A Proposed Quality Control Standard Mixture and Its Uses for Evaluating Nontargeted and Suspect Screening LC/HR-MS Method Performance

Author(s):  
Ann M. Knolhoff ◽  
Jacob H. Premo ◽  
Christine M. Fisher
2021 ◽  
Vol 16 (7) ◽  
pp. 1934578X2110304
Author(s):  
SukJin Lee ◽  
HyeSung Ryu ◽  
WanKyunn Whang

Shilajit has a longstanding use as an anti-aging and memory enhancing drug. It is known to have excellent anti-bacterial effects and is believed to be effective for cognitive enhancement, but is difficult to standardize because of the lack of quality control standards. This study, for the first time, proposes a quality control standard using a simultaneous analytical method for the drug’s multi-compound content using high-performance liquid chromatography-ultraviolet detection (HPLC-UV) as an aid for the internationalization of Mongolian Shilajit. Phenolic compounds 1-6 were isolated from Mongolian Shilajit extract using bioassay-guided isolation, and the isolated compounds were evaluated for cognitive-related anti-Alzheimer’s disease (AD) activities using 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical-scavenging, acetylcholinesterase (AChE), butyrylcholinesterase (BChE), β-site amyloid precursor protein-cleaving enzyme 1 (BACE1), and advanced glycation end-product (AGE) formation assays. The isolated compounds showed good effects for each activity. In addition, the isolated compounds were successfully quantified using a validated quantitative HPLC analysis method. As a result, the isolated compounds were suggested as standard marker compounds for Mongolian Shilajit. Also, we proved that the original material of Mongolian Shilajit is a lichen named Xanthoparmelia somloensis (Gyel.) Hale using HPLC-UV, ultra-high-performance liquid chromatography-electrospray ionization/hybrid linear trap-quadruple-orbitrap-high-resolution mass spectrometry (UHPLC-ESI/LTQ-HRMS).


2020 ◽  
Vol 103 (4) ◽  
pp. 1140-1147
Author(s):  
Isaac Lee ◽  
Jennie Vo ◽  
Quanyin Gao ◽  
Piyush Purohit ◽  
Veronica Zarraga ◽  
...  

Abstract Background A quantitative NMR (qNMR) method can provide rapid analysis compared to chromatographic methods. Sample preparation steps are relatively simpler and run time is shorter. Rapid analysis methods for release tests in quality control laboratories are very important for laboratory efficiency. Here, we describe a single-laboratory validation study for a rapid qNMR analysis of L-arginine, L-citrulline, and taurine in powdered and tablet dietary supplement products. Objectives This validation work is to provide documented evidence for the qNMR method validity as well as method performance. Methods The method used Bruker 400 MHz high-resolution proton NMR spectroscopy for simultaneous determination of L-arginine, L-citrulline, and taurine contents in dietary supplement product 1 (powder) and dietary supplement product 2 (tablet). The absolute NMR quantitation is based on a principle of universal proton response intensity correlation with the number of protons in each target analyte (amino acids) vs. that of a reference standard (maleic acid). Results The test method performance was validated with dietary supplement-1 (powder) and dietary supplement-2 (tablet). The linearity of the method was studied from about 360 mg/g to about 675 mg/g of L-arginine; from about 15 mg/g to about 30 mg/g of L-citrulline; and from about 20 mg/g to about 40 mg/g of taurine in dietary supplement-1, and from about 15 mg/g to about 30 mg/g of taurine in dietary supplement-2. The coefficients of determination (R2) are 1.0000 for L-arginine, 0.9967 for L-citrulline, and 0.9995 for taurine in dietary supplement-1 and 0.9903 for taurine in dietary supplement-2. The accuracies measured from the sample matrices are 102%, 101%, and 100% average recoveries for 80%, 100%, and 120% concentration levels of L-arginine, 105%, 105%, and 103% average recoveries for 80%, 100%, and 120% concentration level of L-citrulline, and 101%, 102%, and 100% average recoveries of taurine for 80%, 100%, 120% concentration levels in dietary supplement-1; and 95, 98%, and 93% average recoveries of taurine for 80%, 100%, 120% concentration levels in dietary supplement-2, respectively. The precisions (RSD) are 1% for L-arginine, 5% for L-citrulline, and 2% for taurine in dietary supplement -1, respectively; and 4% for taurine in dietary supplement-2. The ruggedness of the test method is within 2%, 4%, and 2% for L-arginine, L-citrulline, and taurine for dietary supplement -1, respectively, and within 4% for dietary supplement-2. The method is specific for the quantitation of each nutrient with no background interference from the matrix for the proton peaks of L-arginine, L-citrulline, taurine, and maleic acid (standard). Conclusions The test method is proven to be specific, precise, accurate, rugged, and suitable for intended quantitative analysis of L-arginine, L-citrulline, and taurine in powdered and tablet finished products. Highlights The simultaneous determination of all three nutrients of L-arginine, L-citrulline, and taurine using proton NMR provides rapid analysis for quality control release tests that is more efficient versus that of two HPLC methods. Previously, our laboratory was using one HPLC method to analyze L-arginine and L-citrulline while using a second HPLC method to analyze taurine. That approach required two HPLC instruments and two analysts for parallel analysis that takes 2 days using volatile and flammable solvents for extraction and chemical derivatization. This rapid NMR method can analyze the sample “as is” with results obtained in less than 4 h, and is efficient, safe, and environmentally friendly. The initial higher NMR instrument investment versus two HPLC instruments is rewarded with high returns for continued quality control tests.


2017 ◽  
pp. 1-18
Author(s):  
Marcio Fernando Cobo ◽  
Eleonore J. Deublein ◽  
Agnes Haber ◽  
Rance Kwamen ◽  
Manoj Nimbalkar ◽  
...  

1999 ◽  
Vol 14 (Suppl_3) ◽  
pp. 249-249
Author(s):  
A. Lefebvre ◽  
J. Van der Elst ◽  
C. Qian ◽  
M. Dhont

2006 ◽  
Vol 10 (12) ◽  
pp. 681-685 ◽  
Author(s):  
Queenie Siu Hang Chui ◽  
João Marcos de Almeida Bispo ◽  
Celia Omine Iamashita

Auditor ◽  
2017 ◽  
Vol 3 (2) ◽  
pp. 49-54
Author(s):  
Гоибназаров

The article describes the development and implementation of quality control standard auditor’s work in the Republic of Tajikistan based on the International Standards on Auditing.


2018 ◽  
pp. 1819-1836
Author(s):  
Marcio Fernando Cobo ◽  
Eleonore J. Deublein ◽  
Agnes Haber ◽  
Rance Kwamen ◽  
Manoj Nimbalkar ◽  
...  

2016 ◽  
Vol 9 (2) ◽  
pp. 186-211 ◽  
Author(s):  
Siddhartha Sankar Saha ◽  
Mitrendu Narayan Roy

Quality control of audit procedure has become extremely important in today’s corporate environment in the backdrop of accounting irregularities and audit failures leading to corporate demise. Accounting firms control the quality of audit procedure with the help of the quality control standard (QCS) and specific auditing standard. These standards provide reasonable assurance of compliance with applicable regulation and issuance of the appropriate report by the engagement team. After discussing the international scenario of quality control framework, in this study a comparative analysis of quality control policies and procedures at firm and engagement in three select countries has been presented. The countries selected are the United States of America (USA), the United Kingdom (UK) and India. The study finds that the QCS and the auditing standard in all three countries are designed in line with International Standards on Auditing (ISAs) and International Standards on Quality Control (ISQC)-1. Naturally, quality control policies and procedures in three countries are comparable barring few minor differences. Based on these differences, it can be concluded that the quality control framework in the UK and India is more stringent as compared to the USA.


2017 ◽  
Vol 5 (3) ◽  
Author(s):  
Juliani Sutikno

<p>PT. XYZ is a basic chemical manufacturing company which produces sulphuric acid. Quality<br />standard are reffered to National Standard of Indonesia (SNI). PT. XYZ has certified the use of SNI<br />standard for sulphurid acid product quality. Quality control of product is supervised by technician from<br />PT. XYZ to ensure that only products that meet acceptable standard of quality which may be delivered<br />to customer in order to ensure customer satisfaction. PT. XYZ establish product specifications sulphuric<br />acid in the production process with a concentration of at least 98,5%. Determination of sulphuric acids<br />product specification targets are too high from the referenced standard is loss and optimal quantity of<br />product produced. This study aims to measure the process capability and product specifications of<br />sulphuric acid establishes the right to increase the quantity of products. And then, Designing an<br />appropriate system to control product quality sulphuric acid which has been determined. Determination<br />of the specifications made by processing the sulphuric acids inspection levels. Processing data using<br />analytical tools of quality control, histogram charts, control charts, and a causal diagram. Result of<br />the analysis compared to the quality control standard established by BSN through SNI 0030:2011.<br />From the comparison of the data will be used to set quality standard appropriate levels of sulphuric<br />acid. Quality control system design sulphuric acid starts from the selection of raw material supplier,<br />controlling during the setting process until the sulphuric acid concentration through dilution water.</p>


Sign in / Sign up

Export Citation Format

Share Document