes patients without renal insufficiency. As per FDA reports  only 0.5 % patients have reported hyperkalemia induced by metoprolol [1]. Patient is diabetic and hypertensive. And she is on oral hypoglycemic agents, premixed insulin and on beta blockers along with calcium channel blocker. The potassium value was ranging from 6 to 6.7 mmol/l. Evaluated in detail and no other abnormalities noted in laboratory investigations. Once the offending drug metoprolol is withdrawn the potassium value reaches to normal range in very short period.
本病例报告描述了非常罕见的药物诱导高钾血症与受体阻滞剂的可能性。在文献检索中,仅有2例无肾功能不全的糖尿病患者被报道为琥珀酸美托洛尔所致高钾血症。根据FDA的报告,只有0.5%的患者报告美托洛尔引起的高钾血症。患者有糖尿病和高血压。她正在服用口服降糖药,预混胰岛素和受体阻滞剂以及钙通道阻滞剂。钾值为6 ~ 6.7 mmol/l。详细评估,实验室检查未发现其他异常。一旦停用药物美托洛尔,钾值在很短时间内恢复到正常范围。
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引用次数: 0
COVID-19 Infection and Prevention: A Brief Review COVID-19感染与预防综述
Pub Date : 2022-06-18 DOI: 10.9734/ajrimps/2022/v11i330189
R. S. Kumar, .. Anushree
Corona viruses, a broad group of viruses that have an ability to infect a wide range of animals, or people. It can lead to mild to severe respiratory illnesses. In humans it caused fatal respiratory illness in 2002 and 2012, making it a new concern for public health in the 21st century. Its origin was in Wuhan from where it is rapidly spreading to the rest of the world. In terms of both the number of sick people and the geographic span of epidemic locations, it has crossed the counts of SARS and MERS. The ongoing COVID-19 outbreak has caused a significant threat to worldwide public life.
冠状病毒是一类广泛的病毒,能够感染多种动物或人类。它会导致轻微到严重的呼吸系统疾病。在2002年和2012年,它在人类中引起了致命的呼吸道疾病,使其成为21世纪公共卫生的一个新问题。它起源于武汉,并从那里迅速蔓延到世界其他地区。就患病人数和流行地点的地理跨度而言,它已经超过了SARS和MERS的数量。持续的COVID-19疫情对全球公共生活造成了重大威胁。
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引用次数: 0
Pattern of Some Sperm Proteins, Anti-oxidants, Testosterone, and Prostate-Specific Antigen of Infertile Males with Sperm Cell Deformities in Port Harcourt, Rivers State 一些精子蛋白,抗氧化剂,睾酮和前列腺特异性抗原的模式在哈科特港,河流州不育男性与精子细胞畸形
Pub Date : 2022-06-11 DOI: 10.9734/ajrimps/2022/v11i230186
Aminayanate M. Aworu, A. B. Chioma, I. Elekima, H. Brown, E. Bartimaeus
Aim: Infertility is a global problem affecting both males and females. It is a condition with psychological, economic, and medical implications resulting in trauma and stress, particularly in a society where there is a strong emphasis on childbearing. The study therefore aims to investigate the pattern of some sperm proteins, anti-oxidants, and prostate-specific antigen in the seminal plasma of infertile males with sperm cell deformities. Study Design: The study is a case-control study designed to investigate semen parameters and sperm proteins in infertile males with sperm cell deformities in Port Harcourt, Rivers State. Place and Duration of Study: The study was carried out in the Department of Medical Laboratory Science, Rivers State University, Port Harcourt. However, some of the Laboratory investigations were done in the Chemical Pathology Unit and Medical Microbiology Unit of the University of Port Harcourt Teaching Hospital, Port Harcourt. The Study was between the periods of September 2019 and Feb. 2022. Methodology: A total of 276 males indicated interest to participate in the study of which 193 male subjects were recruited. These subjects were grouped into normospermic males (100), azoospermic (40) and oligospermic males (53). Based on their sperm cell morphology and active motility, they were further classified into asthenozoospermic (40), oligoasthenozoospermic (48), teratozoospermic (26), asthenoteratozoospermic (32), and oligoasthenoteratozoospermic (22). HSP70, PKA, MDA, TAC, and GPX (in seminal plasma), PSA, and testosterone (in serum) were analyzed using ELISA while TAC was done using spectrophotometric methods. Results obtained were statistically analyzed using GraphPad Prism and SPSS. Results: Sperm motility, TSC, and normal sperm morphology were poor in oligospermic subjects but were very severe in OAT subjects. Sperm proteins were altered in subjects with abnormal sperm cell morphologies. HSP70 and PKA were significantly increased while OPN, TAC, and GPX were significantly decreased in the seminal plasma of infertile males with abnormal sperm cells. Testosterone and PSA in blood plasma were significantly lower and higher respectively. Conclusion: Oxidative stress played a significant role in sperm cell deformities and fertility. OAT subjects were the most affected.
目的:不育是一个全球性的问题,影响男性和女性。这是一种具有心理、经济和医学影响的疾病,导致创伤和压力,特别是在一个非常强调生育的社会。因此,本研究旨在探讨精子细胞畸形的不育男性精浆中某些精子蛋白、抗氧化剂和前列腺特异性抗原的模式。研究设计:本研究是一项病例对照研究,旨在调查河流州哈科特港精子细胞畸形的不育男性精液参数和精子蛋白。研究地点和时间:本研究在哈科特港河河州立大学医学检验科学系进行。不过,一些实验室调查是在哈科特港哈科特港大学教学医院的化学病理科和医学微生物科进行的。该研究在2019年9月至2022年2月期间进行。方法:共有276名男性表示有兴趣参与研究,其中193名男性受试者被招募。研究对象分为正常精子男性(100)、无精子男性(40)和少精子男性(53)。根据其精子细胞形态和活跃度,进一步将其分为弱精子型(40例)、少弱精子型(48例)、畸形精子型(26例)、弱异精子型(32例)和少弱异精子型(22例)。ELISA法测定HSP70、PKA、MDA、TAC、GPX(精浆)、PSA、睾酮(血清),分光光度法测定TAC。所得结果采用GraphPad Prism和SPSS进行统计分析。结果:精子活力、TSC和正常精子形态在少精组较差,而在OAT组非常严重。精子细胞形态异常的受试者精子蛋白发生改变。精子细胞异常的不育雄性精浆中HSP70、PKA显著升高,OPN、TAC、GPX显著降低。血浆中睾酮和PSA分别显著降低和升高。结论:氧化应激在精子细胞畸形和生育中起重要作用。OAT受试者受影响最大。
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引用次数: 1
Investigation of Pharmaceutical Care Practice in Two Tertiary Health Care Facilities in Central Monrovia, Liberia 利比里亚蒙罗维亚中部两所三级卫生保健机构药学服务实践调查
Pub Date : 2022-04-26 DOI: 10.9734/ajrimps/2022/v11i230185
C. Sampson K. P., Woode Eric
Aims:  to identify elements of pharmaceutical care and to what extend it is practiced in these hospitals and to identify any drug-related therapeutic problems and determine the perceived importance of pharmaceutical care. Study Design:  A prospective, cross-sectional descriptive survey was carried out among hospital pharmacists and some selected physicians and physician assistants working at two major tertiary healthcare facilities in Liberia. Place and Duration of Study: John F. Kennedy Memorial Hospital, and Eternal Love Winning Africa Hospital, between August, 2021 and October, 2021. Methodology: Pretested structured questionnaires covering demographics and the key elements of pharmaceutical care documentation was administered randomly to 43 health professionals in these hospitals and collected for compilations and analysis. Results: Twenty percent (20.9%) confirmed the documentation of pharmaceutical care elements in both facilities, and 18.6% confirmed the documentations of interventions. Methods used in documentation are paper (13.9%), manual (72.1%) and computers (6.9%) respectively. Unnecessary drug therapy/unwanted indication, adverse drug reactions, drug interactions, need for additional drugs, dosage too high, dosage too low, wrong drugs, and inappropriate compliance are the drug therapy problems that exist at both facilities.  The overall percentage of all the drug therapy problems is twenty-five percent (25.6%), of which most are highlighted at John F. Kennedy Memorial Hospital, though these problems exist at both hospitals. There is an increase in drug therapy problems and a decrease in standard documentation format and method used to document pharmaceutical care at both hospitals. Thirty-nine percent (39.5 %) of the respondents recognized the importance of the documentation of pharmaceutical care (PC).  Conclusion: The study findings revealed that there is semblance of elements of pharmaceutical care activities at the both hospitals, but it is limited. Inadequate documentations of PC interventions coupled with primitive methods of recording PC data are highlighted by respondents. The practice of pharmaceutical care in the Liberia’s healthcare system can greatly improve the quality of pharmaceutical services and enhance the quality of life and therapeutic outcomes to patients/clients.
目的:确定药学服务的要素及其在这些医院的实践范围,确定任何与药物相关的治疗问题,并确定药学服务的感知重要性。研究设计:在利比里亚两家主要三级医疗机构的医院药剂师和一些选定的医生和医生助理中进行了前瞻性横断面描述性调查。学习地点和时间:约翰·肯尼迪纪念医院和永恒的爱赢得非洲医院,2021年8月至2021年10月。方法:对这些医院的43名卫生专业人员随机发放预先测试的结构化问卷,问卷内容涵盖人口统计数据和药学护理文件的关键要素,并收集问卷进行汇编和分析。结果:20%(20.9%)的人确认了两家机构的药学服务要素文件,18.6%的人确认了干预措施文件。文献记录的方法分别为纸质(13.9%)、手工(72.1%)和计算机(6.9%)。不必要的药物治疗/不需要的适应症、药物不良反应、药物相互作用、需要额外的药物、剂量过高、剂量过低、错误的药物和不适当的依从性是两家机构存在的药物治疗问题。所有药物治疗问题的总体百分比为25%(25.6%),其中大多数在约翰·肯尼迪纪念医院突出,尽管这些问题在两家医院都存在。两家医院的药物治疗问题有所增加,用于记录药物护理的标准文件格式和方法有所减少。39%(39.5%)的受访者认识到药学服务文件的重要性。结论:研究结果表明,两家医院的药学服务活动要素具有相似性,但存在局限性。受访者强调了PC干预措施的文件不足以及记录PC数据的原始方法。利比里亚医疗保健系统的药学服务实践可以极大地提高药学服务的质量,提高患者/客户的生活质量和治疗效果。
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引用次数: 0
Oral Spray – A Review on Promising Drug Delivery System for Oral Cavity 口腔喷雾剂——前景广阔的口腔给药系统研究进展
Pub Date : 2022-04-22 DOI: 10.9734/ajrimps/2022/v11i230183
Chirag I Parmar, N. Joshi, Prachi Modi, P. Bhavsar, Nishtha Desai, Adil Patel
Aim: This review aims to compile information related to marketed oral spray preparation along with their formulation and clinical application. Objective: The main objective of this overview is to study the marketed oral spray dosage form for treatment of different diseases and learn about its advantages over the other oral dosage forms e.g. tablet, capsule, patches etc. Description: Oral spray with Mucoadhesive polymers forms small droplets that quickly adheres to the mucosal surface and let the drug permeate into the blood circulation easily. The oral mucosa has shown promising results for the systemic absorption of many drugs owing to the highly permeable nature of the mucosal membrane. Oral sprays are very fast, the most effective and easy way to get daily dose vitamins, minerals, and other nutrients ingredients. Due to this advantage oral sprays have emerged as an effective alternative for bypassing extensive first pass effect. Conclusion: It has been a very well known fact that the oral route of administration is the most popular route of drug administration. However the drwabacks like extensive first pass metabolism and drug degradation in stomach makes this route not suitable for all drugs and thus an alternative oral drug delivery systems are necessary to explaoint benefits of oral route. Many researchers are working to develop oral spray formulations for drugs which need quick permeation followed by quick onset of action and also provide an effective alternative of conventional oral drug delivery systems.
目的:本综述的目的是收集有关市场上销售的口服喷雾剂及其配方和临床应用的信息。目的:本综述的主要目的是研究市场上销售的用于治疗不同疾病的口服喷雾剂型,并了解其相对于其他口服剂型(如片剂、胶囊、贴剂等)的优势。说明:口服喷雾剂,黏附聚合物,形成小液滴,迅速附着在粘膜表面,使药物容易渗透到血液循环中。由于口腔粘膜的高渗透性,口腔粘膜对许多药物的全身吸收显示出有希望的结果。口服喷雾剂是非常快速,最有效和最简单的方式获得每日剂量的维生素,矿物质和其他营养成分。由于这一优势,口服喷雾剂已成为绕过广泛的首次通过效应的有效选择。结论:口服给药途径是最普遍的给药途径,这是众所周知的事实。然而,广泛的首过代谢和药物在胃中的降解等缺点使得该途径并不适用于所有药物,因此需要一种替代的口服给药系统来解释口服给药途径的好处。许多研究人员正在努力开发口服喷雾制剂,以满足快速渗透和快速起效的要求,并提供传统口服给药系统的有效替代方案。
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引用次数: 0
Modulation of Obesity in Sub-Saharan Africa Using Coenzyme Q10 利用辅酶Q10调节撒哈拉以南非洲地区的肥胖
Pub Date : 2022-03-31 DOI: 10.9734/ajrimps/2022/v11i230182
Doris Nnenna Ajibo, Ifeoma Cynthia Ekenna
Obesity is a metabolic disease caused by a large buildup of fat in the body and a deficit in energy consumption compared to energy disposal. It has been related to a shorter life expectancy, has been connected to various cancer types, and has been linked to secondary metabolic illnesses such as diabetes, atherosclerosis, and hypertension. Due to an increase in white adipose tissue deposition, oxidative stress can lead to obesity, and obesity can lead to increased oxidative stress in the body. Coenzyme Q10 (Ubiquinone) is an endogenous anti-oxidant with anti-oxidant properties that aids to reduce oxidative stress. It boosts the anti-oxidant activity of superoxide dismutase and glutathione peroxidase, reduces lipid peroxidation, neutralises free radicals, and promotes vitamin E and C regeneration in the body. It can be found in the form of ubiquinol or ubiquinone. CoQ10 may be found in both diet and supplements. It can be made as a syrup, tablet, soft gel capsule, hard shell capsule, or oral powder as a supplement. It is classified as a biopharmaceutical class II compound with low solubility but good permeability. When CoQ10 supplement is taken with a fatty meal, its bioavailability is increased. CoQ10 slows the evolution of obesity-related atherosclerosis and helps to mitigate the harmful bodily environment caused by obesity.
肥胖是一种代谢性疾病,由体内大量脂肪堆积和能量消耗不足引起。它与较短的预期寿命有关,与各种癌症类型有关,并与糖尿病、动脉粥样硬化和高血压等继发性代谢疾病有关。由于白色脂肪组织沉积的增加,氧化应激可导致肥胖,而肥胖可导致体内氧化应激增加。辅酶Q10(泛醌)是一种内源性抗氧化剂,具有抗氧化特性,有助于减少氧化应激。增强超氧化物歧化酶和谷胱甘肽过氧化物酶的抗氧化活性,减少脂质过氧化,中和自由基,促进体内维生素E和C的再生。它以泛醇或泛醌的形式存在。辅酶q10可以在饮食和补充剂中找到。它可以制成糖浆、片剂、软凝胶胶囊、硬壳胶囊或口服粉末作为补充。它是一种溶解度低但渗透性好的生物制药类化合物。当辅酶q10补充剂与脂肪膳食一起服用时,其生物利用度会增加。辅酶q10减缓肥胖相关动脉粥样硬化的演变,并有助于减轻肥胖造成的有害身体环境。
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引用次数: 0
Formulation Design and Ex Vivo Evaluation of Carbopol -Incorporated Mucoadhesive Thermoreversible gels of Sucralfate for Rectal Drug Delivery 直肠给药用卡波波尔黏附热可逆硫酸盐酸盐凝胶的配方设计及体外评价
Pub Date : 2022-03-23 DOI: 10.9734/ajrimps/2022/v11i130181
S. Firoz, S. Rajasekaran
Aim: The present research is focused on preparation of Thermoreversible gels and screening ex vivo anti-inflammatory activity using croton oil induced hemorrhoid model. Study Design: The animals were divided into four groups, n=8. After overnight fasting, hemorrhoids were induced by inserting sterile cotton swabs soaked in croton oil preparation into the anus of all group animals except normal control group. Place and Duration of Study: Depart of Pharmacology, Sree Vidyanikethan College of Pharmacy, Tirupati. between October 2021 to December 2021 Methodology: Experimental runs for optimization of formulation with the help of 23 factorial designs were designed [1]. Design of Expert program 6.0.6 (Stat-Ease Inc. Minneapolis, MN) was used to create formulations. Formulations were optimized using full factorial de­sign. In situ rectal gel was prepared by the cold meth­od [2]. As shown in Table 1, P188 was dissolved in DDW (de-ionized distilled water) including drug (1% w/v) at room temperature, and it was stored at 4°C for complete solubilization of P188. Carbopol solubilized in DDW, HPMC K4M and other mu­coadhesive polymers were then slowly added to the prepared solution with continuous agitation at 4°C, and were kept for 24 h before their use. The composi­tion of developed gel formulations is summarized in Table 1. Results: Results In the first set of experiment, the application of croton oil to recto anal portion of rats induced significant increase in the Recto anal coefficient and serum level of pro inflammatory cytokines such as IL-6, and TNF (-a) it also showed a significant increase in recto anal portion compared to normal control animals. However, the treatment with Sucralfate containing Thermoreversible gels has maintained the RAC and Interleukin -6 levels near to normal control group. These findings were further supported by histopathological examination wherein the animals treated with optimized formulation showed significant reversal in the severity of inflammation, vasodilatation in the recto anal portion, and presence of inflammatory cells. Conclusion: The findings of the present study suggest that the improved experimental model described in the present work has advantages and the model has a provision for quantifying the inflammatory exudates in the induced experimental hemorrhoids. Also, it was found that, the optimized formulation ameliorated the croton oil-induced hemorrhoids in rats.
目的:研究热可逆凝胶的制备及其体外抗炎作用。研究设计:将动物分为4组,每组8只。禁食一夜后,除正常对照组外,其余各组动物肛门内均插入浸泡过巴豆油制剂的无菌棉签诱导痔疮。学习地点和时间:Tirupati Sree Vidyanikethan药学院药学系。方法学:设计了23个因子设计的配方优化实验运行[1]。专家程序设计6.0.6 (Stat-Ease Inc.)明尼阿波利斯,MN)被用来创建配方。采用全因子设计对配方进行优化。采用冷法制备原位直肠凝胶[2]。如表1所示,将P188溶解在DDW(去离子蒸馏水)中,其中包括药物(1)% w/v) at room temperature, and it was stored at 4°C for complete solubilization of P188. Carbopol solubilized in DDW, HPMC K4M and other mu­coadhesive polymers were then slowly added to the prepared solution with continuous agitation at 4°C, and were kept for 24 h before their use. The composi­tion of developed gel formulations is summarized in Table 1. Results: Results In the first set of experiment, the application of croton oil to recto anal portion of rats induced significant increase in the Recto anal coefficient and serum level of pro inflammatory cytokines such as IL-6, and TNF (-a) it also showed a significant increase in recto anal portion compared to normal control animals. However, the treatment with Sucralfate containing Thermoreversible gels has maintained the RAC and Interleukin -6 levels near to normal control group. These findings were further supported by histopathological examination wherein the animals treated with optimized formulation showed significant reversal in the severity of inflammation, vasodilatation in the recto anal portion, and presence of inflammatory cells. Conclusion: The findings of the present study suggest that the improved experimental model described in the present work has advantages and the model has a provision for quantifying the inflammatory exudates in the induced experimental hemorrhoids. Also, it was found that, the optimized formulation ameliorated the croton oil-induced hemorrhoids in rats.
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引用次数: 0
Formulation and Characterization of Rutin Loaded Chitosan Nanoparticles 负载芦丁的壳聚糖纳米颗粒的制备与表征
Pub Date : 2022-01-20 DOI: 10.9734/ajrimps/2022/v11i130180
M. Raju, M. Srivani, N. V. L. Suvarchala Reddy, G. S. Priya
New drug delivery technologies are transforming drug discovery and development, as well as establishing research and development-focused pharmaceutical firms that are accelerating global progress. The bioactive rutin molecule is used in a wide range of food and medicinal goods. Its limited bioavailability and poor water solubility are major issues. Rutin is a polyphenolic natural compound with antibacterial, anticancer, antioxidant, chemopreventive, and anti-inflammatory activities. However, no research has been published to yet to improve its bioavailability and efficacy. As a result, an attempt was made in this study to load rutin into a nanoparticlulate system in order to improve its bioavailability and efficacy. Six formulations (F1-F6) of nanoparticles were prepared by solvent evaporation technique and were evaluated for particle size and shape using Zeta Sizer, Scanning Electron Microscopy (SEM) and Fourier Transform Infra-Red (FT-IR) Spectroscopy. The optimized formulation was further subjected to in vitro evaluation. Practical percent yield, drug entrapment efficiency and In vitro drug release were evaluated. Out of various formulations F1 have shown best results in particle size 80.71 (1-100 nm), particle shape (spherical nanoparticles with a smoothed surface), average size distribution (105.0), zeta potential (-20.6) percentage yield (70.83), drug entrapment efficiency (83.6%) and drug loading (95%). Pure rutin showed incomplete dissolution of 47.69% in 330 min while Rutin loaded nanoparticles gave 94.75% release in 330 min. It is obvious from the foregoing that rutin chitosan nanoparticles were used as a novel drug delivery technology to improve therapeutic efficacy and sustained release features while overcoming issues such as poor solubility and limited bioavailability.
新的药物输送技术正在改变药物发现和开发,并建立了以研究和开发为重点的制药公司,加速了全球进步。具有生物活性的芦丁分子广泛应用于食品和药品中。其有限的生物利用度和水溶性差是主要问题。芦丁是一种多酚类天然化合物,具有抗菌、抗癌、抗氧化、化学预防和抗炎活性。然而,目前还没有发表任何研究来提高其生物利用度和功效。因此,本研究试图将芦丁加载到纳米颗粒系统中,以提高其生物利用度和功效。采用溶剂蒸发技术制备了6个配方(F1-F6)纳米颗粒,并利用Zeta浆料机、扫描电镜(SEM)和傅里叶变换红外光谱(FT-IR)对纳米颗粒的粒径和形状进行了评价。进一步对优化后的配方进行体外评价。考察了实际收率、包封效率和体外释药效果。在不同的配方中,F1在粒径80.71 (1-100 nm)、颗粒形状(表面光滑的球形纳米颗粒)、平均粒径分布(105.0)、zeta电位(-20.6)、产率(70.83)、包封效率(83.6%)和载药量(95%)方面表现出最佳效果。纯芦丁在330 min内溶出率为47.69%,负载芦丁的纳米颗粒在330 min内释放率为94.75%。综上所述,芦丁壳聚糖纳米颗粒作为一种新型的给药技术,在克服溶解度差和生物利用度有限的同时,提高了药物的治疗效果和缓释特性。
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引用次数: 0
Anti-ulcer Activity of Ethanolic Extract of Alstonia scholaris Bark: An in vivo and in silico Approach 枸杞子树皮乙醇提取物抗溃疡活性的体内和体外实验研究
Pub Date : 2022-01-15 DOI: 10.9734/ajrimps/2022/v11i130179
M. Raju, R. Manisha, V. Reddy, M. Niharika
Aims: The present research is focused on screening in vivo anti-ulcer activity using pylorus ligation and ethanol induced ulcer model.  Study Design: Fourty eight rats, randomly divided into eight groups, were used in this study. Bark of Alstonia scholaris were air-dried, ground into fine powder and used in the preparation of an ethanolic extract. Place and Duration of Study: Department of Pharmacology, Osmania University, Hyderabad between December 2020 and September 2021. Methodology: Ethanol related ulcer was induced using 1 mL/kg b.w, p.o. Treated rats received ethanolic extract of Alstonia scholaris at various doses of 200 and 400 mg/kg b.w. Ulcer index, % ulcer protection were calculated and histological studies were conducted at 6 hr after pylorous ligation respectively. Results: Pharmacological estimations were done by means of 200 mg/kg, b.w. and 400 mg/kg, b.w. The total acidity and free acidity were decreased, pH was increased and ulcer index was decreased by Ethanolic extract of Alstonia scholaris (EEAS 200 and 400 mg/kg b.w., p.o.) in pylorus ligation model. Treatment with EEAS (200 and 400 mg/kg b.w. p.o.) has significantly decreased the ulcer index by ethanol induced ulcer model. To appreciate the ligand-binding attraction of the dynamic ingredients of the excerpt, docking trainings were accomplished for natural compounds against protein data bank (PDB) ID: 5A5N, PDB ID: 6Q2T, PDB ID: 7MBX, PDB ID: 2FV5. The results revealed that vanillic acid, venoterpine, loganetin, dibutyl phthalate, guaia-3,9- diene, 3,6-Bis[2-methylphenyl]-2,5-dihydropyrrolo[3,4-c] pyrrole-1,4- dione, 2H-1-Benzopyran- 2-one,7-acetyl-8-[acetyloxy]-4, n-hexadecanoic acid, stigmasterol, diospyrolide, D- Friedoolean-14-en-3-one, betulin, lupeol acetate, pentanoic acid and standard drug omeprazole had shown highest glide scores with all the selected proteins which indicate a stronger receptor-ligand binding affinity. Conclusion: From in vivo and in silico results it is evident that ethanolic bark extract of Alstonia scholaris possessed significant anti-ulcer activity.
目的:采用幽门结扎法和乙醇诱导的溃疡模型,对其体内抗溃疡活性进行筛选。研究设计:48只大鼠随机分为8组。用风干的方法将Alstonia scholaris树皮磨成细粉,用于制备乙醇提取物。学习地点和时间:2020年12月至2021年9月,海得拉巴Osmania大学药学系。方法:以1 mL/kg b.w, p.o诱导乙醇相关性溃疡,大鼠分别以200、400 mg/kg b.w的不同剂量给药,计算幽门结扎后6小时的溃疡指数、溃疡保护率,并进行组织学观察。结果:以200 mg/kg b.w.和400 mg/kg b.w.对幽门结扎模型进行药理学评价。Alstonia scholaris乙醇提取物(EEAS 200和400 mg/kg b.w., p.o.)可降低幽门结扎模型的总酸度和游离酸度,提高pH,降低溃疡指数。EEAS(200和400 mg/kg b.w.p o)可显著降低乙醇致溃疡模型的溃疡指数。为了了解该摘录的动态成分对配体结合的吸引力,对天然化合物进行了对接训练,以蛋白质数据库(PDB) ID: 5A5N, PDB ID: 6Q2T, PDB ID: 7MBX, PDB ID: 2FV5。结果表明,香草酸、维诺特平、马尾草素、邻苯二甲酸二丁酯、愈伤草-3,9-二烯、3,6-二[2-甲基苯基]-2,5-二氢吡咯- 3,4-c]吡咯-1,4-二酮、2h -1-苯并吡喃-2 - 1,7 -乙酰基-8-[乙酰氧基]-4、正十六酸、豆甾醇、二ospyrolide、D- Friedoolean-14-en-3-one、白桦林、lupeoil acetate、戊酸和标准药物奥美拉唑与所有选择的蛋白质的滑翔得分最高,表明它们具有较强的受体-配体结合亲和力。结论:从体内和体外实验结果可以看出,石桐树皮乙醇提取物具有明显的抗溃疡活性。
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引用次数: 1
COVID-19 Induced Secondary Hemophagocytic Lymphohsitocytosis: A Case Series COVID-19诱导继发性噬血细胞性淋巴组织细胞增多症:一个病例系列
Pub Date : 2022-01-10 DOI: 10.9734/ajrimps/2022/v11i130178
Omelkhir I. Elbanoni, H. A. Elhashmi, Mariam M. Madani, Huda A. Elabbud, Shirin Alougly, Nourz A. Elghariani
Hemophagocytic lymphohistiocytosis (HLH) is a lethal and rapidly progressive hyper-inflammatory state that lead to development of fulminant multi-organ failure. HLH is divided into primary or familial HLH (FHL) and secondary HLH (sHLH). It can be triggered by a variety of agent that affect the immune system, infection is a common triggering agent. Recently, Coronavirus disease (COVID-19) has spread all over the world and was declared a pandemic. COVID-19 infection in children can induce serious hyper-inflammatory syndrome termed multisystem inflammatory syndrome (MIS-C). Clinically MIS-C patients present with features that resemble Kawasaki’s disease or toxic shock syndrome and the clinical and laboratory manifestations may also similar to that of secondary hemophagocytic lymphohistiocytosis, or macrophage activation syndrome (MAS). The reported HLH syndrome in children with COVID-19 increased during 2020-2021. In this case series we present two pediatric patient diagnosed as sHLH post- COVID-19 infection with a brief literature review of similar pediatric patients. 
噬血细胞性淋巴组织细胞增多症(HLH)是一种致死性和快速进展的高炎症状态,可导致暴发性多器官功能衰竭的发展。HLH分为原发性或家族性HLH (FHL)和继发性HLH (sHLH)。它可以由多种影响免疫系统的因素触发,感染是常见的触发因素。最近,冠状病毒病(COVID-19)在全球蔓延,并被宣布为大流行。儿童感染COVID-19可诱发称为多系统炎症综合征(MIS-C)的严重高炎症综合征。临床MIS-C患者表现出类似川崎病或中毒性休克综合征的特征,临床和实验室表现也可能类似于继发性噬血细胞性淋巴组织细胞增多症或巨噬细胞激活综合征(MAS)。报告的COVID-19儿童HLH综合征在2020-2021年期间有所增加。在这个病例系列中,我们报告了两名被诊断为COVID-19感染后sHLH的儿科患者,并简要回顾了类似儿科患者的文献。
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Asian Journal of Research in Medical and Pharmaceutical Sciences
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