Quantitative determination of compound leads in Schiniopsis brasiliensis Engler

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
FHA Fernandes ◽  
RSA Batista ◽  
G Véras ◽  
FS Souza ◽  
ACD Medeiros
Keyword(s):  
Quantitative Determination

Quantitative determination of longitudinal and transverse cross-relaxation rates

1999 ◽  
Vol 96 (9/10) ◽  
pp. 1608-1615
Author(s):  
T. E. Malliavin ◽  
H. Desvaux ◽  
M. A. Delsuc
Keyword(s):  
Quantitative Determination ◽  
Cross Relaxation ◽  
Relaxation Rates

Quantitative Determination of Triperpene Saponins and Alkenated-Phenolics from Labisia pumila by LC-UV/ELSD Method and Confirmation by LC-ESI-TOF

Planta Medica ◽  
2010 ◽  
Vol 76 (05) ◽  
Author(s):  
B Avula ◽  
YH Wang ◽  
Z Ali ◽  
TJ Smillie ◽  
IA Khan
Keyword(s):  
Quantitative Determination ◽  
Labisia Pumila

Quantitative Determination of Gallic acid and Cyanidin-3-O-Glucoside within Sumac Extracts by HPLC-MS/MS

Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
M Koşar ◽  
F Göger ◽  
N Kırımer ◽  
KHC Başer
Keyword(s):  
Quantitative Determination ◽  
Gallic Acid

HPLC-MS/MS Quantitative Determination of Gallic acid and Cyanidin-3-Glucoside Content of Bilberry Fruit Extract from Turkey

Planta Medica ◽  
2011 ◽  
Vol 77 (12) ◽  
Author(s):  
N Kırımer ◽  
F Göger ◽  
KHC Başer
Keyword(s):  
Quantitative Determination ◽  
Gallic Acid ◽  
Fruit Extract

Quantitative Determination of α-Arbutin, β-Arbutin and Hydroquinone from Viburnum, Arctostaphylos, Vaccinium, Pyrus and Ilex Species by HPLC-UV Method

Planta Medica ◽  
2013 ◽  
Vol 79 (05) ◽  
Author(s):  
YH Wang ◽  
C Avonto ◽  
B Avula ◽  
M Wang ◽  
TJ Smillie ◽  
...  
Keyword(s):  
Quantitative Determination

Quantitative determination of five triterpenoid glycosids and chemical profiling of momordica charantia by UHPLC-ELSD/MS

Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
YH Wang ◽  
S Hu ◽  
B Avula ◽  
M Wang ◽  
S Sagi ◽  
...  
Keyword(s):  
Quantitative Determination ◽  
Momordica Charantia ◽  
Chemical Profiling

Quantitative determination of protopine in Hypecoum procumbens subsp. atropunctatum

Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
E Kaynar ◽  
A Emir ◽  
B Bozkurt ◽  
GI Kaya ◽  
MA Onur ◽  
...  
Keyword(s):  
Quantitative Determination

Ionic liquid micellar extraction for quantitative determination of sesquiterpenic acids in Valerianae Radix

Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
I Svinyarov ◽  
A Nedelcheva ◽  
MG Bogdanov
Keyword(s):  
Ionic Liquid ◽  
Quantitative Determination ◽  
Micellar Extraction

Is Quantitative Determination of Fibrin(ogen) Degradation Products and Thrombin-Antithrombin III Complexes Useful to Diagnose Deep Venous Thrombosis in Outpatients?

1989 ◽  
Vol 62 (04) ◽  
pp. 1043-1045 ◽  
Author(s):  
Paul F M M van Bergen ◽  
Eduard A R Knot ◽  
Jan J C Jonker ◽  
Auke C de Boer ◽  
Moniek P M de Maat
Keyword(s):  
Quantitative Determination ◽  
Venous Thrombosis ◽  
Deep Venous Thrombosis ◽  
Antithrombin Iii ◽  
Degradation Products ◽  
Family Doctor ◽  
Diagnostic Value ◽  
Impedance Plethysmography ◽  
Fibrin Degradation Products

SummaryWe studied the diagnostic value of recently introduced ELISA’s for the determination of thrombin-antithrombin III (TAT) complexes, fibrin degradation products (FbDP), fibrinogen degradation products (FgDP) and total degradation products (TDP) for deep venous thrombosis (DVT) in plasma of 239 consecutive outpatients, suspected for DVT by their family doctor. DVT was confirmed by impedance plethysmography in 60 patients. Using the 95th percentile range of 42 healthy volunteers the sensitivity for the detection of DVT was: 37% for TAT, 95% for TDP, 92% for FbDP and 90% for FgDP. Specificity was: 88% for TAT, 16% for TDP, 20% for FbDP and 25% for FgDP.We conclude that these assays are of little value in the diagnosis of DVT in outpatients.

Quantitative Determination of Plasminogen

1970 ◽  
Vol 23 (02) ◽  
pp. 191-201 ◽  
Author(s):  
H. D Bruhn ◽  
L Müller ◽  
F Duckert
Keyword(s):  
Quantitative Determination ◽  
Plasminogen Activator ◽  
Assay System ◽  
Two Stage ◽  
System Activation ◽  
Frozen Plasma

SummaryA modification of the caseinolytic assay for plasminogen is described. This assay system is characterized by the following features :1. Urokinase is used as activator achieving a complete activation of the plasminogen whereas with streptokinase caseinolytically inactive plasminogen-activator complexes are formed.2. All incubation times are reduced to the minimum which is still compatible with accuracy.3. Results are expressed in percent of a standard of ten normal plasmas.4. In this two-stage assay-system (activation of plasminogen to plasmin, digestion of casein by plasmin) both stages proceed simultaneously in the same system, thus the plasmin formed is stabilized “in statu nascendi” by the casein.5. Several conditions (stability of plasminogen in frozen plasma, use of anticoagulants, reproducibility) are defined.

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