Determination of omeprazole via fluorescence‐quenching methodology; application to content uniformity testing

A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered...

Full description

Saved in:
Bibliographic Details
Published in:Luminescence (Chichester, England) Vol. 39; no. 2; pp. e4682 - n/a
Main Authors: Elmansi, Heba, Orbano, Asya, Mashkour, Maram, Shamiya, Heba Abo, Belal, Fathalla
Format: Journal Article
Language:English
Published: England Wiley Subscription Services, Inc 01-02-2024
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered that quenching is proportional to the drug concentration, this dye was used as a sensor for OMP detection. The fluorescence intensity was measured at 518/540 nm, and its linear response ranged from 0.2–10.0 μg/mL with a linear coefficient of 0.9999. The computation yielded a limit of quantification (LOQ) of 0.20 μg/mL and a limit of detection (LOD) of 0.07 μg/mL. Every circumstance and element impacting the reaction product was examined in detail. Pharmacopeial standards carried out the validation. The approved method investigated several commercial preparations and formulations, and the results were favorably compared with those provided by a reference method. According to United States Pharmacopeia (USP) rules, content consistency for two distinct formulations was evaluated. Omeprazole, a proton pump inhibitor, was determined by its quenching effect on the native fluorescence of mercurochrome in acidic medium.
AbstractList A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered that quenching is proportional to the drug concentration, this dye was used as a sensor for OMP detection. The fluorescence intensity was measured at 518/540 nm, and its linear response ranged from 0.2–10.0 μg/mL with a linear coefficient of 0.9999. The computation yielded a limit of quantification (LOQ) of 0.20 μg/mL and a limit of detection (LOD) of 0.07 μg/mL. Every circumstance and element impacting the reaction product was examined in detail. Pharmacopeial standards carried out the validation. The approved method investigated several commercial preparations and formulations, and the results were favorably compared with those provided by a reference method. According to United States Pharmacopeia (USP) rules, content consistency for two distinct formulations was evaluated.
A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered that quenching is proportional to the drug concentration, this dye was used as a sensor for OMP detection. The fluorescence intensity was measured at 518/540 nm, and its linear response ranged from 0.2-10.0 μg/mL with a linear coefficient of 0.9999. The computation yielded a limit of quantification (LOQ) of 0.20 μg/mL and a limit of detection (LOD) of 0.07 μg/mL. Every circumstance and element impacting the reaction product was examined in detail. Pharmacopeial standards carried out the validation. The approved method investigated several commercial preparations and formulations, and the results were favorably compared with those provided by a reference method. According to United States Pharmacopeia (USP) rules, content consistency for two distinct formulations was evaluated.
A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered that quenching is proportional to the drug concentration, this dye was used as a sensor for OMP detection. The fluorescence intensity was measured at 518/540 nm, and its linear response ranged from 0.2–10.0 μg/mL with a linear coefficient of 0.9999. The computation yielded a limit of quantification (LOQ) of 0.20 μg/mL and a limit of detection (LOD) of 0.07 μg/mL. Every circumstance and element impacting the reaction product was examined in detail. Pharmacopeial standards carried out the validation. The approved method investigated several commercial preparations and formulations, and the results were favorably compared with those provided by a reference method. According to United States Pharmacopeia (USP) rules, content consistency for two distinct formulations was evaluated. Omeprazole, a proton pump inhibitor, was determined by its quenching effect on the native fluorescence of mercurochrome in acidic medium.
Abstract A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is based on the ability of OMP to quench the native fluorescence of the mercurochrome dye in an acidic (pH 3.6) solution. Because it was discovered that quenching is proportional to the drug concentration, this dye was used as a sensor for OMP detection. The fluorescence intensity was measured at 518/540 nm, and its linear response ranged from 0.2–10.0 μg/mL with a linear coefficient of 0.9999. The computation yielded a limit of quantification (LOQ) of 0.20 μg/mL and a limit of detection (LOD) of 0.07 μg/mL. Every circumstance and element impacting the reaction product was examined in detail. Pharmacopeial standards carried out the validation. The approved method investigated several commercial preparations and formulations, and the results were favorably compared with those provided by a reference method. According to United States Pharmacopeia (USP) rules, content consistency for two distinct formulations was evaluated.
Author Orbano, Asya
Shamiya, Heba Abo
Belal, Fathalla
Elmansi, Heba
Mashkour, Maram
Author_xml – sequence: 1
  givenname: Heba
  orcidid: 0000-0002-3953-7169
  surname: Elmansi
  fullname: Elmansi, Heba
  email: dr_heba85@hotmail.com
  organization: Mansoura University
– sequence: 2
  givenname: Asya
  surname: Orbano
  fullname: Orbano, Asya
  organization: Mansoura University
– sequence: 3
  givenname: Maram
  surname: Mashkour
  fullname: Mashkour, Maram
  organization: Mansoura University
– sequence: 4
  givenname: Heba Abo
  surname: Shamiya
  fullname: Shamiya, Heba Abo
  organization: Mansoura University
– sequence: 5
  givenname: Fathalla
  surname: Belal
  fullname: Belal, Fathalla
  organization: Mansoura University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38332466$$D View this record in MEDLINE/PubMed
BookMark eNp1kctu1jAQRi1URC8g8QTIEhs2aX1J7ESsoOVSqVI3ZR058bh1lXiC7RT9rPoIPCNPgsvfFgmpq5nFmaOZ-fbJTsAAhLzm7JAzJo4Gj4e1asUzsscbISotarnz2Mtml-yndM0YU0p1L8iubKUUtVJ7BE8gQ5x9MNljoOgozrBE8xMnoDfeUDetGCGNEEb4ffvr-1qaKx8u6Qz5Ci1OeLl5T82yTH7cOjLSEUOGkOkavMNizxuaIeUy9pI8d2ZK8Oq-HpBvnz9dHH-tzs6_nB5_OKtGyZmoxqZrdaMEl9bVLR-c4YqPTEiwtQbBlOXcNYO1MDSdkNw2Gni51DhtlRNCHpB3W-8Sseyccj_7csQ0mQC4pl50ou46zYQu6Nv_0GtcYyjbFUrylrW61f-EY8SUIrh-iX42cdNz1t-F0JcQ-rsQCvrmXrgOM9hH8OHrBai2wA8_weZJUf_x9Pyv8A-Of5Sw
Cites_doi 10.11648/j.ijpc.20170304.11
10.1016/j.jcis.2017.01.116
10.1007/s10895-015-1737-4
10.15406/japlr.2019.08.00309
10.11648/j.ajche.20180601.11
10.1007/978-1-4757-3061-6
10.24297/jac.v15i1.7003
10.1016/j.jpba.2005.09.029
10.1002/jssc.201900726
10.1016/j.chroma.2006.07.001
10.1016/j.microc.2017.04.007
10.7439/ijpc.v2i4.605
10.1080/22297928.2019.1613927
10.1016/j.msec.2014.12.006
10.1080/00387019008054044
10.1007/s10337-014-2827-1
10.1002/bio.3566
ContentType Journal Article
Copyright 2024 John Wiley & Sons Ltd.
2024 John Wiley & Sons, Ltd.
Copyright_xml – notice: 2024 John Wiley & Sons Ltd.
– notice: 2024 John Wiley & Sons, Ltd.
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QF
7QO
7QP
7QQ
7SC
7SE
7SP
7SR
7TA
7TB
7U5
7U7
8BQ
8FD
C1K
F1W
F28
FR3
H8D
H8G
H95
JG9
JQ2
KR7
L.G
L7M
L~C
L~D
P64
7X8
DOI 10.1002/bio.4682
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
Aluminium Industry Abstracts
Biotechnology Research Abstracts
Calcium & Calcified Tissue Abstracts
Ceramic Abstracts
Computer and Information Systems Abstracts
Corrosion Abstracts
Electronics & Communications Abstracts
Engineered Materials Abstracts
Materials Business File
Mechanical & Transportation Engineering Abstracts
Solid State and Superconductivity Abstracts
Toxicology Abstracts
METADEX
Technology Research Database
Environmental Sciences and Pollution Management
ASFA: Aquatic Sciences and Fisheries Abstracts
ANTE: Abstracts in New Technology & Engineering
Engineering Research Database
Aerospace Database
Copper Technical Reference Library
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Materials Research Database
ProQuest Computer Science Collection
Civil Engineering Abstracts
Aquatic Science & Fisheries Abstracts (ASFA) Professional
Advanced Technologies Database with Aerospace
Computer and Information Systems Abstracts – Academic
Computer and Information Systems Abstracts Professional
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
Materials Research Database
Aquatic Science & Fisheries Abstracts (ASFA) Professional
Technology Research Database
Computer and Information Systems Abstracts – Academic
Mechanical & Transportation Engineering Abstracts
ProQuest Computer Science Collection
Computer and Information Systems Abstracts
Materials Business File
Environmental Sciences and Pollution Management
Aerospace Database
Copper Technical Reference Library
Engineered Materials Abstracts
Biotechnology Research Abstracts
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Advanced Technologies Database with Aerospace
ANTE: Abstracts in New Technology & Engineering
Civil Engineering Abstracts
Aluminium Industry Abstracts
Toxicology Abstracts
Electronics & Communications Abstracts
Ceramic Abstracts
METADEX
Biotechnology and BioEngineering Abstracts
Computer and Information Systems Abstracts Professional
ASFA: Aquatic Sciences and Fisheries Abstracts
Solid State and Superconductivity Abstracts
Engineering Research Database
Calcium & Calcified Tissue Abstracts
Corrosion Abstracts
MEDLINE - Academic
DatabaseTitleList Materials Research Database
MEDLINE

MEDLINE - Academic
CrossRef
Database_xml – sequence: 1
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
Biology
EISSN 1522-7243
EndPage n/a
ExternalDocumentID 10_1002_bio_4682
38332466
BIO4682
Genre article
Journal Article
GroupedDBID ---
.3N
.GA
.Y3
05W
0R~
10A
1L6
1OC
31~
33P
3SF
3WU
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACIWK
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADZMN
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFZJQ
AHBTC
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BNHUX
BROTX
BRXPI
BY8
CS3
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRSTM
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
H.T
H.X
HF~
HGLYW
HHY
HVGLF
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2W
P2X
P4D
Q.N
Q11
QB0
QRW
R.K
ROL
RWI
RX1
SUPJJ
SV3
V2E
W8V
W99
WBFHL
WBKPD
WIH
WIK
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XPP
XV2
~IA
~WT
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7QF
7QO
7QP
7QQ
7SC
7SE
7SP
7SR
7TA
7TB
7U5
7U7
8BQ
8FD
AAMNL
C1K
F1W
F28
FR3
H8D
H8G
H95
JG9
JQ2
KR7
L.G
L7M
L~C
L~D
P64
7X8
ID FETCH-LOGICAL-c3102-c598756213df481bfa161c023ed47e206d11f5bddeb59231d57e1723af7d6f223
IEDL.DBID 33P
ISSN 1522-7235
IngestDate Sat Aug 17 01:23:49 EDT 2024
Fri Nov 15 22:45:06 EST 2024
Fri Aug 23 00:54:22 EDT 2024
Sat Nov 02 12:21:03 EDT 2024
Sat Aug 24 01:06:13 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords content uniformity
omeprazole
fluorescence
mercurochrome
Language English
License 2024 John Wiley & Sons Ltd.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3102-c598756213df481bfa161c023ed47e206d11f5bddeb59231d57e1723af7d6f223
Notes Funding information
No funding supported this research.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0002-3953-7169
PMID 38332466
PQID 2931808787
PQPubID 1016397
PageCount 8
ParticipantIDs proquest_miscellaneous_2924997027
proquest_journals_2931808787
crossref_primary_10_1002_bio_4682
pubmed_primary_38332466
wiley_primary_10_1002_bio_4682_BIO4682
PublicationCentury 2000
PublicationDate February 2024
2024-Feb
2024-02-00
20240201
PublicationDateYYYYMMDD 2024-02-01
PublicationDate_xml – month: 02
  year: 2024
  text: February 2024
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: Bognor Regis
PublicationTitle Luminescence (Chichester, England)
PublicationTitleAlternate Luminescence
PublicationYear 2024
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2019; 8
2015; 78
2015; 14
2019; 9
2012; 2012
2017; 3
2013; 2
2006; 1129
2009
1994
2017; 495
2017; 133
1999
2018; 6
2015; 48
2014; 4
2006; 42
1990; 23
2008; 43
2015
2014
2013
2020; 43
2018; 11
2018; 33
2016; 27
2016; 26
2014; 6
2018; 15
U.S.P. Convention (e_1_2_11_19_1) 2015
El‐Kommos M. E. (e_1_2_11_10_1) 2014; 6
e_1_2_11_31_1
Elokely K. (e_1_2_11_9_1) 2012; 2012
Shahrokhian S. (e_1_2_11_11_1) 2015; 14
e_1_2_11_14_1
e_1_2_11_13_1
e_1_2_11_12_1
e_1_2_11_7_1
e_1_2_11_29_1
e_1_2_11_6_1
e_1_2_11_28_1
e_1_2_11_5_1
e_1_2_11_27_1
e_1_2_11_26_1
Christian G. D. (e_1_2_11_30_1) 2014
Sweetman S. C. (e_1_2_11_3_1) 2009
Sudhakararao G. V. (e_1_2_11_4_1) 2014; 4
B.P. Commission (e_1_2_11_18_1) 2013
Sudha T. (e_1_2_11_24_1) 2016; 27
Susithra E. (e_1_2_11_21_1) 2018; 11
e_1_2_11_20_1
e_1_2_11_25_1
e_1_2_11_23_1
e_1_2_11_8_1
e_1_2_11_22_1
e_1_2_11_17_1
e_1_2_11_16_1
e_1_2_11_15_1
DiPiro J. T. (e_1_2_11_2_1) 2008
References_xml – year: 2009
– volume: 6
  start-page: 1
  year: 2018
  publication-title: Am. J Chem. Eng.
– volume: 15
  start-page: 6099
  year: 2018
  publication-title: J Adv. in Chem.
– volume: 9
  start-page: 152
  year: 2019
  publication-title: Anal. Chem. Lett.
– volume: 495
  start-page: 1
  year: 2017
  publication-title: J. Colloid Interface Sci.
– volume: 14
  start-page: 465
  year: 2015
  publication-title: Iran J Pharm Res
– volume: 4
  start-page: 247
  year: 2014
  publication-title: Int. J. Pharm.
– volume: 42
  start-page: 100
  year: 2006
  publication-title: J. Pharm. Biomed. Anal.
– volume: 43
  start-page: 696
  year: 2020
  publication-title: J. Sep. Sci.
– volume: 2012
  start-page: 1
  year: 2012
  publication-title: Chem
– volume: 33
  start-page: 1306
  year: 2018
  publication-title: Luminescence
– volume: 3
  start-page: 52
  year: 2017
  publication-title: Int J Pharm and Chem
– volume: 78
  start-page: 279
  year: 2015
  publication-title: Chromatographia
– volume: 133
  start-page: 398
  year: 2017
  publication-title: J Microc
– year: 2014
– year: 1994
– volume: 26
  start-page: 521
  year: 2016
  publication-title: J Fluoresc
– volume: 2
  start-page: 126
  year: 2013
  publication-title: Int J Pharm Chem
– volume: 48
  start-page: 213
  year: 2015
  publication-title: Mat. Sci. And Eng.: C
– volume: 23
  start-page: 161
  year: 1990
  publication-title: Spectroscopy Lett.
– volume: 11
  start-page: 129
  year: 2018
  publication-title: Asian J Pharm. and Clin. Res.
– volume: 1129
  start-page: 291
  year: 2006
  publication-title: J Chromatogr A.
– volume: 6
  start-page: 212
  year: 2014
  publication-title: Int J Pharm and Pharm Sci.
– volume: 27
  start-page: 80
  year: 2016
  publication-title: Ind. J Pharm.
– volume: 43
  start-page: 395
  year: 2008
– year: 2015
– volume: 8
  start-page: 38
  year: 2019
  publication-title: J Anal Pharm Res.
– year: 2013
– year: 1999
– ident: e_1_2_11_7_1
  doi: 10.11648/j.ijpc.20170304.11
– ident: e_1_2_11_13_1
  doi: 10.1016/j.jcis.2017.01.116
– volume-title: The United States Pharmacopeia: USP 38–NF 33
  year: 2015
  ident: e_1_2_11_19_1
  contributor:
    fullname: U.S.P. Convention
– ident: e_1_2_11_8_1
  doi: 10.1007/s10895-015-1737-4
– ident: e_1_2_11_5_1
  doi: 10.15406/japlr.2019.08.00309
– ident: e_1_2_11_22_1
  doi: 10.11648/j.ajche.20180601.11
– volume: 27
  start-page: 80
  year: 2016
  ident: e_1_2_11_24_1
  publication-title: Ind. J Pharm.
  contributor:
    fullname: Sudha T.
– volume-title: British Pharmacopoeia
  year: 2013
  ident: e_1_2_11_18_1
  contributor:
    fullname: B.P. Commission
– ident: e_1_2_11_31_1
  doi: 10.1007/978-1-4757-3061-6
– ident: e_1_2_11_6_1
  doi: 10.24297/jac.v15i1.7003
– ident: e_1_2_11_17_1
  doi: 10.1016/j.jpba.2005.09.029
– ident: e_1_2_11_23_1
  doi: 10.1002/jssc.201900726
– ident: e_1_2_11_16_1
  doi: 10.1016/j.chroma.2006.07.001
– volume: 4
  start-page: 247
  year: 2014
  ident: e_1_2_11_4_1
  publication-title: Int. J. Pharm.
  contributor:
    fullname: Sudhakararao G. V.
– ident: e_1_2_11_12_1
  doi: 10.1016/j.microc.2017.04.007
– ident: e_1_2_11_29_1
– volume-title: Martindale: the complete drug reference
  year: 2009
  ident: e_1_2_11_3_1
  contributor:
    fullname: Sweetman S. C.
– volume: 2012
  start-page: 1
  year: 2012
  ident: e_1_2_11_9_1
  publication-title: Chem
  contributor:
    fullname: Elokely K.
– ident: e_1_2_11_20_1
  doi: 10.7439/ijpc.v2i4.605
– ident: e_1_2_11_27_1
  doi: 10.1080/22297928.2019.1613927
– ident: e_1_2_11_14_1
  doi: 10.1016/j.msec.2014.12.006
– volume: 11
  start-page: 129
  year: 2018
  ident: e_1_2_11_21_1
  publication-title: Asian J Pharm. and Clin. Res.
  contributor:
    fullname: Susithra E.
– ident: e_1_2_11_28_1
– ident: e_1_2_11_26_1
  doi: 10.1080/00387019008054044
– start-page: 395
  volume-title: Pharmacotherapy: a pathophysiologic approach
  year: 2008
  ident: e_1_2_11_2_1
  contributor:
    fullname: DiPiro J. T.
– volume-title: Analytical chemistry
  year: 2014
  ident: e_1_2_11_30_1
  contributor:
    fullname: Christian G. D.
– ident: e_1_2_11_15_1
  doi: 10.1007/s10337-014-2827-1
– volume: 14
  start-page: 465
  year: 2015
  ident: e_1_2_11_11_1
  publication-title: Iran J Pharm Res
  contributor:
    fullname: Shahrokhian S.
– ident: e_1_2_11_25_1
  doi: 10.1002/bio.3566
– volume: 6
  start-page: 212
  year: 2014
  ident: e_1_2_11_10_1
  publication-title: Int J Pharm and Pharm Sci.
  contributor:
    fullname: El‐Kommos M. E.
SSID ssj0006669
Score 2.376704
Snippet A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative technique is...
Abstract A new, proven, economical spectrofluorimetric approach has been used to determine the proton pump inhibitor omeprazole (OMP). This innovative...
SourceID proquest
crossref
pubmed
wiley
SourceType Aggregation Database
Index Database
Publisher
StartPage e4682
SubjectTerms Computation
content uniformity
Detection
Dyes
Fluorescence
Limit of Detection
mercurochrome
Omeprazole
Proton pump inhibitors
Quenching
Reaction products
Spectrometry, Fluorescence - methods
Tablets - chemistry
Title Determination of omeprazole via fluorescence‐quenching methodology; application to content uniformity testing
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fbio.4682
https://www.ncbi.nlm.nih.gov/pubmed/38332466
https://www.proquest.com/docview/2931808787
https://search.proquest.com/docview/2924997027
Volume 39
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LSwMxEA5aEL34qK9qlQjibe2-stnVk_ZBvaiggrdls0mk0G5K2xX05E_wN_pLnGS71SKC4GkPu5uETGbmm2TyDULHNAk8zpi0bOZBgCJSYkXSFRaoEpGh5zGH6UCxe0evH8NWW9PknJV3YQp-iNmGm9YMY6-1gids3PgiDWU9deoHoTa_ECSY2xve7cwIAyqPDFUqxFrU9UjJO2u7jfLHeU_0A17Oo1Xjbjpr_xnoOlqdgkx8UayKDbQgsipaKspOvlTRcrOs8raJVKvMh9ESwkpiNRDDUfKq-gI_9xIs-7kaGc6nVHy8vZvEa71rhYva06bJc_ztHBxPFNYJ8ODNcJ7pi18DQPp4ouk8sqct9NBp3ze71rQIg5UC8nOtlEQQ0gSu43HpA8aVCWDEFDy94D4Vrh1wx5GEgZVkRINFTqgAUOQlkvJAAvjYRpVMZWIXYRoRG9ZAAj4x8CXIjNHQpixi3JaSk6CGjkqBxMOCayMuWJXdGCYx1pNYQ_VSUvFU28YxQBYntEOwPdDE7DVMpD78SDKhcv0NBJoRhSi8hnYKCc86gSgdcGUAAzgxgvy19_jy6kY_9_764T5acQEFFWnedVSZjHJxgBbHPD806_UTl7Lvtw
link.rule.ids 315,782,786,1408,27935,27936,46066,46490
linkProvider Wiley-Blackwell
linkToHtml http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NTtwwEB6VRRW9AKVQll9XQr0Fkji2E3HiV7vqFpAAiVsUxzZC2o1Xy6ZSe-oj8Iw8CeNkswVVSEicckhiWx7PzDf2-BuAHZFxqqQ0ni8pBig6Z15iQu2hKjETUyoD6QLFzqU4u4mPTxxNzn5zF6bmh5huuDnNqOy1U3C3Ib33jzVU3tndiMdof2cjHiWubgOlF1MzjLg8qchSMdoSIWUN86wf7jV_vvRF_wHMl3i1cjinC-8a6iLMT3AmOagXxmf4oIsl-FhXnvy9BHNHTaG3L2CPm5QYJyRiDbEDPRxlf2xfk193GTH90o4q2qdcP_59qHKv3cYVqctPV03uk2dH4WRsicuBR4dGysLd_Rog2Cdjx-hR3C7D9enJ1VHHm9Rh8HIEf6GXswSjGh4GVJkIYa7JECbm6Oy1ioQOfa6CwDCJhlIyhxcVExpxEc2MUNwg_liBVmELvQpEJMzHZZChW-SRifxYitgXMpHKN0Yx3oZvjUTSYU23kdbEymGKk5i6SWzDRiOqdKJw9ymiliD2YzQ_2MT0NU6kO__ICm1L9w3GmonAQLwNX2sRTzvBQB2hJccBfK8k-Wrv6WH33D3X3vrhNsx1rn720l737Mc6fAoRFNVZ3xvQGo9KvQkz96rcqhbvE58B89g
linkToPdf http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8QwEB584OPi-7E-I4i3un2lafWkrouiqKCCt9I0iQhus-xuBT35E_yN_hIn7XZVRBA89dA2CZnMzDfJ5BuAbZYEnuBcWTb3MECRKbUi5UoLVYmq0PO4w02geHLNLu7CxrGhydmr7sKU_BCDDTejGYW9NgreFqr-SRrKH_SuH4Rofkd9g8LN9Q3vamCFEZZHBVcqBlvM9WhFPGu79erP767oB778DlcLf9Oc_s9IZ2CqjzLJQbksZmFIZnMwVtadfJ6DiaOqzNs86EaVEGNERLQiuiXbneRFP0ry9JAQ9ZjrTkH6lMr317ci89psW5Gy-HTR5D75chBOepqYDHh0ZyTPzM2vFkJ90jN8Htn9Atw2j2-OTqx-FQYrRejnWimNMKYJXMcTykeQqxIEiSm6eil8Jl07EI6jKEczyalBi4IyiajISxQTgUL0sQgjmc7kMhAWURsXQYJOMfCVb4echTbjERe2UoIGNdiqBBK3S7KNuKRVdmOcxNhMYg3WKknFfXXrxohZnNAO0fhgE4PXOJHm9CPJpM7NNxhpRgzD8BoslRIedIJhOgLLAAewUwjy197jw9NL81z564ebMH7VaMbnpxdnqzDpIiIqU77XYKTXyeU6DHdFvlEs3Q_VRvKH
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Determination+of+omeprazole+via+fluorescence%E2%80%90quenching+methodology%3B+application+to+content+uniformity+testing&rft.jtitle=Luminescence+%28Chichester%2C+England%29&rft.au=Elmansi%2C+Heba&rft.au=Orbano%2C+Asya&rft.au=Mashkour%2C+Maram&rft.au=Shamiya%2C+Heba+Abo&rft.date=2024-02-01&rft.issn=1522-7235&rft.eissn=1522-7243&rft.volume=39&rft.issue=2&rft.epage=n%2Fa&rft_id=info:doi/10.1002%2Fbio.4682&rft.externalDBID=10.1002%252Fbio.4682&rft.externalDocID=BIO4682
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1522-7235&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1522-7235&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1522-7235&client=summon