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Phytochemical Composition and Pharmaceutical Potential of Lantana sp: A Review Lantana sp的植物化学成分及药用潜力综述
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3607
L. Ravi
Lantana is a common plant found in around 60 tropical and subtropical countries worldwide. It is a highly invasive species that has tremendously dominated over other species of plants and threaten biodiversity. At present, physical, chemical, and biological agents are in consideration to eradicate this plant to prevent the threat to biodiversity and soil fertility. Lantana is considered as an unwanted plant and its biomass is disposed off. In this review, the pharmaceutical potential of this plant and its phytochemical constituents are discussed. Being source for wide variety of bioactive phytochemicals, Lantana is a valuable pharmaceutical raw material. Hence, instead of eradicating the plant as waste material, its pharmaceutical potentials such as antioxidant, antidiabetic, antimicrobial, anti-inflammatory, and anticancer activities can be exploited for the possible application as therapeutic agent. The modern medicine can take advantage of the fast-growing nature of this plant and use this plant as a tool for biopharming. In traditional medicine, Lantana has been used in formulation along with other plants as a treatment for several ailments. This review concludes that Lantana is a medicinally valuable plant, with huge potential in the pharmaceutical industry.
Lantana是一种常见的植物,在全世界大约60个热带和亚热带国家都有发现。它是一种高度入侵的物种,对其他植物物种有着极大的统治地位,并威胁着生物多样性。目前,为了防止对生物多样性和土壤肥力的威胁,人们正在考虑使用物理、化学和生物制剂来根除这种植物。Lantana被认为是一种不需要的植物,其生物量被处理掉。本文对该植物的药用潜力及其化学成分进行了综述。作为多种具有生物活性的植物化学物质的来源,芒草是一种有价值的药用原料。因此,它的抗氧化、抗糖尿病、抗菌、抗炎和抗癌活性等药物潜力可以被开发为可能的治疗剂,而不是将其作为废物清除。现代医学可以利用这种植物的快速生长特性,并利用这种植物作为生物伤害的工具。在传统医学中,Lantana与其他植物一起用于治疗几种疾病。综上所述,lanthana是一种具有药用价值的植物,在制药工业中具有巨大的潜力。
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引用次数: 0
Application of Response Surface Methodology for Combination of Herbal Extracts Against Antioxidant and Antipsoriatic Activity 响应面法在中药提取物联合抗氧化和抗银屑病活性研究中的应用
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3610
H. Chadha
Aim: The present paper modeled combination of three herbal extracts, extract from the seed of Carica papaya, lyophilized water of Cocos nucifera, and extract from the stem of Ichnocarpus frutescens to evaluate their free radical scavenging activity, using Box-Behnken design response surface methodology (BBD-RSM), a statistical technique designed to optimize compositions that we applied in a novel manner to design combinations of herbal extracts for better antioxidant and antipsoriatic activity. Material and Methods: A BBD-RSM design using three factors and three levels were selected to optimize the ratio of three herbal extracts. Effect of three independent factors, that is, dry weight of C. papaya seed extract (ethanolic), dry weight of lyophilized coconut water, and dry weight of Ichnocarpus extract (hydroalcoholic) was studied on two dependent responses, that is, superoxide dismutase and 2,2-diphenyl-1-picrylhydrazyl activity. Results and Discussion: Combining herbal extracts in optimum ratio have shown synergistic potential against oxidative stress and for free radical scavenging activity. Combination therapy has been shown to be effective in preventing many disorders as compared to their individual potential for cure. The analysis of variance was performed to evaluate the significant differences between the independent variables. BBD-RSM allows for extrapolation of data from three or more compounds in variable ratio combinations. Conclusion: It has been proved that the optimized herbal extracts in a proper amount have significant potential against antioxidant and antipsoriatic activity.
目的:采用Box-Behnken设计响应面法(BBD-RSM),对番木瓜种子提取物、椰子冻干水和鱼皮茎提取物三种草药提取物的组合进行建模,评价其自由基清除活性,一种旨在优化成分的统计技术,我们以一种新的方式应用于设计草药提取物的组合,以获得更好的抗氧化和抗银屑病活性。材料和方法:采用三因素三水平的BBD-RSM设计,优化三种草药提取物的配比。研究了木瓜种子提取物(乙醇)干重、冻干椰子水干重和Ichnocarpus提取物(水醇)干重三个独立因素对超氧化物歧化酶和2,2-二苯基-1-苦丁酰肼活性的影响。结果与讨论:以最佳比例组合草药提取物显示出对抗氧化应激和清除自由基活性的协同潜力。与个体治疗潜力相比,联合治疗已被证明在预防许多疾病方面是有效的。进行方差分析以评估自变量之间的显著差异。BBD-RSM允许从三种或三种以上可变比率组合的化合物中外推数据。结论:经筛选得到的中草药提取物在一定量下具有显著的抗氧化和抗银屑病活性。
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引用次数: 1
The Influence of Propellant on the Technological Qualities of a Floating Aerosol 推进剂对悬浮气溶胶工艺质量的影响
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3626
Davtian Lena
Introduction: The aim of the research was to substantiate the amount of propellant in the composition of the aerosol concentrate, depending on the consumption characteristics of the film formed on the wound surface. The publication experimentally substantiates the concentration of propellant chladon-134a, which is a necessary component for the formation of a film-forming aerosol. Materials and Methods: The authors used modern research methods: Pharmacotechnological and physicochemical – to substantiate the optimal amount of propellant in the composition of the developed aerosol film forming. Results: Studies have shown that the type and amount of propellant affects the film formation. The authors found that depending on the amount of propellant in the balloon, the type of delivery of the solution from the balloon will change – or sprayed, or removed smoothly; the appearance of the film depends on the amount of propellant – smooth, shiny, as well as the percentage of concentrate dispensing from the aerosol container. Discussion and Conclusion: Physicochemical studies have proved the influence of propellant on the technological parameters of the film-forming aerosol: Type of delivery, appearance – colorless film with a smooth shiny surface; film thickness – 10–200 μ; drying time – 10–15 min; and the percentage yield of the contents of the aerosol container – 97.84 ± 2.31%. The use of propellant chladon 134a at a concentration of 10% was found to be optimal. At this concentration, the highest percentage yield of the contents of the aerosol container is ensured, which allows to obtain a film with a smooth type of delivery and satisfactory consumer characteristics.
引言:研究的目的是根据伤口表面形成的薄膜的消耗特性,证实气溶胶浓缩物成分中推进剂的含量。该出版物通过实验证实了推进剂青瓷-134a的浓度,这是形成成膜气溶胶的必要成分。材料和方法:作者使用现代研究方法:药物技术和物理化学-来证实所开发的气溶胶成膜组成中的最佳推进剂量。结果:研究表明,推进剂的种类和用量对成膜有影响。作者发现,根据气球中推进剂的数量,从气球中输送溶液的类型会发生变化——或者被喷洒,或者被顺利移除;薄膜的外观取决于推进剂的数量——光滑、有光泽,以及从气溶胶容器中分配的浓缩物的百分比。讨论与结论:理化研究证明了推进剂对成膜气溶胶工艺参数的影响:发射类型、外观——无色薄膜,表面光滑有光泽;薄膜厚度–10–200μ;干燥时间–10–15分钟;气溶胶容器内容物的产率为97.84±2.31%。发现使用浓度为10%的推进剂青瓷134a是最佳的。在该浓度下,确保了气雾剂容器内容物的最高百分比产率,这允许获得具有平滑输送类型和令人满意的消费者特性的膜。
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引用次数: 0
The Burden of Illness of Acute Exacerbation of Asthma 哮喘急性加重的疾病负担
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3612
M. Iqbal
Objective: The objective of this study was to determine the direct cost of acute exacerbation of asthma (AEXA) among asthmatic patients. Materials and Methods: A total of 111 asthma patients who were admitted to a public hospital with AEXA included in this study. The costs, including investigation charge, unit costs of treatment per bed, medication charge, food costs, transportation costs, and loss of productivity per asthma episode, were calculated. Data were analyzed using Statistical Package for the Social Sciences (SPSS) ver.23.0. Results: A median medical cost of AEXA under the government perspective was USD 105.00 per episode. Medication cost comprised the majority (52.38%) of the total medical costs and lab investigations. A median medical cost of AEXA under the patient’s perspective was USD 22.50 per episode. Conclusion: AEXA and total days stay in the hospital were directly proportional to the total direct costs.
目的:本研究的目的是确定哮喘患者急性发作(AEXA)的直接成本。材料与方法:本研究共纳入公立医院收治的111例AEXA哮喘患者。计算成本,包括调查费用、每张病床的单位治疗费用、药物费用、食品费用、运输费用和每次哮喘发作的生产力损失。数据分析使用社会科学统计软件包(SPSS) ver.23.0。结果:政府视角下AEXA的平均医疗费用为105.00美元/次。用药费用占总医疗费用和实验室调查费用的52.38%。在患者的视角下,AEXA的平均医疗费用为22.50美元/次。结论:AEXA和总住院天数与总直接费用成正比。
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引用次数: 2
Potentiating Antibacterial Effect of Locally Deliver Caffeine Nanoparticles on Systemically Used Antibiotics in Periodontal Treatments 局部递送咖啡因纳米粒子对牙周治疗中系统使用的抗生素的增强抗菌作用
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3618
R. Parmar
Aims: Subinhibitory concentration of antibiotics at periodontal sites may increase the microbial resistance development; hence, this study was carried out to support the hypothesis that antimicrobial as well as anti-inflammatory action of caffeine and its locally deliver nanoparticles, which can deeply penetrate into the periodontal sites might potentiate and synergize the antibacterial effect of systematically used antibiotics for the treatment of periodontitis. Materials and Methods: In this study, the caffeine-loaded low-molecular-weight chitosan nanoparticles were prepared by ionic gelation methodology. Ex vivo antimicrobial activity of prepared nanoparticles was carried out by periodontitis patient’s stimulated saliva sample. Result: Our finding showed that caffeine nanoparticles in combination with amoxicillin affect the growth of periodontitis microorganisms. Periodontitis microorganism grew on a nutrient agar medium in Petri plates. Agar cups were filled in combination of different concentrations of amoxicillin with or without fixed caffeine concentration containing nanoparticles. High amoxicillin concentration (0.5 μg/ml) with 1 mg of caffeine-containing nanoparticles showed maximum zone of inhibition (1.81 ± 0.24 cm). On the other hand, low amoxicillin concentration (0.3 μg/ml) with 1 mg of caffeine-containing nanoparticles demonstrated significant potentiating inhibitory zone (1.54 ± 0.15 cm) as compare to high amoxicillin concentration (0.5 μg/ml) alone (1.50 ± 0.21 cm). Conclusions: It was shown that caffeine nanoparticles potentiate antibacterial effect of amoxicillin.
目的:抗生素在牙周部位的亚抑制浓度可能增加微生物耐药性的发展;因此,本研究旨在支持这样一种假设,即咖啡因及其局部递送的纳米颗粒可以深入牙周部位,具有抗菌和抗炎作用,可能会增强和协同系统使用的抗生素治疗牙周炎的抗菌效果。材料与方法:本研究采用离子凝胶法制备了含咖啡因的低分子量壳聚糖纳米粒子。制备的纳米粒子通过牙周炎患者刺激唾液样品进行体外抗菌活性研究。结果:我们的发现表明,咖啡因纳米颗粒与阿莫西林联合使用会影响牙周炎微生物的生长。牙周炎微生物在培养皿中的营养琼脂培养基上生长。琼脂杯以不同浓度的阿莫西林与含或不含固定咖啡因浓度的纳米颗粒的组合填充。高浓度阿莫西林(0.5μg/ml)和1 mg含咖啡因的纳米颗粒显示出最大抑制区(1.81±0.24 cm)。另一方面,与单独的高阿莫西林浓度(0.5μg/ml)(1.50±0.21 cm)相比,低浓度阿莫西林(0.3μg/ml)和1 mg含咖啡因的纳米颗粒显示出显著的增强抑制区(1.54±0.15 cm)。结论:咖啡因纳米粒子能增强阿莫西林的抗菌作用。
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引用次数: 0
Formulation and Evaluation of Sonidegib Loaded Poly (Ethyl Methacrylate) Nanoparticles for Effective Treatment of Cancer 索地吉负载的聚甲基丙烯酸乙酯纳米颗粒治疗癌症的制备与评价
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3622
A. P. Reddy
Aim: The present research is aimed to develop and evaluate sonidegib loaded poly(ethyl methacrylate) nanoparticles (PEM-NPs) to improve its resistance toward pH and chemical conditions in exposed cancerous lesions. Materials and Methods: The polymer PEM is prepared from ethyl methacrylate (monomer) followed by designing 17 formulations of sonidegib loaded PEM-NPs using 3-factor, 3-level Box–Behnken design, and the results analyzed using Stat-Ease Design Expert® software V8.0.1. Three optimal batches (F1, F2, and F3) with comparable values of observed and predicted values are characterized for particle size, polydispersity index (PDI), zeta potential (ZP), entrapment efficiency, and percentage drug loading. The formulation (F3) with minimum particle size and maximum percentage conversion is further subjected to powder X-ray diffraction (PXRD), Fourier-transform infrared (FTIR), scanning electron microscopy (SEM) studies, drug release, and stability study. Results and Discussion: The particle size of sonidegib PEM-NPs (F1, F2, and F3) ranges between 191.5 ± 42.9 nm to 355 ± 39.7 nm and PDI 0.454 to 0.626. The ZPs are within the acceptable limits of −22.9 ± 2.48 mV–−24.7 ± 1.89 mV. The entrapment efficiency of the NPs ranges between 68.46 ± 0.37% and 70.24 ± 0.18% and percent drug loading between 20.62 ± 2.12% and 21.24 ± 1.72. The in vitro release study indicated an improvement in drug release of formulation F3 (95.878%) in comparison with the pure drug (2.86%). The optimized formulation F3 characterized for FTIR, PXRD, and SEM studies indicated molecular state dispersion of the drug with the polymers. The stability studies conducted for 90 days indicated that the developed formulation is stable. Conclusion: Sonidegib loaded PEM-NPs prepared using 3-factor, 3-level Box–Behnken design with increased solubility and stability.
目的:本研究旨在开发和评估sonidegib负载的聚(甲基丙烯酸乙酯)纳米颗粒(PEM NPs),以提高其在暴露于癌症病变中对pH和化学条件的抵抗力。材料和方法:聚合物PEM由甲基丙烯酸乙酯(单体)制备,然后使用3因素、3级Box-Behnken设计设计17种负载sonidegib的PEM NP配方,并使用Stat Ease design Expert®软件V8.0.1分析结果。对三个最佳批次(F1、F2和F3)的粒径、多分散指数(PDI)、ζ电位(ZP)、包封效率和药物负载百分比进行了表征,观察值和预测值具有可比性。将具有最小粒径和最大转化率的制剂(F3)进一步进行粉末X射线衍射(PXRD)、傅立叶变换红外(FTIR)、扫描电子显微镜(SEM)研究、药物释放和稳定性研究。结果和讨论:sonidegib PEM NPs(F1、F2和F3)的粒径在191.5±42.9nm至355±39.7nm之间,PDI在0.454至0.626之间。ZPs在−22.9±2.48 mV–−24.7±1.89 mV的可接受范围内。NP的包封率在68.46±0.37%和70.24±0.18%之间,载药量百分比在20.62±2.12%和21.24±1.72之间。体外释放研究表明,与纯药物(2.86%)相比,制剂F3的药物释放度提高了95.878%。通过FTIR、PXRD和SEM研究表征的优化制剂F3表明,药物与聚合物的分子状态分散。进行90天的稳定性研究表明,所开发的制剂是稳定的。结论:Sonidegib负载的PEM NPs采用3因子、3级Box-Behnken设计制备,具有增加的溶解度和稳定性。
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引用次数: 0
A Review on Pharmaceutical Potential of Parthenium Plant Parthenium植物的药用潜力综述
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3608
L. Ravi
Parthenium plant, in general, is known to be harmful, dangerous, and invasive in nature. It causes much economic loss to farmers by affecting the cultivation of crops and considered to be a threat to primary production of crops and biodiversity as well. Parthenium hysterophorus a weed belonging to the family Asteraceae, it is an erect short-lived plant and is known for its fleshy growth along sides of abandoned places, roadsides, and uncultivated lands. This weed is found in hot and humid climates around the globe. This invasive species is known with different names in different countries such as carrot weed, star weed, congress grass, wild feverfew, ragweed, bitter weed, and white top. The spread of P. hysterophorus has been found to cause enormous loss to biodiversity by replacing natural ecosystems and sometimes known to cause total habit alternation. In this review article, we discuss P. hysterophorus as a weed, its origin, reproductive bionomics, chemical composition, and its pharmaceutical potential as antibacterial, anti-inflammatory, hypoglycemic, anti-HIV, and antitumor activity in detail.
一般来说,Parthenium是一种有害的、危险的、具有侵入性的植物。它通过影响作物的种植给农民造成很大的经济损失,并被认为是对作物初级生产和生物多样性的威胁。Parthenium hysterophorus是一种属于菊科的杂草,它是一种直立的短命植物,以其肉质生长在废弃的地方、路边和未开垦的土地上而闻名。这种杂草生长在全球炎热潮湿的气候中。这种入侵物种在不同的国家有不同的名字,如胡萝卜草、星草、国会草、野小白菊、豚草、苦草、白顶草。人们已经发现,子宫草的传播通过取代自然生态系统造成巨大的生物多样性损失,有时还会导致完全的习性改变。本文就宫草的来源、生殖生物学、化学成分及其抗菌、抗炎、降血糖、抗艾滋病、抗肿瘤等药理作用作一综述。
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引用次数: 4
Optimization of Chitinase Production from Lake Sediment Inhabitant Bacillus thuringiensis Strain LS1 and Bacillus cereus Strain LS2 苏云金芽孢杆菌菌株LS1和蜡样芽孢杆菌菌株LS2产几丁质酶的优化
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3611
S. Sudha
Objective: Chitinase production from freshwater lake sediment-derived bacteria by submerged fermentation and media optimization. Methodology: Isolation of bacteria from freshwater lake sediment by serial dilution followed by spread plate technique on colloidal chitin agar (CCA). The potential bacterial isolates were detected by qualitative cup plate assay and were identified by 16S rRNA sequencing. Optimization of the chitinase production was done by varying different physicochemical factors one at a time keeping the other factors constant. Results: Two isolates were selected for chitinase production based on the zone of clearance on CCA and were identified as Bacillus thuringiensis strain LS1 (MG948147) and Bacillus cereus strain LS2 (MG948148) based on 16S rRNA sequencing. The enhanced production of chitinase by B. thuringiensis strain LS1 was observed in minimal medium amended with 1% colloidal chitin, glucose as a carbon source, and malt extract as a nitrogen source, in pH 7.0, at 35°C in 72 h of incubation. The optimal condition for chitinase production by B. cereus strain LS2 was minimal medium amended with 1% colloidal chitin, sucrose as carbon source, and yeast extract as nitrogen source with pH 7.0 at 35°C in 96 h of incubation. Conclusion: Lake sediment bacterial community was screened for chitinase production and the potential strains were identified and its 16S rRNA sequences were submitted in GENE BANK.
目的:以淡水湖沉积物来源的细菌为原料,采用深层发酵法生产几丁质酶,并对培养基进行优化。方法:采用胶体几丁质琼脂(CCA)连续稀释扩散板技术从淡水湖沉积物中分离细菌。通过定性杯板法检测潜在的细菌分离株,并通过16S rRNA测序进行鉴定。通过改变不同的物理化学因素来优化几丁质酶的生产,一次一个,保持其他因素不变。结果:根据CCA上的清除区筛选出两株产几丁质酶的菌株,经16S rRNA测序鉴定为苏云金芽孢杆菌菌株LS1(MG948147)和蜡样芽孢杆菌菌株LS2(MG948.148)。苏云金芽孢杆菌菌株LS1在添加1%胶体几丁质、葡萄糖作为碳源和麦芽提取物作为氮源的最低培养基中,在pH 7.0、35°C下培养72小时,观察到几丁质酶的产量增加。蜡状芽孢杆菌菌株LS2产几丁质酶的最佳条件是以1%胶体几丁质、蔗糖为碳源、酵母提取物为氮源,在35°C、pH 7.0的最低培养基中培养96h。结论:对湖泊沉积物细菌群落进行了产几丁质酶的筛选,筛选出了潜在菌株,并将其16S rRNA序列提交到基因库中。
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引用次数: 1
Probiotics and Herbals as a Boom in Treatment of Ulcerative Colitis 益生菌和草药治疗溃疡性结肠炎的热潮
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3627
Sankha Bhattacharya
Ulcerative colitis (UC) is an inflammatory chronic disease primarily affecting the colonic mucosa; the extent and severity of colon involvement are variable. In its most limited form, it may be restricted to the distal rectum, while in its most extended form, the entire colon is involved. UC is identified by mucus diarrhea, tenesmus, bowel distension, and anemia. 5-aminosalicylic acid drugs, steroids, and immunosuppressant are used for therapy of UC. The annual occurrence of disease in Asia, America, and Europe was estimated to be 6.3, 19.2, and 24.3/100,000 people years. The main challenges in the management of the disease are drug-related side effects and local targeting. To overcome these challenges, probiotics overcome drug-related adverse side effects and local targeting. On ingestion, the probiotics can result in health beneficial effects. Probiotics are mainly used as gut modulators but are also nowadays explored for their use in UC.
溃疡性结肠炎(UC)是一种主要影响结肠粘膜的炎症性慢性疾病;结肠受累的程度和严重程度各不相同。在其最有限的形式中,它可能局限于直肠远端,而在其最延伸的形式中则涉及整个结肠。UC可通过粘液性腹泻、里急后重、肠胀和贫血来确定。5-氨基水杨酸药物、类固醇和免疫抑制剂用于UC的治疗。据估计,亚洲、美洲和欧洲的年发病率分别为6.3、19.2和24.3/10万人年。该疾病管理的主要挑战是与药物相关的副作用和局部靶向。为了克服这些挑战,益生菌克服了与药物相关的不良副作用和局部靶向。摄入益生菌后,可产生有益健康的效果。益生菌主要用作肠道调节剂,但目前也在探索其在UC中的应用。
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引用次数: 4
Comparison of the Expression of Antihypertensive Action of Preparation of Different Clinical and Pharmacological Groups 不同临床和药理学组制剂降压作用表达的比较
IF 0.4 Pub Date : 2020-06-09 DOI: 10.22377/ajp.v14i2.3624
V. Ivanna
Introduction: Increased blood pressure (BP) is one of the most significant epidemiological, medical, social, and economic consequences of problems. The results of many studies indicate that in one-third of people in Ukraine, the level of BP exceeds 140/90 mm Hg, it is increased. There is a contradiction between the need to adhere to the current level of therapy, which involves the use of new, as a rule, expensive techniques and drugs, and the constant lack of funding for health care. Materials and Methods: Methods of statistical description, systematic, sociological, economic, and statistical analysis, including variational statistics, correspondence questionnaires, and expert assessments, were used in the research process. The study included 1568 patients diagnosed with hypertension. As a result of the pharmacoepidemiological analysis, it was shown that the most often antihypertensive monotherapy is performed for younger patients with initial lower BP values. Results: A more detailed analysis of the antihypertensive activity of drugs belonging to the main pharmacological groups was performed with arterial hypertension monotherapy. Therefore, it is important to analyze the therapeutic efficacy of antihypertensive drugs from different clinical and pharmacological groups, safety, and their impact on the wellbeing of patients. Discussion and Conclusion: Analysis of the structure of prescriptions revealed the dominant positions of Agriculture Commercialization Equity Fund drugs, and, above all, drugs enalapril, among patients with hypertension in all study groups, regardless of age and gender, as well as regimens of antihypertensive therapy. A retrospective study of the antihypertensive effect of drugs from different clinical and therapeutic groups revealed no significant differences, but significant differences were noted when comparing the original drugs with their reproduced analogs (generics)
血压升高(BP)是最重要的流行病学、医学、社会和经济后果问题之一。许多研究结果表明,在乌克兰三分之一的人,血压水平超过140/90毫米汞柱,它是升高的。必须坚持目前的治疗水平,这通常涉及使用新的、昂贵的技术和药物,而保健资金不断缺乏,两者之间存在矛盾。材料与方法:在研究过程中使用了统计描述、系统、社会学、经济学和统计分析方法,包括变分统计、函电问卷调查和专家评估。该研究包括1568名被诊断为高血压的患者。药物流行病学分析的结果表明,最常见的降压单药治疗是针对初始血压值较低的年轻患者。结果:在动脉高血压单药治疗中,对主要药理组药物的降压活性进行了更详细的分析。因此,分析不同临床和药理组抗高血压药物的疗效、安全性及其对患者健康的影响具有重要意义。讨论与结论:处方结构分析显示,在所有研究组高血压患者中,不论年龄和性别,以及降压治疗方案中,农业商业化股权基金药物占主导地位,以依那普利药物占主导地位。对不同临床和治疗组药物的降压效果进行回顾性研究,结果显示无显著差异,但将原研药物与其复制类似物(仿制药)进行比较,发现有显著差异。
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引用次数: 0
期刊
Asian Journal of Pharmaceutics
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