A quality by design approach with comprehensive green analytical chemistry assessment: Development, validation, and application of a high-performance liquid chromatographic method for quantifying meropenem trihydrate in nanosponges and marketed formu

Meropenem trihydrate (MPN), pivotal in antimicrobial therapeutics, necessitates accurate analytical methods for its quantification across pharmaceutical formulations. The research aimed to develop a Quality by Design (QbD)-driven high-performance liquid chromatography (HPLC) method and validate it for the quantification of MPN in traditional and novel formulations, with a focus on environmental sustainability. The study employed a QbD approach to develop an HPLC method, ensuring its robustness and adaptability. The method’s universality was evaluated in both traditional powders for injection formulation and a novel beta-cyclodextrin nanosponges formulation. Rigorous validation was conducted per the International Conference on Harmonisation Q2 (R1) guidelines, including extensive stability and degradation studies to ascertain the method’s tenacity under multifarious conditions. The QbD-driven HPLC method showcased impeccable precision and accuracy, with a recovery rate of 99% for the marketed product and an encapsulation efficiency of 88.7% for nanosponges. Furthermore, seven different green analytical chemistry tools were used, and they indicated a significant reduction in environmental impact compared to pre-existing methodologies. In conclusion, our QbD-driven HPLC method for MPN quantification melds technical prowess with environmental responsibility, signifying a noteworthy stride in pharmaceutical research. The method’s high precision and stability assessment provide clinicians with a reliable tool for ensuring accurate dosing in critically ill patients, ultimately enhancing therapeutic efficacy and reducing treatment failure risks. Furthermore, the method supports sustainable drug analysis, minimizing ecological hazards associated with pharmaceutical waste. The method’s adaptability and greenness set a benchmark for future analytical methodologies, emphasizing analytical rigor, and ecological conscientiousness.

Authors

Publication Details

Journal
Journal of Applied Pharmaceutical Science
Published
2025-01-01
DOI
https://doi.org/10.7324/japs.2025.236517
Citations
1
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
Field-Weighted Citation Impact
0.75
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article

A quality by design approach with comprehensive green analytical chemistry assessment: Development, validation, and application of a high-performance liquid chromatographic method for quantifying meropenem trihydrate in nanosponges and marketed formu

Yogendra Nayak, Sanjay Garg, T Ashwini, Padmaja A. Shenoy et al.
1 citations
Journal of Applied Pharmaceutical Science
Analytical Methods in Pharmaceuticals
0.75
article

A quality by design approach with comprehensive green analytical chemistry assessment: Development, validation, and application of a high-performance liquid chromatographic method for quantifying meropenem trihydrate in nanosponges and marketed formu

Yogendra Nayak, Sanjay Garg, T Ashwini, Padmaja A. Shenoy, Chandrashekhar Raghu, Usha Y. Nayak
article en
1 citations

Abstract

Meropenem trihydrate (MPN), pivotal in antimicrobial therapeutics, necessitates accurate analytical methods for its quantification across pharmaceutical formulations. The research aimed to develop a Quality by Design (QbD)-driven high-performance liquid chromatography (HPLC) method and validate it for the quantification of MPN in traditional and novel formulations, with a focus on environmental sustainability. The study employed a QbD approach to develop an HPLC method, ensuring its robustness and adaptability. The method’s universality was evaluated in both traditional powders for injection formulation and a novel beta-cyclodextrin nanosponges formulation. Rigorous validation was conducted per the International Conference on Harmonisation Q2 (R1) guidelines, including extensive stability and degradation studies to ascertain the method’s tenacity under multifarious conditions. The QbD-driven HPLC method showcased impeccable precision and accuracy, with a recovery rate of 99% for the marketed product and an encapsulation efficiency of 88.7% for nanosponges. Furthermore, seven different green analytical chemistry tools were used, and they indicated a significant reduction in environmental impact compared to pre-existing methodologies. In conclusion, our QbD-driven HPLC method for MPN quantification melds technical prowess with environmental responsibility, signifying a noteworthy stride in pharmaceutical research. The method’s high precision and stability assessment provide clinicians with a reliable tool for ensuring accurate dosing in critically ill patients, ultimately enhancing therapeutic efficacy and reducing treatment failure risks. Furthermore, the method supports sustainable drug analysis, minimizing ecological hazards associated with pharmaceutical waste. The method’s adaptability and greenness set a benchmark for future analytical methodologies, emphasizing analytical rigor, and ecological conscientiousness.

Journal of Applied Pharmaceutical Science
Openalex Percentile: Top 35%
Analytical Methods in Pharmaceuticals
0.75
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