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Pharmacokinetic characteristics of[14C]CHMFL-FLT3-122 in rats
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Dong-yang LI1, 3, Xiao WANG2, Xiao-rong LU2, Jin YANG1, *, Hong-zhang SUN3, *
Acta Pharmaceutica Sinica | 2019, 54(4) : 714 - 719
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Acta Pharmaceutica Sinica | 2019, 54(4): 714-719
Original Articles
Pharmacokinetic characteristics of[14C]CHMFL-FLT3-122 in rats
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Dong-yang LI1, 3, Xiao WANG2, Xiao-rong LU2, Jin YANG1, *, Hong-zhang SUN3, *
Affiliations
  • 1. China Pharmaceutical University, Nanjing 210009, China
  • 2. Hefei Blooming Drug Safety Evaluation, Co. LTD., Hefei 230031, China
  • 3. Hefei Cosource Pharmaceuticals Inc., Hefei 230031, China
Published: 2019-04-12 doi: 10.16438/j.0513-4870.2018-1109
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The study was conducted to characterize the pharmacokinetics, distribution, metabolism and excretion of CHMFL-FLT3-122 after a single oral dose of 50 mg·kg-1[14C] labeled CHMFL-FLT3-122 in rats. Isotope tracing techniques were used to analyze drug concentration and identify the distribution of drugs in tissues and metabolites in biological samples. The experiments were approved by the Animal Ethics Committee of XenoBiotic Laboratories-China, Inc. The absolute bioavailability in male and female rats were 45.83% and 50.92% respectively. The parent drug and its metabolites were extensively distributed in the stomach, intestine, liver and lung, and were eliminated completely in 48 h. The majority of radioactivity was excreted through the feces at 92.34% of the dose with a small fraction through urine at 3.99% of the dose. The parent drug was the most significant circulating component, representing 49.23% and 70.65% over the 0-48 h collection time interval in the plasma of male and female. Two major metabolites, M553 (sulfate conjugate) and M457 (N-dealkyl product), were identified in plasma. Metabolites of CHMFL-FLT3-122, including ten phase Ⅰ and four phase Ⅱ metabolites, were identified. The metabolic pathways of CHMFL-FLT3-122 were proposed as N-dealkylation, oxidation, amide hydrolysis, sulfate conjugation, and glucuronic conjugation.

CHMFL-FLT3-122  /  acute myelocytic leukemia  /  in vivo metabolism  /  ADME  /  radiolabelling
Dong-yang LI, Xiao WANG, Xiao-rong LU, Jin YANG, Hong-zhang SUN. Pharmacokinetic characteristics of[14C]CHMFL-FLT3-122 in rats[J]. Acta Pharmaceutica Sinica, 2019 , 54 (4) : 714 -719 . DOI: 10.16438/j.0513-4870.2018-1109
Year 2019 volume 54 Issue 4
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Article Info
doi: 10.16438/j.0513-4870.2018-1109
  • Receive Date:2018-12-12
  • Online Date:2026-01-26
  • Published:2019-04-12
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History
  • Received:2018-12-12
  • Revised:2019-02-11
Affiliations
    1. China Pharmaceutical University, Nanjing 210009, China
    2. Hefei Blooming Drug Safety Evaluation, Co. LTD., Hefei 230031, China
    3. Hefei Cosource Pharmaceuticals Inc., Hefei 230031, 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
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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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