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Pharmacokinetics of two kinds of nimodipine crystal tablets in rhesus monkey
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Qi-meng ZHOU1, Jun-ke SONG1, Cheng XING2, Jin-hua WANG1, Yang LÜ2, Guan-hua DU1, *
Acta Pharmaceutica Sinica | 2017, 52(12) : 1918 - 1923
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Acta Pharmaceutica Sinica | 2017, 52(12): 1918-1923
ORIGINAL ARTICLES
Pharmacokinetics of two kinds of nimodipine crystal tablets in rhesus monkey
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Qi-meng ZHOU1, Jun-ke SONG1, Cheng XING2, Jin-hua WANG1, Yang LÜ2, Guan-hua DU1, *
Affiliations
  • 1. Beijing Key Laboratory of Drug Target and Screening Research, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
  • 2. Research Centre of Polymorphic Drugs, Beijing Key Laboratory of Polymorphic Drugs, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Published: 2017-12-12 doi: 10.16438/j.0513-4870.2017-0638
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Nimodipine is a selective calcium channel antagonist of cerebral vessels smooth muscle and also has polymorphs. It hasn't been reported that different crystal forms influence the metabolism process in huge animals like rhesus monkeys in vivo. This article may provide reference in the control of the quality of nimodipine and quality consistency evaluation. The powder X-ray diffraction (PXRD) method was used to identify different crystal forms and the dissolution test in vitro was used to detect the dissolution. The LC-MS method of assay nimodipine in rhesus monkey plasm was established to determine pharmacokinetics characters of different tablets from different crystal forms in rhesus monkey in vivo. As a result, the tablets inherit difference crystal forms and the dissolution of reference tablets is 1.3% higher than crystal tablets. However, the maximal blood concentration (Cmax) of crystal tablet was 37.3% higher than reference tablet and AUC of crystal tablet was 29.8% higher than reference tablet. After administrated 2.5 mg·kg-1 orally, calculated pharmacokinetics characters were observed as following:Cmax was 381.4 ±327.3 and 178.0 ±214.8 μg·L-1; AUC0-t was 853.1 ±500.7 and 646.5 ±430.3 μg·L-1·h respectively. The serum concentration result of different nimodipine tablets in rhesus monkeys in vivo suggests that polymorphs has a significantly distinction, which points out that controlling the crystal forms of nimodipine is essential to ensure the therapeutic efficacy. It is essential to execute quality consistency evaluation.

nimodipine  /  powder X-ray diffraction  /  rhesus  /  pharmacokinetics  /  LC-MS
Qi-meng ZHOU, Jun-ke SONG, Cheng XING, Jin-hua WANG, Yang LÜ, Guan-hua DU. Pharmacokinetics of two kinds of nimodipine crystal tablets in rhesus monkey[J]. Acta Pharmaceutica Sinica, 2017 , 52 (12) : 1918 -1923 . DOI: 10.16438/j.0513-4870.2017-0638
Year 2017 volume 52 Issue 12
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Article Info
doi: 10.16438/j.0513-4870.2017-0638
  • Receive Date:2017-07-15
  • Online Date:2026-01-14
  • Published:2017-12-12
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History
  • Received:2017-07-15
  • Revised:2017-09-15
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Affiliations
    1. Beijing Key Laboratory of Drug Target and Screening Research, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
    2. Research Centre of Polymorphic Drugs, Beijing Key Laboratory of Polymorphic Drugs, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, 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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