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Pharmacokinetics of FGF21-164 fusion protein in mice using UHPLC-MS/MS method
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Zhen-dong CHEN1, Yu-xiong GAO1, Hao XUE1, Yuan-dong ZHENG1, Rong WANG2, Mei-jia YANG3, *, Da-fang ZHONG1, *
Acta Pharmaceutica Sinica | 2021, 56(9) : 2372 - 2377
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Acta Pharmaceutica Sinica | 2021, 56(9): 2372-2377
Special Reports: Bioanalysis for Drug
Pharmacokinetics of FGF21-164 fusion protein in mice using UHPLC-MS/MS method
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Zhen-dong CHEN1, Yu-xiong GAO1, Hao XUE1, Yuan-dong ZHENG1, Rong WANG2, Mei-jia YANG3, *, Da-fang ZHONG1, *
Affiliations
  • 1. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China
  • 2. China Pharmaceutical University, Nanjing 210009, China
  • 3. Jiangsu Cell Tech Medical Research Institute, Nanjing 211103, China
Published: 2021-09-12 doi: 10.16438/j.0513-4870.2021-0637
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FGF21-164 is a fusion protein obtained by structural modification and coupling of endogenous FGF21. It is a candidate drug used in the treatment of glucose and lipid metabolic disorders caused by obesity. In this study, the candidate peptide mass spectrometry information of the protein hydrolyzed by trypsin was predicted by Skyline software and verified by high resolution mass spectrometry. The specific surrogate peptide (YLYTDDAQQTEAHLEIR) with the best mass response was selected after optimizing ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Under ESI positive ion mode, the parent ion m/z 689.3 with 3 charge and the product ion m/z 738.4 with single charge can be monitored. After dilution by PBS, the serum samples were denatured under 60℃ and alkylated to reduce the matrix effect, then incubated with trypsin at 37℃ for 2 h, to obtain the surrogate peptide. The chromatographic separation was carried out on an EclipsePlus C18 column (2.1 mm×50 mm, 1.8 μm) using aqueous solution containing 0.1% formic acid (phase A) and acetonitrile solution containing 0.1% formic acid (phase B). Finally, the concentration of FGF21-164 fusion protein in mouse serum was quantitatively analyzed by external standard method by monitoring the above ion pairs using triple quadrupole mass spectrometer. This method showed a good linearity in the range of 2.50-500 μg·mL-1 (r=0.998 8), and was successfully applied to the pharmacokinetic study of FGF21-164 fusion protein in mice. This experiment was approved by the Experimental Animal Ethics Committee of Shanghai Institute of Materia Medica, Chinese Academy of Sciences (batch number: 20180004040450). Compared with the endogenous FGF21, the t1/2 of FGF21-164 fusion protein was prolonged from 0.5 h to 2.6 h, which is expected to prolong the therapeutic efficacy of this protein.

LC-MS/MS  /  FGF21-164 fusion protein  /  pharmacokinetics
Zhen-dong CHEN, Yu-xiong GAO, Hao XUE, Yuan-dong ZHENG, Rong WANG, Mei-jia YANG, Da-fang ZHONG. Pharmacokinetics of FGF21-164 fusion protein in mice using UHPLC-MS/MS method[J]. Acta Pharmaceutica Sinica, 2021 , 56 (9) : 2372 -2377 . DOI: 10.16438/j.0513-4870.2021-0637
Year 2021 volume 56 Issue 9
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Article Info
doi: 10.16438/j.0513-4870.2021-0637
  • Receive Date:2021-04-27
  • Online Date:2025-12-18
  • Published:2021-09-12
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  • Received:2021-04-27
  • Revised:2021-07-19
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Affiliations
    1. Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China
    2. China Pharmaceutical University, Nanjing 210009, China
    3. Jiangsu Cell Tech Medical Research Institute, Nanjing 211103, 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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