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Esomeprazole

Manufactured by AstraZeneca
Sourced in Sweden, China, United Kingdom

Esomeprazole is a proton pump inhibitor (PPI) medication used for the treatment of acid-related disorders, such as gastroesophageal reflux disease (GERD) and peptic ulcers. It works by reducing the production of stomach acid, which can help to heal and prevent further damage to the esophagus and stomach lining.

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11 protocols using esomeprazole

1

Comparison of Helicobacter pylori Eradication Regimens

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Eligible patients at each center were randomly assigned to two groups for 14-day treatment: (1) HDDT: esomeprazole 40 mg thrice daily (before breakfast/lunch/dinner) and amoxicillin 1000 mg thrice daily (after breakfast/lunch/dinner); or (2) TFEB: esomeprazole 40 mg twice daily (before breakfast/dinner), bismuth potassium citrate 220 mg twice daily (before breakfast/dinner), tetracycline 500 mg thrice daily (after breakfast/lunch/dinner), and furazolidone 100 mg twice daily (after breakfast/dinner).
The drug information is as follows: esomeprazole (AstraZeneca Pharmaceutical, Södertälje, Sweden), bismuth potassium citrate capsules (Sinopharm Shantou Jinshi Pharmaceutical, Shantou, Guangdong Province, China), amoxicillin (Zhuhai United Laboratories, Zhuhai, Guangdong Province, China), tetracycline (Guangdong Huanan Pharmaceutical, Dongguan, Guangdong Province, China), and furazolidone (Yunpeng Pharmaceutical, Linfen, Shanxi Province, China).
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2

Comparing Dual and Quadruple Therapies for H. pylori

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The eligible subjects were randomly divided into two groups according to the ratio of 1:1 by a computer-generated randomized digital table. The treatment group (dual therapy) received of 20 mg esomeprazole AstraZeneca Pharmaceutical Co., Ltd., Cambridge, UK, www.astrazeneca.com.cn) four times daily and 750 mg amoxicillin (Kunming Baker Norton Pharmaceutical Co., Ltd., Kunming, China, www.kbn.com.cn) four times daily for 14 days. Control group (bismuth-containing quadruple therapy) received of 220 mg bismuth potassium citrate (Lizhu Group Lizhu Pharmaceutical Factory, Guangzhou, China, www.livzon.com.cn) twice daily, 20 mg esomeprazole (AstraZeneca Pharmaceutical Co., Ltd., Cambridge, UK, www.astrazeneca.com.cn) twice daily, 1000 mg amoxicillin (Kunming Baker Norton Pharmaceutical Co., Ltd., Kunming, China, www.kbn.com.cn) twice daily and 250 mg clarithromycin capsule (Shanghai Abbott Pharmaceutical Co., Ltd., Shanghai, China, www.abbott.com.cn) twice daily for 14 days. Bismuth potassium citrate and esomeprazole were taken half an hour before meals, while amoxicillin and clarithromycin were taken half an hour after meals.
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3

Evaluation of Combination Therapy

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Drugs used in this study were as follows: FZD was from Yunpeng Pharmaceutical Co. Ltd, Shanxi, China; esomeprazole was from AstraZeneca Pharmaceutical Co. Ltd, Jiangsu, China; AMX was from Zhuhai Federal Pharmaceutical Co. Ltd, Guangdong, China; bismuth potassium citrate was from Furen Pharmaceutical Group Co. Ltd, Henan, China; and CLA was from Yangtze River Pharmaceutical Group Co. Ltd, Jiangsu, China. All drugs were routinely prescribed in hospital pharmacy.
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4

Paclitaxel-Resistant Ovarian Cancer Cell Line

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Human ovarian cancer cell line (paclitaxelresistant cell line) was purchased from Shanghai Yanjing Biotechnology Co. Ltd. Esomeprazole was product of Astrazeneca Pharmaceuticals Ltd, while Taxol was purchased from Jiangsu Osaikang Pharmaceutical Co. Ltd. RPMI160, DMEM culture medium, and 0.25 % trypsin containing EDTA were purchased from Hyclone, USA. TRIzol was purchased from Shanghai Terui Biological Engineering Co. Ltd. Antibody against V-ATPase was obtained from Santa Cruz Company, United States, while BCA protein quantitative assay kit was purchased from Biyuntian Institute of Technology.
Optical microscopes were products of Olympus, Japan. Super clean worktable was purchased from Beijing Semiconductor Equipment no. 1 Plant. Gel imager was obtained from Shanghai Tanon Company. Instrument for RT-PCR and pipettes were purchased from Eppendorf, Germany.
Low-temperature, high-speed centrifuge was purchased from Sigma Company. Enzyme marker was bought from Thermo Fisher Technology Co. Ltd, while Flow cytometer was product of Becton Dikinson, USA.
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5

Quadruple Therapy for H. pylori with S. boulardii

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This was a randomized, parallel-group study. Three hundred and sixty H. pylori-infected patients were recruited in the study and randomly assigned by a computer program into two groups: standard quadruple therapy group (Group A) and quadruple therapy plus S. bouladii (Group B). Computer-generated randomization assignments were centralized using the block randomization method (block size of 8) by a data manager who was not involved in the data analysis or patient enrollment. Patients assigned to Group A received esomeprazole (AstraZeneca Pharmaceutical, Co. Ltd., Cambridge, United Kingdom) 20 mg two times a day (bid); amoxicillin (Baker Norton Pharmaceutical, Co., Ltd., Kunming, China) 1.0 g bid; clarithromycin (Abbott Laboratories Ltd., Shanghai, China) 500 mg bid; and Bismuth Potassium Citrate (Livzon Pharmaceutical Group, Inc., Zhuhai, China) 600 mg bid for 14 days. Patients assigned to Group B received the same quadruple therapy for 14 days, Additionally, S. boulardii sachets (Laboratories Biocodex, Inc., France) of 500 mg was given a bid to Group B for 14 days. Serious diarrhea patients (mushy stools or watery stools > two times a day) were additionally given montmorillonite powder 3 g tid. Considering the high resistance rate of metronidazole in the Center China population, we took amoxicillin and clarithromycin as our antibiotic choice (9 (link), 39 (link)).
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6

Anchorage-Independent Growth of Melanoma Cells

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In order to simulate anchorage-independent growth conditions, we performed two different tests culturing melanoma cells in dishes coated with agarose or rocking the cells in tubes.
Culture dishes were coated with 1.5 % agarose (Promega, San Luis Obispo, California).
5x104 cells were plated in agarose-coated petri dishes in complete medium and after 5 days colonies were counted. At the end of the experiments, cells from colonies were centrifuged and used for western blot analysis, invasion assay, and Wound Healing Assay.
In rocking test, 5x104 cells were left rocking in tubes on the Mini Rocker Shaker (Biosan), at room temperature in Dulbecco's D-Mem Nutrient mix F12 (DME/F12-HEPES EuroClone, MI, Italy). In some experiment cells were treated with esomeprazole (Astra Zeneca, Sweden) and everolimus (MedChemExpress, Stockholm Sweden) during the rocking period. After 48h of rocking, cells were centrifuged, counted, and used for western blot analysis, invasion assay, and Wound Healing Assay.
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7

Postoperative Monitoring and Management

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Postoperative observations included recording of complaints of abdominal/chest pain, dyspnea, abdominal distention, changes in vital signs, and an abdominal/chest examination. If there were no complications, an oral diet was suspended for 1 day after the procedure. Esomeprazole (40 mg twice daily, AstraZeneca, Sodertalje, Sweden) was administered intravenously during the patient's hospital stay and then orally for another 8 weeks. If mediastinal emphysema or pneumothorax was found during or after the procedure, conservative treatments, including the intravenous infusion of Esomeprazole and antibiotics, were implemented.
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8

Enhancing Paclitaxel Sensitivity with siRNA and Esomeprazole

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V-ATPase V1C1 small interfering RNA (siRNA) and negative control siRNA were obtained from Santa Cruz Biotechnology. Cells were seeded at 5×103 cells/well in a 96-well microplate in RPMI 1640 with 10% FBS. All siRNAs were transfected into the cells using Lipofectamine 2000 (Invitrogen, San Diego, CA) according to the manufacturer’s protocol. After 24 hours of siRNA transfection, cells were treated with various concentrations of paclitaxel (Sigma-Aldrich) and then incubated at 37°C for 48 hours. Esomeprazole (AstraZeneca, Mol̈ndal, Sweden) was resuspended in normal saline at a concentration of 5 mg/mL. Cells were seeded at 3×103 cells/well in a 96-well microplate in RPMI 1640 with 10% FBS. Cells were pretreated or not with Esomeprazole (20-30 mg/mL) based on the protocols in previous reports [12 (link),13 (link)]. After 24 hours of treatment, cells were treated with various concentrations of paclitaxel and incubated at 37°C for 48 hours.
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9

Endoscopic Variceal Obliteration and Banding

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An endoscope (GIF-Q260J; Olympus Optical Co., Ltd., Tokyo, Japan), injection needle (Olympus NM-200L-423; Olympus), histoacryl blue (Beijing Fu’aile Technology Development Co., Ltd., Beijing, China), and lauromacrogol (Tianyu Pharmaceutical, Zhejiang, China) were used for EVO treatment employing the sandwich technique. Histoacryl glue (0.5 mL) with lauromacrogol (2 mL) was injected into the GV before and after tissue adhesive injection. The injection was stopped when the varices became engorged. Reinjection was performed in any residual GV while maintaining blood flow (depressive at palpation with the catheter) every 3 to 4 weeks until eradication. After EVO of GV, EBL was performed for concomitant EV.
To hasten the healing of ulcers induced by endoscopic therapy, a proton pump inhibitor and protective agent for the gastric mucosa were routinely administered to patients in both groups. After each endoscopic treatment session, the patients received esomeprazole 40 mg (AstraZeneca Pharmaceutical Co., Ltd, Wuxi, China) once daily via intravenous injection, and teprenone 50 mg (Weicai Pharmaceutical Co., Ltd, Suzhou, China) 3 times per day after meals.
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10

Comparative Helicobacter pylori Eradication Regimens

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Minocycline-containing BQT comprised bismuth potassium citrate 110 mg four times daily (before breakfast/lunch/dinner/bedtime), esomeprazole 20 mg twice daily (before breakfast/dinner), metronidazole 400 mg four times daily (after breakfast/lunch/dinner and before bedtime), and minocycline 100 mg twice daily (after breakfast/dinner) for 14 days.
Tetracycline-containing BQT comprised bismuth potassium citrate/esomeprazole/metronidazole with doses same as above and tetracycline 500 mg four times daily (after breakfast/lunch/dinner and before bedtime) for 14 days. Treatment allocation was not blinded.
The study drug information was as follows: bismuth potassium citrate (bismuth potassium citrate capsules 110 mg/capsule; Group Li Zhu Pharmaceutical Factory, Zhuhai, China), esomeprazole (esomeprazole magnesium enteric-coated tablets 20 mg/tablet; AstraZeneca Pharmaceutical Co., Ltd, Wuxi, China), metronidazole (metronidazole tablets 400 mg/tablet; Yabao Pharmaceutical Group Co., Ltd, Yunzhou, China), tetracycline (tetracycline tablets 250 mg/tablet; Hubei Yuancheng Saichuang Technology Co., Ltd, Wuhan, China), and minocycline (minocycline 50 mg/capsule; Wyeth Pharmaceutical Co., Ltd, Suzhou, China).
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