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Determination of related substances in eldecalcitol soft capsules by solid phase extraction-HPLC*
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Jie LI, Qing-ting WANG, Li-min ZHANG, Jia-hong ZHANG, Zhen-fei LIU, Yang-sheng CHEN**
Chinese Journal of Pharmaceutical Analysis | 2024, 44(6) : 1009 - 1016
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Chinese Journal of Pharmaceutical Analysis | 2024, 44(6): 1009-1016
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Determination of related substances in eldecalcitol soft capsules by solid phase extraction-HPLC*
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Jie LI, Qing-ting WANG, Li-min ZHANG, Jia-hong ZHANG, Zhen-fei LIU, Yang-sheng CHEN**
Affiliations
  • CP Pharmaceutical Qingdao Co, Ltd, Qingdao 266000, China
Published: 2024-06-30 doi: 10.16155/j.0254-1793.2024.06.11
Outline
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Objective:

To establish an amino solid-phase extraction-HPLC method for the determination of three related substances in eldecalcitol soft capsules.

Methods:

The eldecalcitol soft capsules were extracted by an amino solid-phase extraction method, followed by eluting with ethyl acetate: n-hexane and anhydrous ethanol. The residue was then dissolved with acetonitrile and water after vacuum evaporation. An ODS column (250 mm×4.6 mm, 5 μm) was used. Water-acetonitrile with gradient elution was employed. The flow rate was 1.0 mL·min-1, the injection volume was 50 μL, and the detection wavelength was set at 265 nm.

Results:

Interference from blank excipients was eliminated with pretreatment. Baseline separation and good selectivity of eldecalcitol and other impurities was achieved. The stability of the test and reference solution was investigated at 4 ℃. The area change percentage of the impurities in the test solution were 98.6%-102.3% at 24 h. The area change percentage of the impurities in the reference solution were 101.2%, 96.9%, 98.5% and 96.2% at 24 h, respectively. The quantitation limits of eldecalcitol, trans impurity, pre-eldecalcitol and tachy impurity were 0.107 μg·mL-1, 0.102 μg·mL-1, 0.128 μg·mL-1 and 0.063 μg·mL-1, respectively. The detection limits were 0.054 μg·mL-1, 0.051 μg·mL-1, 0.064 μg·mL-1, 0.031 μg·mL-1, respectively. The linear ranges of 4 components were 0.1-6.3 μg·mL-, 0.1-1.2 μg·mL-, 0.1-5.6 μg·mL-and 0.1-1.1 μg·mL-1, respectively. The correlation coefficients(n=5) were 0.999 9, 1.000, 1.000 and 0.999 4, respectively. The average recoveries (n=6)of tachy impurity, pre-eldecalcitol and trans impurity were 106.6%, 88.6% and 102.8% with RSDs of 6.7%, 3.1% and 2.1%, respectively. In the three batches of samples, no impurities were detected except pre-eldecalcitol. The contents of pre-eldecalcitol were 5.0%, 5.0% and 5.1%, respectively.

Conclusion:

The method is simple to operate, economical and practical with high safety, strong specificity, good repeatability and high accuracy. The method provides a reliable basis for the study of drug quality such as eldecalcitol soft capsules and drugs with similar oily substrate.

solid-phase extraction  /  eldecalcitol soft capsules  /  oily substrate  /  activated vitamin D  /  structural isomer  /  related substances
Jie LI, Qing-ting WANG, Li-min ZHANG, Jia-hong ZHANG, Zhen-fei LIU, Yang-sheng CHEN. Determination of related substances in eldecalcitol soft capsules by solid phase extraction-HPLC*[J]. Chinese Journal of Pharmaceutical Analysis, 2024 , 44 (6) : 1009 -1016 . DOI: 10.16155/j.0254-1793.2024.06.11
Year 2024 volume 44 Issue 6
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doi: 10.16155/j.0254-1793.2024.06.11
  • Receive Date:2023-12-28
  • Online Date:2026-03-13
  • Published:2024-06-30
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  • Received:2023-12-28
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    CP Pharmaceutical Qingdao Co, Ltd, Qingdao 266000, 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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