• Application Note

HPLC Method Transfer for Analysis of Metoclopramide HCl and Related Substances from an Agilent 1100 Series LC System to an ACQUITY Arc System

HPLC Method Transfer for Analysis of Metoclopramide HCl and Related Substances from an Agilent 1100 Series LC System to an ACQUITY Arc System

  • Margaret Maziarz
  • Mark Wrona
  • Waters Corporation

This is an Application Brief and does not contain a detailed Experimental section.

Abstract

This application brief demonstrates to transfer an HPLC method for related substances of metoclopramide HCl from an Agilent 1100 Series LC System to an ACQUITY Arc System, replicating the chromatographic separation and meeting system suitability specifications.

Benefits

The ACQUITY Arc System successfully reproduced chromatographic separation obtained on the Agilent 1100 Series LC System, generating reliable, robust, and accurate results.

Introduction

Analytical methods used for testing of pharmaceutical raw materials and finished products are often transferred across organizations or to contract partners that utilize instruments from different vendors. It is therefore essential for the analytical laboratories to successfully transfer these methods, to ensure product consistency and compliance with regulations. Effective method transfer generates equivalent results for the same analysis, independent of the instrument, laboratory, or the resources. This is important to eliminate the need to revalidate the method, which is time consuming and costly.

Here, we present a transfer of the HPLC method for related substances analysis of metoclopramide HCl from an Agilent 1100 Series LC System to an ACQUITY Arc System. The success of the method transfer to the new instrumentation will be measured by examining the chromatographic separation for comparable results, and verifying that the system suitability results meet the specifications defined in the USP General Chapter <621> Chromatography.1

Results and Discussion

The related compounds of metoclopramide HCl used in this study are listed in Table 1. Separate stock solutions were prepared in methanol at 1.0 mg/mL. A metoclopramide stock solution was diluted with water to 0.5 mg/mL and spiked with related substances at 1.0% level. For a system suitability solution, each stock solution was transferred to one vial and diluted with water to 0.05 mg/mL concentration of each analyte. The mixture was then diluted with standard diluent (50:50 methanol/water) to 15 μg/mL concentration for system suitability determination.

Table 1. List of the USP specified related substances of metoclopramide HCl for method transfer.

The HPLC method was first run on an Agilent 1100 Series LC System and then transferred to an ACQUITY Arc System. The ACQUITY Arc System offers a novel Multi-flow path technology, which enables efficient method transfer of legacy methods developed on previous generations of LC instrumentation. Instrument conditions for transfer of the HPLC method are listed in Figure 1.

Figure 1. Instrument conditions for transfer of the HPLC method for metoclopramide HCl and its USP-related substances from an Agilent 1100 Series LC System to an ACQUITY Arc System.

The chromatographic data of a sample containing metaclopramide API at 0.5 mg/mL with 1.0% of related substance acquired on both the Agilent 1100 Series LC and ACQUITY Arc Systems is displayed in Figure 2. The data shows that the ACQUITY Arc System reproduced chromatographic separation acquired on the Agilent 1100 Series LC System.

Figure 2. Chromatographic data of the metoclopramide API at 0.5 mg/mL with 1.0% of related substances for the method transfer from an Agilent 1100 Series LC System to an ACQUITY Arc System.

The mass spectral data acquired using an ACQUITY QDa Detector coupled to an ACQUITY Arc System was used to confirm identity of metoclopramide and related substances by mass detection. The mass analysis window from Empower 3 Software (Figure 3) shows UV and mass spectral data from a single result. This UV detection enhanced with MS spectral data was used to quickly confirm identity of the sample components.

Figure 3. Confirming peak identity by mass detection using mass spectral data acquired with an ACQUITY QDa Detector. Mass analysis window from Empower 3 Software shows UV and mass spectral data from a single result.

Performance of the HPLC method on the ACQUITY Arc System was verified by evaluating system suitability of five replicate injections of the system suitability solution according to the requirements defined in the USP General Chapter <621> Chromatography1 and compared to the results obtained on the Agilent 1100 Series LC System. Results of the method system suitability acquired on both systems passed the USP specifications and are summarized in Table 2. The retention times and peak areas repeatability of the method run on the ACQUITY Arc System were substantially lower than the USP specifications of less than 2.0% RSD and comparable to the Agilent 1100 Series LC System. The USP resolution values between all the peaks were comparable on both systems, indicating no loss in resolution for method transfer. The USP peak tailing factors were also comparable.

Table 2. System suitability results of five replicate injection of the system suitability solution for method transfer between Agilent 1100 Series LC and ACQUITY Arc systems.

Enabled by a unique Multi-flow path technology, the ACQUITY Arc System easily accepts and replicates methods from a variety of platforms, without compromising method integrity.2 The ACQUITY Arc System provides powerful LC performance and secures the lab’s investment by ensuring integration with new technologies such as the ACQUITY QDa Detector and the Empower Chromatography Data System (CDS) Software.

Conclusion

The HPLC method for metoclopramide and its related substances was successfully transferred from an Agilent 1100 Series LC System to an ACQUITY Arc System. The ACQUITY Arc System successfully replicated the quality of chromatographic separation obtained on the Agilent 1100 Series LC System and met the USP specifications for system suitability. Meeting the system suitability requirements is essential for laboratories to remain in compliance with the current Good Laboratory Practices regulations. Moreover, the ACQUITY QDa Detector in conjunction with UV detection enabled quick confirmation of peak identity by mass detection. Overall, the ACQUITY Arc System delivers reliable, robust, and reproducible results, which are key elements to enhance throughput and laboratory efficiency for routine testing in the QC laboratory.

References

  1. USP General Chapter, <621> Chromatography, USP 37-NF 32, The United States Pharmacopeia Convention, Official December 1, 2014.
  2. ACQUITY Arc System, http://www.waters.com/waters/nav.htm?cid=134844390

720005467, August 2015

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