Institution
King Faisal Specialist Hospital & Research Centre
Healthcare•Riyadh, Saudi Arabia•
About: King Faisal Specialist Hospital & Research Centre is a healthcare organization based out in Riyadh, Saudi Arabia. It is known for research contribution in the topics: Medicine & Detection limit. The organization has 58 authors who have published 157 publications receiving 3527 citations.
Topics: Medicine, Detection limit, High-performance liquid chromatography, Chiral resolution, Enantiomer
Papers published on a yearly basis
Papers
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TL;DR: In this article, the antioxidant properties of marshmallow (Althaea officinalis L, Fam. Malvaceae) ethanolic extract was evaluated using different antioxidant tests, including reducing power, free radical scavenging, superoxide anion radical scavenges, and metal chelating activities.
Abstract: The antioxidant properties of marshmallow (Althaea officinalis L., Fam. Malvaceae) ethanolic extract was evaluated using different antioxidant tests, including reducing power, free radical scavenging, superoxide anion radical scavenging, and metal chelating activities. The extract of marshmallow (A. officinalis L.) exhibited strong total antioxidant activity. The concentration of 50, 100, and 250 µg/mL of ethanol extract of marshmallow (A. officinalis L.) showed 85.5%, 91.2%, and 96.4% inhibition on peroxidation of linoleic acid emulsion, respectively. On the other hand, 100 µg/mL of standard antioxidant such as butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), and α‐tocopherol exhibited 94.5%, 99.1%, and 80% inhibition on peroxidation of linoleic acid emulsion, respectively. The extract of marshmallow (A. officinalis L.) had effective reducing power, free radical scavenging, superoxide anion radical scavenging, and metal chelating activities at same concentration (50, 100, and 250 ...
60 citations
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TL;DR: The acidosis of this enzyme deficiency progresses rapidly, leading to cardiopulmonary arrest and death within hours of onset unless treated promptlyunless treated promptly, in four surviving infants diagnosed and treated early.
Abstract: Deficiency of 3-hydroxy-3-methylglutaryl-CoA lyase has been studied in 11 Saudi infants. The diagnosis was established by the measurement of enzyme activity in lymphocytes, in fibroblasts and, in seven patients, by the gas chromatography/mass spectrometer pattern of excreted organic acids in the urine. In seven infants the disease caused a devastating acidotic attack within the first day of life, while in two the crisis occurred by the third day of life. In two infants from one family the disease appeared later in infancy. The clinical presentation of an acidotic attack is lethargy, hyperpnoea, tachypnoea and seizures, either at birth (two infants), following first feeding (in five infants), or following vomiting or refusal of food in later infancy. The acidotic attacks recurred later in life following minor illness or refusal to eat. The acidosis of this enzyme deficiency progresses rapidly, leading to cardiopulmonary arrest and death within hours of onset unless treated promptly. In four surviving infants diagnosed and treated early, development is normal. Magnetic resonance and computerized tomography brain scans in these infants, however, show white matter lesions and mild atrophy.
56 citations
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TL;DR: In this article, the authors present the instrumentation involved in their design, including light detection and flow injection analysis system used for the analysis of inorganic and organic compounds from gaseous samples and solutions indicate that these sensors are used with good reproducibility and selectivity of the analytes at low concentration level.
Abstract: Chemiluminescence sensors are important tools in analytical chemistry due to their high sensitivity selectivity. This review presents the instrumentation involved in their design, including light detection and flow injection analysis system used. Various applications for the analysis of inorganic and organic compounds from gaseous samples and solutions indicate that these sensors are used with good reproducibility and selectivity of the analytes at low concentration level.
52 citations
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TL;DR: Structures and related enantioselectivities of the respective chiral derivatization reagents for drugEnantioseparation by high-performance chromatography based upon pre-column derivatized and diastereomeric formation are reviewed.
Abstract: Structures and related enantioselectivities of the respective chiral derivatization reagents (CDRs) for drug enantioseparation by high-performance chromatography based upon pre-column derivatization and diastereomeric formation are reviewed. The elution order of diastereomers caused reaction of some CDRs with enantiomeric amino acids and carboxylic acids. The development of new CDRs available for indirect HPLC methods is also discussed. Copyright © 2001 John Wiley & Sons, Ltd.
Abbreviations used:
ABD-APy
4-(aminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
Ace-L-Cys
N-acetyl-L-cysteine
Ace-D-Pen
N-acetyl-D-penicillamine
AITC
2,3,4-tri-O-acetyl-α-D-arabinopyranosyl isothiocyanate
AEA
1-(1-anthryl)ethylamine or 1-(2-anthryl)ethylamine
APH
2-amino-7-phosphonoheptanoic acid
APB
2-amino-4-phosphonobutanoic acid
APV
2-amino-5-phosphonvaleric acid
APMB
2-[4-(1-aminoethyl)phenyl]-6-methoxybenzoxazole
Boc-L-Cys
N-tert-butoxycarbonyl-L-cysteine
Bz-L-Cys
N-benzoyl-L-cysteine
But-But
tert-butyl 3-(chloroformoxy)butyrate
BZOP-Cl
benoxaprofen chloride
BEIT
1-(2-naphthyl)ethyl isothiocyanate
BGIT
2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
CAZT-Ala-NH2
N2-[2-(4-chloro-6-(4-phenylazoanilino)-1,3,5-triazinyl)]-L-alanine amide
2-Chl-L-ISMN
2-chlorocarbonyl-L-isosorbide 5-mononitrate
5-Chl-L-ISMN
5-chlorocarbonyl-L-isosorbide 2-mononitrate
5-Chl-L-IMMN
5-chlorocarbonyl-L-isomannide 2-mononitrate
5-Chl-L-ISMA
5-chlorocarbonyl-L-isosorbide 2-monoacetate
CMNT-Ala-NH2
N2-[2-(4-chloro-6-(4-methoxy-1-naphthyl)-1,3,5-triazinyl)]-L-alanine amide
CMOT-Ala-NH2
N2-[2-(4-chloro-6-methoxy-1,3,5-triazinyl)]-L-alanine amide
CNOT-Ala-NH2
N2-[2-(4-chloro-6-(2-naphthoxy)-1,3,5-triazinyl)]-L-alanine amide
DATAAAN
(R,R)-O,O-diacetyl tartaric acid anhydride
DBOSAAN
(R,R)-O,O-dibenzyl tartaric acid anhydride
DBTAAN
(R,R)-O,O-dibenzoyl tartaric acid anhydride
DEOSAAN
(R,R)-O,O-diethyl tartaric acid anhydride
DMTAAN
(R,R)-O,O-dimethyl tartaric acid anhydride
DTTAAN
(R,R)-O,O-di-p-toluoyl tartaric acid anhydride
DANE
1-(4-dimethylamino-1-naphthyl)ethylamine
DBD-Apy
4-(N,N-dimethylaminosulfonyl)-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
DBD-CO-Hz
N-hydra-zinoformylmethyl-N-methylamino-4,4-N,N-dimethylamino sulphonyl-2,1,3-benzoxadiazole
DBD-Pz
4-N,N-dimethylamino sulphonyl-7-piperazino-2,1,3-benzoxadiazole
DBD-Pro
4-(2-carboxypyrrolidin-1-yl)-7-(N,N-dimethylamino-sulphonyl)-2,1,3-benzoxadiazole
DBD-N-Me-Ala
4-(N-1-carboxyethyl-N-methyl)amino-7-N,N-dimethylamino-2,1,3-benzoxadiazole
DBD-Pro-COCl
4-(N,N-dimethyl aminosulfonyl)-7-(2-chloroformylpyrrolidin-1-yl)-2,1,3-benzoxadiazole
DBD-PyNCS
4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole
ECF
1-(cyclohexyl)ethyl chloroformate
Eth-But
ethyl 3-(chloroformoxy)butyrate
FLEC
(+)-1-(9-fluorenyl)ethyl chloroformate
FLOP-Cl
flunoxaprofen chloride
FDNP-Ala-NH2
N2-(5-fluoro-2,4-dinitrophenyl)-L-alanine amide
FDNP-Phe-NH2
N2-(5-fluoro-2,4-dinitrophenyl)-L-phenylalanine amide
FDNP-Pro-NH2
N2-(5-fluoro-2,4-dinitrophenyl)-L-proline amide
FAZT-Ala-NH2
N2-[2-(4-fluoro-6-(4-phenylazoanilino)-1,3,5-triazinyl)]-L-alanine amide
FMOC-L-Pro
9-fluorenylmethyl chloroformate-L-proline
FMOC-L-Phe
9-fluorenylmethyl chloroformate-L-phenylalanine
FLOPIC
flunoxaprofen isocyanate
FDNP-Val-NH2
N2-(5-fluoro-2,4-dinitrophenyl)-L-valine amide
GITC
2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate
i-But-L-Cys
N-isobutanoyl-L-cysteine
i-Val-L-Cys
N-isovaleroyl-L-cysteine
LA
leucinamide
methy-BNCC
2′-methyl-1,1′-binaphthalene-2-carbonyl cyanide
MCF
(−)-methyl chloroformate
Me-But
methyl 3-(chloroformoxy) butyrate
MDL
methylated N ϵ -dansyl-L-lysine
MDNE-OTf
1-methyl-2-(6,7-dimethoxy-2,3-naphthalimido)ethyl trifluoromethane sulfonate
methoxy-BNCC
2′-methoxy-1,1′-binaphthalene-2-carbonyl cyanide
MeDAP
2-amino- ω - phosphonoalkanoic acid
MNE-OTf
1-methyl-2-(2,3-naphthalimido)ethyl trifluoromethane sulfonate
n-But-L-Cys
N-butanoyl-L-cysteine
NBD-Pro
4-(2-carboxypyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole
N-AA
N-[2-(chloroformoxy)propyl]acetamide
NBD-N-Me-Ala
4-(N-1-carboxyethyl-N-methyl)-amino-7-nitro-2,1,3-benzoxadiazole
NBD-Pro-COCl
4-(2-chloroformylpyrrolidin-1-nyl)-7-nitro-2,1,3-benzoxadiazole
NAP-IC
1-(6-methoxy-2-naphthyl)ethyl isocyanate
NAP-IT
1-(6-methoxy-2-naphthyl)ethyl isothiocyanate
NEIT
1-(1-naphthyl)ethyl isothiocyanate
NEIC
1-(1-naphthyl)ethyl isocyanate
NBD-PyNCS
4-(3-isothiocyanatopyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole
NEA
1-(1-naphthyl)ethylamine
NBD-APy
4-nitro-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole
NPSP-Cl
4-nitrophenylsulfonyl-(s)-prolyl chloride
β-ODAP
ω-N-oxalyl derivative of L-α, β-diaminopropanoic acid
γ-ODAB
ω-N-oxalyl derivative of L-α, γ-diminobutanoic acid
δ-OORN
ω-N-oxalyl derivative of orinithine
ϵ-OLYS
ω-N-oxalyl derivative of lysine
PEA
1-phenylethylamine
PEIC
1-phenylethyl isocyanate
PEIT
1-phenylethyl isothiocyanate
PAA
phenyl alanine amide
PAME
phenyl alanine methyl ester
PGIT
2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl isothiocyanate
Pro-L-Cys
N-propanoyl-L-cysteine
Tma-L-Cys
N-trimethylacetyl-L-cysteine
TFCF
tetrahydro-3-furanyl chloroformate
Val-L-Cys
N-valeroyl-L-cysteine
47 citations
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TL;DR: A simple and reliable HPLC method for the chiral resolution of o, p‐DDT and o,p‐DDD is described and the enantiomeric resolution has been achieved on Chiralpak AD‐R, Chiralcel OD‐ R, and Chiral Cel OJ‐R chiral stationary phases.
Abstract: A simple and reliable HPLC method for the chiral resolution of o,p-DDT and o,p-DDD is described. The enantiomeric resolution of o,p-DDT and o,p-DDD has been achieved on Chiralpak AD-R, Chiralcel OD-R, and Chiralcel OJ-R chiral stationary phases. The mobile phases used were acetonitrile-water (50:50 [v/v]) and acetonitrile-2-propanol (50:50 [v/v]) at a flow rate of 1.0 mL/min. For both pesticides detection was done at 220 nm. The values for o,p-DDT of alpha and R(s) varied from 1.24 to 2.52 and from 0.80 to 2.47, respectively. The values of alpha and R(s) for o,p-DDD were 1.26 and 0.60, respectively.
46 citations
Authors
Showing all 81 results
Name | H-index | Papers | Citations |
---|---|---|---|
Hassan Y. Aboul-Enein | 56 | 876 | 16492 |
Roger W. Byard | 54 | 1002 | 16437 |
Shahrukh K. Hashmi | 33 | 268 | 4176 |
Ashraf Ghanem | 32 | 117 | 3166 |
Abderrezak Bouchama | 31 | 70 | 5690 |
Pinar Ozand | 26 | 160 | 2273 |
Claire Simons | 23 | 90 | 2018 |
Asim F. Belgaumi | 16 | 54 | 1009 |
Saeed Ahmed | 16 | 67 | 716 |
Christer Ullbro | 13 | 22 | 746 |
Imran Ali | 13 | 36 | 848 |
Gael E. Phillips | 13 | 24 | 629 |
J. Brismar | 11 | 12 | 356 |
Tariq Ali | 11 | 15 | 1704 |
Yunus M. Siddiqui | 11 | 15 | 445 |