scholarly journals Micro-Droplet Platform for Exploring the Mechanism of Mixed Field Agglutination in B3 Subtype

Biosensors ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 276
Author(s):  
Ding-Ping Chen ◽  
Chen Chen ◽  
Pei-Yu Wu ◽  
Yen-Heng Lin ◽  
Wei-Tzu Lin ◽  
...  
Keyword(s):  
Blood Sample ◽  
Reaction Times ◽  
Type B ◽  
Dilution Ratio ◽  
Taiwanese Population ◽  
High Reproducibility ◽  
Blood Samples ◽  
Gene Variation ◽  
Mixed Field ◽  
Group B

B3 is the most common subtype of blood group B in the Taiwanese population, and most of the B3 individuals in the Taiwanese population have the IVS3 + 5 G > A (rs55852701) gene variation. Additionally, a typical mixed field agglutination is observed when the B3 subtype is tested with anti-B antibody or anti-AB antibody. The molecular biology of the gene variation in the B3 subtype has been identified, however, the mechanism of the mixed field agglutination caused by the type B3 blood samples is still unclear. Therefore, the purpose of this study was to understand the reason for the mixed field agglutination caused by B3. A micro-droplet platform was used to observe the agglutination of type B and type B3 blood samples in different blood sample concentrations, antibody concentrations, and at reaction times. We found that the agglutination reaction in every droplet slowed down with an increase in the dilution ratio of blood sample and antibody, whether type B blood or type B3 blood was used. However, as the reaction time increased, the complete agglutination in the droplet was seen in type B blood, while the mixed field agglutination still occurred in B3 within 1 min. In addition, the degree of agglutination was similar in each droplet, which showed high reproducibility. As a result, we inferred that there are two types of cells in the B3 subtype that simultaneously create a mixed field agglutination, rather than each red blood cell carrying a small amount of antigen, resulting in less agglutination.

Blood types in Bengal cats in the UK

2009 ◽  
Vol 11 (10) ◽  
pp. 826-828 ◽  
Author(s):  
Danièlle A. Gunn-Moore ◽  
Kerry E. Simpson ◽  
Michael J. Day
Keyword(s):  
Blood Sample ◽  
Type A ◽  
Blood Type ◽  
Type B ◽  
Microtitre Plate ◽  
Blood Typing ◽  
Blood Samples ◽  
Microtitre Plate Assay ◽  
The Uk ◽  
Type Ab

Blood samples from 100 adult Bengal cats from the UK were submitted for assessment of blood type using RapidVet-H Feline blood typing cards (dms Laboratories), with further assessment by standard blood typing in a microtitre plate assay when card typing was inconclusive or revealed blood type B or AB. Ninety-eight cats were found to be type A when assessed using the blood typing cards. One cat initially tested as type AB but was found to be type A on testing a second blood sample using the blood typing cards. One cat initially tested as type B but was found to be type A when a second sample was tested by standard blood typing assay. Finding that 100% of the cats were blood type A is in contrast with previous studies that reported 10 Bengal cats to be type A, four to be type AB and one to be type B.

A Cross Sectional Survey of Chicken Astroviruses Antibody in Broiler and Sonali (Cross-Bred) Chickens in Selected Areas in Bangladesh

2020 ◽  
Vol 43 (1) ◽  
pp. 75-80
Author(s):  
Md Zulfekar Ali ◽  
Mohammad Moktader Moula ◽  
Zafar Ahmed Bhuiyan ◽  
Muhammad Tariq Javed
Keyword(s):  
Age Groups ◽  
Winter Season ◽  
Cross Sectional Survey ◽  
Cross Sectional ◽  
Blood Samples ◽  
Elisa Kit ◽  
Published Report ◽  
Poultry Birds ◽  
Wide Range ◽  
Group B

AbstractChicken astroviruses (CAstV) are enteric viruses of poultry causing gastroenteritis, malabsorption, gout and white chick disease commonly known as runting-stunting syndrome (RSS). It can affect the wide range of poultry birds, especially chicken, turkey and duck worldwide. To our best knowledge there is no published report on presence of antibodies against CAstV in Bangladesh. Therefore, the study aimed to detect the presence of CAstV antibodies in broilers and sonali chickens (a cross-bread) in Bangladesh through a cross-sectional survey. A total of 454 blood samples from 66 flocks of broiler (n=343) and sonali chickens (n=111) of different ages were obtained during 2017 from four districts. The birds were healthy but were not vaccinated against CAstV. The samples were tested for specific antibodies against CAstV Group B by using commercially available ELISA kit. Overall, 16.74% (76/454) samples and 34.84% (23/66) flocks were positive for CAstV antibodies. The seroprevalence of CAstV was significantly (p=0.001) higher in sonali chickens (36.96%) than broiler (10.20%), while it was significantly higher (p=0.001) in birds of Bogura district (36.94%) than the other three districts. Regarding the age groups, seroprevalence was insignificantly (p=0.192) higher in sonali chicken before laying age (45%) than during laying age (27.45%). Regarding the seasons, CAstV infection was prevalent significantly (p=0.001) higher in winter season. Thus, the present study indicated the presence of CAstV in poultry in Bangladesh, so further studies are required to find out the magnitude of the problem in the country.

scholarly journals Development of a blood sample detector for multi-tracer positron emission tomography using gamma spectroscopy

2019 ◽  
Vol 6 (1) ◽  
Author(s):  
Carlos Velasco ◽  
Adriana Mota-Cobián ◽  
Jesús Mateo ◽  
Samuel España
Keyword(s):  
Positron Emission Tomography ◽  
Blood Sample ◽  
Pet Imaging ◽  
Spectroscopic Analysis ◽  
Gamma Spectroscopy ◽  
Emission Tomography ◽  
Blood Samples ◽  
Positron Emission

Abstract Background Multi-tracer positron emission tomography (PET) imaging can be accomplished by applying multi-tracer compartment modeling. Recently, a method has been proposed in which the arterial input functions (AIFs) of the multi-tracer PET scan are explicitly derived. For that purpose, a gamma spectroscopic analysis is performed on blood samples manually withdrawn from the patient when at least one of the co-injected tracers is based on a non-pure positron emitter. Alternatively, these blood samples required for the spectroscopic analysis may be obtained and analyzed on site by an automated detection device, thus minimizing analysis time and radiation exposure of the operating personnel. In this work, a new automated blood sample detector based on silicon photomultipliers (SiPMs) for single- and multi-tracer PET imaging is presented, characterized, and tested in vitro and in vivo. Results The detector presented in this work stores and analyzes on-the-fly single and coincidence detected events. A sensitivity of 22.6 cps/(kBq/mL) and 1.7 cps/(kBq/mL) was obtained for single and coincidence events respectively. An energy resolution of 35% full-width-half-maximum (FWHM) at 511 keV and a minimum detectable activity of 0.30 ± 0.08 kBq/mL in single mode were obtained. The in vivo AIFs obtained with the detector show an excellent Pearson’s correlation (r = 0.996, p < 0.0001) with the ones obtained from well counter analysis of discrete blood samples. Moreover, in vitro experiments demonstrate the capability of the detector to apply the gamma spectroscopic analysis on a mixture of 68Ga and 18F and separate the individual signal emitted from each one. Conclusions Characterization and in vivo evaluation under realistic experimental conditions showed that the detector proposed in this work offers excellent sensibility and stability. The device also showed to successfully separate individual signals emitted from a mixture of radioisotopes. Therefore, the blood sample detector presented in this study allows fully automatic AIFs measurements during single- and multi-tracer PET studies.

scholarly journals Microsphere-Based Microfluidic Device for Plasma Separation and Potential Biochemistry Analysis Applications

Micromachines ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 487
Author(s):  
Hongyan Xu ◽  
Zhangying Wu ◽  
Jinan Deng ◽  
Jun Qiu ◽  
Ning Hu ◽  
...  
Keyword(s):  
Blood Sample ◽  
Microfluidic Device ◽  
Biochemical Analysis ◽  
Cost Effective ◽  
Clinical Diagnostics ◽  
Correction Factors ◽  
Separation Device ◽  
Blood Samples ◽  
Plasma Separation ◽  
Blood Biochemical

The development of a simple, portable, and cost-effective plasma separation platform for blood biochemical analysis is of great interest in clinical diagnostics. We represent a plasma separation microfluidic device using microspheres with different sizes as the separation barrier. This plasma separation device, with 18 capillary microchannels, can extract about 3 μL of plasma from a 50 μL blood sample in about 55 min. The effects of evaporation and the microsphere barrier on the plasma biochemical analysis results were studied. Correction factors were applied to compensate for these two effects. The feasibility of the device in plasma biochemical analysis was validated with clinical blood samples.

scholarly journals Molecular identification by multiplex polymerase chain reaction of Pasteurella multocida in cattle and buffaloes in Baghdad

2014 ◽  
Vol 38 (1) ◽  
pp. 99-106
Author(s):  
Ihab G. M. AL-Shemmari
Keyword(s):  
Polymerase Chain Reaction ◽  
Multiplex Pcr ◽  
Multiplex Polymerase Chain Reaction ◽  
Pasteurella Multocida ◽  
Type B ◽  
Chain Reaction ◽  
Blood Samples ◽  
Nasal Swabs ◽  
Polymerase Chain ◽  
B 31

The aim of this study was to identify pasteurella multocida and their types by PCR in cattle’s and buffaloesi bagdad from March to August 2012 on 204 animals , including 102 cattle and 102 buffaloes at slaughter houses from Baghdad .Blood samples and nasal swaps were collected , before slaughtering and lung tissues of slaughtered animal , and from 54 clinically suspected cases of pasteurellosis , including 27 bovines ,and 27 buffaloes the samples taken included blood and nasal swabs . Pasteurellamultocida were isolated from 94 animals include 49 cattle 45 buffaloes. The typing of the isolates by multiplex PCR for genotyping Pasteuerllamultocida revealed 93 isolates of type B , 31 from cattle and 62 from buffaloes ,and 81 isolates of type A , 55 from cattle and 26 from buffaloes .

Serological survey of the Berlin population

1934 ◽  
Vol 30 (11-12) ◽  
pp. 1206-1206
Author(s):  
Т. Charbet
Keyword(s):  
Serological Survey ◽  
Blood Samples ◽  
Group A ◽  
Group B

Over the course of 11 years, 30,000 blood samples from inpatients were examined. The distribution by group gives the following result: Group 0-31.6%, Group A-42.2%, Group B- 14.7%, and Group AB-6.5%. There was no difference in the groups with regard to gender. For the indicated period of time the percentage, the ratio of groups did not change significantly.

Use of Values for Calcium and Protein Serum, and of a Derived Index Obtained from a Probability Population Sample

1978 ◽  
Vol 24 (3) ◽  
pp. 506-506
Author(s):  
Anthea Kelly ◽  
Louis Munan ◽  
Claude PetitClerc ◽  
Kok Ping Ho ◽  
Bernard Billon
Keyword(s):  
Body Weight ◽  
Ursodeoxycholic Acid ◽  
Blood Sample ◽  
Cholic Acid ◽  
Amylase Activity ◽  
Population Sample ◽  
Blood Samples ◽  
Annual Index ◽  
Protein Serum

Abstract Volume 22 p 1726: In the footnote to Table 3, the last half of the sentence should read " for SI units, the index becomes (80 calcium - 120)/protein." Volume 23 p 1779: In column two of "corrections," the word "malate" should be substituted for "maleate." p 2127: In column two, last line, change "chinic" to "chenodeoxycholic." On the next page, change the last part of the sub-legend to Figure 7 to read "(5) ursodeoxycholic acid, (6) cholic acid." p 2205: col. two, line 32. For "mg/g body weight" read "mg/kg body weight." p 2288: In the last sentence of the abstract, change ".... 0.3 to 7.8 mole..." to "... 0.3 to 7.8 mmol...." p 2289: Table 1, footnote a should read: "Millimoles of 4NP injected/270 x 10-3 moles of 4NPP. This is calculated as if the 4NP were present in 270 nmol of 4NPP...." p 2290: In Table 2, in column A "7.76d" should read "7.76c" p 2356: The reader may incorrectly infer that the "Gamma-Coat Kit" (CA 535, 536; 555, 556) is intended for the analysis of dried blood samples on paper in screening for congenital hypothyroidism in infants. Actually, that kit is intended for serum thyroxine assay. A modified kit dedicated to dried blood-sample screening for hypothyroidism is currently under development and will be introduced shortly as CA-538, 558. Further, in Tables and text, the "3.5-mm" disks referred to should read "3.18 mm" (⅛''). This is of significance, because the error in diameter produces a 20% error in the apparent blood volume or thyroxine content per disk in the Tables. Inadvertent omissions from the list of invited reviewers (p 2360) and our annual index are, respectively: Jocelyn M. Hicks and Royden Rand and "Direct Spectrophotometric Determination of α-Amylase Activity in Saliva, with p-Nitrophenyl α-Maltoside as Substrate," by Baiba K. Gillard, Henry C. Markman, and Stephen A. Feig. (p 2279)

Changing the Time of Blood Collection to Determine Vancomycin Concentrations in Intensive Care Unit Patients

2018 ◽  
Vol 38 (1) ◽  
pp. 24-28
Author(s):  
Drayton A. Hammond ◽  
Taylor B. James ◽  
Lexis N. Atkinson ◽  
Jacob T. Painter ◽  
Katherine Lusardi
Keyword(s):  
Intensive Care Unit ◽  
Intensive Care ◽  
Blood Sample ◽  
Medical Intensive Care Unit ◽  
Sample Collection ◽  
Blood Samples ◽  
Significant Difference ◽  
Vancomycin Trough ◽  
Medical Intensive Care ◽  
Trough Levels

BACKGROUND Clinical practice guidelines for initiation and therapeutic drug monitoring, but not timing, of vancomycin dosing exist at many institutions. Scheduling vancomycin trough measurements and doses around the morning blood sample collection could yield more interpretable troughs and increase patient safety. OBJECTIVE To evaluate the appropriateness of blood sample collection times for vancomycin trough measurements before and after an initiative to change the timing of blood sampling to determine vancomycin doses and trough levels in a medical intensive care unit. METHODS A retrospective cohort study was conducted of patients in a medical intensive care unit who received intravenous vancomycin at a scheduled interval. Differences in continuous and categorical data were compared between pre- and postintervention groups. The primary outcome was proportion of blood samples collected for vancomycin trough measurements within 30 minutes of the next scheduled vancomycin dose. RESULTS Baseline characteristics were similar between the preintervention (n = 68) and postintervention (n = 176) groups except for the percentage of blood samples drawn for trough measurements and morning laboratory tests (6% vs 81%; P &lt; .001). Frequency of loading doses was similar between patients in the pre- and postintervention groups, as was weight-based maintenance dosing. There was no significant difference in the percentage of blood samples collected to measure vancomycin trough levels appropriately at 30, 60, or 75 minutes from the next scheduled dose. CONCLUSION Measuring vancomycin trough levels in morning blood samples did not affect the percentage of inappropriately collected blood samples used to measure vancomycin trough levels.

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