Feng Zhiqiang, Zhou Jie, Shang Xueying, Kuang Guojun, Han Jian, Lu Liping, Zhang Lei
a College of Pharmacy , Third Military Medical University , Chongqing , P. R. China.
b College of Chinese Traditional Medicine , Guangzhou University of Traditional Chinese Medicine , Guangzhou , Guangdong , P. R. China.
Pharm Biol. 2017 Dec;55(1):1177-1184. doi: 10.1080/13880209.2017.1285321.
Baicalin (BL) and baicalein (B) as the major flavonoids of Scutellaria baicalensis Georgi (Lamiaceae) have been investigated intensively, and shown to possess a multitude of pharmacological activities.
This study systematically evaluates the stability of BL and B in monomer and total flavonoid fraction (FSR) form in vitro, and further studies whether the protective measures are effective to make B and BL stable enough to meet the requirement of quantitative analysis in various biological samples.
The stability of BL and B was evaluated by investigating the influence factors such as pH (2.0, 3.0, 4.5, 6.8, 7.4 and 9.0), temperature (4, 25 and 40 °C), antioxidant (vitamin C and NaSO) and sunlight. After the protective measures were taken, stability of BL and B in plasma, urine and tissue homogenates was evaluated through post-preparative stability (stored at 4 °C for 24 h), three freeze-thaw cycles stability and long-term stability test (stored in refrigerator at -20 °C for 15 days). In addition, by comparing the degradation parameters of BL and B obtained from the monomer administration group with those of the FSR administration group, drug-drug interaction of coexistent components in FSR on the stability of BL and B was discussed.
The degradation of BL and B was both pH- and temperature-dependent with their correlation coefficents for first-order kinetics equation larger than 0.99, and acidic environment (pH 2-4.5), lower temperature (<4 °C) and acidic antioxidant (e.g. vitamin C) were conducive to stabilize B and BL. Furthermore, coexistent components in FSR were proved to have function on inhibiting the degradation of BL and B in our study for the first time, which was characteristic of prolonging their biological half-life (t) significantly, e.g., from 2.89 h to indefinite for BL (pH 6.8, 25 °C), from 2.63 h to 4.48 h for B (pH 6.8, 25 °C) and so on. Antioxidant of NaSO could inhibit the degradation of BL with t increasing from 1.8 h to 3.5 h, but aggravate the bio-transformation of B with t decreasing from 0.92 h to 0.29 h. Our research proved that BL monomer, and BL and B in FSR form could be stabilized enough to meet the requirement of biological quantitative analysis under the protection of coexistent components in FSR.
The results obtained indicated that the stability of BL and B was affected not only by its environmental parameters, but also by the coexistent components in the effective total flavonoids fractions.
黄芩苷(BL)和黄芩素(B)作为唇形科植物黄芩的主要黄酮类化合物,已得到深入研究,并显示出多种药理活性。
本研究系统评价了BL和B单体及总黄酮组分(FSR)形式在体外的稳定性,并进一步研究保护措施是否能有效使B和BL稳定到足以满足各种生物样品定量分析的要求。
通过考察pH(2.0、3.0、4.5、6.8、7.4和9.0)、温度(4、25和40℃)、抗氧化剂(维生素C和NaSO)和光照等影响因素来评价BL和B的稳定性。采取保护措施后,通过制备后稳定性(4℃储存24小时)、三个冻融循环稳定性和长期稳定性试验(-20℃冰箱储存15天)评价BL和B在血浆、尿液和组织匀浆中的稳定性。此外,通过比较单体给药组与FSR给药组获得的BL和B的降解参数,探讨FSR中共存成分对BL和B稳定性的药物相互作用。
BL和B的降解均依赖于pH和温度,其一级动力学方程的相关系数大于0.99,酸性环境(pH 2 - 4.5)、较低温度(<4℃)和酸性抗氧化剂(如维生素C)有利于稳定B和BL。此外,本研究首次证明FSR中的共存成分具有抑制BL和B降解的作用,其特点是显著延长它们的生物半衰期(t),例如,BL在pH 6.8、25℃时从2.89小时延长至无限长,B在pH 6.8、25℃时从2.63小时延长至4.48小时等。NaSO抗氧化剂可抑制BL的降解,t从1.8小时增加到3.5小时,但会加剧B的生物转化,t从0.92小时降至0.29小时。我们的研究证明,在FSR中共存成分的保护下,BL单体以及FSR形式的BL和B可以稳定到足以满足生物定量分析的要求。
所得结果表明,BL和B的稳定性不仅受其环境参数影响,还受有效总黄酮组分中共存成分的影响。