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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Main Authors: Neelkant Prasad, Roshan Issarani, Badri Prakash Nagori
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Journal of Spectroscopy
Online Access:http://dx.doi.org/10.1155/2013/836372
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spelling 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
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AT roshanissarani ultravioletspectrophotometricmethodfordeterminationofglipizideinpresenceofliposomalproliposomalturbidity
AT badriprakashnagori ultravioletspectrophotometricmethodfordeterminationofglipizideinpresenceofliposomalproliposomalturbidity
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