Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity
A simple and sensitive ultraviolet spectrophotometric method for quantitative estimation of glipizide in presence of lipid turbidity is described to avoid false estimation due to diffraction by turbidity. UV detection was performed at 230 nm, 225 nm, and 235 nm, and the calibration curve was plotted...
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2013-01-01
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Series: | Journal of Spectroscopy |
Online Access: | http://dx.doi.org/10.1155/2013/836372 |
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doaj-8ca31467153c4c409791b8c558fbc26b2020-11-24T23:48:38ZengHindawi LimitedJournal of Spectroscopy2314-49202314-49392013-01-01201310.1155/2013/836372836372Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal TurbidityNeelkant Prasad0Roshan Issarani1Badri Prakash Nagori2Lachoo Memorial College of Science and Technology, Pharmacy Wing, Sector-A, Shastri Nagar, Jodhpur, Rajasthan 342003, IndiaLachoo Memorial College of Science and Technology, Pharmacy Wing, Sector-A, Shastri Nagar, Jodhpur, Rajasthan 342003, IndiaLachoo Memorial College of Science and Technology, Pharmacy Wing, Sector-A, Shastri Nagar, Jodhpur, Rajasthan 342003, IndiaA simple and sensitive ultraviolet spectrophotometric method for quantitative estimation of glipizide in presence of lipid turbidity is described to avoid false estimation due to diffraction by turbidity. UV detection was performed at 230 nm, 225 nm, and 235 nm, and the calibration curve was plotted between resultant of absorbance of [230 nm − (225 nm + 235 nm)/2] and concentration of analyte. The calibration curve was linear over the concentration range tested (1–20 μg/mL) with limit of detection of 0.27 μg/mL and limit of quantification of 0.82 μg/mL. Percent relative standard deviations and percent relative mean error, representing precision and accuracy, respectively, for clear as well as turbid solutions, were found to be within acceptable limits, that is, always less than 0.69 and 0.41, respectively, for clear solution and 0.65 and 0.47, respectively, for turbid solution. Conclusively, our method was successfully applied for the determination of glipizide in clear as well as turbid solutions, and it was found that the drug analyte in both types of solutions can be detected from the same calibration curve accurately and precisely and glipizide entrapped in the liposomes or in proliposomal matrix was not detected.http://dx.doi.org/10.1155/2013/836372 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Neelkant Prasad Roshan Issarani Badri Prakash Nagori |
spellingShingle |
Neelkant Prasad Roshan Issarani Badri Prakash Nagori Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity Journal of Spectroscopy |
author_facet |
Neelkant Prasad Roshan Issarani Badri Prakash Nagori |
author_sort |
Neelkant Prasad |
title |
Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity |
title_short |
Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity |
title_full |
Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity |
title_fullStr |
Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity |
title_full_unstemmed |
Ultraviolet Spectrophotometric Method for Determination of Glipizide in Presence of Liposomal/Proliposomal Turbidity |
title_sort |
ultraviolet spectrophotometric method for determination of glipizide in presence of liposomal/proliposomal turbidity |
publisher |
Hindawi Limited |
series |
Journal of Spectroscopy |
issn |
2314-4920 2314-4939 |
publishDate |
2013-01-01 |
description |
A simple and sensitive ultraviolet spectrophotometric method for quantitative estimation of glipizide in presence of lipid turbidity is described to avoid false estimation due to diffraction by turbidity. UV detection was performed at 230 nm, 225 nm, and 235 nm, and the calibration curve was plotted between resultant of absorbance of [230 nm − (225 nm + 235 nm)/2] and concentration of analyte. The calibration curve was linear over the concentration range tested (1–20 μg/mL) with limit of detection of 0.27 μg/mL and limit of quantification of 0.82 μg/mL. Percent relative standard deviations and percent relative mean error, representing precision and accuracy, respectively, for clear as well as turbid solutions, were found to be within acceptable limits, that is, always less than 0.69 and 0.41, respectively, for clear solution and 0.65 and 0.47, respectively, for turbid solution. Conclusively, our method was successfully applied for the determination of glipizide in clear as well as turbid solutions, and it was found that the drug analyte in both types of solutions can be detected from the same calibration curve accurately and precisely and glipizide entrapped in the liposomes or in proliposomal matrix was not detected. |
url |
http://dx.doi.org/10.1155/2013/836372 |
work_keys_str_mv |
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