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Investigation of In Vitro Cytotoxic Effects of Flumethrin by Using Brine Shrimp Lethality Assay 用盐水对虾致死试验研究氟氯菊酯体外细胞毒作用
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000174
Ufuk Mercan Yücel
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引用次数: 0
Prevalence of Antibiotic Resistant Bacteria in Urine Culture from Two Medical Laboratories in Benghazi 班加西两个医学实验室尿液培养中抗生素耐药菌的流行情况
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000196
Samia Elzwi
Background: Urinary tract infection is the most common bacterial infection and is the second after respiratory tract infection in antibiotic prescription. The treatment of UTI is becoming difficult because of the increasing drug resistance against the common bacteria associated with UTI. Objective: This study aimed to determine the bacteria, and their antimicrobial drug resistance, associated with UTI in the Libyan population in the city of Benghazi. Materials and Methods: We performed a retrospective analysis of data of urine culture (2019 -2020) taken from two Medical Laboratories in Benghazi. A total of 1031 urine samples; 318 male, 713 females were analyzed. Result: In this study, Escherichia coli was the most prevalent bacterial uropathogen with (59.84%), followed by Klebsiella pneumoniae (11.58%) and pseudomonas aeruginosa (10%). Then, Proteus and streptococcus pneumoniae had the same prevalence value (3.86%), Enterococcusfaecalis (2.7%), and Staphylococcus aureus (2.3%). Neisseria gonorrhea had the lowest (.038). Furthermore, E coli is highly resistance to imipenem, nalidixic acid and nitrofurantoin, and Klebsiella pneumoniae is highly resistance to, imipenem, nitrofurantoin, levofloxacin and ciprofloxacin, pseudomonas is resistance to imipenem, levofloxacin, and ciprofloxacin, proteus mirabilis is resistance to nitrofurantoin, Augmentin and gentamicin. Antibiotics purchasing without prescriptions remains a major problem in Libya. Based on these findings, we recommend appropriate initiatives to monitor and control the use of antibiotics.
背景:尿路感染是最常见的细菌感染,是抗生素处方中仅次于呼吸道感染的第二大细菌感染。由于对与尿路感染相关的常见细菌的耐药性日益增加,治疗尿路感染变得越来越困难。目的:本研究旨在确定班加西利比亚人群中与尿路感染相关的细菌及其抗菌药物耐药性。材料和方法:我们对班加西两个医学实验室的尿液培养数据(2019 -2020)进行了回顾性分析。共1031份尿样;男性318例,女性713例。结果:以大肠杆菌(59.84%)为主,其次为肺炎克雷伯菌(11.58%)和铜绿假单胞菌(10%)。其次,变形杆菌和肺炎链球菌、粪肠球菌和金黄色葡萄球菌的患病率相同(3.86%),分别为2.7%和2.3%。淋病奈瑟菌最低(0.038)。此外,大肠杆菌对亚胺培南、萘啶酸和呋喃妥因具有高度耐药,肺炎克雷伯菌对亚胺培南、呋喃妥因、左氧氟沙星和环丙沙星具有高度耐药,假单胞菌对亚胺培南、左氧氟沙星和环丙沙星具有耐药,奇异变形杆菌对呋喃妥因、奥格门汀和庆大霉素具有耐药。在利比亚,无处方购买抗生素仍然是一个主要问题。基于这些发现,我们建议采取适当的措施来监测和控制抗生素的使用。
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引用次数: 0
Convection-Enhanced Delivery of Alkaloid - Loaded Maghemite Nanoparticles against 9L - Gliomass Cell Line 负载生物碱的磁赤铁矿纳米颗粒对9L -胶质瘤细胞系的对流增强递送
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000210
Mahendra Kumar Sahu
Convection Enhanced Delivery (CED) is a novel approach to synthesize and facilitate targeted delivery of phytocontituents/ pharmaceuticals to the brain. The CED procedure involves a minimally invasive surgical exposure of the brain, followed by placement of small diameter catheters directly into the brain tumor. The study was designed to synthesize unique, sustained release, targeted delivery with no toxicity of piperidine alkaloids along with maghemite (γ-Fe2O3), poly-ethylene glycol and human serum albumin conjugation using 9L-gliomass cell line. Subsequently different nanoparticles (NPs) were prepared Naked NPs and HSA- or polyethylene glycol (PEG)-coated NPs with/without piperidine alkaloid were studied. In vitro results showed no toxicity and a similar cell-kill efficacy of the piperidine alkaloid-loaded particles via HSA coating to that of free piperidine alkaloid, while piperidine alkaloid-loaded particles via PEG coating showed low efficacy
对流增强输送(CED)是一种合成和促进植物成分/药物靶向输送到大脑的新方法。CED手术包括微创手术暴露大脑,随后将小直径导管直接置入脑肿瘤。本研究旨在利用9l -胶质质细胞系,与磁赤铁矿(γ-Fe2O3)、聚乙二醇和人血清白蛋白偶联物合成独特、缓释、无毒性的哌啶类生物碱。随后制备了不同的纳米颗粒(NPs),并研究了HSA或聚乙二醇(PEG)包被/不包被胡椒碱生物碱的NPs。体外实验结果表明,经HSA包被的胡椒碱生物碱负载颗粒与游离胡椒碱的细胞杀伤效果相似,无毒性,而PEG包被的胡椒碱生物碱负载颗粒的细胞杀伤效果较低
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引用次数: 0
Zanthoxylum Armatum: A Systemic Review of its EthnoMedicinal Properties, Phytochemistry, Pharmacology and Toxicology 花椒:民族药用特性、植物化学、药理学和毒理学的系统综述
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000162
A. Bhattacharjee
Background: Zanthoxylum armatum DC., a popular spice and traditional medicine is widely distributed throughout North Eastern region of India. The plant has been used in different indigenous medicinal practices to cure several diseases associated with digestive and nervous system. Aim: The aim of this paper is to provide a systematic review on taxonomy, ethnomedicinal properties, phytochemistry, pharmacology, and toxicology of this plant. Furthermore, the possible development and perspectives for future research on this plant are also discussed. Materials and methods: Upto date information was gathered through a search of different books, journals, articles, annual reports, proceedings and web-based materials. Result: The different plant parts like leaves, fruits, stem, bark, seeds and roots are enriched with various secondary metabolites viz. alkaloids, sterols, phenolics, lignins, coumarins, terpenoids and flavonoids. It is considered as one of the most valued commercial trade medicinal plant due to its multidirectional therapeutic applications in Ayurveda and other traditional system of medicine. Pharmacological findings revealed its potential as nootropic, antioxidant, antiinflammatory, cytotoxic, insecticidal/larvicidal drug. Conclusion: Zanthoxylum armatum is one of the important folklore medicinal plants cultivated in North Eastern region of India. Its diverse therapeutic applications can be associated with the presence of various secondary metabolites. The various ethno-pharmacological applications of Zanthoxylum armatum have been verified by several related researches. More extensive study on the individual specific phyto-component can lead to novel innovations for the well-being of
背景:Zanthoxylum armatum DC。是一种流行的香料和传统药物,广泛分布在印度东北部地区。这种植物在不同的土著医学实践中被用来治疗与消化和神经系统有关的几种疾病。目的:对该植物的分类、民族药特性、植物化学、药理及毒理学等方面进行系统综述。并对该植物的研究前景进行了展望。材料和方法:通过搜索不同的书籍、期刊、文章、年度报告、会议记录和网络材料来收集最新的信息。结果:植物的叶、果、茎、皮、种子、根等不同部位富含生物碱、甾醇、酚类、木质素、香豆素、萜类、黄酮类等多种次生代谢产物。它被认为是最有价值的商业贸易药用植物之一,因为它在阿育吠陀和其他传统医学系统中的多向治疗应用。药理研究表明其具有促智、抗氧化、抗炎、细胞毒、杀虫/杀幼虫等药理作用。结论:花椒是印度东北地区重要的民间药用植物之一。其不同的治疗应用可能与各种次级代谢物的存在有关。花椒的多种民族药理学应用已被多项相关研究证实。对单个特定植物成分进行更广泛的研究可以为人类的福祉带来新的创新
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引用次数: 0
The Bioactive Flavonoid Taxifolin Inhibits Differentiation and the Production of the Inflammatory Cytokine Interleukin-6 in Cultured Human Adipocytes 生物活性类黄酮杉木素抑制体外培养的人脂肪细胞的分化和炎性细胞因子白细胞介素-6的产生
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000195
Mami Sakurai
Background: Taxifolin, a bioactive flavonoid that possesses potent antioxidant activity, has been reported to show multiple pharmacological properties, including protective effects against obesity-related diabetic nephropathy and diabetic cardiomyopathy. However, knowledge regarding the effects of taxifolin on adipocytes, which are closely associated with obesity and diabetes, is insufficient. Objective: This study aimed to explore the direct effects of taxifolin on differentiation and inflammation adipocytes by culturing human preadepocytes (HPAds). Methods: HPAds were cultured for 16 days in a differentiation medium with or without taxifolin to examine its effect on differentiation. On day 16, levels of lipid and differentiation-related gene expression (PPARγ, C/EBPα, adiponectin, CD36, and GLUT4 mRNAs) in adipocytes were measured using the Oil Red O assay and the real-time polymerase chain reaction assay, respectively. Adiponectin levels in the medium were measured using an enzyme-linked immunosorbent assay (ELISA). The taxifolin effect on inflammation was assessed using mature adipocytes differentiated for 15 days. After incubating mature adipocytes in a differentiation medium containing tumor necrosis factor-α (TNF-α) or TNF-α + taxifolin for three hours, the level of interleukin-6 (IL-6), an inflammatory cytokine in the medium, was measured using ELISA. Results: Exposure of taxifolin to adipocytes during differentiation decreased the levels of lipid in adipocytes and adiponectin in the medium. It also decreased the expression levels of C/EBPα, adiponectin, CD36, and GLUT4 mRNAs, but not PPARγ mRNA. Taxifolin inhibited the increase in IL-6 levels in the medium induced by TNF-α in mature adipocytes. Conclusion: These results suggest that taxifolin has anti-differentiation and anti-inflammatory effects on adipocytes. Additionally, taxifolin is expected to have the potential as a therapeutic drug for obesity and metabolic syndrome.
背景:杉木素是一种具有生物活性的类黄酮,具有强大的抗氧化活性,已被报道显示出多种药理特性,包括对肥胖相关的糖尿病肾病和糖尿病性心肌病的保护作用。然而,关于taxifolin对与肥胖和糖尿病密切相关的脂肪细胞的影响的知识还不够。目的:通过培养人前脂肪细胞(hpad),探讨taxifolin对脂肪细胞分化和炎症的直接影响。方法:将hpad在加或不加taxifolin的分化培养基中培养16 d,观察其对分化的影响。第16天,分别采用油红O法和实时聚合酶链反应法检测脂肪细胞的脂质水平和分化相关基因表达(PPARγ、C/EBPα、脂联素、CD36和GLUT4 mrna)。采用酶联免疫吸附试验(ELISA)测定培养基中的脂联素水平。使用分化15天的成熟脂肪细胞来评估杉木素对炎症的影响。成熟脂肪细胞在含肿瘤坏死因子-α (TNF-α)或TNF-α + taxifolin的分化培养基中培养3小时后,采用ELISA法检测培养基中炎症细胞因子白细胞介素-6 (IL-6)的水平。结果:在分化过程中,taxifolin暴露于脂肪细胞中,降低了脂肪细胞中的脂质水平和培养基中的脂联素。同时降低了C/EBPα、脂联素、CD36和GLUT4 mRNA的表达水平,但没有降低PPARγ mRNA的表达水平。Taxifolin抑制TNF-α诱导的成熟脂肪细胞IL-6水平升高。结论:杉木素对脂肪细胞具有抗分化和抗炎作用。此外,taxifolin有望成为肥胖和代谢综合征的治疗药物。
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引用次数: 1
Adverse Effects of Bisoprolol in Rats 比索洛尔对大鼠的不良反应
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000164
Alsadek H Bogzil
The present study was designed to investigate the adverse effect of Bisoprolol and protective effect of Vitamin E and To Show the result of the combination between Bisorprolol and Vit. E on hepatic and renal disturbance induced in rats by Bisorprolol. Experimental design: After one week of acclimatization, eighty rats randomly allocated into 4 equal groups, each of 20 rats. The 1st group: Rats in this group were not medicated and left as control and received Nacl as avehicle. The 2nd group (VE): Rats in this group treated with vitamin E (1.8mg/kg b.wt. once daily) per os for Successive 21 days. The 3rd group (B): Rats in this group treated orally with Bisoprolol (1.8mg/kg b.wt. once daily) for successive 21 days as standard. The 4th group (VE+B): Rats in this group received orally a combination of vitamin E (1.8mg/kg b.wt. once daily) with Bisoprolol (1.8mg/kg b.wt. once daily) for Successive 21 day. At the end of the experiment, all rats were sacrificed, Liver and kidney samples were taken and blood was taken to centrifuged to gain serum for biochemical investigations. Effect of Bisoprolol, Vit.E and their combination on liver parameter (ALT, AST, ALP, Total serum proteins, Serum albumin, serum globulin). Oral administration of Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) Showed a significant increase in (ALT, AST, ALP) while total serum proteins, serum albumin, and serum globulin showed a significant decrease compared with control group. Administration of Vit.E (1.8mg/kg b.wt. once daily for 21 days) and its combination with Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a decrease in (ALT, SAT, ALP) while total serum proteins, serum albumin, and serum globulin showed an increased compared with Bisoprolol group. 2Effect of Bisoprolol, Vit.E and their combination on kidney parameters (creatinine and uric acid). Oral administration of bisoprolol (1.8mg/kg b.wt. once daily for 21 days) Showed a significant increase in (Creatinine and uric acid) compared with control group. Administration of Vit E (1.8mg/ kg b.wt. once daily for 21 days and its combination with bisoprolol (1.8mg /kg b.wt. once daily for 21 days) Showed a decrease in (creatinine and uric acid compared with bisoprolol group. 3Effect of Bisoprolol and vit. E on antioxidant activites aCAT, SOD and GPX activity Administration of Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a significant decrease in CAT, SOD and GPX activity compared with control group. Administration of Vit.E (1.8mg/kg b.wt. once daily for 21 days) and its combination with bisoprolol showed a significant increase in CAT, SOD and GPX activity compared with bisoprolol group. bLipid peroxidation (MDA) Oral administration of bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a significant increase in MDA activity compared with control group. Research Article
本研究旨在探讨比索洛尔的不良反应和维生素E的保护作用,并展示比索洛尔与维生素E联合使用的效果。E对比索洛尔致大鼠肝肾损害的影响。实验设计:适应1周后,80只大鼠随机分为4组,每组20只。第一组:不给药,留用为对照,以Nacl为载药剂。第二组(VE):给予维生素E (1.8mg/kg b.w.t);每天一次),连续21天。第三组(B):该组大鼠口服比索洛尔(1.8mg/kg b.wt)。每天一次),连续21天为标准。第四组(VE+B):该组大鼠口服维生素E (1.8mg/kg b.wt)。比索洛尔(1.8mg/kg b.wt)。每天一次),连续21天。实验结束时,处死大鼠,取肝肾标本,离心取血,得到血清进行生化检查。比索洛尔的效果。E及其联合作用对肝脏各项指标(ALT、AST、ALP、血清总蛋白、血清白蛋白、血清球蛋白)的影响。口服比索洛尔(1.8mg/kg b.wt)。(1次/ d,连用21 d)血清ALT、AST、ALP显著高于对照组,血清总蛋白、白蛋白、球蛋白显著低于对照组。Vit的管理E(1.8毫克/公斤体重)每日1次,连用21天),并与比索洛尔(1.8mg/kg b.w.t)合用。与比索洛尔组相比,1次/天,连续21天,ALT、SAT、ALP均下降,血清总蛋白、血清白蛋白、血清球蛋白均升高。比索洛尔的疗效。E及其联合对肾脏参数(肌酐、尿酸)的影响。口服比索洛尔(1.8mg/kg b.wt)。每日1次,连续21天)与对照组相比,肌酐和尿酸显著升高。给药Vit E (1.8mg/ kg b.wt)。每日一次,连用21天,并与比索洛尔(1.8mg /kg b.wt)合用。每日1次,连续21天)与比索洛尔组相比,肌酐和尿酸均下降。比索洛尔与维特的疗效。比洛尔(1.8mg/kg b.wt)对抗氧化活性、aCAT、SOD和GPX活性的影响与对照组相比,CAT、SOD和GPX活性显著降低。Vit的管理E(1.8毫克/公斤体重)每日1次,连用21 d),与比索洛尔组相比,其与比索洛尔组的CAT、SOD和GPX活性均显著升高。脂质过氧化(MDA)口服比索洛尔(1.8mg/kg b.wt)。1次/ d,连续21 d), MDA活性显著高于对照组。研究文章
{"title":"Adverse Effects of Bisoprolol in Rats","authors":"Alsadek H Bogzil","doi":"10.23880/apct-16000164","DOIUrl":"https://doi.org/10.23880/apct-16000164","url":null,"abstract":"The present study was designed to investigate the adverse effect of Bisoprolol and protective effect of Vitamin E and To Show the result of the combination between Bisorprolol and Vit. E on hepatic and renal disturbance induced in rats by Bisorprolol. Experimental design: After one week of acclimatization, eighty rats randomly allocated into 4 equal groups, each of 20 rats. The 1st group: Rats in this group were not medicated and left as control and received Nacl as avehicle. The 2nd group (VE): Rats in this group treated with vitamin E (1.8mg/kg b.wt. once daily) per os for Successive 21 days. The 3rd group (B): Rats in this group treated orally with Bisoprolol (1.8mg/kg b.wt. once daily) for successive 21 days as standard. The 4th group (VE+B): Rats in this group received orally a combination of vitamin E (1.8mg/kg b.wt. once daily) with Bisoprolol (1.8mg/kg b.wt. once daily) for Successive 21 day. At the end of the experiment, all rats were sacrificed, Liver and kidney samples were taken and blood was taken to centrifuged to gain serum for biochemical investigations. Effect of Bisoprolol, Vit.E and their combination on liver parameter (ALT, AST, ALP, Total serum proteins, Serum albumin, serum globulin). Oral administration of Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) Showed a significant increase in (ALT, AST, ALP) while total serum proteins, serum albumin, and serum globulin showed a significant decrease compared with control group. Administration of Vit.E (1.8mg/kg b.wt. once daily for 21 days) and its combination with Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a decrease in (ALT, SAT, ALP) while total serum proteins, serum albumin, and serum globulin showed an increased compared with Bisoprolol group. 2Effect of Bisoprolol, Vit.E and their combination on kidney parameters (creatinine and uric acid). Oral administration of bisoprolol (1.8mg/kg b.wt. once daily for 21 days) Showed a significant increase in (Creatinine and uric acid) compared with control group. Administration of Vit E (1.8mg/ kg b.wt. once daily for 21 days and its combination with bisoprolol (1.8mg /kg b.wt. once daily for 21 days) Showed a decrease in (creatinine and uric acid compared with bisoprolol group. 3Effect of Bisoprolol and vit. E on antioxidant activites aCAT, SOD and GPX activity Administration of Bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a significant decrease in CAT, SOD and GPX activity compared with control group. Administration of Vit.E (1.8mg/kg b.wt. once daily for 21 days) and its combination with bisoprolol showed a significant increase in CAT, SOD and GPX activity compared with bisoprolol group. bLipid peroxidation (MDA) Oral administration of bisoprolol (1.8mg/kg b.wt. once daily for 21 days) showed a significant increase in MDA activity compared with control group. Research Article","PeriodicalId":313915,"journal":{"name":"Advances in Pharmacology & Clinical Trials","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126876465","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
Pathophysiology and Management of Bacterial Meningitis in Pediatrics 儿科细菌性脑膜炎的病理生理学和治疗
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000198
Gudisa Bereda
Bacterial meningitis in children and infants is correlated with substantial morbidity and mortality. Bacterial meningitis is one of the most frequent central nervous system infections, which is prevalent in low-income countries. There are three types of neonatal meningitis such as early-onset meningitis (from 0–6 days); late-onset meningitis (from 7–29 days) and extremely late-onset meningitis (from 30–90 days). The intense inflammation within the subarachnoid space noted in lumbar cerebrospinal fluid, and the resulting neurological damage, are not the direct result of the pathogenic bacteria but rather of activation of the host’s inflammatory pathways by the microorganisms or their products. All children who are suspected of having meningitis should have their cerebrospinal fluid examined unless lumbar puncture is contraindicated. The critical elements of managing pediatric meningitis involve prompt initiation of therapy, use of the appropriate antimicrobial with correct dosing and duration, attention to expected complications, and appropriate follow-up. In neonates, the primary empiric regimen used conventionally has been ampicillin and gentamycin. For infants whose cerebrospinal fluid is suspicious for bacterial meningitis, ampicillin (300 mg/kg per day divided every 6 hrs) and cefotaxime (200 to 300 mg/kg per day divided every 6 hrs) is appropriate.
儿童和婴儿细菌性脑膜炎与大量发病率和死亡率相关。细菌性脑膜炎是最常见的中枢神经系统感染之一,在低收入国家普遍存在。新生儿脑膜炎有三种类型,如早发性脑膜炎(0-6天);迟发性脑膜炎(7-29天)和极迟发性脑膜炎(30-90天)。腰椎脑脊液蛛网膜下腔内的剧烈炎症以及由此引起的神经损伤不是致病菌的直接结果,而是微生物或其产物激活宿主炎症通路的结果。所有怀疑患有脑膜炎的儿童都应检查脑脊液,除非有腰椎穿刺的禁忌。管理儿童脑膜炎的关键要素包括及时开始治疗,使用适当的抗微生物药物,正确剂量和持续时间,注意预期的并发症,以及适当的随访。在新生儿中,常规使用的主要经验性方案是氨苄西林和庆大霉素。对于脑脊液疑似细菌性脑膜炎的婴儿,宜使用氨苄西林(每天300毫克/公斤,每6小时分一次)和头孢噻肟(每天200至300毫克/公斤,每6小时分一次)。
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引用次数: 0
Difloxacin Disposition and Residues in Broiler Chickens 双氟沙星在肉鸡体内的处理和残留
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000214
C. Errecalde
Difloxacin disposition in broiler chickens was studied, with the objective of establishing pharmacokinetic parameters in plasma and tissues and estimating a withdrawal period. Forty-two adult chickens were divided into 14 groups of 3 individuals each, which received a 10 mg/kg single oral dose of difloxacin after a period of fasting between 12 hours before and 3 hours after administration. Each batch was sacrificed at pre-established times, and blood, muscle lung, liver, skin and kidney samples were obtained in a period up to 120 hours post application. Assay consisted in the extraction of the analyte, its separation and quantification by high performance liquid chromatography (HPLC). Mean plasma and tissue concentrations of difloxacin by time were analyzed with the PK Solution software. Oral application determines rapid absorption, moderate plasmatic permanence and extensive tissue distribution. The analysis of residual concentrations in tissues using WT 1.4 software calculated the withdrawal period, based on maximum residue limits (MRL) of 300, 1900, 400, 600 and 300 µg/kg, established for muscle, liver, skin, kidney and lung, respectively, a withdrawal period of 3 days is estimated for muscle, liver and skin and 5 days for kidney and lung.
研究了双氟沙星在肉鸡体内的分布,建立了双氟沙星在血浆和组织中的药动学参数,并估计了停药期。将42只成年鸡分为14组,每组3只,在给药前12小时至给药后3小时禁食,给予10 mg/kg双氟沙星单次口服。每批在预先设定的时间处死,并在应用后120小时内获得血液、肌肉肺、肝脏、皮肤和肾脏样本。分析包括分析物的提取、分离和高效液相色谱(HPLC)定量。用PK Solution软件分析双氟沙星随时间变化的平均血浆和组织浓度。口服决定快速吸收,适度的血浆持久性和广泛的组织分布。使用WT 1.4软件分析组织中残留浓度,根据肌肉、肝脏、皮肤、肾脏和肺的最大残留限量(MRL)分别为300、1900、400、600和300µg/kg,计算停药期,估计肌肉、肝脏和皮肤的停药期为3天,肾脏和肺的停药期为5天。
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引用次数: 0
Faropenem, a Stable and Orally Bioavailable β-Lactam, to Counteract Resistant Pathogens and Infectious Diseases 法罗培南:一种稳定的口服生物可利用β-内酰胺,用于抵抗耐药病原体和传染病
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000216
Amit Bhalla
Antimicrobial resistance is a huge challenge for the effective prevention and treatment of infectious diseases worldwide. Community-onset infections with extended-spectrum β-lactamases (ESBL) producing bacteria are a challenge. In various studies, ESBL-producing isolates were consistently susceptible only to carbapenems. When treatment with other antibiotics fails, carbapenems are used as the last-line antibiotics for treating severe and/or resistant bacterial infections. In this narrative review, we aim to present the pharmacology of Faropenem, which is an orally administered penem antibiotic with a broad-spectrum activity against many Gram-positive and Gram-negative aerobes, and anaerobes. Faropenem is effective in the treatment of uncomplicated cystitis and is a potential solution to combat the emergence of resistance among respiratory tract pathogens. It is an alternative to fluoroquinolones or macrolides/ketolides when there is a concern with resistant pathogens.
抗微生物药物耐药性是世界范围内有效预防和治疗传染病的巨大挑战。社区发生的广谱β-内酰胺酶(ESBL)产生细菌感染是一个挑战。在各种研究中,产生esbl的分离株始终只对碳青霉烯类敏感。当用其他抗生素治疗失败时,碳青霉烯类被用作治疗严重和/或耐药细菌感染的最后一线抗生素。在这篇叙述性综述中,我们的目的是介绍法罗培南的药物学,法罗培南是一种口服给药的培南抗生素,对许多革兰氏阳性和革兰氏阴性需氧菌和厌氧菌具有广谱活性。法罗培南在治疗无并发症的膀胱炎方面是有效的,并且是对抗呼吸道病原体耐药性出现的潜在解决方案。当涉及耐药病原体时,它是氟喹诺酮类药物或大环内酯类/酮类药物的替代品。
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引用次数: 0
Medicinal Herbal Plants and Allopathic Drugs to Treat Diabetes Mellitus: A glance 治疗糖尿病的草药植物和对抗药物:概览
Pub Date : 1900-01-01 DOI: 10.23880/apct-16000151
Saurabh Nimesh
The present study was based on Diabetes Mellitus, its cure using herbal drugs over allopathic drugs. According to the official World Health Organisation (WHO) data, India tops the list of countries with the highest number of diabetics; China, America, Indonesia, Japan, Pakistan, Russia, Brazil, Italy and Bangladesh follow. In the year 2000, the total number of diabetics in India stood at 31.7 million and is expected to rise by more than 100% in the year 2030 to account to a whopping 79.4 million. Despite the use of advanced Allopathic drugs for the treatment, use of herbal remedies is gaining higher importance because of Allopathic drugs have drawbacks and limitations. Natural herbs have been highly esteemed source of medicine throughout the human history. They are widely used today indicating that herbs are a growing part of modern high-tech medicine. The herbal drugs with anti-diabetic activity are extensively formulated commercially because of easy availability, affordability and less side effects as compared to the synthetic anti-diabetic drugs. The WHO has listed 21,000 plants, which are used for medicinal purposes around the world. A list of medicinal herbal plants with proven anti-diabetic and related beneficial effects and of herbal drugs used in treatment of diabetes is compiled. Thus, this review article undertakes the attempt for providing updated information on the type of diabetes and herbal formulations which will enhance the existing knowledge of the researchers.
本研究以糖尿病为研究对象,以中药治疗糖尿病为研究对象。根据世界卫生组织(WHO)的官方数据,印度是糖尿病患者人数最多的国家;中国、美国、印度尼西亚、日本、巴基斯坦、俄罗斯、巴西、意大利和孟加拉国紧随其后。2000年,印度糖尿病患者总数为3170万,预计到2030年将增长100%以上,达到7940万。尽管使用了先进的对抗疗法药物进行治疗,但由于对抗疗法药物有缺点和局限性,使用草药疗法变得越来越重要。在整个人类历史上,天然草药一直是备受推崇的药物来源。它们在今天被广泛使用,这表明草药是现代高科技医学中日益增长的一部分。与合成的抗糖尿病药物相比,具有抗糖尿病活性的草药由于容易获得、负担得起和副作用小而被广泛地商业化配制。世界卫生组织列出了全球2.1万种药用植物。编制了经证实具有抗糖尿病和相关有益作用的草药植物清单以及用于治疗糖尿病的草药。因此,这篇综述文章试图提供关于糖尿病类型和草药配方的最新信息,以提高研究人员的现有知识。
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引用次数: 2
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Advances in Pharmacology & Clinical Trials
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