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Improved Stability of a Stable Crystal Form C of 6S-5-Methyltetrahydrofolate Calcium Salt,Method Development and Validation of an LC–MS/MS Method for Rat Pharmacokinetic Comparison
Authors:Zenglin Lian  Hong Chen  Kang Liu  Qianghua Jia  Feng Qiu  Yongzhi Cheng
Institution:1.Beijing Jinkang Hexin Pharmaceutical Technology Co., Ltd., Beijing 101111, China;2.Beijing Key Lab of TCM Collateral Disease Theory Research, School of Traditional Chinese Medicine, Capital Medical University, Beijing 100069, China;3.Lianyungang Jinkang Hexin Pharmaceutical Co., Ltd., Lianyungang 222115, China;4.Chinese Medicine DongFang College, Beijing University, Beijing 100029, China;
Abstract:Folate is a vitamin beneficial for humans that plays an important role in metabolism, but it cannot be well supplemented by food; it is necessary to supplement it in other ways. Based on this consideration, a novel crystal form C of 6S-5-methyltetrahydrofolate calcium salt (MTHF CAC) was obtained. To explore the difference between MTHF CAC and the crystal form Ⅰ of 6S-5-methyltetrahydrofolate calcium salt (MTHF CA) as well as an amorphous product of 6S-5-methyltetrahydrofolate glucosamine salt (MTHF GA), their stability and pharmacokinetic behaviours were compared. The results of high-performance liquid chromatography coupled with ultraviolet detection analysis indicated that MTHF CAC showed a better stability than MTHF CA and MTHF GA. After oral administration of MTHF CAC, MTHF CA, and MTHF GA to male rats, the MTHF concentrations were analysed using a validated liquid chromatography–tandem mass spectrometry, and the pharmacokinetic parameters were compared. The mean residence times (0–t) of MTHF CAC, MTHF CA, and MTHF GA were 3.7 ± 1.9 h, 1.0 ± 0.2 h (p < 0.01), and 1.5 ± 0.3 h (p < 0.05), respectively. The relative bioavailability of MTHF CAC was calculated to be 351% and 218% compared with MTHF CA and MTHF GA, respectively, which suggests that MTHF CAC can be better absorbed and utilized for a longer period of time.
Keywords:6S-5-methyltetrahydrofolate  crystal form C  stability  pharmacokinetics  LC–  MS/MS
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