HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities
Calactin, a doubly-linked cardenolide, is commonly found in Apocynaceae family including Calotropis gigantea (L.) Dryand. (Niu jiao gua, C. gigantea). This phytochemical has gained recognition for its potential as an anticancer agent and a marker for anticancer properties. Our previous reports demon...
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Elsevier
2025-02-01
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| author | Naphat Kaewpaeng Sudaporn Wongwan Khemmachat Pansooksan Chanakan Chailom Pattaraporn Chaisupasakul Dumrongsak Pekthong Nitra Nuengchamnong Zhi-Hong Jiang Li-Ping Bai Piyarat Srisawang Supawadee Parhira |
| author_facet | Naphat Kaewpaeng Sudaporn Wongwan Khemmachat Pansooksan Chanakan Chailom Pattaraporn Chaisupasakul Dumrongsak Pekthong Nitra Nuengchamnong Zhi-Hong Jiang Li-Ping Bai Piyarat Srisawang Supawadee Parhira |
| author_sort | Naphat Kaewpaeng |
| collection | DOAJ |
| description | Calactin, a doubly-linked cardenolide, is commonly found in Apocynaceae family including Calotropis gigantea (L.) Dryand. (Niu jiao gua, C. gigantea). This phytochemical has gained recognition for its potential as an anticancer agent and a marker for anticancer properties. Our previous reports demonstrated the remarkable anti-liver and anti-colon cancer activities both in vitro and in vivo of the dichloromethane fraction from the stem barks of C. gigantea (CGD). However, quantitative analysis of calactin content in CGD by using a high-performance liquid chromatography (HPLC) – ultraviolet (UV) method was limited. Therefore, this study aimed to develop more sensitive and reliable method for measurement of calactin in CGD by using a HPLC- electrospray ionization mass spectrometry (ESI-MS) for its application on quality control and prediction of anticancer activity of CGD. The study utilized a HPLC-ESI-MS system, negative mode, for standardization and validation. An octadecylsilane column and a mixture of acetonitrile and water containing 0.1 % formic acid in gradient system were used as a stationary phase and a mobile phase, respectively. The method was validated in terms of linearity, accuracy, precision, recovery, limit of detection (LOD), and limit of quantitation (LOQ). The linearity of the developed technique was verified within the calactin concentrations range from 1 to 50 μg/mL, exhibiting a linear coefficient of determination (R2) greater than 0.998. The LOD and LOQ were 0.1 and 1 μg/mL, respectively. The proposed methodology met the acceptance criteria according to the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline Q2(R1). Therefore, the method was suitable for the quality control of CGD. Additionally, we suggest applying the established protocol to quantify the calactin contents in CGDs collected over a period of one year (12 months) to investigate the correlation to their cytotoxicities against human cell lines derived from colon cancer (HCT116), human hepatoblastoma (HepG2) and human cell line derived from stomach cancer metastasized to liver (MKN74). This will help in predicting its cytotoxicity against HCT116, HepG2 and MKN74. In summary, the established HPLC-ESI-MS method is suitable for both quality control and predicting of CGD anticancer activities for further utilization. |
| format | Article |
| id | doaj-art-559207c542114d91a8ee09412713d8d1 |
| institution | Kabale University |
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| language | English |
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| series | Heliyon |
| spelling | doaj-art-559207c542114d91a8ee09412713d8d12025-01-27T04:22:02ZengElsevierHeliyon2405-84402025-02-01113e41963HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activitiesNaphat Kaewpaeng0Sudaporn Wongwan1Khemmachat Pansooksan2Chanakan Chailom3Pattaraporn Chaisupasakul4Dumrongsak Pekthong5Nitra Nuengchamnong6Zhi-Hong Jiang7Li-Ping Bai8Piyarat Srisawang9Supawadee Parhira10Department of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, ThailandDepartment of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, ThailandDepartment of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, ThailandDepartment of Pharmaceutical Chemistry and Pharmacognosy, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, ThailandCenter of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, Thailand; Department of Physiology, Faculty of Medical Science, Naresuan University, 65000, Phitsanulok, ThailandCenter of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, Thailand; Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence for Environmental Health and Toxicology, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, ThailandFaculty of Science, Naresuan University, 65000, Phitsanulok, ThailandState Key Laboratory of Quality Research in Chinese Medicine, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Disease, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau, ChinaState Key Laboratory of Quality Research in Chinese Medicine, Guangdong-Hong Kong-Macao Joint Laboratory of Respiratory Infectious Disease, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Macau, ChinaCenter of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, Thailand; Department of Physiology, Faculty of Medical Science, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence in Medical Biotechnology, Faculty of Medical Science, Naresuan University, 65000, Phitsanulok, Thailand; Corresponding author. Department of Physiology, Faculty of Medical Science, Naresuan University, 65000, Phitsanulok, Thailand.Center of Excellence for Innovation in Chemistry, Naresuan University, 65000, Phitsanulok, Thailand; Center of Excellence for Environmental Health and Toxicology, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand; Corresponding author. Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Naresuan University, 65000, Phitsanulok, Thailand.Calactin, a doubly-linked cardenolide, is commonly found in Apocynaceae family including Calotropis gigantea (L.) Dryand. (Niu jiao gua, C. gigantea). This phytochemical has gained recognition for its potential as an anticancer agent and a marker for anticancer properties. Our previous reports demonstrated the remarkable anti-liver and anti-colon cancer activities both in vitro and in vivo of the dichloromethane fraction from the stem barks of C. gigantea (CGD). However, quantitative analysis of calactin content in CGD by using a high-performance liquid chromatography (HPLC) – ultraviolet (UV) method was limited. Therefore, this study aimed to develop more sensitive and reliable method for measurement of calactin in CGD by using a HPLC- electrospray ionization mass spectrometry (ESI-MS) for its application on quality control and prediction of anticancer activity of CGD. The study utilized a HPLC-ESI-MS system, negative mode, for standardization and validation. An octadecylsilane column and a mixture of acetonitrile and water containing 0.1 % formic acid in gradient system were used as a stationary phase and a mobile phase, respectively. The method was validated in terms of linearity, accuracy, precision, recovery, limit of detection (LOD), and limit of quantitation (LOQ). The linearity of the developed technique was verified within the calactin concentrations range from 1 to 50 μg/mL, exhibiting a linear coefficient of determination (R2) greater than 0.998. The LOD and LOQ were 0.1 and 1 μg/mL, respectively. The proposed methodology met the acceptance criteria according to the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline Q2(R1). Therefore, the method was suitable for the quality control of CGD. Additionally, we suggest applying the established protocol to quantify the calactin contents in CGDs collected over a period of one year (12 months) to investigate the correlation to their cytotoxicities against human cell lines derived from colon cancer (HCT116), human hepatoblastoma (HepG2) and human cell line derived from stomach cancer metastasized to liver (MKN74). This will help in predicting its cytotoxicity against HCT116, HepG2 and MKN74. In summary, the established HPLC-ESI-MS method is suitable for both quality control and predicting of CGD anticancer activities for further utilization.http://www.sciencedirect.com/science/article/pii/S2405844025003433Calotropis giganteaCalactinAnticancerStandardizationApplication |
| spellingShingle | Naphat Kaewpaeng Sudaporn Wongwan Khemmachat Pansooksan Chanakan Chailom Pattaraporn Chaisupasakul Dumrongsak Pekthong Nitra Nuengchamnong Zhi-Hong Jiang Li-Ping Bai Piyarat Srisawang Supawadee Parhira HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities Heliyon Calotropis gigantea Calactin Anticancer Standardization Application |
| title | HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities |
| title_full | HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities |
| title_fullStr | HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities |
| title_full_unstemmed | HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities |
| title_short | HPLC-MS standardization and validation methods for determination of calactin content in dichloromethane fraction of Calotropis gigantea (L.) Dryand. (Niu jiao gua) stem bark and its application in prediction of anticancer activities |
| title_sort | hplc ms standardization and validation methods for determination of calactin content in dichloromethane fraction of calotropis gigantea l dryand niu jiao gua stem bark and its application in prediction of anticancer activities |
| topic | Calotropis gigantea Calactin Anticancer Standardization Application |
| url | http://www.sciencedirect.com/science/article/pii/S2405844025003433 |
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