Application of the external standard method with a correction for absorption in the srxrf analysis of biological tissue

Author(s):  
V. A. Trunova ◽  
A. V. Sidorina ◽  
K. V. Zolotarev ◽  
V. V. Kriventsov
2013 ◽  
Vol 821-822 ◽  
pp. 1005-1008
Author(s):  
Li Min Ma ◽  
Li Cui ◽  
Yu Hang Zhao

Detection of 9а-OH-AD prepared by biotransformation by RP-HPLC directly was studied.The detection is performed on a Kromasil 100-5C18(4.6×250mm) column, using methanol:water(7:3,v/v)as mobile phase,0.8mL•min-1flow rate and external standard method,deteced at 242nm.There is a good line correlaction between peak and content in range of 0.01-0.20g/L,the correlation coefficient is 0.9942,the average recovery is 99.09% with a relative stand deviation of 0.89%(n=5).The method is simple,stable,accurate and reliable for quality control of 9а-OH-AD.


2018 ◽  
Vol 101 (1) ◽  
pp. 242-248
Author(s):  
Nathan P Stern ◽  
Jatinder Rana ◽  
Amitabh Chandra ◽  
John Balles

Abstract A quantitative ultra-performance LC (UPLC) method was developed and validated to successfully separate, identify, and quantitate the major polyphenolic compounds present in different varieties of sorghum (Sorghum bicolor) feedstock. The method was linear from 3.2 to 320 ppm, with an r2 of 0.99999 when using luteolinidin chloride as the external standard. Method accuracy was determined to be 99.5%, and precision of replicate preparations was less than 1% RSD. Characterization by UPLC-MS determined that the predominant polyphenolic components of the sorghum varietals were 3-deoxyanthocyanidins (3-DXAs). High-throughput screening for 3-DXA identified four unique classes within the sorghum varieties. Certain feedstock varieties have been found to have a high potential to not only be plant-based colorants, but also provide significant amounts of bioactive 3-DXAs, making them of unique interest to the dietary supplement industry.


2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Yang Xu ◽  
Yuejie Wang ◽  
Shengnan Bi ◽  
Yanxue Jia ◽  
Huiwei Bao

Objective. To establish a quantitative analysis of multicomponents by single marker (QAMS) method for the simultaneous determination of 4 active components such as protocatechuic acid, catechin, quercetin, and luteolin in Plantago depressa. Method. 4 active components in Plantago depressa were studied. Quercetin was used as an internal reference to establish the relative correction factors among protocatechuic acid, catechin, and luteolin and calculate the contents of each component; the results were compared with those measured by the external standard method. Results. 4 components showed a good linear relationship in their respective concentration ranges (r > 0.9995). The relative correction factors (fs/k) of protocatechuic acid, catechin, and luteolin were 1.1992, 0.8613, and 1.6069, respectively. The method had good durability. The contents of protocatechuic acid, catechin, and luteolin calculated by QAMS were not significantly different from those measured by the external standard method. Conclusion. QAMS can be used to determine the content of 4 components in Plantago depressa at the same time, and the method is simple, accurate, and can be used for quality control.


2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Dan Xu ◽  
Sicen Wang ◽  
Xiaofang Hou ◽  
Changshan Sun

Tianwang Buxin pill (TWBXP) is an ancient Chinese classic prescription. Liquiritin, deoxyschizandrin, and tanshinone II A are three bioactive components in TWBXP, which have been proven to be closely related to the therapy effect of neurodegenerative disease. Their contents are very low in TWBXP. In this study, we used a diode array detector (DAD) to perform a full wavelength scanning in order to choose a most suitable detection wavelength to establish an HPLC method for the simultaneous determination of these three components in TWBXP. Various chromatographic conditions were investigated to verify its applicability. Finally, a Kromasil C18 column (250 × 4.6 mm, 5 μm) thermostated at 30°C, mobile phase as 0.2% phosphoric acid solution (eluent A), and 0.1% phosphoric acid-acetonitrile solution (eluent B) were used. Both external standard method and internal standard method were used for quantification. The results showed that both methods were simple and convenient in operation without special pretreatment and exhibits excellent precision, repeatability (RSD < 3.0%), good linearity (R2 > 0.9990), and good recoveries (recovery value between 95% and 105%). Because of the low contents in samples, the internal standard method provided a better accurate result than the external standard method. The stability results showed the sample became stable within 24 hours at room temperature. The method provides a convenient and effective way for the quality control of TWBXP, and it can help the research about AD in the future.


2000 ◽  
Vol 15 (3) ◽  
pp. 173-174
Author(s):  
Wu Wanguo ◽  
Ruan Yuzhong

An external standard method using mica for angular calibration of powder diffractometers is described. This is useful especially when standard referee materials certified by the US National Institute of Standards and Technology are not accessible.


2016 ◽  
Vol 29 (6) ◽  
pp. 261-268
Author(s):  
Jinkyu Park ◽  
Ranhee Park ◽  
Sun Ho Han ◽  
Sang Ho Lim ◽  
Chi Gyu Lee ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5374
Author(s):  
Ruru Ren ◽  
Yanting Li ◽  
Huan Chen ◽  
Yingli Wang ◽  
Lingling Yang ◽  
...  

Given the standard substances of zeaxanthin and its homologues obtained from Lycium barbarum L. (LB) are extremely scarce and unstable, a novel quantitative analysis of carotenoids by single marker method, named QAMS, was established. Four carotenoids including lutein, zeaxanthin, β-carotene, and zeaxanthin dipalmitate were determined simultaneously by employing trans-β-apo-8′-carotenal, a carotenoid component which did not exist in LB, as standard reference. Meanwhile, β-carotene, another carotenoid constituent which existed in LB, was determined as contrast. The QAMS methods were fully verified and exhibited low standard method difference with the external standard method (ESM), evidenced by the contents of four carotenoids in 34 batches of LB samples determined using ESM and QAMS methods, respectively. HCA, PCA, and OPLS-DA analysis disclosed that LB samples could be clearly differentiated into two groups: one contained LB samples collected from Ningxia and Gansu; the other was from Qinghai, which was directly related to the different geographical location. Once exposed under high humidity (RH 75 ± 5%) at a high temperature (45 ± 5 °C) as compared with ambient temperature (25 ± 5 °C), from day 0 to day 28, zeaxanthin dipalmitate content was significantly decreased, and ultimately, all the decrease rates reached about 80%, regardless of the storage condition. Our results provide a good basis for improving the quality control of LB.


2014 ◽  
Vol 881-883 ◽  
pp. 781-784
Author(s):  
Zhi Guo Huang ◽  
Chun Hui Wei ◽  
Hui Bo Luo ◽  
Yan Mei Liu ◽  
Jie Deng

In order to fully exploit the truffle resources, this article took fresh and mature truffles as raw material, studied on extraction and detection of α-androstenol. The experiment used acetone as extracting agent and used ultrasonic wave extraction method to extract α-androstenol. Then the extracting solution was concentrated by Termovap Sample Concentrator, and was detected by GC-MS. The results showed that: using acetone as extraction agent, ultrasonic temperature at 50°C, ultrasonic frequency in 40KHZ, time for 60min, after concentrated and detected by external standard method for quantitative. The detected results showed that: in mature truffles, the content of α-androstenol was 0.0193μg/100g, the content of its isomeric compounds was 0.707μg/100g; in immature truffles, the content of α-androstenol was 0.0087μg/100g, the content of its isomeric compounds was 0.238μg/100g.


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