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  • ZHANG Ming-fa, SHEN Ya-qin
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    Gastric cancer is an important killer that threatens people's life and health, and its morbidity and mortality rank third among various malignant tumors in China. In addition to its anti-inflammatory, anti-infective, and cardiovascular regulating effects, berberine has good effects on liver cancer, colorectal cancer, brain tumors, head and neck tumors, urinary system tumors, etc. Therefore, it may be a potential anti-tumor drug. In this article, the prevention of gastric cancer with berberine, and the inhibition and induction of apoptosis of human gastric cancer cells such as SGC7901, BGC-823, and MKN-45 are mainly reviewed to provide a reference for the clinical development of berberine in the future.
  • WANG Yu, CHEN Tong, WANG Hui
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    Objective: To establish the quality standard of Qinggan Mixture, and to provide reference for the quality control of manufacture of Qinggan Mixture. Methods: Three kinds of medicinal materials in Qinggan Mixture, namely, cortex moutan, radix scutellariae and fructus gardeniae, were identified qualitatively by thin-layer chromatography (TLC), and the content of baicalin in Qinggan Mixture was determined by high performance liquid chromatography (HPLC). Results: The TLC map of cortex moutan, radix scutellariae and fructus gardeniae was clear in spots, with good separation effect, and strong specificity, and there was no interference from the negative control. When the mass concentration of baicalin was 16.125-258 μg/mL, it exhibited a good linear relationship with the peak response value (Apeak response value=22 655 ρμg/mL–99 737, r2=0.999 4, n=5). The average spiked recovery rate was 100.55% (RSD=1.92%); the average content of baicalin in three batches of Qinggan Mixture was 1.20 μg/mL. Conclusion: Cortex moutan, radix scutellariae and fructus gardeniae in the Qinggan Mixture can be qualitatively identified by TLC; HPLC has good specificity, precision, repeatability and stability in quantitative determination of baicalin in the Qinggan Mixture, and can be used for quantitative quality control of baicalin in the Qinggan Mixture.
  • ZHANG Xiao-ning, LI Qiu-feng, LI Jun-wei
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    Objective: To analyze the clinical diagnosis and treatment process of a patient with diabetic ketoacidosis accompanied by mucormycosis, and to provide reference for the diagnosis and treatment of patients with such complicated infection. Methods and Results: The patient was admitted to the hospital due to ''cough and expectoration for 1 week''. However, the next day, due to the critical value in the blood glucose report, the patient was considered diabetic ketoacidosis, and was transferred to a higher hospital for treatment. The patient's chest CT showed pulmonary infection, so doxycycline + cefoperazone sulbactam sodium + amikacin was given empirically. However, after more than ten days of anti-infection treatment, the infection was still controlled poorly, so experts were invited for consultation. Experts considered a high possibility of fungal infection in the patient, so amphotericin B for injection was added, and then fungal clumps (preferring mucor) were found in the bronchial mucosa tissue. Later, the anti-infection treatment regimen was adjusted to amphotericin B cholesterol sulfate complex for injection + posaconazole suspension oral liquid + cefoperazone sulbactam sodium. However, after more than one month of anti-infection treatment, the infection was still not completely controlled, so the clinical pharmacist was invited for consultation, who suggested adjusting the anti-infection treatment regimen to isavuconazole for injection + meropenem based on the patient's condition, previous medication and relevant diagnosis and treatment guidelines, and the doctor adopted the suggestion. After that, the cough, expectoration, fever and other infectious symptoms of the patient were significantly relieved, and chest CT also showed that the lung lesions were obviously absorbed. Conclusion: For complicated and refractory infectious diseases, the possibility of fungal infection should be fully considered in clinical practice, and the pathogen should be actively explored. In targeted treatment, the varieties and dosage forms of drugs should also be optimized, and their efficacy should be observed in real time to ensure timely and effective treatment on patients.
  • SUN Li-yun, GONG Jian, CHEN Yuan-sen, LI Xia, YANG Xiao-yu
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    Objective: To analyze the treatment process and pharmaceutical care of two patients with lung injury clinically treated with sivelestat sodium, and to provide reference for the safe and reasonable clinical use of sivelestat sodium. Methods and Results: Case 1 was admitted to the hospital for treatment because of "headache, dizziness and disturbance of consciousness for 2h caused by traffic accident". Right lateral ventricle drainage and drainage needle implantation were performed, and symptomatic treatment was given after the operation. On Day 21 after admission, the patient was transferred to ICU, and levofloxacin and meropenem were used in combination to strengthen anti-infection. On Day 22 after admission, the patient developed ARDS, and the doctor consulted the clinical pharmacist about the precautions for using sivelestat sodium before dissolving 0.3 g sivelestat sodium in 50 mL 0.9% sodium chloride injection, for pumping into the patient at a rate of 2 mL/h. Other pharmacists' suggestions were adopted by the doctor, but the patient was still poor in condition, and then transferred to a superior hospital for further treatment. Case 2 was admitted to the hospital for treatment because of "general weakness accompanied by sore throat and fever for 2 days", and the symptoms did not improve significantly after symptomatic treatment. After the consultation of ICU experts, the patient was transferred to ICU for treatment. On Day 3 after admission, the patient was diagnosed with multiple organ dysfunction syndrome (heart, lung and kidney), and experts from the superior hospital suggested anti-inflammatory and continuous renal replacement treatment, with intravenous drip of 0.2 g sivelestat sodium for 7 days, q24h. The clinical pharmacist suggested that sivelestat sodium should be used within 72 hours of lung injury. If there was another organ dysfunction in the elderly patient, it was recommended to discontinue the drug. If the improvement after 5 days of medication was not ideal, the drug could be discontinued. On Day 11 after admission, the inflammatory reaction of both lungs of the patient worsened, and sivelestat sodium had been used for more than 5 days, so the clinical pharmacist suggested discontinuing the drug, and the doctor adopted this suggestion. During this period, no adverse drug reactions (ADRs) occurred. Conclusion: Clinical pharmacists participate in clinical treatment, learn the latest pharmaceutical knowledge, put forward medication suggestions for unused drugs in time, analyze the advantages and disadvantages, and implement pharmaceutical care to avoid the occurrence of ADRs.
  • CAI Fang-qing, CHEN Ming-yu, WANG Ling, RUAN Jun-shan
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    Objective: To analyze the occurrence and treatment process of systemic muscle pain in one patient after using ceftizoxime sodium for Injection, and to provide reference for clinical medication safety of ceftizoxime. Methods and Results: The patient was referred to the gastrointestinal surgery department of our hospital because of repeated middle and upper abdominal pain and discomfort for more than 20 days, and gastric cancer (cardiac adenocarcinoma) detected by other hospital. The clinic considered elective surgery, so ceftizoxime sodium for Injection was preventively used. However, shortly after medication, the patient complained of systemic muscle soreness, night sweating, joint discomfort, and extensive pain in the back and waist, with a heart rate of 104 times/min and a visual analysis scale (VAS) of 8 points. Based on the previous condition and current medication of the patient, it was initially suspected that the adverse drug reactions were caused by ceftizoxime sodium for Injection, so ceftizoxime sodium for Injection was stopped. Soon, the patient complained that the systemic myalgia was relieved and VAS was reduced to 3 points, so it was determined that the myalgia was probably caused by ceftizoxime sodium for Injection. Conclusion: Systemic muscle pain caused by ceftizoxime sodium for Injection is rarely reported in clinical practice. Clinical pharmacists should integrate patients' condition and medication when carrying out pharmaceutical practice to help doctors make accurate judgments, so as to effectively deal with situations and ensure the medication safety of patients.
  • LIU Ying, CAO Jia, XU Ya-zhou
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    Objective: To analyze the correlation between the use of antibacterial drugs and imipenem-resistant Acinetobacter Baumannii in tertiary teaching hospitals in Xuzhou and Nanjing, Jiangsu Province, and to provide reference for clinical reduction of imipenem-resistant Acinetobacter baumannii (IRAB). Methods: A total of 15 434 strains of Acinetobacter baumannii detected from inpatient specimen from two tertiary teaching hospitals in Xuzhou and four tertiary teaching hospitals in Nanjing from January 2019 to December 2021 were used as the research objects, and the correlation between the use of antibacterial drugs and IRAB in hospitals of Nanjing and Xuzhou in three years was analyzed using the correlation coefficient method and linear regression method. Results: From 2019 to 2021, the composition ratio of IRAB in Xuzhou and Nanjing showed a significant increase trend, while the use of carbapenems, β-lactams and fluoroquinolones was significantly related to the composition ratio of IRAB (P<0.05). Conclusion: Reducing the use of carbapenems, piperacillin tazobactam sodium, fluoroquinolones and other antibacterial drugs may help to reduce IRAB.
  • FAN Xiao-dong, ZHANG Jie, XIE Xing-xing, LUO Zong-wei
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    Objective: To compare and analyze the clinical efficacy and safety of glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs in patients with chronic hepatitis B (CHB). Methods: Randomized controlled trials on the clinical efficacy and safety of glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs in patients with CHB were searched from the database establishment date to October 2023 in the databases such as Pubmed, Embase, CNKI, Wanfang Medical Network, and VIP. The Stata1 and Revman software were used to perform a network meta-analysis of the clinical efficacy and safety of glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs in patients with CHB. Results: After screening, 42 articles were included, involving a total of 3 991 cases. The results of the network meta-analysis showed that the efficacy of glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs in CHB patients was superior to nucleoside (nucleotide) analogs alone in terms of the indexes such as ALT, AST and total bilirubin (P<0.05). In terms of medication safety, the difference of incidence of adverse drug reactions between glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs and nucleoside (nucleotide) analogs alone was not statistically significant (P>0.05). Conclusion: The efficacy of glycyrrhizic acid preparations combined with nucleoside (nucleotide) analogs is more definite in CHB patients with a high safety.
  • SUN Jia-bin, ZHANG Ya-yun, OUYANG Ba-si
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    Objective: To explore the active ingredients and action mechanism of Wind-dispersing and Shufeng Huoluo Pills in the treatment of rheumatoid arthritis (RA) based on network pharmacology and molecular simulation docking technology. Methods: The active ingredients and targets of Wind-dispersing and Shufeng Huoluo Pills were retrieved through TCMSP and PubChem databases, and the gene sites for RA treatment were retrieved through GeneCards and DisGeNET databases. The common targets were obtained by intersection of the above two, and the core compounds and core targets were obtained through the network topology algorithm with the visualization of Cytoscape software. A protein-protein interaction (PPI) network was established through STRING platform to obtain important targets for GO and KEGG enrichment analysis. The core targets and core compounds were verified by molecular docking. Results: 158 main active compounds of Wind-dispersing and Shufeng Huoluo Pills were screened, including 49 core compounds such as quercetin, ursolic acid and luteolin, and 248 targets of Wind-dispersing and Shufeng Huoluo Pills for RA treatment were selected, including 84 important targets. The GO function enrichment and KEGG pathway enrichment analysis showed that Wind-dispersing and Shufeng Huoluo Pills mainly regulated the biological processes of inflammation, immune response, cell proliferation, apoptosis and so on, and played a therapeutic role mainly by regulating tumor necrosis factor signaling pathway, cytokine-cytokine receptor interaction signaling pathway, NOD like receptor signaling pathway and so on. Molecular docking results showed that three core compounds (quercetin, ursolic acid, luteolin) in Wind-dispersing and Shufeng Huoluo Pills had strong affinity with three core targets (IL-6, MAPK14, GSK3B). Conclusion: Quercetin, ursolic acid, luteolin and other main active ingredients in Wind-dispersing and Shufeng Huoluo Pills may regulate the body's multiple signaling pathways through core targets such as MAPK14, GSK3B and IL-6, and play a therapeutic role in RA.