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Pharmacokinetics and preliminary safety evaluation of a novel DPP-4 inhibitor LGT-6
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Li-hong HE1, 2, Yu ZHANG3, Wei-ke LIAO1, 2, *, Lei TANG1, 2, *
Acta Pharmaceutica Sinica | 2026, 61(7) : 2675 - 2681
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Acta Pharmaceutica Sinica | 2026, 61(7): 2675-2681
• Original Articles •
Pharmacokinetics and preliminary safety evaluation of a novel DPP-4 inhibitor LGT-6
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Li-hong HE1, 2, Yu ZHANG3, Wei-ke LIAO1, 2, *, Lei TANG1, 2, *
Affiliations
  • 1State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University, Guiyang 550004, China
  • 2Guizhou Provincial Engineering Technology Research Center for Chemical Drug R & D, Guizhou Medical University, Guiyang 550004, China
  • 3Central Laboratory of Tongren People's Hospital, Tongren 554300, China
Published: 2026-07-12 doi: 10.16438/j.0513-4870.2026-0236
Outline
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To evaluate the excretion pathway, pharmacokinetic properties, and cardiac safety of the dipeptidyl peptidase-4 (DPP-4) inhibitor LGT-6 in rats, an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was used to determine drug concentrations in biological samples, in combination with an automated patch-clamp technique (automated patch clamp, APC) to assess the risk of human ether-à-go-go-related gene (hERG) potassium channel inhibition. The results showed that LGT-6 is primarily excreted via the biliary route in rats, with a cumulative excretion rate of approximately 82.4%. Following single-dose administration via tail vein injection (5 mg·kg-1) or oral gavage (5 mg·kg-1), the absolute bioavailability of LGT-6 was 77.2%. The IC50 of LGT-6 against the hERG potassium channel was greater than 30 μmol·L-1. The analytical methods established in this project for quantifying various target components in in vivo and in vitro biological samples all complied with relevant regulatory technical requirements. These data indicate that LGT-6 exhibits absorption, distribution, metabolism, and excretion (ADME) characteristics dominated by biliary excretion and high oral absorption efficiency, along with a low cardiac safety risk, thereby providing key experimental evidence to support its further preclinical safety evaluation and subsequent development. This experiment was approved by the Animal Ethics Committee of Guizhou Medical University (Grant No: 1900912).

dipeptidyl peptidase-4 inhibitor  /  excretion pathway  /  pharmacokinetics  /  human ether-à-go-go-related gene inhibition activity
何立虹, 张宇, 廖伟科, 汤磊. 新型DPP-4抑制剂LGT-6的药代动力学及初步安全性研究. 药学学报, 2026 , 61 (7) : 2675 -2681 . DOI: 10.16438/j.0513-4870.2026-0236
Li-hong HE, Yu ZHANG, Wei-ke LIAO, Lei TANG. Pharmacokinetics and preliminary safety evaluation of a novel DPP-4 inhibitor LGT-6[J]. Acta Pharmaceutica Sinica, 2026 , 61 (7) : 2675 -2681 . DOI: 10.16438/j.0513-4870.2026-0236
Year 2026 volume 61 Issue 7
228
110
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Article Info
doi: 10.16438/j.0513-4870.2026-0236
  • Receive Date:2026-03-04
  • Online Date:2026-09-21
  • Published:2026-07-12
Article Data
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History
  • Received:2026-03-04
  • Revised:2026-05-29
Affiliations
    1State Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University, Guiyang 550004, China
    2Guizhou Provincial Engineering Technology Research Center for Chemical Drug R & D, Guizhou Medical University, Guiyang 550004, China
    3Central Laboratory of Tongren People's Hospital, Tongren 554300, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
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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