Sakshi N. Sonawane , Bhaskar K. Kurangi , Omkar A. Shelar , Abhilash A. Jalalpure , Nikhil Gawas , Rahul Koli
{"title":"通过质量设计,建立了一种稳定性指示的反相高效液相色谱法,用于评价转移体和上市产品中橙皮苷的含量","authors":"Sakshi N. Sonawane , Bhaskar K. Kurangi , Omkar A. Shelar , Abhilash A. Jalalpure , Nikhil Gawas , Rahul Koli","doi":"10.1016/j.jics.2024.101521","DOIUrl":null,"url":null,"abstract":"<div><div>The present study aimed to develop and validate a Quality by Design (QbD)-assisted simple stability-indicating reverse-phase high-performance liquid chromatography (RP-HPLC) method for the estimation of hesperidin in transfersomes and marketed formulations. This QbD strategic approach is innovative as it allows for optimization with minimal trial and error, making the HPLC method more efficient while enhancing robustness, reliability, and regulatory compliance. Hesperidin is a naturally occurring polyphenolic flavonoid widely distributed in citrus species, including oranges and lemons. Due to its extensive and attractive therapeutic potential, an efficient, accurate, and specialized HPLC technique was developed and validated according to ICH guidelines. A central composite design was employed for the analysis, offering the advantage of using a reduced number of design points and experimental runs. Using a C18 column (4.6 mm × 250 mm, 5 μm) and acetonitrile (0.1 % orthophosphoric acid) (70:30) as the mobile phase, chromatographic separation was performed at a wavelength of 284 nm and a flow rate of 1 ml/min. Hesperidin peaked around 4.6 min using the innovative analytical method. The method was found to be linear over a concentration range of 0.5–16 μg/ml. The developed method was robust, precise, and accurate, with a 98 % recovery. The limit of detection (LOD) was 0.453 μg/ml, and the limit of quantification (LOQ) was 1.375 μg/ml, with a relative standard deviation (RSD) of less than 2 %. Moreover, forced degradation studies of hesperidin were conducted, and the relevance of the developed method was evaluated on transfersome nanoformulations and marketed formulations, demonstrating its versatility and broad applicability. The hesperidin peak was well separated in the presence of degradation products. It was found that the developed method was adequate, sensitive, and specific. This research provides a comprehensive and innovative approach to hesperidin estimation, which can significantly impact quality control and formulation development.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 1","pages":"Article 101521"},"PeriodicalIF":3.4000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quality by design assisted a stability indicating RP-HPLC method for the estimation of hesperidin in transfersome and marketed product\",\"authors\":\"Sakshi N. Sonawane , Bhaskar K. Kurangi , Omkar A. Shelar , Abhilash A. Jalalpure , Nikhil Gawas , Rahul Koli\",\"doi\":\"10.1016/j.jics.2024.101521\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The present study aimed to develop and validate a Quality by Design (QbD)-assisted simple stability-indicating reverse-phase high-performance liquid chromatography (RP-HPLC) method for the estimation of hesperidin in transfersomes and marketed formulations. This QbD strategic approach is innovative as it allows for optimization with minimal trial and error, making the HPLC method more efficient while enhancing robustness, reliability, and regulatory compliance. Hesperidin is a naturally occurring polyphenolic flavonoid widely distributed in citrus species, including oranges and lemons. Due to its extensive and attractive therapeutic potential, an efficient, accurate, and specialized HPLC technique was developed and validated according to ICH guidelines. A central composite design was employed for the analysis, offering the advantage of using a reduced number of design points and experimental runs. Using a C18 column (4.6 mm × 250 mm, 5 μm) and acetonitrile (0.1 % orthophosphoric acid) (70:30) as the mobile phase, chromatographic separation was performed at a wavelength of 284 nm and a flow rate of 1 ml/min. Hesperidin peaked around 4.6 min using the innovative analytical method. The method was found to be linear over a concentration range of 0.5–16 μg/ml. The developed method was robust, precise, and accurate, with a 98 % recovery. The limit of detection (LOD) was 0.453 μg/ml, and the limit of quantification (LOQ) was 1.375 μg/ml, with a relative standard deviation (RSD) of less than 2 %. Moreover, forced degradation studies of hesperidin were conducted, and the relevance of the developed method was evaluated on transfersome nanoformulations and marketed formulations, demonstrating its versatility and broad applicability. The hesperidin peak was well separated in the presence of degradation products. It was found that the developed method was adequate, sensitive, and specific. 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引用次数: 0
摘要
本研究旨在建立并验证一种质量设计(QbD)辅助的简单稳定性指示反相高效液相色谱(RP-HPLC)方法,用于转移体和市售制剂中橙皮苷的含量测定。这种QbD策略方法具有创新性,因为它允许以最小的试验和错误进行优化,使HPLC方法更高效,同时增强了鲁棒性、可靠性和法规遵从性。橙皮苷是一种天然存在的多酚类黄酮,广泛存在于柑橘类植物中,包括橙子和柠檬。由于其广泛而有吸引力的治疗潜力,根据ICH指南开发了一种高效、准确和专门的HPLC技术并进行了验证。采用中心复合设计进行分析,减少了设计点和实验运行的数量。色谱柱为C18柱(4.6 mm × 250 mm, 5 μm),流动相为乙腈(0.1%正磷酸)(70:30),波长为284 nm,流速为1 ml/min。采用创新的分析方法,橙皮苷在4.6 min左右达到峰值。该方法在0.5 ~ 16 μg/ml浓度范围内呈线性。该方法鲁棒性好,精密度高,准确度高,回收率达98%。检测限(LOD)为0.453 μg/ml,定量限(LOQ)为1.375 μg/ml,相对标准偏差(RSD)小于2%。此外,进行了橙皮苷的强制降解研究,并对所开发的方法在转移纳米制剂和上市制剂上的相关性进行了评估,证明了其通用性和广泛的适用性。在降解产物存在的情况下,橙皮苷峰分离良好。结果表明,所建立的方法充分、灵敏、特异。本研究提供了一种全面、创新的橙皮苷评价方法,对橙皮苷的质量控制和制剂开发具有重要意义。
Quality by design assisted a stability indicating RP-HPLC method for the estimation of hesperidin in transfersome and marketed product
The present study aimed to develop and validate a Quality by Design (QbD)-assisted simple stability-indicating reverse-phase high-performance liquid chromatography (RP-HPLC) method for the estimation of hesperidin in transfersomes and marketed formulations. This QbD strategic approach is innovative as it allows for optimization with minimal trial and error, making the HPLC method more efficient while enhancing robustness, reliability, and regulatory compliance. Hesperidin is a naturally occurring polyphenolic flavonoid widely distributed in citrus species, including oranges and lemons. Due to its extensive and attractive therapeutic potential, an efficient, accurate, and specialized HPLC technique was developed and validated according to ICH guidelines. A central composite design was employed for the analysis, offering the advantage of using a reduced number of design points and experimental runs. Using a C18 column (4.6 mm × 250 mm, 5 μm) and acetonitrile (0.1 % orthophosphoric acid) (70:30) as the mobile phase, chromatographic separation was performed at a wavelength of 284 nm and a flow rate of 1 ml/min. Hesperidin peaked around 4.6 min using the innovative analytical method. The method was found to be linear over a concentration range of 0.5–16 μg/ml. The developed method was robust, precise, and accurate, with a 98 % recovery. The limit of detection (LOD) was 0.453 μg/ml, and the limit of quantification (LOQ) was 1.375 μg/ml, with a relative standard deviation (RSD) of less than 2 %. Moreover, forced degradation studies of hesperidin were conducted, and the relevance of the developed method was evaluated on transfersome nanoformulations and marketed formulations, demonstrating its versatility and broad applicability. The hesperidin peak was well separated in the presence of degradation products. It was found that the developed method was adequate, sensitive, and specific. This research provides a comprehensive and innovative approach to hesperidin estimation, which can significantly impact quality control and formulation development.
期刊介绍:
The Journal of the Indian Chemical Society publishes original, fundamental, theorical, experimental research work of highest quality in all areas of chemistry, biochemistry, medicinal chemistry, electrochemistry, agrochemistry, chemical engineering and technology, food chemistry, environmental chemistry, etc.