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Tablets of paliperidone using compression-coated technology for controlled ascending release 被引量:1
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作者 Yingying Tang Huan Teng +5 位作者 Yanan Shi Haibing He Yu Zhang Tian Yin Cuifang Cai Xing Tang 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2018年第2期143-154,共12页
The aim of this work was to prepare ascending release compression-coated(CC) tablets with paliperidone(PAL) using a simple manufacturing technique and short manufacturing process.The release behavior and mechanisms in... The aim of this work was to prepare ascending release compression-coated(CC) tablets with paliperidone(PAL) using a simple manufacturing technique and short manufacturing process.The release behavior and mechanisms in vitro of the final tablets was investigated and evaluated. The PAL CC tablets were comprised of a core layer of high viscosity hydroxypropyl cellulose(HPC-H) and a coating layer of high viscosity hydroxypropyl methylcellulose(HPMCK100 M). Several factors such as materials and core tablet compositions were studied for their influence in the formulation procedure. The drug release mechanism was studied using gravimetric analysis. The data could be fitted to the Peppas model. The ascending drug release results were expressed in terms of the slope of the release curve at different time points.Results showed that the formulation could achieve a good ascending drug release when the weight ratio of PAL was 5:1(core:layer). The fraction of HPC and HPMC was 33 %, and the combination of Eudragit RL-PO was 10%. The ascending release mechanism was due to solvent penetration into the PAL CC tablets, and subsequent drug dissolution from the gelatinous HPC and HPMC matrix erosion. The release mechanism was therefore a combination of diffusion and erosion. This work demonstrated that the compression-coated tablets could achieve controlled ascending release over 24 h for the oral administration systems. 展开更多
关键词 PALIPERIDONE compression-coated tablet Ascending RELEASE CONTROLLED RELEASE
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The Qilin Delivers a Jade Tablet to Confucius’Mother
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《China Today》 2026年第2期69-69,共1页
Confucius’imminent birth is heralded by the appearance of the qilin.The mythical one-horned animal came to his mother at the door and cast out of its mouth a jade tablet bearing an inscription saying that she would g... Confucius’imminent birth is heralded by the appearance of the qilin.The mythical one-horned animal came to his mother at the door and cast out of its mouth a jade tablet bearing an inscription saying that she would give birth to“the son of the refinement of water,and that he would succeed the Zhou Dynasty,but as a king without a throne(su wang).”Stunned,Yan Zhengzai–Confucius’mother–tied an embroidered ribbon around the horn of the qilin,and the animal stayed for two nights. 展开更多
关键词 qilin refinement water mythical animal CONFUCIUS jade tablet zhou dynasty INSCRIPTION imminent birth
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A time-released osmotic pump fabricated by compression-coated method: Formulation screen, mechanism research and pharmacokinetic study 被引量:4
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作者 Tiegang Xin Yang Zhao +5 位作者 Hengpan Jing Wenji Zhang Yunyun Gao Xinggang Yang Xukai Qu Weisan Pan 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2014年第4期208-217,共10页
In this investigation,time-released monolithic osmotic pump(TMOP)tablets containing diltiazem hydrochloride(DIL)were prepared on the basis of osmotic pumping mechanism.The developed dosage forms were coated by Kollido... In this investigation,time-released monolithic osmotic pump(TMOP)tablets containing diltiazem hydrochloride(DIL)were prepared on the basis of osmotic pumping mechanism.The developed dosage forms were coated by Kollidon®SR-Polyethylene Glycol(PEG)mixtures via compression-coated technology instead of spray-coating method to form the outer membrane.For more efficient formulation screening,a three-factor five-level central composite design(CCD)was introduced to explore the optimal TMOP formulation during the experiments.The in vitro tests showed that the optimized formulation of DIL-loaded TMOP had a lag time of 4 h and a following 20-h drug release at an approximate zero-order rate.Moreover,the releasemechanismwas proven based on osmotic pressure and its profile could be well simulated by a dynamic equation.After oral administration by beagle dogs,the comparison of parameters with the TMOP tablets and reference preparations show no significant differences for C_(max)(111.56±20.42,128.38±29.46 ng/ml)and AUC_(0-48 h)(1654.97±283.77,1625.10±313.58 ng h/ml)but show significant differences for T_(max)(13.00±1.16,4.00±0.82 h).These pharmacokinetic parameters were consistent with the dissolution tests that the TMOP tablets had turned out to prolong the lag time of DIL release. 展开更多
关键词 Time-released Osmotic pump compression-coated Central composite design PHARMACOKINETIC
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Efficacy and safety of Tripterygium wilfordii glycosides tablets combined with Western medicine for patients with rheumatic immune diseases
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作者 Hang Shu Xiao-Yu Chen +2 位作者 Jie Zhao Pin Li Zhen Sun 《World Journal of Clinical Cases》 SCIE 2025年第6期14-23,共10页
BACKGROUND Rheumatic immune diseases are a group of chronic inflammatory diseases charac-terized by joint and systemic multi-organ involvement,including rheumatoid arthritis,systemic lupus erythematosus,and Sjogren’s... BACKGROUND Rheumatic immune diseases are a group of chronic inflammatory diseases charac-terized by joint and systemic multi-organ involvement,including rheumatoid arthritis,systemic lupus erythematosus,and Sjogren’s syndrome,among others.The pathogenesis of these diseases is related to the abnormal activation and regulatory imbalance of the immune system.The prevalence and morbidity of rheumatic immune diseases are high,imposing a significant burden on patients'quality of life and socio-economic costs.Currently,the treatment of rheumatic immune diseases mainly relies on Western medicine,such as non-steroidal anti-inflammatory drugs,glucocorticoids,disease-modifying antirheumatic drugs,and biologics.However,the therapeutic effects of Western medicine are not ideal,some patients poorly respond or are resistant to Western medicine,and long-term use often causes various adverse reactions.AIM To systematically evaluate the efficacy and safety of Tripterygium wilfordii gly-cosides tablets combined with Western medicine in the treatment of patients with rheumatic immune diseases.METHODS This study conducted a meta-analysis to systematically evaluate the efficacy and safety of Tripterygium wilfordii glycosides tablets combined with Western medicine for patients with rheumatic immune diseases.Chinese and English databases were searched for randomized controlled trials(RCTs)on the treatment of rheumatic immune diseases with Tripterygium wilfordii glycosides tablets combined with Western medicine.The quality of the included studies was assessed using the Cochrane risk of bias assessment tool.Meta-analysis was performed using RevMan 5.4 software.RESULTS The meta-analysis included 11 RCTs involving 1026 patients with rheumatic immune diseases.The combined treatment significantly reduced the risk of disease recurrence(relative risk=1.07,95%confidence interval:1.01-1.15,P<0.05)and showed no significant heterogeneity(I2=0%,P=0.53),indicating that Tripterygium wilfordii glycosides tablets combined with Western medicine is an effective method to reduce the possibility of postoperative recurrence in patients with rheumatic immune diseases.However,due to the limited number and quality of the studies included,these results should be interpreted with caution.CONCLUSION Tripterygium wilfordii glycosides tablets combined with Western medicine is an effective and safe treatment option for patients with rheumatic immune diseases and can be considered a clinical choice.However,more high-quality research is needed to validate this conclusion and provide more solid evidence for clinical practice. 展开更多
关键词 Rheumatic immune diseases Tripterygium wilfordii polyglycosides tablets Western medicine treatment Systematic review META-ANALYSIS
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Efficacy and Safety Study of Rasagiline Tablets in the Treatment of Parkinson’s Disease
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作者 Lu Zhang Jin Xu +1 位作者 Ling Liu Haiyan Tang 《Journal of Clinical and Nursing Research》 2025年第11期344-349,共6页
Objective:To evaluate the efficacy and safety of rasagiline tablets in the treatment of Parkinson’s disease,in order to provide a more scientific basis for the application of the drug in Parkinson’s disease.Methods:... Objective:To evaluate the efficacy and safety of rasagiline tablets in the treatment of Parkinson’s disease,in order to provide a more scientific basis for the application of the drug in Parkinson’s disease.Methods:This study is a single-arm,prospective,observational study.The trial collected patients with primary Parkinson’s disease who met the inclusion and exclusion criteria after being assessed by the investigator to evaluate the efficacy and safety of rasagiline tablets in the treatment of Parkinson’s disease patients through UPDRSIII and UPDRSII scales,and evaluated the efficacy and safety of rasagiline tablets in the treatment of Parkinson’s disease patients.Results:A total of 3560 patients were included in this study.44.1%of patients had early Parkinson’s disease,52.4%had intermediate Parkinson’s disease,and 3.5%had advanced Parkinson’s disease.The UPDRSIII(exercise capacity)score was 26.76 at baseline,25.47 at 1 month,24.18 at 2 months,and 23.39 at 3 months after treatment,and scores significantly improved over time(P<0.001).The UPDRSII(ability to perform daily living)score was an average of 23.60 at baseline,22.49 at 1 month,21.53 at 2 months,and 21.09 at 3 months after treatment,with statistically significant differences in scores between months(P<0.001).A total of 18 adverse events/reactions occurred in this study,and adverse symptoms eventually disappeared or resolved,without termination due to adverse events/reactions or patient discharge.Conclusion:Rasagiline tablets have significant efficacy in improving daily exercise capacity and living ability in patients with Parkinson’s disease,and have a certain safety,which supports the effectiveness of rasagiline as a treatment for Parkinson’s disease and provides new evidence for its clinical application. 展开更多
关键词 Parkinson’s disease Rasagiline tablets UPDRS score
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Clinical Study on the Combination Therapy of Diosmin Tablets and Mayinglong Musk Hemorrhoids Ointment for Patients with Acute Hemorrhoids
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作者 Quanchang Sun 《Journal of Clinical and Nursing Research》 2025年第6期286-292,共7页
Objective:To evaluate the clinical effect of combined therapy with Diosmin Tablets and Mayinglong Musk Hemorrhoids Ointment for patients with acute hemorrhoids.Methods:A total of 50 patients with acute hemorrhoids who... Objective:To evaluate the clinical effect of combined therapy with Diosmin Tablets and Mayinglong Musk Hemorrhoids Ointment for patients with acute hemorrhoids.Methods:A total of 50 patients with acute hemorrhoids who visited the hospital from January 2023 to January 2025 were selected as samples and randomly divided into two groups.Group A was treated with Diosmin Tablets combined with Mayinglong Musk Hemorrhoids Ointment,while Group B was treated with Mayinglong Musk Hemorrhoids Ointment only.The efficacy,wound recovery time,perianal pain score,hemorrhoid symptom score,and stress indicators were compared between the two groups.Results:The efficacy of Group A was higher than that of Group B(P<0.05).The postoperative perianal edema time and wound healing time in Group A were shorter than those in Group B,and the Visual Analog Scale(VAS)score was lower than that in Group B(P<0.05).The hemorrhoid symptom score in Group A was lower than that in Group B(P<0.05).The stress level in Group A was lower than that in Group B(P<0.05).Conclusion:The combination therapy of Diosmin Tablets and Mayinglong Musk Hemorrhoids Ointment for postoperative treatment of acute hemorrhoids can effectively relieve perianal pain,shorten the duration of hemorrhoids,and is highly feasible. 展开更多
关键词 Acute hemorrhoids Mayinglong musk hemorrhoids ointment Diosmin tablets EFFICACY
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Effect of Bifidobacterium Triple Viable Bacteria Tablets on Neonatal Necrotizing Enterocolitis and Its Impact on Serum Factors of the Patients
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作者 Xiaoyan Ding 《Journal of Clinical and Nursing Research》 2025年第8期292-297,共6页
Objective:To analyze the efficacy of Bifidobacterium triple viable bacteria tablets on neonatal necrotizing enterocolitis(NEC)and its impact on serum factors of the patients.Methods:From January 2021 to May 2025,88 ne... Objective:To analyze the efficacy of Bifidobacterium triple viable bacteria tablets on neonatal necrotizing enterocolitis(NEC)and its impact on serum factors of the patients.Methods:From January 2021 to May 2025,88 neonates with NEC admitted to our hospital were selected as study subjects.During the study,these 88 patients were evenly divided into two groups,namely the observation group and the control group,with 44 patients in each group based on the random number table method.In terms of treatment,the control group was treated with meropenem,while the observation group received additional treatment with Bifidobacterium triple viable bacteria powder based on the treatment plan of the control group.The clinical efficacy and differences in serum inflammatory factor levels between the two groups were compared.Results:The efficacy of the observation group(90.91%)was better than that of the control group(72.73%)(P<0.05).After treatment,the levels of C-reactive protein(CRP)and procalcitonin(PCT)in both groups decreased compared to those before treatment,and the values of the above indicators in the observation group were lower than those in the control group(P<0.05).Conclusion:Based on conventional treatment for NEC neonates,the use of Bifidobacterium triple viable bacteria tablets has significant efficacy and can effectively reduce serum inflammatory factor levels. 展开更多
关键词 Bifidobacterium triple viable bacteria tablets Necrotizing enterocolitis NEONATES Serum factors
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Hypolipidemic effect and mechanism of Hedan tablet (荷丹片) based on network pharmacology
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作者 HU Huiming WENG Jiajun +6 位作者 TANG Fangrui WANG Yaqi FAN Shengxian WANG Xuecheng CUI Can SHAO Feng ZHU Yanchen 《Journal of Traditional Chinese Medicine》 2025年第2期408-421,共14页
OBJECTIVE:To examine Hedan tablet(HDT,荷丹片)'s potential mechanisms in hyperlipidemic rats induced by a high-fat diet(HFD),as well as its regulatory effects and primary active constituents.METHODS:By using ultra-... OBJECTIVE:To examine Hedan tablet(HDT,荷丹片)'s potential mechanisms in hyperlipidemic rats induced by a high-fat diet(HFD),as well as its regulatory effects and primary active constituents.METHODS:By using ultra-performance liquid chromatography(UPLC)-quadrupole-time-of-flight(QTOF)-tandem mass spectrometry(MS/MS),the components of HDT that can enter the circulatory system were found,aiming to investigate its active constituents with pharmacological effects.Based on network pharmacology approaches,the relevant HDT targets in the therapy of hyperlipidemia were anticipated.The possible mechanism of HDT for hyperlipidemia treatment was verified by in-vivo experiments,and the main active components of HDT for hyperlipidemia treatment were analyzed via in-vitro experiments.RESULTS:UPLC-QTOF-MS/MS identified 30 components of HDT entering the circulatory system,primarily consisting of flavonoids,diterpenoids and alkaloids.The results of a network pharmacology study revealed that 30 active components mostly target 74 genes associated with hyperlipidemia.The primary active ingredients may include quercetin,kaempferol,and epicatechin,and the main gene targets may be tumor necrosis factor(TNF),interleukin-6(IL-6),interleukin 1 beta(IL-1β),etc.The results of animal experiments demonstrated that HDT can significantly regulate the blood lipid level in rats with HFD,improve the degree of inflammatory infiltration in rat liver cells,lower TNF-α,Creactive protein(CRP),IL-6,matrix metalloproteinase 9(MMP9) and malondialdehyde(MDA) levels while raising total superoxide dismutase(T-SOD) level.Meanwhile,HDT can considerably lower the expression of sterol regulatory element-binding transcription factor 2(SREBF2),3-hydroxy-3-methylglutaryl-CoA reductase(HMGCR),and MMP9 while significantly increasing the expression of peroxisome proliferator-activated receptor alpha(PPAR-α) and PPAR-γ.In vitro study confirmed that quercetin and kaempferol could reduce the levels of IL-6,IL1B,MMP9 and HMGCR in the high-fat model of hepatoma G2 cells.CONCLUSIONS:The mechanism by which HDT treats hyperlipidemia involves modification of the lipid metabolism targets such as downregulating SREBF2,HMGCR and MMP9,and upregulating PPAR-α and PPAR-γ,as well as anti-inflammatory and antioxidant actions.This study provides a pharmacological and biological rationale for the use of HDT in clinical hyperlipidemia management. 展开更多
关键词 HYPERLIPIDEMIA MECHANISM network pharmacology ultra-performance liquid chromatography-quadrupole-time-offlight-tandem mass spectrometry Hedan tablet
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Clinical Efficacy and Mechanism of Qinjin Tablet in Treating Unstable Angina with Phlegm-Stasis Syndrome Based on the HDL-C/MMP-9 Signaling Axis
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作者 Yuan WANG Jingru GAO Hongjun ZHU 《Medicinal Plant》 2025年第6期49-53,63,共6页
[Objectives]To explore the clinical efficacy of Qinjin Tablet in treating unstable angina with phlegm-stasis syndrome and preliminarily explore its intervention mechanism.[Methods]Sixty unstable angina patients with p... [Objectives]To explore the clinical efficacy of Qinjin Tablet in treating unstable angina with phlegm-stasis syndrome and preliminarily explore its intervention mechanism.[Methods]Sixty unstable angina patients with phlegm-stasis syndrome were randomly divided into a treatment group and a control group(30 each).The control group received standardized Western medicine treatment,while the treatment group also took Qinjin Tablet.After a 4-week treatment,comparisons were made on improvement of angina symptoms,TCM syndrome scores,blood stasis scores,reduction/cessation of short-acting anti-angina drugs,Seattle Angina Questionnaire(SAQ)scores,blood lipid levels,and matrix metalloproteinase-9(MMP-9)concentrations between the two groups.[Results]No statistical differences existed in baseline data like age,gender,and disease duration between the two groups(P>0.05).The treatment group showed significantly better efficacy than the control group in improving angina symptoms,TCM syndrome scores,blood stasis scores,and reduction or discontinuation of short-acting anti-anginal drugs(P<0.05).The SAQ score increase was more significant in the treatment group(P<0.05).The control group significantly reduced low-density lipoprotein cholesterol(LDL-C)(P<0.05),while the treatment group markedly increased high-density lipoprotein cholesterol(HDL-C)(P<0.05).Post-treatment,the treatment group had a marked reduction in serum MMP-9(P<0.05),with no significant change in the control group.[Conclusions]Qinjin Tablet can significantly alleviate clinical symptoms and improve quality of life in UA patients by modulating the HDL-C/MMP-9 signaling pathway. 展开更多
关键词 Qinjin tablet Unstable angina Phlegm-stasis interlocking syndrome High-density lipoprotein cholesterol Matrix metalloproteinase-9
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Exploring the mechanism of Shenhua tablet(肾华片)alleviating renal injury by regulating macrophage glycolysis via hypoxia-inducible factor-1α/pyruvate kinase M2 signaling pathway in diabetic kidney disease mice
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作者 CHEN Yuanchun JING Jiaxing +5 位作者 LI Qingmin ZHOU Xiaohong JIN Xiaofei GAO Weijuan CHEN Xiangmei YU Wentao 《Journal of Traditional Chinese Medicine》 2025年第3期528-537,共10页
OBJECTIVE:To investigate the impact of Shenhua tablet(肾华片,SHT)on renal macrophage polarization and renal injury in mice with diabetic kidney disease(DKD)and to explore the potential mechanism involving the hypoxia-... OBJECTIVE:To investigate the impact of Shenhua tablet(肾华片,SHT)on renal macrophage polarization and renal injury in mice with diabetic kidney disease(DKD)and to explore the potential mechanism involving the hypoxia-inducible factor-1α(HIF-1α)and pyruvate kinase M2(PKM2)signaling pathway,along with the glycolysis metabolism pathway.METHODS:The animals were divided into the following groups:Model,Control,dapagliflozin,SHT low-dose,SHT medium-dose,and SHT high-dose.We assessed 24-hour urine protein(24 h-UTP)levels,urinary albuminto-creatinine ratio,and regularly monitored fasting blood glucose during the treatment period.After treatment,we examined renal tissue structure,renal function(urea nitrogen,uric acid,creatinine,cystatin C,β2-microglobulin),and glycolysis in renal macrophages.Additionally,we observed macrophage polarization in renal tissue and measured inflammatory factors(tumor necrosis factor-α,interleukin-1β,interleukin-6,interleukin-10,monocyte chemoattractant protein-1)to assess the immunoinflammatory status of the renal tissue.Finally,we investigated the expression of the HIF-1α/PKM2 signaling pathway in macrophages to explore its role in the glycolysis process.RESULTS:SHT shows a beneficial effect in treating DKD by reducing 24 h-UTP,regulating blood glucose levels,improving renal tissue structure,protecting renal function,inhibiting macrophage glycolysis,reducing macrophage transformation to the M1 state,and suppressing the expression of the HIF-1α/PKM2 signaling pathway.CONCLUSION:SHT may exert renoprotective effects by inhibiting macrophage glycolysis via the HIF-1α/PKM2 signaling pathway.This inhibition decreases macrophage M1 polarization and reduces immunoinflammatory injury in the renal tissue of DKD mice. 展开更多
关键词 diabetic kidney disease MACROPHAGES GLYCOLYSIS hypoxia-inducible factor-1α pyruvate kinase M2 Shenhua tablet
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A Case Study of Heart Failure Resulting from Dilated Cardiomyopathy Treated with Sacubitril Valsartan Sodium Tablets in Combination with Qiliqiangxin Capsules
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作者 Qiuwen FU Li XU 《Medicinal Plant》 2025年第3期75-79,共5页
This article presents a case study of a 20-year-old male patient diagnosed with dilated cardiomyopathy(DCM)(NYHA IV).This condition was diagnosed as"heart failure disease"(water overflowing due to yang defic... This article presents a case study of a 20-year-old male patient diagnosed with dilated cardiomyopathy(DCM)(NYHA IV).This condition was diagnosed as"heart failure disease"(water overflowing due to yang deficiency,intermingled phlegm and stasis)in traditional Chinese medicine(TCM).The treatment approach employed a combination of TCM and Western medicine.Western medicine involved the administration of sacubitril valsartan sodium tablets to inhibit ventricular remodeling,in conjunction with diuretics and cardiotonic agents.Initially,TCM utilized a static infusion of Shenfu injection,which was subsequently supplemented with Qiliqiangxin capsules to invigorate qi,warm yang,activate blood circulation,and promote diuresis.After a follow-up period of 3 years,the patient's ejection fraction(EF)improved from 23%to 51%,and the left ventricular end diastolic diameter(LVed)decreased from 68 to 52 mm,accompanied by a significant alleviation of symptoms.These findings indicate that the combined treatment of TCM and Western medicine can synergistically enhance cardiac function and impede the progression of the disease,thereby offering valuable insights for the optimal management of DCM. 展开更多
关键词 DILATED cardiomyopathy (DCM) Heart failure Sacubitril VALSARTAN SODIUM tabletS Qiliqiangxin capsules Chest TIGHTNESS Shortness of BREATH
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Application of Shexiang Baoxin Pill Combined with Rosuvastatin Calcium Tablets in the Treatment of Angina Pectoris due to Coronary Atherosclerotic Heart Disease
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作者 Jingjiao Hui 《Journal of Clinical and Nursing Research》 2025年第11期230-236,共7页
Objective:To analyze the therapeutic efficacy of Shexiang Baoxin Pill combined with Rosuvastatin Calcium Tablets(ROS)in patients with angina pectoris due to coronary atherosclerotic heart disease(CHD-AP).Methods:Eight... Objective:To analyze the therapeutic efficacy of Shexiang Baoxin Pill combined with Rosuvastatin Calcium Tablets(ROS)in patients with angina pectoris due to coronary atherosclerotic heart disease(CHD-AP).Methods:Eighty CHD-AP patients admitted for treatment from January 2023 to December 2024 were selected and evenly divided using a random number table.The combined group(40 cases)received treatment with Shexiang Baoxin Pill combined with ROS,while the reference group(40 cases)received ROS monotherapy.The overall response rate,frequency and duration of AP attacks,blood lipid levels,and cardiac function indicators were compared between the two groups.Results:The combined group exhibited a higher overall response rate than the reference group.After treatment,the frequency and duration of AP attacks were lower in the combined group than in the reference group.Additionally,blood lipid levels and cardiac function indicators were superior in the combined group(p<0.05).Conclusion:The combination of Shexiang Baoxin Pill and ROS demonstrates favorable therapeutic effects in CHD-AP patients,effectively preventing AP attacks,regulating blood lipid levels,protecting cardiac function,and reducing disease risk. 展开更多
关键词 Shexiang Baoxin pill Rosuvastatin calcium tablets Coronary atherosclerotic heart disease Angina Pectoris
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参郁宁神片(宁郁异形片)治疗轻度至中度抑郁症的随机、双盲、安慰剂/盐酸氟西汀对照、多中心Ⅲ期临床试验
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作者 赵阳 曾美桦 +3 位作者 杨巧宁 高洪阳 李涛 高蕊 《中国新药杂志》 北大核心 2026年第3期318-324,共7页
目的:评估参郁宁神片(宁郁异形片)治疗轻度至中度抑郁症患者的临床疗效和安全性。方法:采用多中心、随机、双盲双模拟设计,纳入572例符合中国精神障碍分类方案与诊断标准(The Chinese Classification of Mental Disorders, Third Editio... 目的:评估参郁宁神片(宁郁异形片)治疗轻度至中度抑郁症患者的临床疗效和安全性。方法:采用多中心、随机、双盲双模拟设计,纳入572例符合中国精神障碍分类方案与诊断标准(The Chinese Classification of Mental Disorders, Third Edition, CCMD-3)且基线汉密尔顿抑郁量表(Hamilton Depression Rating Scale, HAMD)-17评分为14~24分的受试者,随机分为3组:参郁宁神片组(2.4 g,tid,n=344)、盐酸氟西汀组(10 mg·d^(-1)首周,20 mg·d^(-1)后续7周,n=115)及安慰剂组(n=113),持续治疗8周。主要终点为HAMD-17评分自基线至第8周的组间差异,采用改良意向治疗分析集,与阳性药组进行非劣效性检验(非劣效界值=2.5),与安慰剂进行差异性检验。结果:治疗8周后,参郁宁神片组HAMD-17评分较基线降低(10.50±4.46)分,显著优于安慰剂组[(7.03±5.07),P<0.05],与盐酸氟西汀组(10.13±3.94)的组间差异为-0.25(95%CI[-1.18,0.68]),达到非劣效标准。安全性分析显示,参郁宁神片组未报告药物相关不良事件(0%vs盐酸氟西汀组8.8%)。结论:参郁宁神片在改善轻中度抑郁症状方面呈现与盐酸氟西汀相当的临床疗效,且具有更优的安全性特征。该结果为参郁宁神片在抑郁症治疗领域的应用提供了高级别循证医学证据。 展开更多
关键词 中成药 参郁宁神片 宁郁异形片 抑郁 临床试验
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地榆升白片联合粒细胞集落刺激因子对儿童急性淋巴细胞白血病化疗后粒细胞缺乏的疗效
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作者 刘志强 刘福稳 +1 位作者 卢娟 范小菊 《实用医学杂志》 北大核心 2026年第4期663-667,共5页
目的 探讨地榆升白片联合粒细胞集落刺激因子(G-CSF)对儿童急性淋巴细胞白血病化疗后粒细胞缺乏的效果。方法 选取2022年1月至2024年1月在医院接受治疗化疗的148例急性淋巴细胞白血病患儿为研究对象,所有患儿均出现粒细胞缺乏。随机数... 目的 探讨地榆升白片联合粒细胞集落刺激因子(G-CSF)对儿童急性淋巴细胞白血病化疗后粒细胞缺乏的效果。方法 选取2022年1月至2024年1月在医院接受治疗化疗的148例急性淋巴细胞白血病患儿为研究对象,所有患儿均出现粒细胞缺乏。随机数字表法将患儿分为观察组和对照组,每组74例。对照组接受G-CSF治疗,观察组在对照组的基础上联合应用地榆升白片。记录患儿rhG-CSF用药剂量及用药时间。在用药后第4、8、14、21天检测外周血中白细胞(WBC)数、中性粒细胞(NE)数、红细胞(RBC)数和血小板(PLT)数,并比较两组用药前后的血清谷丙转氨酶(ALT)、谷草转氨酶(AST)、肌酐(Cre)和尿素氮(Urea)。记录骨痛、发热、皮疹等不良反应发生情况。结果 观察组的rhG-CSF用药剂量和用药时间均低于对照组;观察组在用药后第4、8、14、21天的WBC、NE、RBC和PLT均高于对照组,且用药后ALT、AST、Cre、Urea数值低于对照组(P<0.05)。两组不良反应情况相比,差异无统计学意义(P>0.05)。结论 地榆升白片联合G-CSF治疗儿童急性淋巴细胞白血病化疗后粒细胞缺乏,能更快提升外周血粒细胞水平,且对肝肾功能未见额外负担。 展开更多
关键词 急性淋巴细胞白血病 粒细胞缺乏 地榆升白片 粒细胞集落刺激因子
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红花逍遥片联合常规疗法治疗乳腺炎的成本-效果分析
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作者 陈雯 张然 +4 位作者 封昭 侯新 朱丽 吴东盼 任晓明 《临床药物治疗杂志》 2026年第1期55-60,共6页
目的评估红花逍遥片联合常规疗法治疗乳腺炎的经济性,以期为临床合理用药提供参考。方法系统检索中国知网、万方数据知识服务平台、维普资讯、中国生物医学数据库PubMed,Embase及Cochrane Library等中英文数据库中红花逍遥片治疗乳腺炎... 目的评估红花逍遥片联合常规疗法治疗乳腺炎的经济性,以期为临床合理用药提供参考。方法系统检索中国知网、万方数据知识服务平台、维普资讯、中国生物医学数据库PubMed,Embase及Cochrane Library等中英文数据库中红花逍遥片治疗乳腺炎相关文献,检索时限为建库至2024年11月30日。以常规疗法为对照,对红花逍遥片联合治疗乳腺炎的文献进行系统梳理和meta分析。基于决策树模型,从中国卫生系统角度出发,计算增量成本-效果比(ICER),并进行敏感性分析。结果基础分析显示,红花逍遥片联合治疗方案每多治疗1例有效的乳腺炎患者需多花费1014.84元,ICER值小于本研究的意愿支付阈值(2024年我国人均GDP)。敏感性分析显示研究结果较为稳健。结论对于乳腺炎患者,红花逍遥片联合治疗方案比常规治疗方案更具经济性。 展开更多
关键词 红花逍遥片 乳腺炎 成本-效果分析 药物经济学
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心阴片激活SIRT1抑制内皮间质转化改善慢性心力衰竭大鼠心肌纤维化的作用及机制
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作者 李巧 褚庆民 +2 位作者 叶桃春 刘树林 刘敏 《中药新药与临床药理》 北大核心 2026年第2期199-207,共9页
目的探讨心阴片激活沉默信息调节因子1(SIRT1)抑制内皮间质转化(EndMT)改善慢性心力衰竭大鼠心肌纤维化的作用及机制。方法采用主动脉弓缩窄术复制压力负荷型慢性心力衰竭大鼠模型。将60只SD大鼠随机分为假手术组、模型组、心阴片低剂量... 目的探讨心阴片激活沉默信息调节因子1(SIRT1)抑制内皮间质转化(EndMT)改善慢性心力衰竭大鼠心肌纤维化的作用及机制。方法采用主动脉弓缩窄术复制压力负荷型慢性心力衰竭大鼠模型。将60只SD大鼠随机分为假手术组、模型组、心阴片低剂量组(0.315 g·kg^(-1))、心阴片中剂量组(0.63 g·kg^(-1))、心阴片高剂量组(1.26 g·kg^(-1))、EX527组[1.26 g·kg^(-1)心阴片+5 mg·kg^(-1)EX527(SIRT1抑制剂)],每组10只。各给药组按照上述设定剂量灌胃给药,每天1次,连续8周。采用超声心动图检测大鼠心功能,包括左室射血分数(LVEF)、左室短轴缩短率(LVFS)、舒张末期左室内径(LVIDd)、收缩末期左室内径(LVIDs)等心功能指标;HE、Masson染色法观察大鼠心肌组织病理变化,分析心肌组织的胶原纤维相对面积占比;Western Blot法检测心肌组织相关蛋白的表达水平;qRT-PCR法检测心肌组织相关基因的表达水平。结果与假手术组比较,模型组大鼠的LVEF、LVFS水平明显降低(P<0.05),LVIDd、LVIDs水平明显升高(P<0.05);心肌细胞增大,并有大量的炎性细胞浸润,肌原纤维紊乱,胶原纤维沉积增多,胶原纤维相对面积占比明显升高(P<0.05);心肌组织CollagenⅠ、CollagenⅢ蛋白表达量明显增加(P<0.05),SIRT1、CD31、VE-cadherin蛋白表达明显下调(P<0.05),α-SMA、FSP1、TGF-β1、p-Smad2/3蛋白表达明显上调(P<0.05);心肌组织SIRT1、VE-cadherin mRNA表达明显下调(P<0.05),α-SMA、TGF-β1、Smad2/3 mRNA表达明显上调(P<0.05)。与模型组比较,心阴片中、高剂量组大鼠的LVEF、LVFS水平明显升高(P<0.05),心肌组织CD31、VE-cadherin蛋白表达明显上调(P<0.05),α-SMA、FSP1蛋白表达明显下调(P<0.05)。心阴片各剂量组大鼠的LVIDd、LVIDs水平明显降低(P<0.05);心肌细胞明显缩小,炎性细胞浸润及胶原纤维沉积明显减轻,胶原纤维相对面积占比明显降低(P<0.05);心肌组织CollagenⅠ、CollagenⅢ蛋白表达量明显减少(P<0.05),SIRT1蛋白表达明显上调(P<0.05),TGF-β1、p-Smad2/3蛋白表达明显下调(P<0.05);心肌组织SIRT1、VE-cadherin mRNA表达明显上调(P<0.05),α-SMA、TGF-β1、Smad2/3 mRNA表达明显下调(P<0.05)。与模型组比较,EX527组大鼠的心功能、心肌组织病理变化及其他检测指标均无明显变化(P>0.05)。结论心阴片能够有效防治慢性心力衰竭大鼠的心肌纤维化,明显改善其心功能,其机制可能是通过激活SIRT1调控TGF-β1/Smad2/3信号通路,从而抑制EndMT的发生。 展开更多
关键词 心阴片 慢性心力衰竭 心肌纤维化 内皮间质转化 沉默信息调节因子1 TGF-β1/Smad2/3信号通路 大鼠
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坤泰胶囊联合雌二醇/雌二醇地屈孕酮治疗肾虚型卵巢储备功能下降及卵巢早衰临床疗效
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作者 沙海林 陈启霞 《中国计划生育学杂志》 2026年第2期239-243,共5页
目的:探究坤泰胶囊联合雌二醇片/雌二醇地屈孕酮片治疗肾虚型卵巢储备功能下降及卵巢早衰患者疗效。方法:纳入2023年6月—2025年6月本院收治的卵巢储备功能下降及卵巢早衰患者136例,随机数字表法分为雌二醇组(n=68,给予雌二醇片雌二醇... 目的:探究坤泰胶囊联合雌二醇片/雌二醇地屈孕酮片治疗肾虚型卵巢储备功能下降及卵巢早衰患者疗效。方法:纳入2023年6月—2025年6月本院收治的卵巢储备功能下降及卵巢早衰患者136例,随机数字表法分为雌二醇组(n=68,给予雌二醇片雌二醇地屈孕酮片治疗)与坤泰胶囊组(n=68,给予坤泰胶囊联合雌二醇片/雌二醇地屈孕酮片治疗)。对比两组临床疗效,治疗前后卵巢情况、性激素水平、血脂水平变化,药物不良反应。结果:治疗后,坤泰胶囊组临床疗效(95.6%)高于雌二醇组(85.3%),两组子宫内膜厚度、卵巢体积、窦卵泡数量均升高,E_(2)、HDL-C水平升高,FSH、LH、LDL-C均下降,且坤泰胶囊组变化幅度大于雌二醇组(均P<0.05);不良反应坤泰胶囊组(11.8%)与雌二醇组(8.8%)无差异(P>0.05)。结论:坤泰胶囊联合雌二醇片/雌二醇地屈孕酮片治疗卵巢早衰,提高临床疗效、卵巢储备功能,改善患者子宫内膜厚度、血清性激素和血脂水平,未增加药物不良反应。 展开更多
关键词 卵巢早衰 卵巢储备功能 雌二醇片/雌二醇地屈孕酮片 坤泰胶囊 子宫内膜 卵巢指标 性激素 不良反应
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秦洞庭、苍梧二郡创设新证
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作者 陈伟 《武汉大学学报(哲学社会科学版)》 北大核心 2026年第1期51-56,共6页
出土简牍所见的秦洞庭、苍梧二郡,大致分别相当于史籍中的黔中郡和长沙郡。近期刊布的里耶秦简中编号为7-1、7-12的两枚木牍,包含有这两个郡初创之时的重要信息。在里耶秦简7-1中,长沙县属于洞庭郡,并且可能是郡治所在的县。而在里耶秦... 出土简牍所见的秦洞庭、苍梧二郡,大致分别相当于史籍中的黔中郡和长沙郡。近期刊布的里耶秦简中编号为7-1、7-12的两枚木牍,包含有这两个郡初创之时的重要信息。在里耶秦简7-1中,长沙县属于洞庭郡,并且可能是郡治所在的县。而在里耶秦简7-12中,长沙县和新武陵县分别是洞庭郡内两个地区的中心。由此推断,大约在秦始皇二十五年十一月或稍早,建有洞庭郡,长沙县为郡治。其后,继续向南用兵。约在二十六年十月或稍迟,将以长沙为中心的地区从洞庭郡中分割出来,连同南方新开拓之地,设置苍梧郡。 展开更多
关键词 里耶秦简 洞庭郡 苍梧郡 长沙县
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苗药糖宁通络片治疗糖尿病前期患者的多中心、随机、双盲、安慰剂对照试验
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作者 赵能江 李津 +15 位作者 夏文 张智海 袁乔英 杨娟 陈杰 杨倩 王世东 孙新宇 王秀阁 周玉森 钱锐 赵进东 田国庆 陆灏 黄延芹 杨叔禹 《中医杂志》 北大核心 2026年第2期166-172,共7页
目的观察苗药糖宁通络片治疗糖尿病前期患者的有效性和安全性,为糖尿病早期干预提供依据。方法采用随机、双盲、安慰剂对照的试验设计,纳入全国14家医院180例糖尿病前期患者,分为糖宁通络组与安慰剂组各90例。糖宁通络组采用糖宁通络片... 目的观察苗药糖宁通络片治疗糖尿病前期患者的有效性和安全性,为糖尿病早期干预提供依据。方法采用随机、双盲、安慰剂对照的试验设计,纳入全国14家医院180例糖尿病前期患者,分为糖宁通络组与安慰剂组各90例。糖宁通络组采用糖宁通络片+生活方式干预,安慰剂组给与安慰剂+生活方式干预,两组疗程均为12周。治疗后观察主要疗效指标(从首次用药开始12周内进展为2型糖尿病的发病率)、次要疗效指标[包括治疗前后体重、体重指数(BMI)、腰臀比、空腹血糖(FPG)、餐后2 h血糖(2hPG)、糖化血红蛋白(HbA1c)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、尿酸(UA)、尿白蛋白/肌酐比值(UACR)、胰岛素抵抗指数(HOMA-IR)、0~120分血糖曲线下面积(AUC_(0~120 min))];评价肝肾功能等安全性指标;采用多因素Logistic回归分析和多元线性回归分析评价糖宁通络片对各结局指标的影响;并根据BMI进行探索性亚组分析。结果糖宁通络组和安慰剂组分别有85例和79例完成研究。治疗3个月后,糖宁通络组和安慰剂组2型糖尿病发病率分别为4.71%(4/85)和13.92%(11/79),差异有统计学意义(P<0.05)。Logistic回归分析提示,糖宁通络片能降低糖尿病发生风险74.4%[OR=0.256,95%CI(0.066,0.812),P<0.05]。两组患者次要疗效指标及安全性指标比较差异均无统计学意义(P>0.05)。亚组分析显示,在BMI<24 kg/m^(2)亚组患者中,糖宁通络组的FPG和AUC_(0~120 min)较安慰剂组降低(P<0.05)。结论糖宁通络片可降低糖尿病前期患者进展为2型糖尿病的发病率,具有较好的安全性,且在BMI<24 kg/m2的患者中降糖效果更佳。 展开更多
关键词 糖尿病前期 2型糖尿病 糖宁通络片 苗药 随机对照试验
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羟乙磺酸哌柏西利片制备工艺优化研究
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作者 周敏 王静 +1 位作者 王文萱 魏蔚 《山东化工》 2026年第3期10-14,共5页
为了建立并优化羟乙磺酸哌柏西利片的制备工艺,采用对比实验及单因素试验,比较元素差异对处方制备的影响。以中间体的流动性、可填充性和溶出行为等为指标进行考察。结果显示,最优处方为填充剂m(微晶纤维素)∶m(乳糖)为2∶1,崩解剂的用... 为了建立并优化羟乙磺酸哌柏西利片的制备工艺,采用对比实验及单因素试验,比较元素差异对处方制备的影响。以中间体的流动性、可填充性和溶出行为等为指标进行考察。结果显示,最优处方为填充剂m(微晶纤维素)∶m(乳糖)为2∶1,崩解剂的用量为6%,硬脂酸镁作为润滑剂的用量为2%。采用干法制粒的工艺,以送料速度6 r/min,压辊转速4 r/min,压辊压力为30 kg/cm 3,一级整粒筛为2.0 mm,二级整粒筛为1.0 mm,建立了一套完整的羟乙磺酸哌柏西利片制备工艺。最终获得了羟乙磺酸哌柏西利片最优处方与制备工艺,符合质量与稳定要求,可在生产上推广。 展开更多
关键词 羟乙磺酸哌柏西利片 单因素 处方优化 工艺改进
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