Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques
Alpha glucoside inhibitors used to treat type-2 diabetes mellitus (DM) are likely to be safe and effective. These agents are most effective for postprandial hyperglycemia. Miglitol is a type of drug used to treat type-2 DM. A simple, selective, linear, precise and accurate reversed-phase high-perfor...
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| Format: | Article |
| Language: | English |
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MDPI AG
2016-10-01
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| Series: | Scientia Pharmaceutica |
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| Online Access: | http://www.mdpi.com/2218-0532/84/4/654 |
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| author | Kesavan Balakumaran Mosesbabu Janagili Nagaraju Rajana Sureshbabu Papureddy Jayashree Anireddy |
| author_facet | Kesavan Balakumaran Mosesbabu Janagili Nagaraju Rajana Sureshbabu Papureddy Jayashree Anireddy |
| author_sort | Kesavan Balakumaran |
| collection | DOAJ |
| description | Alpha glucoside inhibitors used to treat type-2 diabetes mellitus (DM) are likely to be safe and effective. These agents are most effective for postprandial hyperglycemia. Miglitol is a type of drug used to treat type-2 DM. A simple, selective, linear, precise and accurate reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed and validated for a related substance of miglitol and its identification, and characterization was done by different mass spectrometry techniques. The gradient method at a flow rate of 1.0 mL/min was employed on a prevail carbohydrate ES column (250 × 4.6 mm, 5 μm particle size) at a temperature of 35 °C. Mobile phase A consisted of 10 mM dipotassium hydrogen orthophosphate adjusted to pH 8.0 using concentrated phosphoric acid and mobile phase B consisted of acetonitrile. The ultraviolet detection wavelength was 210 nm and 20 μL of the sample were injected. The retention time for miglitol was about 24.0 min. Forced degradation of the miglitol sample was conducted in accordance with the International Conference on Harmonisation (ICH) guidelines. Acidic, basic, neutral, and oxidative hydrolysis, thermal stress, and photolytic degradation were used to assess the stability-indicating the power of the method. Substantial degradation was observed during oxidative hydrolysis. No degradation was observed under the other stress conditions. The method was optimized using samples generated by forced degradation and sample solutions spiked with impurities and epimers. Good resolution of the analyte peak from peaks, corresponding to process-related impurities, epimers and degradation products, was achieved and the method was validated as per the ICH guidelines. The method can successfully be applied for routine analysis of miglitol. |
| first_indexed | 2024-12-10T07:21:55Z |
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| id | doaj.art-d6d9ac42d7c745a7ac43b7ae9947e59f |
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| issn | 2218-0532 |
| language | English |
| last_indexed | 2024-12-10T07:21:55Z |
| publishDate | 2016-10-01 |
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| series | Scientia Pharmaceutica |
| spelling | doaj.art-d6d9ac42d7c745a7ac43b7ae9947e59f2022-12-22T01:57:47ZengMDPI AGScientia Pharmaceutica2218-05322016-10-0184465467010.3390/scipharm84040654scipharm84040654Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry TechniquesKesavan Balakumaran0Mosesbabu Janagili1Nagaraju Rajana2Sureshbabu Papureddy3Jayashree Anireddy4Analytical Research, Custom Pharmaceutical Services, Dr. Reddy’s Laboratories Ltd., Bollaram Road, Miyapur, Hyderabad 500049, IndiaAnalytical Research, Custom Pharmaceutical Services, Dr. Reddy’s Laboratories Ltd., Bollaram Road, Miyapur, Hyderabad 500049, IndiaAnalytical Research, Custom Pharmaceutical Services, Dr. Reddy’s Laboratories Ltd., Bollaram Road, Miyapur, Hyderabad 500049, IndiaAnalytical Research, Custom Pharmaceutical Services, Dr. Reddy’s Laboratories Ltd., Bollaram Road, Miyapur, Hyderabad 500049, IndiaCentre for Chemical Sciences & Technology, Institute of Science and Technology, Jawaharlal Nehru Technological University, Kukatpally, Hyderabad 500085, IndiaAlpha glucoside inhibitors used to treat type-2 diabetes mellitus (DM) are likely to be safe and effective. These agents are most effective for postprandial hyperglycemia. Miglitol is a type of drug used to treat type-2 DM. A simple, selective, linear, precise and accurate reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed and validated for a related substance of miglitol and its identification, and characterization was done by different mass spectrometry techniques. The gradient method at a flow rate of 1.0 mL/min was employed on a prevail carbohydrate ES column (250 × 4.6 mm, 5 μm particle size) at a temperature of 35 °C. Mobile phase A consisted of 10 mM dipotassium hydrogen orthophosphate adjusted to pH 8.0 using concentrated phosphoric acid and mobile phase B consisted of acetonitrile. The ultraviolet detection wavelength was 210 nm and 20 μL of the sample were injected. The retention time for miglitol was about 24.0 min. Forced degradation of the miglitol sample was conducted in accordance with the International Conference on Harmonisation (ICH) guidelines. Acidic, basic, neutral, and oxidative hydrolysis, thermal stress, and photolytic degradation were used to assess the stability-indicating the power of the method. Substantial degradation was observed during oxidative hydrolysis. No degradation was observed under the other stress conditions. The method was optimized using samples generated by forced degradation and sample solutions spiked with impurities and epimers. Good resolution of the analyte peak from peaks, corresponding to process-related impurities, epimers and degradation products, was achieved and the method was validated as per the ICH guidelines. The method can successfully be applied for routine analysis of miglitol.http://www.mdpi.com/2218-0532/84/4/654reverse phase liquid chromatographymiglitolstability-indicating methodsforced degradationhigh performance liquid chromatographyDNJ (1-deoxynojirimycin)mass spectrometry |
| spellingShingle | Kesavan Balakumaran Mosesbabu Janagili Nagaraju Rajana Sureshbabu Papureddy Jayashree Anireddy Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques Scientia Pharmaceutica reverse phase liquid chromatography miglitol stability-indicating methods forced degradation high performance liquid chromatography DNJ (1-deoxynojirimycin) mass spectrometry |
| title | Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques |
| title_full | Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques |
| title_fullStr | Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques |
| title_full_unstemmed | Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques |
| title_short | Development and Validation of Miglitol and Its Impurities by RP-HPLC and Characterization Using Mass Spectrometry Techniques |
| title_sort | development and validation of miglitol and its impurities by rp hplc and characterization using mass spectrometry techniques |
| topic | reverse phase liquid chromatography miglitol stability-indicating methods forced degradation high performance liquid chromatography DNJ (1-deoxynojirimycin) mass spectrometry |
| url | http://www.mdpi.com/2218-0532/84/4/654 |
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