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...
Saved in:
Published in: | Luminescence (Chichester, England) Vol. 39; no. 2; pp. e4682 - n/a |
---|---|
Main Authors: | , , , , |
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 |