DEVELOPMENT AND VALIDATION OF SENSITIVE LC-ESI-MS/M S METHOD FOR THE SIMULTANEOUS ESTIMATION OF DAPAGLIFLOZIN AND SAXAGL IPTIN IN HUMAN PLASMA (Record no. 11176)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200212095756.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200212b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12114
Author Adluri, Phanindra
245 ## - TITLE STATEMENT
Title DEVELOPMENT AND VALIDATION OF SENSITIVE LC-ESI-MS/M S METHOD FOR THE SIMULTANEOUS ESTIMATION OF DAPAGLIFLOZIN AND SAXAGL IPTIN IN HUMAN PLASMA
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(4)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 55-59p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective
:
To develop and validate a sensitive liquid chromato
graphy-electrospray ionization-tandem mass spectrom
etric (LC-ESI-MS/MS)
technique for the quantification of dapagliflozin a
nd saxagliptin in plasma by linagliptin as internal
standard.
Methods
:
Chromatography was achieved on hypersil C
18
(50 mmx4 mm) 5 μ analytical column with 0.1% formi
c acid and acetonitrile (25:75 V/V)
as mobile phase at 0.7 ml/min flow rate. Dapagliflo
zin, saxagliptin, and linagliptin were detected at
m/z 409.14/135.0, m/z 316.2/180.13 and m/z
472.54/456.21 respectively. Drugs and internal stan
dard were extracted by LLE (liquid-liquid extractio
n).
Results
:
Developed technique was validated over 0.5-1500.0 n
g/ml linear concentration range for dapagliflozin a
nd 2.00-2000.0 ng/ml for
saxagliptin. This method established with intra-bat
ch and inter-batch precision within 2.44-8.12% and
1.25-7.14 % for dapagliflozin and 1.84-7.5 %
and 1.02–6.00 % for saxagliptin. This method establ
ished with intra-batch and inter-batch accuracy for
dapagliflozin within 98.86-103% and 96.98-
102 % respectively and for saxagliptin within 98.05
-109.06 % and 97.00-104.00 % respectively.
Conclusion
:
Both dapagliflozin and saxagliptin were stable duri
ng three freeze-thaw cycles, long term and bench-to
p stability studies. The
developed method was useful for the routine analysi
s of dapagliflozin and saxagliptin simultaneously i
n plasma samples.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 12115
Co-Author Shravan Kumar Y.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
International Standard Serial Number 2656-0097
Title International journal of pharmacy and pharmaceutical science
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/31249/19668
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2020-02-12 2020909 2020-02-12 2020-02-12 Articles Abstract Database
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