Please use this identifier to cite or link to this item: https://hdl.handle.net/10321/3813
Title: Smart spectrophotometric method development for simultaneous estimation of antidiabetic drugs in formulations
Authors: Attimarad, Mahesh
Venugopala, Katharigatta Narayanaswamy
Shafi, Sheeba 
Balgoname, Abdulmalek Ahmed 
Altaysan, Abdulrahman Ibrahim 
Keywords: 1115 Pharmacology and Pharmaceutical Sciences;Antidiabetics;Vildagliptin;Remogliflozin;Derivative spectrophotometry
Issue Date: 12-Jan-2022
Publisher: EManuscript Technologies
Source: Attimarad, M, Venugopala, K.N., Shafi, S., Balgoname, A.A. and Altaysan, A.I. 2022. Smart spectrophotometric method development for simultaneous estimation of antidiabetic drugs in formulations. Indian Journal of Pharmaceutical Education and Research. 56(1): 224-231. doi:10.5530/ijper.56.1.26
Journal: Indian Journal of Pharmaceutical Education and Research; Vol. 56, Issue 1 
Abstract: 
An anti-diabetic formulation consisting of vildagliptin and remogliflozin was
prescribed for better glycemic control. In the present study a simple, rapid derivative
spectrophotometric methods were evolved to analyze these two analytes from the
formulations. Methods: Two processed UV spectrophotometric methods were established
by measuring the peak amplitude at zero-crossing of second derivative spectra of
analytes. The second procedure comprehends the generation of zero - order spectra from
the mixture of analyte spectra by division and multiplication by the pure analyte spectra
to remove the effect of one of the analytes. Results: Both methods showed linearity
concentrations in the range of 2-75 µg/ml for RGF and 2-50 µg/ml for VGT. The low
LOD and LOQ found for RGF and VGT by both methods indicated the good sensitivity of
the methods. The mean percentage recovery was 98.60 % and 100.78%, for RGF and
98.81 % and 99.15 % for VGT, with low percent relative error. The % RSD for intra and
inter-day precision was less than ±2%. Finally, the planned methods were employed
for the assay of the VGT and RGF from the medicine and the outcomes were matched
with the reported methods. Conclusion: The assay results of the formulation were in
agreement with the concentration of labeled amount and no significant difference was
observed in the results when compared to the reported method. Hence, the anticipated
procedures could be applied for the routine quality control of formulations consisting of
VGT and RGF.
URI: https://hdl.handle.net/10321/3813
ISSN: 0019-5464 (Online)
DOI: 10.5530/ijper.56.1.26
Appears in Collections:Research Publications (Applied Sciences)

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