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Effect of Compound Lactobacillus Acidophilus Tablet Combined with Omeprazole Enteric-coated Tablet on Acute Gastroenteritis
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作者 CHEN Xiaoyu 《外文科技期刊数据库(文摘版)医药卫生》 2021年第9期414-415,共4页
Objective: to analyze the effect of compound lactobacillus acidophilus tablet combined with omeprazole enteric-coated tablet on disease control in patients with acute gastroenteritis. Methods: patients with acute gast... Objective: to analyze the effect of compound lactobacillus acidophilus tablet combined with omeprazole enteric-coated tablet on disease control in patients with acute gastroenteritis. Methods: patients with acute gastroenteritis were selected as the subjects of the study, and the patients admitted from June 2019 to August 2020 were selected for the period of time. The patients were divided into two groups by random number method for comparative exploration, and the changes of the condition of 100 patients were recorded. The control group was given compound lactobacillus acidophilus tablet, and the observation group was given compound Lactobacillus acidophilus tablet combined with omeprazole enteric-coated tablet. The therapeutic effect was analyzed. Results: from the quality of treatment, the treatment effect of observation group was 90%, the control group was 78%, the difference between the groups was significant, with statistical significance (P < 0.05). At the same time, the incidence of adverse events in the observation group was 4% (2/50), significantly lower than that in the control group (10%, 5/50), and the difference was statistically significant. Conclusion: the combination of compound Lactobacillus acidophilus tablets and omeprazole enteric-coated tablets in the treatment of acute gastroenteritis can not only manage the disease and improve the therapeutic effect, but also have high safety guarantee and clinical promotion value. 展开更多
关键词 compound lactobacillus acidophilus tablet omeprazole enteric-coated tablet acute gastroenteritis
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Formulation Development of Generic Omeprazole 20 mg Enteric Coated Tablets
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作者 Christopher Oswald Migoha Eliangiringa Kaale Godliver Kagashe 《Pharmacology & Pharmacy》 2015年第7期293-301,共9页
Omeprazole is a potent proton pump inhibitor with powerful inhibition of secretion of gastric juice. Oral site-specific drug delivery systems have recently attracted a great interest for the local treatment of bowel d... Omeprazole is a potent proton pump inhibitor with powerful inhibition of secretion of gastric juice. Oral site-specific drug delivery systems have recently attracted a great interest for the local treatment of bowel disease and for improving systemic absorption of drugs which are unstable in the stomach. However, microenvironment in the gastrointestinal tract and varying absorption mechanisms cause hindrance for the formulation and optimization of oral drug delivery. The objective of the study was to develop and optimize enteric coating process for omeprazole tablets. Different batches of core tablets were sub coated, one set sub coated with opadry and another with a mixture of light magnesium oxide, magnesium stearate and absolute alcohol omeprazole magnesium. Seal coating was applied by using opadry to achieve certain weight gain and to protect omeprazole from acidic coating polymers. A comparative dissolution test was performed. The variation of thickness and diameter were observed to be minimal with a weight gain of 3% - 4% of enteric polymer. Disintegration test showed that in each tested batch the enteric coated layer remained intact in 0.1N HCl for 2 hours and when exposed to alkaline media of phosphate buffer pH 6.8, it dissolved within few minutes. Dissolution release was 98.8% to 102.4% within two hours when the product was exposed to phosphate buffer pH 6.8 after 2 hours. The similarity and dis-similarity factors were calculated and observed to be 54 to 61 and 4 to 5 respectively. Therefore a simple and good enteric coating process was developed and tested with potential for transfer this technology into local pharmaceutical industries using cheap and easily available materials. 展开更多
关键词 omeprazole Magnesium ENTERIC Coating tablets Kollicoat (Methacrylic Acid/Ethyl ACRYLATE Copolymers) (MAE)
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Clinical Effect of Ilaprazole Enteric-Coated Tablets in Patients with Peptic Ulcer
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作者 Fanghui Chen 《Journal of Biosciences and Medicines》 2024年第9期155-160,共6页
Objective: To discuss the actual effect of ilaprazole enteric-coated tablets in the treatment of peptic ulcer patients. Methods: 200 peptic ulcer patients who received treatment from January to December 2023 were sele... Objective: To discuss the actual effect of ilaprazole enteric-coated tablets in the treatment of peptic ulcer patients. Methods: 200 peptic ulcer patients who received treatment from January to December 2023 were selected as the study sample, and all patients were randomly and evenly divided into the study group (n = 100) and the control group (n = 100), and the serum inflammatory factors and the disappearance time of symptoms were compared. Results: After treatment, the serum inflammatory factors in the observation group were better than those in the control group, and the time of belching and burning sensation in the observation group was shorter than that in the control group, all of which were statistically significant (P Conclusion: Ilaprazole enteric-coated tablets in the treatment of peptic ulcer have a good effect and can effectively improve the symptoms of patients with clinical signs, with reference significance. 展开更多
关键词 Ilaprazole enteric-coated tablets Peptic Ulcer SYMPTOMS
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Exploration on the Efficacy of Rebeprazole Sodium Enteric-soluble Tablets and Omeprazole in Gastric Ulcer Treatment
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作者 ZHOUXueqiang 《外文科技期刊数据库(文摘版)医药卫生》 2022年第4期132-136,共5页
Objective: to explore the clinical value of rebeprazole and omeprazole in gastric ulcer. Methods: patients with gastric ulcer were recorded in this experiment. Experiments began in July 2010 and ended in July 2021.A t... Objective: to explore the clinical value of rebeprazole and omeprazole in gastric ulcer. Methods: patients with gastric ulcer were recorded in this experiment. Experiments began in July 2010 and ended in July 2021.A total of 94 patients, equally divided to different groups, were based on the lottery method. Reference group: 47 patients were treated together with omeprazole, clarithromycin, amoxicillin, and colloidal pectin, bismuth. Test group: rebeprazole sodium enteric-coated tablets, clarithromycin, amoxicillin, colloidal pectin and bismuth therapy. Observation index: Improvement of clinical symptoms score of group 2 gastric ulcer patients, improvement of gastrointestinal hormone level, improvement of ulcer area and pain score;and occurrence of adverse reactions. Results: (1) Before treatment, the difference of clinical symptoms was weak, with P-value was 0.05.After treatment, the points of stomach pain, abdominal distension, acid reflux and poor appetite were decreased, and the test group had lower points, and the P-value was less than 0.05. (2) Before the treatment, the distribution of gastrointestinal hormone levels was relatively balanced, with a large P-value ratio of 0.05.After treatment, gastrin level and motility level decreased in each group, and the test group had lower data with a P value less than 0.05. (3) Before treatment, the ulcer area and pain score were similar, with a large P-value ratio of 0.05.After treatment, the ulcer area and pain score in each group showed a downward trend, and the value of the test group was smaller, and the P-value was less than 0.05. (4) In The reference group, the probability of adverse reactions such as gastric spasm, nausea and dizziness was higher than that of the test group, and the P-value was less than 0.05. Conclusion: based on the treatment of gastric ulcer.The improvement of symptom integral and the improvement of gastrointestinal hormone level were more obvious, and the ulcer area was reduced, and the pain was relieved. 展开更多
关键词 gastric ulcer rebeprazole sodium enteric-soluble tablets omeprazole clinical effect
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Analyze the Effect of Omeprazole Enteric Coated Tablets and Compound Lactobacillus Acidophilus Tablets in the Treatment of Acute Gastroenteritis
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作者 LI Jiansheng 《外文科技期刊数据库(文摘版)医药卫生》 2020年第2期089-091,共5页
Objective: to investigate the clinical effect of compound Lactobacillus acidophilus tablets and omeprazole enteric coated tablets combined with compound Lactobacillus acidophilus tablets in patients with acute gastroe... Objective: to investigate the clinical effect of compound Lactobacillus acidophilus tablets and omeprazole enteric coated tablets combined with compound Lactobacillus acidophilus tablets in patients with acute gastroenteritis. Methods: the period from May 2018 to May 2020 was selected as the research period and 106 patients with acute gastroenteritis in our hospital during this period were selected for study. All the patients were randomly divided into control group and treatment group, 53 cases in each group. The control group was given compound Lactobacillus acidophilus tablets and the treatment group was given compound Lactobacillus acidophilus tablets combined with omeprazole enteric coated tablets. After 2 weeks of continuous treatment, the improvement of clinical symptoms and the overall curative effect were compared between the two groups. Results: compared with the control group, the clinical symptom score of the treatment group was lower (P < 0.05), and the overall efficacy was higher (P < 0.05). Conclusion: Omeprazole enteric coated tablets combined with compound Lactobacillus acidophilus tablets in the treatment of acute gastroenteritis can effectively relieve symptoms and acute inflammatory reaction, with definite curative effect and good feasible value. 展开更多
关键词 acute gastroenteritis omeprazole enteric coated tablets compound Lactobacillus acidophilus tablets
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Analysis of the Therapeutic Effect of Clopidogrel Bisulfate Tablets + Aspirin Enteric-Coated Tablets on Acute Myocardial Infarction
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作者 Yiru Chen 《Journal of Clinical and Nursing Research》 2024年第6期290-294,共5页
Objective:To investigate and analyze the clinical effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on acute myocardial infarction(AMI)patients.Methods:The study period was from Janu... Objective:To investigate and analyze the clinical effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on acute myocardial infarction(AMI)patients.Methods:The study period was from January 2020 to December 2023,the sample source was 82 AMI patients admitted to our hospital,grouped into an observation group(n=41)and a control group(n=41)by the numerical table method.The patients in the control group were treated with aspirin enteric-coated tablets,and the patients in the observation group were treated with aspirin enteric-coated tablets combined with clopidogrel bisulfate.The clinical efficacy,coagulation indexes,and the incidence of cardiovascular adverse events between the two groups were compared.Results:The clinical efficacy of the observation group was higher than that of the control group(P<0.05);the platelet aggregation rate(PAR)of the observation group was lower than that of the con-trol group after treatment(P<0.05),and there was no significant difference in the prothrombin time(PT)and activated partial thromboplastin time(APTT)between the two groups(P>0.05).The incidence of cardiovascular adverse events in the observation group was lower than that of the control group(P<0.05).Conclusion:The treatment effect of clopidogrel bisulfate tablets combined with aspirin enteric-coated tablets on AMI patients is remarkable.It reduces the PAR and the incidence of cardiovascular adverse events,so this treatment method should be popularized. 展开更多
关键词 Clopidogrel bisulfate Aspirin enteric-coated tablets Acute myocardial infarction
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Analysis of Therapeutic Effect of Mesalazine Enteric-coated Tablet Combined with Bifidum Triple Viable Capsule in Treatment of Ulcerative Colitis
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作者 XIE Xiaodong YU Haodong 《外文科技期刊数据库(文摘版)医药卫生》 2021年第12期542-544,共5页
Objective: to study the therapeutic effect of mesalazine enteric-coated tablet combined with bifidobacterium triple viable capsule in the treatment of ulcerative colitis. Methods: the therapeutic effect of mesalazine ... Objective: to study the therapeutic effect of mesalazine enteric-coated tablet combined with bifidobacterium triple viable capsule in the treatment of ulcerative colitis. Methods: the therapeutic effect of mesalazine enteric-coated tablets combined with bifidum triple viable capsule was analyzed in 100 patients with ulcerative colitis from January 2020 to July 2021. Results: the experimental group (χ2=6.5236, P=0.0234) had higher curative effect (P < 0.05). Adverse reactions (χ2=4.5236, P=0.0011) were lower,P < 0.05. IL-6 (t=8.5241, P=0.0000) and TNF-α (t=10.2531, P=0.0000) were lower, P < 0.05. D-lactic acid (t5.2362 =,P=0.0000) and botulinum toxin (t=12.5246, P=0.0000) were lower (P < 0.05). Conclusion: mesalazine enteric-coated tablet combined with bifidum triple living capsule is effective and safe. 展开更多
关键词 mesalazine enteric-coated tablets bifidum triple living capsule adverse reactions
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Gradient high performance liquid chromatography method for simultaneous determination of ilaprazole and its related impurities in commercial tablets 被引量:2
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作者 Shang Wang Dong Zhang +3 位作者 Yingli Wang Xiaohong Liu Yan Liu Lu Xu 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2015年第2期146-151,共6页
A methodology(HPLC)proposed in this paper for simultaneously quantitative determination of ilaprazole and its related impurities in commercial tablets was developed and validated.The chromatographic separation was car... A methodology(HPLC)proposed in this paper for simultaneously quantitative determination of ilaprazole and its related impurities in commercial tablets was developed and validated.The chromatographic separation was carried out by gradient elution using an Agilent C8 column(4.6 mm×250 mm,5 mm)which was maintained at 25℃.The mobile phase composed of solvent A(methanol)and solvent B(solution consisting 0.02 mmol/l monopotassium phosphate and 0.025 mmol/l sodium hydroxide)was at a flow rate of 1.0 ml/min.The samples were detected and quantified at 237 nm using an ultraviolet absorbance detector.Calibration curves of all analytes from 0.5 to 3.5 mg/ml were good linearity(r≥0.9990)and recovery was greater than 99.5%for each analyte.The lower limit of detection(LLOD)and quantification(LOQ)of this analytical method were 10 ng/ml and 25 ng/ml for all impurities,respectively.The stress studies indicated that the degradation products could not interfere with the detection of ilaprazole and its related impurities and the assay can thus be considered stability-indicating.The method precisions were in the range of 0.41-1.21 while the instrument precisions were in the range of 0.38-0.95 in terms of peak area RSD%for all impurities,respectively.This method is considered stabilityindicating and is applicable for accurate and simultaneous measuring of the ilaprazole and its related impurities in commercial enteric-coated tablets. 展开更多
关键词 Ilaprazole enteric-coated tablets Related impurities HPLC Validation
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胃复春片联合常规西医疗法治疗气虚血瘀型胃肠上皮化生的效果分析
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作者 刘晓伟 季静岳 《中国社区医师》 2026年第1期49-51,共3页
目的:探讨胃复春片联合常规西医疗法治疗气虚血瘀型胃肠上皮化生(GIM)的效果。方法:选取2024年1—12月于无锡市锡山区中医医院就诊的气虚血瘀型GIM患者62例作为研究对象,按照随机数字表法分为对照组(31例)和观察组(31例)。对照组采用常... 目的:探讨胃复春片联合常规西医疗法治疗气虚血瘀型胃肠上皮化生(GIM)的效果。方法:选取2024年1—12月于无锡市锡山区中医医院就诊的气虚血瘀型GIM患者62例作为研究对象,按照随机数字表法分为对照组(31例)和观察组(31例)。对照组采用常规西医疗法,观察组在对照组基础上给予胃复春片治疗。比较两组治疗效果。结果:治疗后,两组胃部隐痛或刺痛、神疲乏力、胃部嘈杂、嗳气泛酸、舌质瘀斑评分均低于治疗前,且观察组低于对照组(P<0.001)。治疗后,两组胃黏膜表皮生长因子、表皮生长因子受体免疫组化半定量评分均下降,且观察组低于对照组(P<0.05)。治疗后,两组肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6水平均降低,且观察组低于对照组(P<0.001)。观察组治疗总有效率高于对照组(P=0.041)。结论:胃复春片联合常规西医疗法治疗气虚血瘀型GIM的效果良好,可减轻患者临床症状,下调表皮生长因子、表皮生长因子受体表达水平,减轻炎性反应。 展开更多
关键词 胃肠上皮化生 气虚血瘀 胃复春片 胃镜下氩离子凝固术 奥美拉唑 替普瑞酮
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Delayed-release oral mesalamine tablet mimicking a small jejunal gastrointestinal stromal tumor:A case report
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作者 Fabio Frosio Emanuele Rausa +2 位作者 Paolo Marra Marie-Christine Boutron-Ruault Alessandro Lucianetti 《World Journal of Clinical Cases》 SCIE 2022年第19期6710-6715,共6页
BACKGROUND Enteric-coated medications are supposed to pass intact through the gastric environment and to release the drug content into the small intestine or the colon.Before dissolution of the enteric coating,they ma... BACKGROUND Enteric-coated medications are supposed to pass intact through the gastric environment and to release the drug content into the small intestine or the colon.Before dissolution of the enteric coating,they may appear hyperdense on computed tomography(CT).Unfortunately,few reports have been published on this topic so far.In this case report,the hyperdense appearance on contrastenhanced CT of an enteric-coated mesalamine tablet was initially misinterpreted as a jejunal gastrointestinal stromal tumor(GIST).CASE SUMMARY An asymptomatic 81-year-old male patient,who had undergone laparoscopic right nephrectomy four years earlier for stage 1 renal carcinoma,was diagnosed with a jejunal GIST at the 4-year follow-up thoraco-abdominal CT scan.He was referred to our hub hospital for gastroenterological evaluation,and subsequently underwent 18-fluorodeoxyglucose positron emission tomography,abdominal magnetic resonance imaging,and video capsule endoscopy.None of these examinations detected any lesion of the small intestine.After reviewing all the CT images in a multidisciplinary setting,the panel estimated that the hyperdense jejunal image was consistent with a tablet rather than a GIST.The tablet was an 800 mg delayed-release enteric-coated oral mesalamine tablet(Asacol®),which had been prescribed for non-specific colitis,while not informing the hospital physicians.CONCLUSION Delayed-release oral mesalamine(Asacol®),like other enteric-coated medications,can appear as a hyperdense image on a CT scan,mimicking a small intestinal GIST.Therefore,adetailed knowledge of the patients’medications and a multidisciplinary review of the images areessential. 展开更多
关键词 MESALAMINE enteric-coating Asacol tablet Gastrointestinal stromal tumor Case report
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复方嗜酸乳杆菌片联合奥美拉唑肠溶片治疗对急性肠胃炎患者症状改善情况及不良反应的影响 被引量:2
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作者 何永涛 吕伟超 《系统医学》 2025年第4期187-190,共4页
目的探究奥美拉唑肠溶片、复方嗜酸乳杆菌片治疗急性肠胃炎的效果。方法非随机选取2021年2月—2023年2月于菏泽市第三人民医院就诊治疗的88例急性肠胃炎患者为研究对象,按治疗方法不同分为对照组(n=44,奥美拉唑肠溶片治疗)和观察组(n=44... 目的探究奥美拉唑肠溶片、复方嗜酸乳杆菌片治疗急性肠胃炎的效果。方法非随机选取2021年2月—2023年2月于菏泽市第三人民医院就诊治疗的88例急性肠胃炎患者为研究对象,按治疗方法不同分为对照组(n=44,奥美拉唑肠溶片治疗)和观察组(n=44,在对照组基础上结合复方嗜酸乳杆菌片治疗)。比较两组症状改善情况、炎性因子水平及不良反应发生情况。结果与对照组相比,观察组症状(腹痛、腹泻、呕吐、发热)消退时间较对照组短,炎性因子水平较对照组低,差异有统计学意义(P均<0.05)。与对照组9.10%(4/44)相比,观察组不良反应总发生率(0)更低,差异有统计学意义(χ^(2)=4.190,P<0.05)。结论应用奥美拉唑肠溶片、复方嗜酸乳杆菌片治疗后,急性肠胃炎临床症状能进一步改善,且不良反应较少。 展开更多
关键词 复方嗜酸乳杆菌片联合奥美拉唑肠溶片 奥美拉唑肠溶片 复方嗜酸乳杆菌片 急性肠胃炎 不良反应 炎症因子 治疗效果
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双歧杆菌四联活菌片联合奥美拉唑治疗幽门螺杆菌阳性消化性溃疡的临床疗效观察
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作者 张毛 牛思 邵阿康 《四川生理科学杂志》 2025年第10期2243-2245,2249,共4页
目的:探讨不同药物方案治疗幽门螺杆菌阳性消化性溃疡的临床疗效。方法:选取我院收治的幽门螺杆菌阳性消化性溃疡患者90例,选取时间为2023年1月至2023年7月,根据信封法分为试验组和参照组,参照组采用奥美拉唑治疗,试验组在此基础上采用... 目的:探讨不同药物方案治疗幽门螺杆菌阳性消化性溃疡的临床疗效。方法:选取我院收治的幽门螺杆菌阳性消化性溃疡患者90例,选取时间为2023年1月至2023年7月,根据信封法分为试验组和参照组,参照组采用奥美拉唑治疗,试验组在此基础上采用双歧杆菌四联活菌片联合治疗,比较两组患者临床疗效,观察两组患者Hp清除率、Hp清除时间和溃疡愈合时间,并比较两组患者治疗前后胃肠激素和炎性因子水平,观察两组患者不良反应发生情况。结果:试验组治疗总有效率(95.56%)高于参照组(80.00%)(χ^(2)=6.535,P=0.011)。与参照组(77.78%)比较,试验组患者Hp清除率(93.33%)高于参照组,Hp清除时间和溃疡愈合时间更短(P<0.05)。治疗后试验组患者MTL和GAS水平更低,CGRP水平更高(P<0.05)。治疗后试验组患者TNF-α、IL-6和CRP水平更低(P<0.05)。两组不良反应发生率(13.33%vs 11.11%)无明显差异(χ^(2)=0.104,P=0.747)。结论:奥美拉唑基础上采用双歧杆菌四联活菌片联合治疗幽门螺杆菌阳性消化性溃疡的临床疗效显著,可提高Hp清除率,改善胃肠功能,减轻炎症反应,安全性高。 展开更多
关键词 双歧杆菌四联活菌片 奥美拉唑 幽门螺杆菌阳性消化性溃疡 临床疗效
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硫糖铝分散片联合奥美拉唑肠溶胶囊治疗隆起糜烂性胃炎患者的临床疗效 被引量:1
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作者 罗酩 《中国现代药物应用》 2025年第12期87-90,共4页
目的探析硫糖铝分散片联合奥美拉唑肠溶胶囊治疗隆起糜烂性胃炎(REG)患者的临床疗效。方法100例REG患者,依据治疗方案不同分为对照组(50例)及观察组(50例)。对照组予以奥美拉唑肠溶胶囊治疗,观察组予以奥美拉唑肠溶胶囊联合硫糖铝分散... 目的探析硫糖铝分散片联合奥美拉唑肠溶胶囊治疗隆起糜烂性胃炎(REG)患者的临床疗效。方法100例REG患者,依据治疗方案不同分为对照组(50例)及观察组(50例)。对照组予以奥美拉唑肠溶胶囊治疗,观察组予以奥美拉唑肠溶胶囊联合硫糖铝分散片治疗。比较两组症状评分、胃黏膜功能指标[胃蛋白酶原Ⅰ(PGⅠ)、胃蛋白酶原Ⅱ(PGⅡ)、胃泌素-17(GAS-17)]、炎症因子[白细胞介素-6(IL-6)]水平、临床疗效。结果治疗后,观察组腹痛、饱胀、恶心、呕吐评分均低于对照组(P<0.05)。治疗后,观察组PGⅠ(98.51±8.42)μg/L、GAS-17(6.72±1.13)pmol/L高于对照组的(90.39±6.64)μg/L、(5.18±0.85)pmol/L,PGⅡ(9.01±1.75)μg/L低于对照组的(10.13±1.96)μg/L(P<0.05)。治疗后,观察组IL-6(14.05±2.23)ng/L低于对照组的(16.11±3.82)ng/L(P<0.05)。观察组治疗总有效率96.00%高于对照组的84.00%(P<0.05)。结论与单用奥美拉唑肠溶胶囊相比,采用硫糖铝分散片联合奥美拉唑肠溶胶囊用药方案治疗REG,可以更好地改善患者症状、胃黏膜功能、炎症因子水平,且有助于明显提升临床疗效。 展开更多
关键词 隆起糜烂性胃炎 奥美拉唑肠溶胶囊 硫糖铝分散片 胃黏膜功能 炎症因子 临床疗效
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口服抗胃食管反流药物临床综合评价
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作者 赵玲 高媛 +2 位作者 李赛楠 陈佳 李从欣 《药物评价研究》 北大核心 2025年第11期3273-3282,共10页
目的将新型抑酸药富马酸伏诺拉生与经典治疗胃食管反流的口服质子泵抑制剂(PPI)类药物(奥美拉唑、雷贝拉唑钠、泮托拉唑钠等)进行临床综合评价,以期为医疗机构的安全、合理用药提供参考及循证依据。方法基于《中国医疗机构药品评价与遴... 目的将新型抑酸药富马酸伏诺拉生与经典治疗胃食管反流的口服质子泵抑制剂(PPI)类药物(奥美拉唑、雷贝拉唑钠、泮托拉唑钠等)进行临床综合评价,以期为医疗机构的安全、合理用药提供参考及循证依据。方法基于《中国医疗机构药品评价与遴选快速指南(第二版)》,制定百分制评估体系,通过查阅万方数据库(Wanfang Data)、维普生物医学数据库(VIP)、中国学术期刊全文数据库(CNKI)、PubMed、Embase、Cochrane Library等数据库相关文献,以及参考药品说明书、临床指南,从有效性、药学特性、安全性、经济性、国家医保、基本药物情况、全球使用情况及药品生产企业状况等方面对富马酸伏诺拉生片、奥美拉唑肠溶胶囊2种、艾司奥美拉唑镁肠溶胶囊2种、雷贝拉唑钠肠溶片2种、泮托拉唑钠肠溶片2种、艾普拉唑肠溶片共10个品种进行量化评分,并根据评分结果划分推荐级别。结果评价结果显示在胃食管反流的治疗方面,所评价药物的综合得分分别为富马酸伏诺拉生片80.1分,奥美拉唑肠溶胶囊(10 mg)83.8分,奥美拉唑肠溶胶囊(20 mg)80.3分,艾司奥美拉唑镁肠溶胶囊(石药)79.8分,艾司奥美拉唑镁肠溶胶囊(东阳光)79.6分,雷贝拉唑钠肠溶片(卫材)77.2分,雷贝拉唑钠肠溶片(晋城)74.8分,泮托拉唑钠肠溶片(武田)80.8分,泮托拉唑钠肠溶片(华纳)81分,艾普拉唑肠溶片73.6分。结论所有品种得分均在70分以上,均建议为强推荐,且其中奥美拉唑肠溶胶囊、泮托拉唑钠肠溶片及富马酸伏诺拉生片作为胃食管反流治疗的优选药物。 展开更多
关键词 药品遴选 胃食管反流 富马酸伏诺拉生片 奥美拉唑肠溶胶囊 泮托拉唑钠肠溶片
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保济口服液联合奥美拉唑肠溶片治疗急性胃肠炎患者的临床评价 被引量:1
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作者 邹济源 武琛 +3 位作者 王辉 陈林 焦云涛 左瑞菊 《中国药物应用与监测》 2025年第5期899-903,共5页
目的探究保济口服液联合奥美拉唑肠溶片治疗急性胃肠炎患者的效果及对胃肠激素和血清可溶性白细胞介素2受体(sIL-2R)、白细胞介素2(IL-2)与C反应蛋白(CRP)水平的影响。方法经随机数字表法将2023年1月至2024年5月北京中医医院顺义医院收... 目的探究保济口服液联合奥美拉唑肠溶片治疗急性胃肠炎患者的效果及对胃肠激素和血清可溶性白细胞介素2受体(sIL-2R)、白细胞介素2(IL-2)与C反应蛋白(CRP)水平的影响。方法经随机数字表法将2023年1月至2024年5月北京中医医院顺义医院收治的106例急性胃肠炎患者分成对照组与观察组,各53例。对照组口服奥美拉唑肠溶片治疗,观察组在此基础上使用保济口服液治疗,比较两组治疗7 d后的临床疗效、临床症状消失时间、治疗前后的胃肠激素(胃泌素、胃动素、胃蛋白酶原Ⅰ和胃蛋白酶原Ⅱ)水平、血清炎症因子(sIL-2R、IL-2与CRP)水平及不良反应发生情况。结果治疗后,与对照组(79.25%,42/53)比较,观察组的总有效率(94.34%,50/53)较高(χ^(2)=5.267,P<0.05)。与对照组比较,观察组治疗后腹痛、腹泻、呕吐及发热症状消失时间均较早(P<0.05)。治疗后,观察组胃泌素、胃动素、胃蛋白酶原Ⅰ、胃蛋白酶原Ⅱ水平[分别为(133.59±22.57)ng·L^(-1)、(382.23±64.49)ng·L^(-1)、(128.38±21.42)ng·L^(-1)、(13.74±2.49)ng·L^(-1)]均较对照组[分别为(171.16±26.84)ng·L^(-1)、(326.72±51.65)ng·L^(-1)、(104.86±19.53)ng·L^(-1)、(17.95±3.27)ng·L^(-1)]有明显的改善(t=7.799、4.891、5.907、7.457,均P<0.05)。治疗后,两组血清sIL-2R与CRP水平均较治疗前降低,IL-2水平均较治疗前升高,且观察组sIL-2R、CRP、IL-2水平[分别为(304.52±40.96)kU·L^(-1)、(8.48±1.45)mg·L^(-1)、(71.29±12.73)ng·L^(-1)]均优于对照组[分别为(335.17±41.15)kU·L^(-1)、(12.19±3.29)mg·L^(-1)、(53.62±9.54)ng·L^(-1)],差异均有统计学意义(t=3.843、7.512、8.086,均P<0.05)。两组服药期间出现不良反应的总发生率对比差异无统计学意义(P>0.05)。结论用保济口服液配合奥美拉唑肠溶片治疗急性胃肠炎可快速缓解患者的临床症状,改善其胃肠功能,减轻机体的炎症反应,疗效突出,且不良反应少。 展开更多
关键词 保济口服液 奥美拉唑肠溶片 急性胃肠炎 胃肠激素水平 可溶性白细胞介素2受体 白细胞介素2 C反应蛋白
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CYP2C19基因多态性对奥美拉唑药代动力学影响
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作者 朱琦涛 姜敏生 +3 位作者 尹咸淼 宋欢 丁峰 甘方良 《湖北科技学院学报(医学版)》 2025年第2期98-102,106,共6页
目的研究中国成人受试者体内不同CYP2C19基因型对奥美拉唑镁肠溶片药代动力学影响。方法招募32例中国健康成人受试者空腹单次服用奥美拉唑镁肠溶片参比制剂并进行基因检测,采用单中心、随机、开放、单剂量、两制剂、四周期、两序列完全... 目的研究中国成人受试者体内不同CYP2C19基因型对奥美拉唑镁肠溶片药代动力学影响。方法招募32例中国健康成人受试者空腹单次服用奥美拉唑镁肠溶片参比制剂并进行基因检测,采用单中心、随机、开放、单剂量、两制剂、四周期、两序列完全重复交叉设计,受试者口服受试制剂20mg或参比制剂20 mg,抽取空腹组血样至给药后14h。用超高效液相色谱-串联质谱(UPLC-MS/MS)法测定血样中奥美拉唑镁的浓度,并采用Phoenix WinNonlin 8.2统计软件,以非房室模型(NCA模块)计算奥美拉唑镁主要PK参数并评价不同CYP2C19基因对于药物代谢的影响。结果服用受试制剂正常代谢组、中间代谢组、慢代谢组的C_(max)和AUC_(0-t)分别为(286.2±75.7)μg/L,(511.9±198.5)μg·h/L;(542.8±123.6)μg/L,(1075.58±476.21)μg·h/L;(1209.1±165.6)μg/L,(4539.83±1064.55)μg·h/L;3组间差异均存在显著性(P<0.05)。服用参比制剂空腹条件下,正常代谢组、中间代谢组、慢代谢组的C_(max)和AUC_(0-t)分别为(264.1±84.7)μg/L,(545.11±229.8)μg·h/L;(538.7±183.1)μg/L,(1110.66±826.33)μg·h/L;(1234.4±182.1)μg/L,(4308.98±1500.34)μg·h/L;3组间差异均存在显著性(P<0.05)。两制剂主要药动学参数(C_(max)、AUC_(0-t)、AUC_(0-∞))的几何均值比90%置信区间均落于80.00%~125.00%。结论不同个体内CYP2C19基因存在差异,从而导致CYP2C19酶活性的不同,并会影响奥美拉唑镁肠溶片在人体内的血药浓度以及药动学过程。 展开更多
关键词 奥美拉唑镁 CYP2C19 基因组学 药代动力学 肠溶片
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奥美拉唑肠溶片降解产物F和G转化物的研究
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作者 杨永 姚娜 +4 位作者 崔祥祯 解元元 王肖 于龙环 郝贵周 《中南药学》 2025年第11期3342-3346,共5页
目的明确奥美拉唑肠溶片中F和G混合物高温转化物的化学结构,并用对照品建立其HPLC检测方法。方法通过对奥美拉唑肠溶片中F和G转化物的产生机制进行分析,结合质谱、杂质对照品的峰定位及PDA最大吸收波长,明确了F和G混合物高温转化物的结... 目的明确奥美拉唑肠溶片中F和G混合物高温转化物的化学结构,并用对照品建立其HPLC检测方法。方法通过对奥美拉唑肠溶片中F和G转化物的产生机制进行分析,结合质谱、杂质对照品的峰定位及PDA最大吸收波长,明确了F和G混合物高温转化物的结构。参考《美国药典》奥美拉唑肠溶胶囊有关物质色谱条件,以艾司奥美拉唑钠杂质Ⅱ为对照品建立了奥美拉唑肠溶片中该杂质的研究方法。结果F和G转化物与艾司奥美拉唑钠杂质Ⅱ的保留时间、最大吸收波长、分子量均一致;奥美拉唑肠溶片的强制降解试验表明本法专属性良好,艾司奥美拉唑钠杂质Ⅱ在0.049~1.98μg·mL^(-1)与峰面积线性关系良好(r=0.9999),低、中、高浓度的平均回收率分别为99.6%、101.2%、100.9%(n=3),RSD分别为3.6%、1.2%、0.099%,检测限为0.025μg·mL^(-1),定量限为0.05μg·mL^(-1)。结论艾司奥美拉唑钠杂质Ⅱ即杂质F和G转化物,将前者用于系统适用性研究,节省了分析时间,提高了分析效率。 展开更多
关键词 F和G转化物 艾司奥美拉唑钠杂质Ⅱ 奥美拉唑肠溶片
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老年浅表性胃炎患者使用雷贝拉唑钠肠溶片治疗的效果研究
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作者 刘媛媛 《中国医药指南》 2025年第20期93-95,共3页
目的探讨雷贝拉唑钠肠溶片治疗老年浅表性胃炎的临床效果及安全性,并与奥美拉唑进行对比分析。方法选取辽宁省军区营口离职干部休养所于2022年1月至2025年1月老年浅表性胃炎患者共计30例,按照随机数字表法分为观察组15例和对照组15例,... 目的探讨雷贝拉唑钠肠溶片治疗老年浅表性胃炎的临床效果及安全性,并与奥美拉唑进行对比分析。方法选取辽宁省军区营口离职干部休养所于2022年1月至2025年1月老年浅表性胃炎患者共计30例,按照随机数字表法分为观察组15例和对照组15例,患者均服用阿莫西林克拉维酸钾片。在此基础上,观察组加用雷贝拉唑钠肠溶片;对照组加用奥美拉唑肠溶片。对比两组治疗前后炎症因子[肿瘤坏死因子(TNF-α)、超敏C-反应蛋白(hs-CRP)、白细胞介素-6(IL-6)]、胃肠激素[血清胃泌素(GAS)、生长抑素(SS)、表皮生长因子(EGF)]、胃黏膜恢复效果的差异,以及总有效率与不良反应发生率的差异。结果治疗后,观察组TNF-α、hs-CRP、IL-6、GAS、SS以及活动性炎症评分、慢性炎症评分均低于对照组(P<0.05),EGF为高于对照组(P<0.05)。且治疗后观察组胃黏膜中重度患者比例少于对照组(P<0.05)。观察组总有效率和不良反应发生率均优于对照组(P<0.05)。结论雷贝拉唑钠肠溶片可进一步改善老年浅表性胃炎患者的炎症反应及胃肠功能,疗效优于奥美拉唑肠溶片,且安全性更高。 展开更多
关键词 老年浅表性胃炎 雷贝拉唑钠肠溶片 奥美拉唑 炎症因子 安全性
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奥美拉唑肠溶微丸片的制备及体外释放度考察 被引量:8
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作者 李宝红 韩芸 +2 位作者 吴君 邓妙丽 吴劲东 《西北药学杂志》 CAS 2013年第1期63-65,共3页
目的制备一种奥美拉唑肠溶片剂。方法采用挤出-滚圆法制备奥美拉唑微丸,将奥美拉唑微丸与辅料压片,再对片剂分别用HPMC E50和EudragitRL30D-55包衣,制成奥美拉唑肠溶片。结果体外释放度实验显示,制备的奥美拉唑片在酸性介质中2h稳定... 目的制备一种奥美拉唑肠溶片剂。方法采用挤出-滚圆法制备奥美拉唑微丸,将奥美拉唑微丸与辅料压片,再对片剂分别用HPMC E50和EudragitRL30D-55包衣,制成奥美拉唑肠溶片。结果体外释放度实验显示,制备的奥美拉唑片在酸性介质中2h稳定性良好,在碱性介质中45min基本释药完全。结论用该方法制备奥美拉唑肠溶片,稳定性好,工艺简便,易于操作。 展开更多
关键词 奥美拉唑 挤出-滚圆法 丙烯酸树脂 奥美拉唑肠溶微丸片 体外释放度
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奥美拉唑镁肠溶片与奥美拉唑胶囊治疗消化性溃疡的临床随机对照研究 被引量:3
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作者 冯常炜 李振峰 +2 位作者 赵治国 唐芙爱 段芳龄 《胃肠病学和肝病学杂志》 CAS 2004年第4期414-416,共3页
目的 验证奥美拉唑镁肠溶片与奥美拉唑胶囊治疗消化性溃疡的生物等效性及评价其不良反应。方法 采用随机对照和开放试验的方法治疗经胃镜检查证实的消化性溃疡共 171例 ,其中奥美拉唑镁肠溶片组 (试验组 ) 68例 ,胃溃疡 2 1例 ,十二... 目的 验证奥美拉唑镁肠溶片与奥美拉唑胶囊治疗消化性溃疡的生物等效性及评价其不良反应。方法 采用随机对照和开放试验的方法治疗经胃镜检查证实的消化性溃疡共 171例 ,其中奥美拉唑镁肠溶片组 (试验组 ) 68例 ,胃溃疡 2 1例 ,十二指肠溃疡 47例 ;奥美拉唑胶囊组 (对照组 ) 67例 ,其中胃溃疡 2 1例 ,十二指肠溃疡 46例 ;开放试验组 3 6例 ,其中十二指肠溃疡 2 9例 ,胃溃疡 7例。结果 试验组中胃溃疡的愈合率和总有效率分别为 80 9%和 10 0 %十二指肠溃疡的愈合率和总有效率分别为87 2 %和 97 8% ;对照组中胃溃疡的愈合率和总有效率为 85 7%和 95 2 % ,十二指肠溃疡的愈合率和总有效率为 84 7%和 97 8% ;开放试验组中胃溃疡的愈合率和总有效率均为 10 0 0 %十二指肠溃疡的愈合率和总有效率分别为 86 2 %和 10 0 % ;试验组中疼痛消失率及其他消化道症状的消失率在胃溃疡为 95 2 %和 89 0 %在十二指肠溃疡则为 97 8%和 98 3 % ;对照组中疼痛及其他消化道症状的消失率在胃溃疡为 95 2 %和 92 7% ,在十二指肠溃疡为 97 8%和 98 7%。两组在愈合率、总有效率、疼痛消失率和其他消化道症状消失率方面相比均无显著差别 (P >O 0 5 )。两组在治疗过程中均未见明显的不良反应。 展开更多
关键词 奥美拉唑镁肠溶片 奥美拉唑胶囊 胃溃疡 十二指肠溃疡
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