scholarly journals Recovery and Stability of Δ9-Tetrahydrocannabinol Using the Oral-Eze®Oral Fluid Collection System and Intercept®Oral Specimen Collection Device

2015 ◽  
Vol 39 (8) ◽  
pp. 648-654 ◽  
Author(s):  
Kimberly L. Samano ◽  
Lakshmi Anne ◽  
Ted Johnson ◽  
Kenneth Tang ◽  
R.H. Barry Sample
2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Hu Suk Lee ◽  
Vuong Nghia Bui ◽  
Duy Tung Dao ◽  
Ngoc Anh Bui ◽  
Thanh Duy Le ◽  
...  

Abstract Background African swine fever (ASF), caused by the ASF virus (ASFV), was first reported in Vietnam in 2019 and spread rapidly thereafter. Better insights into ASFV characteristics and early detection by surveillance could help control its spread. However, the pathogenicity and methods for early detection of ASFV isolates from Vietnam have not been established. Therefore, we investigated the pathogenicity of ASFV and explored alternative sampling methods for early detection. Results Ten pigs were intramuscularly inoculated with an ASFV strain from Vietnam (titer, 103.5 HAD50/mL), and their temperature, clinical signs, and virus excretion patterns were recorded. In addition, herd and environmental samples were collected daily. The pigs died 5–8 days-post-inoculation (dpi), and the incubation period was 3.7 ± 0.5 dpi. ASFV genome was first detected in the blood (2.2 ± 0.8) and then in rectal (3.1 ± 0.7), nasal (3.2 ± 0.4), and oral (3.6 ± 0.7 dpi) swab samples. ASFV was detected in oral fluid samples collected using a chewed rope from 3 dpi. The liver showed the highest viral loads, and ear tissue also exhibited high viral loads among 11 tissues obtained from dead pigs. Overall, ASFV from Vietnam was classified as peracute to acute form. The rope-based oral fluid collection method could be useful for early ASFV detection and allows successful ASF surveillance in large pig farms. Furthermore, ear tissue samples might be a simple alternative specimen for diagnosing ASF infection in dead pigs. Conclusions Our data provide valuable insights into the characteristics of a typical ASFV strain isolated in Vietnam and suggest an alternative, non-invasive specimen collection strategy for early detection.


2006 ◽  
Vol 30 (8) ◽  
pp. 614-616 ◽  
Author(s):  
O. Quintela ◽  
D. J. Crouch ◽  
D. M. Andrenyak

2007 ◽  
Vol 170 (2-3) ◽  
pp. 117-120 ◽  
Author(s):  
T. Speedy ◽  
D. Baldwin ◽  
G. Jowett ◽  
M. Gallina ◽  
A. Jehanli

2017 ◽  
Vol 4 (suppl_1) ◽  
pp. S107-S108 ◽  
Author(s):  
Chelsea Shannon ◽  
Claire Bristow ◽  
Sasha Herbst De Cortina ◽  
Jennifer Chang ◽  
Jeffrey Klausner

Abstract Background From 2014 to 2015, the syphilis rate in the United States increased by 19%, reaching its highest rate since 1994. Currently, point-of-care syphilis assays use fingerstick or venipuncture whole blood to identify Treponema pallidum (TP) antibodies by qualitative immunoassay. However, patients and providers prefer oral fluid testing to whole blood testing. In this study, we aimed to determine whether a rapid syphilis test intended for use on whole blood could be used to detect TP antibodies in oral fluid. Methods Oral fluid was collected from 72 participants using the Super•SAL™ Oral Fluid Collection Device (Oasis Diagnostics®, Vancouver, WA). The device uses an absorbent cylindrical pad to collect and filter ~1 mlml of oral fluid. Oral fluid filtrate was tested using the SD Bioline Syphilis 3.0 rapid test (Alere Diagnostics, MA) following manufacturer directions for whole blood. TP particle agglutination (TPPA) and rapid plasma reagin (RPR) results derived from participants’ medical records were used as reference values. We used three different definitions as comparators: 1: TPPA reactive; 2: TPPA and RPR reactive and 3: TPPA reactive and RPR titer >1:4. Those with non-reactive TPPA and RPR results were considered seronegative. We calculated the sensitivity and specificity for definition 1 and sensitivity for definitions 2 and 3. We used the exact binomial method to determine 95% confidence intervals (CI). Results With definitions 1, 2, and 3, respectively, sensitivity was 83.3% (CI: 67.2, 93.6), 86.4% (CI: 65.1, 97.1), and 100% (CI: 71.5, 100). Specificity was 47.2% (CI: 36.5, 75.5). Conclusion The high sensitivity of the SD Bioline Syphilis 3.0 test using oral fluid suggests a strong potential for the development of accurate rapid oral syphilis tests. Sensitivity increased with higher RPR titer. False positive results may be due to the presence of non-venereal treponemal antibodies in oral fluid. Further research and development are needed to optimize specificity. Disclosures All authors: No reported disclosures.


2010 ◽  
Vol 34 (9) ◽  
pp. 590-593 ◽  
Author(s):  
Hallvard Gjerde ◽  
Elisabeth L. Øiestad ◽  
Åse Marit L. Øiestad ◽  
Marit Langødegård ◽  
Ingebjørg Gustavsen ◽  
...  

Author(s):  
Melanie A. MacMullan ◽  
Prithivi Chellamuthu ◽  
Aubree Mades ◽  
Sudipta Das ◽  
Fred Turner ◽  
...  

Current commercially available methods for reliably detecting antibodies against SARS-CoV-2 remain expensive and inaccessible due to the need for whole blood collection by highly trained phlebotomists using personal protective equipment (PPE). We have evaluated an antibody detection approach using the OraSure Technologies’ Oral Antibody Collection Device (OACD) and their proprietary SARS-CoV-2 total antibody detection enzyme-linked immunosorbent assay (ELISA). We found that the OraSure test for total antibody detection in oral fluid had comparable sensitivity and specificity to commercially available serum-based ELISAs for SARS-CoV-2 antibody detection while allowing for a more accessible specimen collection with the potential for self-collection.


2014 ◽  
Vol 39 (2) ◽  
pp. 140-143 ◽  
Author(s):  
Ashley-Jane Hall ◽  
Janet V. Warner ◽  
Michael G. Henman ◽  
Wendy E. Ferguson

2014 ◽  
Vol 7 (2) ◽  
pp. 114-120 ◽  
Author(s):  
Sébastien Anizan ◽  
Mateus M. Bergamaschi ◽  
Allan J. Barnes ◽  
Garry Milman ◽  
Nathalie Desrosiers ◽  
...  

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