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Bioequivalence study of duloxetine hydrochloride enteric-coated tablets in healthy Chinese subjects
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Zhen ZHANG1a, Xiu-jin ZHANG1b, Ping ZHONG1b, Wen-ling ZHU1b, Jian-feng LIU1b
Chinese Journal of Clinical Pharmacology | 2025, 41(4) : 533 - 537
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Chinese Journal of Clinical Pharmacology | 2025, 41(4): 533-537
Pharmacokinetics and Bioequivalence Study
Bioequivalence study of duloxetine hydrochloride enteric-coated tablets in healthy Chinese subjects
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Zhen ZHANG1a, Xiu-jin ZHANG1b, Ping ZHONG1b, Wen-ling ZHU1b, Jian-feng LIU1b
Affiliations
  • 1a.Drug Clinical Trial Institution, The First Affiliated Hospital of Xiamen University, Xiamen 361003, Fujian Province, China
  • 1b.BE/Phase I Clinical Center, The First Affiliated Hospital of Xiamen University, Xiamen 361003, Fujian Province, China
Published: 2025-02-28 doi: 10.13699/j.cnki.1001-6821.2025.04.017
Outline
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Objective

To evaluate the bioequivalence of domestic duloxetine hydrochloride enteric-coated tablets and original enteric-coated capsules in Chinese healthy subjects.

Methods

In a random, open, two periods, two sequence, self-crossover study, 40 cases healthy subjects in fasting test and 48 cases healthy subjects in fed test were given single oral test preparation and reference preparation 20 mg of duloxetine hydrochloride. The concentrations of duloxetine hydrochloride in plasma were determined by high performance liquid chromatography tandem mass spectrometry. The pharmacokinetic parameters were calculated using Phonenix WinNolin 8.0 software, and the bioequivalence of the test and the reference duloxetine hydrochloride was evaluated.

Results

The main pharmacokinetic parameters of the test and the reference duloxetine hydrochloride in fasting test were as follows: Cmax were (16.70±5.94) and (16.70±7.10) ng·mL-1; AUC0-t were (217.28±98.82) and (222.42±117.98) ng·h·mL-1; AUC0-∞ were (225.91±100.35) and (229.40±119.34) ng·h·mL-1. The main pharmacokinetic parameters of the test and the reference duloxetine hydrochloride in fed test were as follows: Cmax were (20.10±9.56) and (21.30±10.90) ng·mL-1; AUC0-t were (266.99±146.66) and (273.22±168.09) ng·h·mL-1; AUC0-∞ were (277.83±154.73) and (283.51±174.63) ng·h·mL-1. The 90% confidence intervals of the main pharmacokinetic parameters of the test and reference preparations in fasting and fed tests were between 80.00%-125.00%.

Conclusion

The test and the reference duloxetine hydrochloride were bioequivalent under fasting and fed conditions.

duloxetine hydrochloride enteric-coated tablet  /  Chinese healthy subject  /  bioequivalence  /  high performance liquid chromatography tandem mass spectrometry
Zhen ZHANG, Xiu-jin ZHANG, Ping ZHONG, Wen-ling ZHU, Jian-feng LIU. Bioequivalence study of duloxetine hydrochloride enteric-coated tablets in healthy Chinese subjects[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (4) : 533 -537 . DOI: 10.13699/j.cnki.1001-6821.2025.04.017
Year 2025 volume 41 Issue 4
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doi: 10.13699/j.cnki.1001-6821.2025.04.017
  • Receive Date:2024-08-15
  • Online Date:2026-08-04
  • Published:2025-02-28
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History
  • Received:2024-08-15
Affiliations
    1a.Drug Clinical Trial Institution, The First Affiliated Hospital of Xiamen University, Xiamen 361003, Fujian Province, China
    1b.BE/Phase I Clinical Center, The First Affiliated Hospital of Xiamen University, Xiamen 361003, Fujian Province, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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