Literature DB >> 10716597

Analysis of the stability and degradation products of triptolide.

Y P Mao1, X L Tao, P E Lipsky.   

Abstract

Triptolide is the major active ingredient of the Chinese herbal remedy Tripterygium wilfordii Hook F. (TwHF). As triptolide content is used to estimate the potency of preparations of TwHF, assessment of its stability is warranted. The accelerated stability of triptolide was investigated in 5% ethanol solution in a light-protected environment at pH 6.9, within a temperature range of 60-90 degrees C. The observed degradation rate followed first-order kinetics. The degradation rate constant (K25 degrees C) obtained by trending line analysis of Arrhenius plots of triptolide was 1.4125 x 10(-4) h(-1). The times to degrade 10% (t1/10) and 50% (t1/2) at 25 degrees C were 31 and 204 days, respectively. Stability tests of triptolide in different solvents and different pH conditions (pH4-10) in a light-protected environment at room temperature demonstrated that basic medium and a hydrophilic solvent were the major factors that accelerated the degradation of triptolide. Triptolide exhibited the fastest degradation rate at pH 10 and the slowest rate at pH 6. In a solvent comparison, triptolide was found to be very stable in chloroform. The stability of triptolide in organic polar solvents tested at both 100% and 90% concentration was greater in ethanol than in methanol than in dimethylsulphoxide. Stability was also greater in a mixture of solvent:pH6 buffer (9:1) than in 100% solvent alone. An exception was ethyl acetate, which is less polar than the other solvents tested, but permitted more rapid degradation of triptolide. Two of the degradation products of triptolide were isolated and identified by HPLC and mass spectroscopy as triptriolide and triptonide. This suggested that the decomposition of triptolide occurred at the C12 and C13 epoxy group and the C14 hydroxyl. The opening of the C12 and C13 epoxy is an irreversible reaction, but the reaction occurring on the C14 hydroxyl is reversible. These results show that the major degradation pathway of triptolide involves decomposition of the C12 and C13 epoxy group. Since this reaction is very slow at 4 degrees C at pH 6, stability is enhanced under these conditions.

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Year:  2000        PMID: 10716597     DOI: 10.1211/0022357001773625

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  3 in total

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Authors:  Iqbal Ahmad; Zubair Anwar; Sofia Ahmed; Muhammad Ali Sheraz; Raheela Bano; Ambreen Hafeez
Journal:  AAPS PharmSciTech       Date:  2015-02-21       Impact factor: 3.246

2.  Studies on calcium dependence reveal multiple modes of action for triptolide.

Authors:  Stephanie J Leuenroth; Craig M Crews
Journal:  Chem Biol       Date:  2005-12

3.  Tripterygium polyglycosid attenuates the established airway inflammation in asthmatic mice.

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Journal:  Chin J Integr Med       Date:  2013-01-15       Impact factor: 1.978

  3 in total

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