DEVELOPMENT AND VALIDATION OF ANALYTICAL SPECTROPHO TOMETRIC AND RP-HPLC METHODS FOR THE SIMULTANEOUS ESTIMATION OF HYDROQUI NONE, HYDROCORTISONE AND TRETINOIN TERNARY MIXTURE IN TOPICAL FORMULATION (Record no. 11098)

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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200207111915.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200207b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 11991
Author Marwa, AlJamal K.
245 ## - TITLE STATEMENT
Title DEVELOPMENT AND VALIDATION OF ANALYTICAL SPECTROPHO TOMETRIC AND RP-HPLC METHODS FOR THE SIMULTANEOUS ESTIMATION OF HYDROQUI NONE, HYDROCORTISONE AND TRETINOIN TERNARY MIXTURE IN TOPICAL FORMULATION
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(11)
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 10-16p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective:
Development and validation of spectrophotometric an
d RP-HPLC methods for the simultaneous determination
of Hydroquinone (HQ),
Hydrocortisone (HC) and Tretinoin (TRT) ternary combi
nation in pharmaceutical preparation.
Methods:
The proposed spectrophotometric method was able to
determine TRT directly from its absorption spectrum
at 362 nm, however, HQ and
HC from their first derivative spectra at 284 nm and
252 nm, respectively, without any separation step.
The RP-HPLC method was developed using a
C
18
Sunfire
©
waters column with a mobile phase composed of acet
onitrile: phosphate buffer (adjusted to pH 6.1 using
ortho-phosphoric acid) in the
ratio of 30:70 %, v/v, respectively at a flow rate
of 0.8 ml/min. Quantification was based on measurin
g peak areas at 260 nm.
Results:
The spectrophotometric method was able to selective
ly quantify each of HQ, HC and TRT in the ranges of
10-50 μg/ml, 2-10 μg/ml and 0.5-5 μg/ml,
respectively. The RP-HPLC method was able to produc
e well-resolved peaks after 3.0, 8.2 and 20.2 min,
in the ranges of 2-10 μg/ml, 0.1-1 μg/ml and 0.05-2
μg/ml, for HQ, HC and TRT, respectively. The obtain
ed A, D
1
or peak areas values plotted against the concentra
tion of each of the three components showed
linear response in the stated ranges. Both methods
were validated in terms of linearity, LOD, LOQ, pre
cision, accuracy and selectivity.
Conclusion:
Both developed proposed methods were applied for th
e determination of the active ingredients in the ph
armaceutical formulation and
the common excipients did not interfere in the anal
ysis. The RP-HPLC method proved to be more sensitiv
e when compared to the applied
spectrophotometric method. However, the applied spe
ctrophotometric methods, considered as green analyt
ical chemistry, is a simple, time-saving
method that requires minimal use of a hazardous sol
vent.
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) 11992
Co-Author Gazy, Azza A.
773 0# - HOST ITEM ENTRY
Title International journal of pharmacy and pharmaceutical science
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
International Standard Serial Number 2656-0097
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/35188/21008
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 2020-02-07 2020850 2020-02-07 2020-02-07 Articles Abstract Database
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