Quantitative Open-Access HPLC Analysis - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Quantitative Open-Access HPLC Analysis
The authors discuss the approach taken to develop a new calibration approach, its associated protocols, and how it can be used to calculate data.


Pharmaceutical Technology
Volume 34, pp. s6-s11

Benzophenone was chosen as the external standard because it is stable, can be weighed out accurately, and is commercially available at high purity. Benzophenone is also very soluble in compatible solvents, has good chromatographic properties on open-access gradient HPLC methods, and has a high extinction coefficient at its λmax of 254 nm.


Figure 1: Sample log-on interface of the Yieldaliser software (GlaxoSmithKline, GSK). (ALL FIGURES ARE COURTESY OF BORMAN ET AL.)
Integrating a standardized approach. To ensure that the HPLC system is functioning satisfactorily, a test mixture and blank solution are automatically injected early in the day. Immediately afterward, six standard vials of a solution of benzophenone of known concentration (typically 0.35 mg/mL made up in methanol [MeOH]) are injected and the percentage relative standard deviation (i.e., measure of injector precision) and average response of the benzophenone (i.e., measure of accuracy) are checked against predetermined limits. If the performance does not fall within these limits, then the system will automatically repeat the standardization. If the calibration fails again, then the lead user is notified by email and the system is checked for problems such as poor column performance, solvent leaks, or autosampler issues. The assay functionality is disabled if the standardization criteria are not met. Figure 1 shows a screenshot of the customized interface on the laboratory computer that is connected to the instrument. The user selects either the 3- or 8-minute gradient method and then chooses to perform an analysis of impurities or assay (the assay analysis option is highlighted in red in Figure 1 and only runs on the 8-minute gradient).

Developing sample preparation protocols

Two protocols were developed to enable the analysis of liquid samples (for generating yield in solution data) and solid samples (assay data). These protocols were created to meet users' expectations. For example, sample preparation had to be quick, easy to follow, and use vessels that could be disposed of at minimal cost. Chemists needed to be able to to generate data that were sufficiently precise (within ± 3% w/w of the actual purity) for the majority of their applications. Trained analytical chemists can perform assays with greater precision (e.g., typically ± 0.5% w/w), however this is far more resource intensive.


ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
What is the single greatest threat to maintaining manufacturing processes at your facility?
Quality issues
Facility/environment problems
Process development problems
Production equipment downtime
Raw material supply problems
Regulatory restrictions
Business decisions to limit production
Quality issues
100%
Facility/environment problems
0%
Process development problems
0%
Production equipment downtime
0%
Raw material supply problems
0%
Regulatory restrictions
0%
Business decisions to limit production
0%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Praise and Perils for Biotechnology Patent Policy
Risk-Mitigation Strategies in Drug Manufacturing for Emerging Markets
Quality Focus: Ensuring Raw Material Transparency
Advertising of Prescription Drugs  Keeping it Honest and Balanced
Key Ways for Ensuring Global Regulatory Compliance
Source: Pharmaceutical Technology,
Click here