The interferon-induced enzyme oligo-isoadenylate synthetase: Rapid determination of its in vitro products

1981 ◽  
Vol 110 (1) ◽  
pp. 190-196 ◽  
Author(s):  
Gilles Merlin ◽  
Michel Revel ◽  
David Wallach
Keyword(s):  
Author(s):  
Do Thi Thuy Linh ◽  
Hoang Thanh Duong ◽  
Nguyen Tuan Hiep ◽  
Pham Thanh Huyen ◽  
Nguyen Minh Khoi ◽  
...  

 This study develops a high performance liquid chromatography with ultraviolet detection (HPLC-UV) for simultaneous quantification of hederacoside C and α-hederin in Hedera nepalensis K. Koch. The method proposed in this study was validated in terms of the analytical parameters such as high repeatability, high accuracy and good sensitivity. The method was used to determine the content of hederacoside C and α-hederin in Hedera nepalensis K. Koch, which had been collected in Ha Giang, Lao Cai and Lai Chau. The study results show that the content of hederacoside C and the content of α-hederin ranged from 0.40 to 4.01% and 0.21 – 0.54% based on absolute dry mass, respectively. Keywords Hedera nepalensis K. Koch, hederacoside C, α-hederin, HPLC-UV. References [1] L. Jafri, et al, In vitro assessment of antioxidant potential and determination of polyphenolic compounds of Hedera nepalensis K. Koch, Arabian Journal of Chemistry. 10 (2017) 3699-3706. https://doi.org/10.1016/j.arabjc.2014.05.002.[2] S. Saleem, et al, Plants Fagonia cretica L, and Hedera nepalensis K. Koch contain natural compounds with potent dipeptidyl peptidase-4 (DPP-4) inhibitory activity, Journal of ethnopharmacology. 156 (2014) 26-32. https://doi.org/10.1016/j.jep.2014.08.017[3] D.H. Bich, Medicinal plants and animals for medicine in Vietnam, Vol 1, Science and Technics Publishing House, Hanoi, 2006 (in Vietnamese).[4] National Institute Of Medicinal Materials, List of medicinal plants in Vietnam, Science and Technics Publishing House, Hanoi, 2016 (in Vietnamese).[5] L. Jafri, et al, Hedera nepalensis K. Koch: A Novel Source of Natural Cancer Chemopreventive and Anticancerous Compounds, Phytotherapy research. 30(3) (2016) 447-453. https://doi.org/10.1002/ptr.5546. [6] S. Kanwal, et al, Antioxidant, antitumor activities and phytochemical investigation of Hedera nepalensis K. Koch, an important medicinal plant from Pakistan, Pakistan Journal of Botany. 43 (2011) 85-89. [7] G. Uddin, et al, Biological screening of ethyl acetate extract of Hedera nepalensis stem, African Journal of Pharmacy and Pharmacology. 6(42) (2012) 2934-2937. https://doi.org/10.5897/AJPP12.828 [8] H. Kizu, et al, Studies on Nepalese Crude Drugs, III, On the Saponins of Hedera nepalensis K. Koch, Chemical and Pharmaceutical Bulletin. 33(8) (1985) 3324-3329. https://doi.org/0.1248/cpb.33.3324[9] X. Tong, et al, Extraction and GC-MS Analysis of Volatile Oil from Hedera nepalensis var sinensis, Fine Chemicals. 24(6) (2007) 559-561. [10] EDQM, European Pharmacopoeia, fifth ed., Council of Europe, France, 2015. [11] N.T.H. Mai, et al, Simultaneous Quantification of Hederacoside C and α-Hederin from the Leaves of Hedera helix L. by HPLC, Journal of Medicinal Material. 21(6) (2016). (in Vietnamese).[12] L. Havlíková, et al, Rapid Determination of α-Hederin and Hederacoside C in Extracts of Hedera helix Leaves Available in the Czech Republic and Poland, Natural product communications. 10(9) (2015). https://doi.org/10.1177/1934578X1501000910[13] M. Yu, et al, Determination of Saponins and Flavonoids in Ivy Leaf Extracts Using HPLC-DAD, Journal of Chromatographic Science. 53(4) (2014) 478-483. https://doi.org/10.1093/chromsci/bmu068.[14] EMEA, Validation of analytical procedures: text and methodology Q2 (R1), in International conference on harmonization, Geneva, Switzerland, 2005. [15] W. Horwitz, Official methods of analysis, 12 ed., Vol 1, Association of Official Analytical Chemists, Washington DC, 1975.


1983 ◽  
Vol 63 (1) ◽  
pp. 233-237 ◽  
Author(s):  
W. C. SAUER ◽  
H. JØRGENSEN ◽  
R. BERZINS

A method for measuring protein digestibility of small feed samples was developed with growing pigs fitted with a single cannula in the duodenum. Feed was ground through a 0.8-mm mesh screen and 1-g samples were enclosed in 25 × 40-mm monofilament nylon bags (50-μm mesh). Following pre-digestion in vitro to simulate gastric digestion (0.01 N HCI; pepsin 1 g/L; 2.5 h), the bags were inserted into the small intestine via the duodenal cannula, recovered in feces within 48 h, frozen, lyophilized and analyzed for protein. Apparent protein digestibility of soybean meal and meat-and-bone meal were 88.1 and 80.9%, respectively, compared with 90.0 and 79.1, respectively, determined conventionally. Protein digestibility (nylon bag vs. conventional technique) for three barley samples were 63.2 vs. 65.2%, 62.8 vs. 67.6% and 62.3 vs. 67.5%. The pigs were fed a 16% crude protein grower diet during the nylon bag studies. Preliminary studies showed no recovery of nylon bags in feces, unless the pig was starved for 1 day, when these were administered via a gastric cannula. The nylon bag technique, when samples are inserted via the duodenal cannula, appears to be a promising approach for rapid determination of protein digestibilities in small samples of feedstuffs. Key words: Nylon bag, digestibility, protein, cannula, pigs


2009 ◽  
Vol 63 (3) ◽  
Author(s):  
Gai Zhang ◽  
Jianbo Liu ◽  
Zuchao Meng ◽  
Xin Wang

AbstractA rapid and simple as well as sensitive inductively coupled plasma mass spectrometry (ICP-MS) method for the determination of cobalamin is described. Cobalamin in human urine and medicine tablet solutions was converted on-line into free cobalt ions in acid medium, the cobalt ions were then detected by ICP-MS. Cobalamin was determined by measuring the increase of integral counts per second intensity, which was linear over the cobalamin concentration range of 1.0 × 10−10 g mL−1 to 8.0 × 10−5 g mL−1, and the limit of detection was 0.05 ng mL−1 (3σ). At the pump rate of 30 rotations per minute, one analysis cycle of cobalamin, including sampling and washing, could be accomplished in 0.5 min with the relative standard deviations of less than 5 %. The proposed procedure was applied successfully in monitoring cobalamin in human urine without any pretreatment process and in rapid determination of cobalamin in multivitamin tablets.


1996 ◽  
Vol 36 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Sang Bae Han ◽  
Goo Taeg Oh ◽  
Yeo-Pyo Yun ◽  
Byung Kil Min ◽  
Byung Hwa Hyun ◽  
...  

1997 ◽  
Vol 41 (7) ◽  
pp. 1537-1540 ◽  
Author(s):  
F Peyron ◽  
A Favel ◽  
H Guiraud-Dauriac ◽  
M El Mzibri ◽  
C Chastin ◽  
...  

A rapid-flow cytofluorometric susceptibility test for in vitro amphotericin B testing of yeasts was evaluated and compared to the National Committee for Clinical Laboratory Standards (NCCLS) M27-T reference broth macrodilution method. The flow cytofluorometric method is based on the detection of decreased green fluorescence intensity of cells stained with DiOC5(3), a membrane potential-sensitive cationic dye, after drug treatment. Testing was performed on 134 clinical isolates (Candida spp. and Torulopsis glabrata). From the dose-response curve obtained for each isolate, three endpoints were calculated by computer analysis (the concentrations at which the fluorescence intensity was reduced by 50, 80, and 90%, i.e., 50% inhibitory concentration [IC50], IC80, and IC90, respectively). A regression analysis correlating these endpoints with the M27-T MICs showed that the best agreement was obtained with IC80. The flow cytofluorometric method showed good reproducibility with control strains. These initial results suggest that the flow cytofluorometric method is a valid alternative to the NCCLS reference method.


Bioanalysis ◽  
2013 ◽  
Vol 5 (11) ◽  
pp. 1353-1362 ◽  
Author(s):  
Wanlong Zhou ◽  
Perry G Wang ◽  
Oluwatosin A Ogunsola ◽  
Margaret EK Kraeling

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