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DC Field | Value | Language |
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dc.contributor.author | Munde, Manojkumar K. | - |
dc.contributor.author | Kulkarni, Nilesh S. | - |
dc.contributor.author | Rukhe, Nikita B. | - |
dc.contributor.author | Sen, Dhanya B. | - |
dc.date.accessioned | 2021-09-22T08:40:30Z | - |
dc.date.available | 2021-09-22T08:40:30Z | - |
dc.date.issued | 2020 | - |
dc.identifier.issn | 0974-3618 | - |
dc.identifier.uri | http://172.20.40.131:80/jspui/handle/123456789/3305 | - |
dc.description | FULL TEXT : https://rjptonline.org/AbstractView.aspx?PID=2020-13-7-76 | en_US |
dc.description.abstract | SGLT-2 is the newly developed class of antidiabetic medicine also called as gliflozins. Empagliflozin, dapagliflozin and canagliflozin are the SGLT-2 class inhibitors for the treatment of type II diabetes mellitus. SGLT-2 inhibitors shows the 82% of plasma protein binding, 36.8% of partitioning of red blood cells, 78% of bioavailability, 5.6 to 13.1 hrs half life in oral route of administration. In this review we complied analytical methods for the development and determination of the SGLT-2 inhibitors. Table no. 1, 2, 3 shows the analytical method development and validation of empagliflozin dapagliflozin and canagliflozin alone and with its combination by the HPLC method respectively also table no. 4 shows the various formulations available in SGLT-2 Inhibitors. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Research Journal of Pharmacy and Technology | en_US |
dc.subject | Empagliflozin | en_US |
dc.subject | dapagliflozin | en_US |
dc.subject | canagliflozin | en_US |
dc.subject | pharmacokinetic parameters | en_US |
dc.subject | pharmacodynamic parameters | en_US |
dc.subject | HPLC method | en_US |
dc.title | A Comprehensive Review on Analytical Method Development and Validation for SGLT-2 Inhibitors by HPLC in Its API and Dosage Form | en_US |
dc.type | Article | en_US |
Appears in Collections: | Faculty Publications |
Files in This Item:
File | Description | Size | Format | |
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1627 Dhanya B. Sen.docx | 13.72 kB | Microsoft Word XML | View/Open |
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