Relevant bibliographies by topics / Blood plasma

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Blood plasma'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 July 2024

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Journal articles on the topic "Blood plasma"

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Vahidi, Mehrnoosh, Hamidreza Fallah Haghmohammadi, Masoumesadat Peyghambarzadeh, and Erfan Niazi. "Experimental Estimation of Human Blood Plasma Viscosity." International Journal of Pharma Medicine and Biological Sciences 8, no. 1 (January 2019): 1–6. http://dx.doi.org/10.18178/ijpmbs.8.1.1-6.

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UDOVENKO, A. V. "DETERMINATION OF THROMBIN AND PLASMIN ACTIVITY IN HUMAN BLOOD PLASMA USING THE TURBIDIMETRIC CURVE OF CLOT FORMATION AND DISSOLUTION." Biotechnologia Acta 16, no. 2 (April 28, 2023): 50–52. http://dx.doi.org/10.15407/biotech16.02.050.

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The aim of the study was to develop a method for determination the activity of thrombin, which is based on the turbidimetry curve of the formation and dissolution of a blood plasma clot. Methods. Donor blood samples were collected in 3.8% sodium citrate (1 part of sodium citrate and 9 parts of blood, pH 7.4). Plasma was separated from blood cells within 1 hour after blood collection by centrifugation the latter at 1200 g for 20 minutes. Aliquots of plasma were stored at -20 °C. Results. To determine the concentrations of thrombin and plasmin, TDCs of the formation and dissolution of blood plasma clots, initiated by the APTT reagent, were used. Based on the values of τ obtained, a calibration curve was constructed in the coordinates 1/τ – [Thr] (the rate of protofibrils formation in s-1 vs thrombin concentration in NIH units in 1 ml). Conclusion. The proposed methods to determine the activity of thrombin and plasmin made it possible to quantitatively calculate the rate of prothrombin activation in the lag period, the concentration and activity of thrombin based on the rate of fibrin and protofibrils formation as well as the activity and concentration of plasmin at the point of the complete clot dissolution,
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Golovanova, Olga. "Kinetic characteristics of crystallization in prototypes of human blood plasma." Bulletin of the Karaganda University. "Chemistry" series 85, no. 1 (March 29, 2017): 48–58. http://dx.doi.org/10.31489/2017ch1/48-58.

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Forrest, A. R., S. Morton, and C. Lambardarios. "Blood or plasma lactate?" British Journal of Sports Medicine 24, no. 2 (June 1, 1990): 132. http://dx.doi.org/10.1136/bjsm.24.2.132.

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Adams, G. "Microwave Blood Plasma Defroster." Journal of Microwave Power and Electromagnetic Energy 26, no. 3 (January 1991): 156–59. http://dx.doi.org/10.1080/08327823.1991.11688152.

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Jacobs, Anne C., and Jeanne M. Fair. "Bacteria-killing ability of fresh blood plasma compared to frozen blood plasma." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 191 (January 2016): 115–18. http://dx.doi.org/10.1016/j.cbpa.2015.10.004.

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Kriger-, Olga. "Advantages of Porcine Blood Plasma as a Component of Functional Drinks." Foods and Raw Materials 2, no. 2 (September 1, 2014): 26–32. http://dx.doi.org/10.12737/5456.

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Tomin, Tamara, Natalie Bordag, Elmar Zügner, Abdullah Al-Baghdadi, Maximilian Schinagl, Ruth Birner-Gruenberger, and Matthias Schittmayer. "Blood Plasma Quality Control by Plasma Glutathione Status." Antioxidants 10, no. 6 (May 27, 2021): 864. http://dx.doi.org/10.3390/antiox10060864.

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Timely centrifugation of blood for plasma preparation is a key step to ensure high plasma quality for analytics. Delays during preparation can significantly influence readouts of key clinical parameters. However, in a routine clinical environment, a strictly controlled timeline is often not feasible. The next best approach is to control for sample preparation delays by a marker that provides a readout of the time-dependent degradation of the sample. In this study, we explored the usefulness of glutathione status as potential marker of plasma preparation delay. As the concentration of glutathione in erythrocytes is at least two orders of magnitude higher than in plasma, even the slightest leakage of glutathione from the cells can be readily observed. Over the 3 h observation period employed in this study, we observed a linear increase of plasma concentrations of both reduced (GSH) and oxidized glutathione (GSSG). Artificial oxidation of GSH is prevented by rapid alkylation with N-ethylmaleimide directly in the blood sampling vessel as recently published. The observed relative leakage of GSH was significantly higher than that of GSSG. A direct comparison with plasma lactate dehydrogenase activity, a widely employed hemolysis marker, clearly demonstrated the superiority of our approach for quality control. Moreover, we show that the addition of the thiol alkylating reagent NEM directly to the blood tubes does not influence downstream analysis of other clinical parameters. In conclusion, we report that GSH gives an excellent readout of the duration of plasma preparation and the associated pre-analytical errors.
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Emsley, Jonas. "Plasma kallikrein's low gear." Blood 135, no. 8 (February 20, 2020): 518–19. http://dx.doi.org/10.1182/blood.2019004339.

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Shuai, Wen, and Shaoying Li. "CD138− plasma cell myeloma." Blood 134, no. 11 (September 12, 2019): 906. http://dx.doi.org/10.1182/blood.2019001845.

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Dissertations / Theses on the topic "Blood plasma"

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Lal, Ritu Anilkumar 1968. "Plasma protein binding and blood to plasma partitioning studies of methamphetamine." Thesis, The University of Arizona, 1991. http://hdl.handle.net/10150/277954.

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Methamphetamine is a sympathomimetic drug with CNS, cardiovascular and anorectic effects. We examined the Blood to Plasma (Blood/Plasma) partitioning and plasma protein binding (PB) of d-Methamphetamine (d-MAP), using whole rat blood. The mean Blood/Plasma ratio was around 1.2 and the fraction unbound (fᵤ) was 0.8. Further, we studied the influence of concentration, pH and the presence of 1-MAP on the Blood/Plasma ratio and PB of d-MAP. There was no significant change in the Blood/Plasma ratio and the PB values at different concentrations of d-MAP or in the presence of 1-MAP. There was a slight increase in the Blood/Plasma ratio and a slight but insignificant decrease in fᵤ with pH. The equilibrium binding constants (KA) of d-MAP with human serum albumin and α₁ -acid glycoprotein were also determined and they were found to be 213 and 2461 M⁻¹ respectively.
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Finning, Kirstin M. "Prediction of fetal RhD blood group status using fetal genetic material in maternal blood." Thesis, University of the West of England, Bristol, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275889.

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Urbenjapol, Supanee. "Changes in plasma nitrate concentrations, liver and kidney flavin-containing monooxygenase, cytochrome P450 2a5 and metal contents in cadmium and bacterial endotoxin exposed mice /." [St. Lucia, Qld.], 2001. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe16190.pdf.

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Bergdahl, Ingvar A. "Lead in blood ICP-MS studies of lead in plasma, blood and erythrocyte proteins /." Lund : Dept. of Occupational and Environmental Medicine, Institute of Laboratory Medicine, Lund University, 1997. http://catalog.hathitrust.org/api/volumes/oclc/39159416.html.

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Suontaka, Anna-Maija. "Haemostatic changes in plasma for transfusion during preparation and storage /." Stockholm, 2006. http://diss.kib.ki.se/2006/91-7140-449-X/.

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Wang, Haiyao. "Antiplasmin the main plasmin inhibitor in blood plasma : studies on structure-function relationships /." Stockholm : Department of Surgical Sciences, Division of Clincal Chemistry and Blood Coagulation, Karolinska University, 2005. http://diss.kib.ki.se/2005/91-7140-278-0/.

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Al-Othman, Abdullah Abdulrahman 1961. "Influence of copper deficiency on plasma lipoproteins and the development of enlarged plasma volume and cholesterol pool size." Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277117.

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Two studies were designed to investigate the time course development of enlarged plasma volume and cholesterol pool size in copper (Cu)-deficient rats as well as influence of Cu deficiency on the lipid composition of lipoproteins. Rats were randomly assigned to three dietary Cu treatments (deficient, marginal, and adequate) in the Study I and two dietary Cu treatments (deficient and adequate) in Study II. Enlargement of plasma volume and cholesterol pool size were established prior to the increase in plasma cholesterol concentration. Cu concentration was decreased, whereas iron and zinc concentrations were increased in the organs of Cu-deficient and Cu-marginal rats. The plasma pool size of VLDL triglyceride was elevated 6-fold, protein and phospholipid were unaltered, and cholesterol was reduced 36%. The plasma pool size of lipid and protein components of HDL and LDL fractions were markedly elevated in Cu-deficient rats.
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Shatova, Tatyana A. "Portable blood plasma separation for point of care diagnostics." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/103847.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2015.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 127-136).
Point of care testing is expanding the healthcare field towards personalized and early-detection medicine. Microfluidic platforms present an opportunity for low cost, portable diagnostic sensors through manipulation of small volumes of fluids on isolated, compact devices. One of the challenges of microfluidic sensors is the biological sample pretreatment steps that are manually performed prior to on-chip loading and sensing. This issue is especially prominent for human blood, which contains about a billion cells in one milliliter total volume. These blood cells can rupture, clog devices, block optical readouts, and foul electrodes. At the same time, the liquid portion of human blood, plasma, is rich in a variety of disease indicators, many of which have not yet been identified, and thus is an essential part in the diagnostic field. This thesis focuses on the design of a small, around 1 cm long, microfluidic device that separates out blood plasma from undiluted human blood. This design does not require any external field or equipment, beyond a loading syringe and collection tubing. The separation results show 10-100 times improvement in plasma purity over the literature values for passive separation designs. This separation system was then combined with a colorimetric malaria sensor that produced a visually detectable colored result with a 7.5 nM limit of detection in whole blood. This thesis details the design of a low power point of care diagnostic process that is capable of blood processing and detection, and which eliminates the need for any external laboratory-scale equipment. Advantages and challenges of other low power, microfluidic sensor constructs are also discussed.
by Tatyana A. Shatova.
Ph. D.
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Owen, Alice. "The effects of estrogens and phytoestrogens on the metabolism and oxidation of plasma lipoproteins /." Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09pho968.pdf.

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GIORGI, G. BAGNAGATTI DE. "PRELIMINARY EVALUATION OF THE QUALITY OF BLOOD COMPONENTS FOR TRANSFUSION USE (WHOLE BLOOD, PACKED RED BLOOD CELLS, FRESH FROZEN PLASMA) IN CANINE, FELINE AND BOVINE BLOOD PRODUCTS, AND PREPARATION OF BLOOD COMPONENT FOR NON-TRANSFUSION USE (PLATELET RICH PLASMA)IN DOG." Doctoral thesis, Università degli Studi di Milano, 2013. http://hdl.handle.net/2434/219125.

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Evaluation of hematological parameters, ammonia concentration and microbial contamination in Canine Packed Red Blood Cells stored in CPD-SAGM for 42 days. Abstract Canine transfusion medicine practices have been growing rapidly over the past few decades and the use of specific blood components (packed red cells, plasma) has permitted to optimized the canine blood donations. The study was undertaken to evaluated the changes in RBC, MCV, Ht, RDW, WBC and ammonia concentration in canine PRBC stored in CPD-SAGM for 42 days. Also the presence of bacterial contamination was evaluated with blood culture. PRBC units were stored in a routine manner and were examined every 2-3 weeks. Hematological parameters changed significantly with increase of MCV, Ht and RDW, while WBC decreased. Also ammonia concentration increased significantly during the storage. RBC and WBC deteriorated somewhat during storage and ammonia concentration increased similar to what reported in canine and human in vitro studies. No bacterial contamination was reported. The results obtained in this study agree mostly with what previously is reported in canine and human medicine. Further studies are needed to better evaluated how the reported alterations influence viability of blood cells in canine PRBC. The safety and quality of feline whole blood units collected with an open system and the effect of storage on hematological parameters and ammonia concentration Abstract The veterinary transfusion medicine is constantly in progress but still now feline blood donation, collection, and conservation of whole blood and blood products present some problems. Feline whole blood collected with open system and stored in CPDA1 for 35 days at 4°C was evaluated for hematological parameters, ammonia concentration and sterility during the storage period. Statistical analysis resulted in significant increase in ammonia concentration and decrease of WBC. No other significant changes resulted in hematological parameters (RBC, Ht, MCV, RDW). No units presented bacterial contamination during storage. The use a standardized protocol during blood collection, preparation and storage of feline whole blood permit to obtain a product without microbial contamination, minimum changes in haematological parameters but with a very high ammonia concentration. Preliminary Evaluation on the Stability of Protein in Bovine Fresh Frozen Plasma Abstract The aim of this study were to evaluating preliminary stability of glucose, urea, total protein and protein fractions in bovine fresh frozen plasma (FFP). Blood was collected into human sterile double-pack blood collection system containing citrate-phosphate-dextrose-adenine (CPDA) and after centrifugation the plasma units were stored within 8 hours from blood collection at – 19°C obtaining FFP. The analysis of biochemical parameters were performed on fresh plasma after centrifugation of whole blood unit and on thawed FFP after 1 and 6 months of storage. Pre and post storage results were compared using a one way repeated measures ANOVA. Seven FFP were obtained from 7 different whole blood units. There was no significant changes in the concentrations of glucose, urea, total protein and protein fraction during the entire period of storage. This preliminary study showed that during 6 months of storage no significant changes were appeared in the evaluate biochemical parameters in bovine FFP. Effectiveness of manual double centrifugation method for preparation of Canine Platelet-Rich Plasma Abstract The platelet-rich plasma (PRP) is a product derived from whole blood with a platelet concentration higher than normal range in a small amount of plasma. Regenerative capacities of PRP deriving from platelet growth factors. For this reason PRP is used in human and veterinary medicine for its capacity to stimulate cell proliferation, angiogenesis, wound healing, production of fibroblasts, collagen, osteoblasts and to accelerate the healing process. In veterinary medicine the methods use to produce PRP are not standardized and extremely numerous. The aim of this study was to describe and evaluate a manual double centrifugation method to produce canine PRP. 28 blood samples (5-10 ml with 1 ml of sodium citrate) from 28 healthy dogs were analyzed. The first centrifugation (2500 rpm for 10’) resulted in two components, blood cell component in the bottom and serum component (SEC) in the upper fraction of the tube. All SEC, the buffy coat and the first 2 mm of red blood cell was submitted to a second centrifugation (4000 rpm for 15’) and resulted in two components, platelet poor plasma (PPP) and platelet pellet in the bottom. The amount of PPP used to resuspend platelet pellet was calculated considering that all platelets previously present in the SEC was in platelet pellet. Then 50% of the calculated PPP was used to resuspend platelet pellet with the aim to obtain the final platelet concentration of about 1 million /µl. The method proposed in this study permitted in 14/28 samples of PRP (50%) to reach the human target of 1 milion platelets/µl ± 20% and/or the target of three to six fold platelet concentration in whole blood. According to a part of human literature the concentration of platelet in PRP does not seem to be necessarily linked to its effectiveness. For this reason to complete the evaluation of the proposed method will be necessary assess the platelet viability and after apply the PRP in vivo.
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Books on the topic "Blood plasma"

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R, Harris James, ed. Blood separation and plasma fractionation. New York: Wiley-Liss, 1991.

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1924-, Scanu Angelo M., and Spector Arthur A. 1936-, eds. Biochemistry and biology of plasma lipoproteins. New York: Dekker, 1986.

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Smit Sibinga, C. Th, P. C. Das, and S. Seidl, eds. Plasma Fractionation and Blood Transfusion. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2631-1.

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Lundblad, Roger L. Biotechnology of plasma proteins. Boca Raton: Taylor & Francis, 2012.

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Symposium on Blood and its Derivatives (1984 Cartagena, Colombia). Seminar on Symposium on Blood and its Derivatives, Cartagena, Colombia, 25-30 November 1984: Report. [Vienna]: United Nations Industrial Development Organization, 1985.

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Human plasma proteins: Their investigation in pathological conditions. 2nd ed. Chichester: Wiley, 1987.

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Serum/plasma proteomics: Methods and protocols. New York: Humana Press, 2011.

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A, Kreisberg Robert, and Segrest Jere P, eds. Plasma lipoproteins and coronary artery disease. Boston: Blackwell Scientific Publications, 1992.

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Rita, Cornelis, ed. Trace elements in human plasma or serum. Boca Raton, Fla: CRC Press, 1989.

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Bertolini, Joseph, Neil Goss, and J. M. Curling. Production of plasma proteins for therapeutic use. Hoboken, N.J: John Wiley & Sons, 2013.

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Book chapters on the topic "Blood plasma"

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Mesko, D., and R. Pullmann. "Blood — Plasma — Serum." In Differential Diagnosis by Laboratory Medicine, 40–368. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-55600-5_2.

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Jaworski, Peter M. "Blood and plasma." In The Routledge Handbook of Commodification, 262–77. London: Routledge, 2023. http://dx.doi.org/10.4324/9781003188742-23.

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Ghosh, S. "Blood Products: Fresh-frozen Plasma, Albumin Preparations and Plasma Substitutes." In Handbook of Blood and Blood Products, 21–28. London: Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-19289-2_4.

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Hoffman, Christopher Ryan, Alexander Huynh, and Henry Liu. "Plasma Substitutes." In Blood Substitutes and Oxygen Biotherapeutics, 185–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-95975-3_18.

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Joseph, Nisha S., and Sagar Lonial. "Plasma Cell Leukemia." In Neoplastic Diseases of the Blood, 639–44. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-64263-5_34.

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Eguchi, Yutaka. "Plasma Dia-Filtration for Severe Sepsis." In Acute Blood Purification, 142–49. Basel: KARGER, 2010. http://dx.doi.org/10.1159/000314864.

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Wardrop, K. Jane, and Marjory Brooks. "Plasma Products." In Manual of Veterinary Transfusion Medicine and Blood Banking, 43–54. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781118933053.ch4.

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Baele, Philippe L. "Plasma and Albumin." In Alternatives to Blood Transfusion in Transfusion Medicine, 83–108. Oxford, UK: Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9781444319583.ch8.

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Fiehn, Oliver, and Tobias Kind. "Metabolite Profiling in Blood Plasma." In Metabolomics, 3–17. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-244-1_1.

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Lista, Simone, Ina Giegling, and Dan Rujescu. "Schizophrenia: Blood-Serum-Plasma Metabolomics." In Advances in Biological Psychiatry, 27. Basel: S. KARGER AG, 2014. http://dx.doi.org/10.1159/000358024.

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Conference papers on the topic "Blood plasma"

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Vikinge, Trine P., Kenny M. Hansson, Johan Benesch, Knut Johansen, Mats Ranby, Tomas L. Lindahl, Ingemar Lundstroem, and Pentti Tengvall. "Blood plasma coagulation studied by surface plasmon resonance." In BiOS Europe '98, edited by Francesco Baldini, Nathan I. Croitoru, Martin Frenz, Ingemar Lundstroem, Mitsunobu Miyagi, Riccardo Pratesi, and Otto S. Wolfbeis. SPIE, 1999. http://dx.doi.org/10.1117/12.336920.

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Kiriakidis, Kiriakos, and Richard O'Brien. "Optimal Estimation of Blood Insulin From Blood Glucose." In ASME 2006 International Mechanical Engineering Congress and Exposition. ASMEDC, 2006. http://dx.doi.org/10.1115/imece2006-14776.

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Plasma insulin estimation from plasma glucose has been proposed in order to avoid hyperinsulinemia in the control of diabetes. This paper presents an estimator with error feedback based on measured and predicted plasma glucose designed to tolerate measurement noise as well as discretization error by means of the H∞ criterion. The proposed estimator is tested and evaluated using synthetic patient data.
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Minkyung Lee, Hyunchul Kim, Yunjung Kim, Won Young Lee, Ku Youn Baik, N. K. Kaushik, and Guangsup Cho. "Blood coagulation with atmospheric-plasma jets." In 2012 IEEE 39th International Conference on Plasma Sciences (ICOPS). IEEE, 2012. http://dx.doi.org/10.1109/plasma.2012.6383715.

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Huang, N. "Surface Modification of Blood Contacting Biomedical Implants by Plasma Processes." In PLASMA PHYSICS: 11th International Congress on Plasma Physics: ICPP2002. AIP, 2003. http://dx.doi.org/10.1063/1.1593932.

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Miura, T., M. Inagaki, M. Taki, N. Saito, T. Meguro, and K. Yamada. "GRANULOCYTE ELASTASE RELEASE DURING BLOOD COAGULATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643166.

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Granulocyte elastase (ELP) has a high-potency fibrinolytic activity. Hence, there is a possibility that ELP acts as a thrombolytic enzyme like plasmin in thrombolysis. We investigated the release of ELP from granulocytes, especially during blood coagulation.The biological activity of ELP was measured using a synthetic substrate, Suc-Ala-Tyr-Leu-Val-pNA. The immunological activity assayed as an alpha-l-antitrypsin-ELP complex was measured using an anti-ELP antibody (Merck), because more than 90% of ELP in blood forms alpha-l-antitrypsin-ELP complexes.The ELP activity in granulocytes extracted by 2 mol/1 KSCN was 10 mU/106 cells. This fibrinolytic activity corresponds to 1-2 U of plasmin in the fibrin plate method.The ELP release from separated granulocytes was observed by adding Ca2+, and the release was increased by Ca ionophore A 23187. The release was dose-dependent as far as 10 mM Ca2+ (final concentration) and the maximum release was obtained within 15 minutes. However, the ELP release was not produced by thrombin.The level of alpha-l-antitrypsin-ELP complex in serum was twice higher and that in heparinized plasma was 1.5 times higher than that in sodium citrated plasma. ELP was not released from granulocytes incubated in both prekallikrein deficient plasma and Factor XII deficient plasma containing 10 mM Ca2+. But addition of normal plasma (about 10%) resulted in ELP releaseThese results suggest that the ELP release from granulocytes is dependent on Ca2+ and the release is relevant to the blood coagulation system, especially to contact factors.
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Khumpuang, S., T. Tanaka, F. Aita, Z. Meng, K. Ooe, M. Ikeda, Y. Omori, et al. "Blood Plasma Separation Device using Capillary Phenomenon." In TRANSDUCERS '07 & Eurosensors XXI. 2007 14th International Conference on Solid-State Sensors, Actuators and Microsystems. IEEE, 2007. http://dx.doi.org/10.1109/sensor.2007.4300546.

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Topsakal, Erdem, Tutku Karacolak, and Elaine C. Moreland. "Glucose-dependent dielectric properties of blood plasma." In 2011 XXXth URSI General Assembly and Scientific Symposium. IEEE, 2011. http://dx.doi.org/10.1109/ursigass.2011.6051324.

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Baranova, L. N., and V. E. Kholmogorov. "Blood plasma: the inner filter for erythrocytes during UV irradiation of the blood." In Radiofrequency and Optical Methods of Biomedical Diagnostics and Therapy, edited by Valery V. Tuchin. SPIE, 1993. http://dx.doi.org/10.1117/12.146464.

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Kim, Y. H., H. S. Rhim, H. S. Uhm, and E. H. Choi. "Atmospheric pressure air plasma jet assisted blood coagulation." In 2011 IEEE 38th International Conference on Plasma Sciences (ICOPS). IEEE, 2011. http://dx.doi.org/10.1109/plasma.2011.5993283.

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Lenk, G., J. Hansson, W. van der Wijngaart, G. Stemme, and N. Roxhed. "Capillary driven and volume-metred blood-plasma separation." In TRANSDUCERS 2015 - 2015 18th International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2015. http://dx.doi.org/10.1109/transducers.2015.7180929.

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Reports on the topic "Blood plasma"

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Cortés Ortigosa, Francisco, and María Pascual Mora. Characterization of the extraction method of extracellular vesicles by HDL and LDL contamination. Fundación Avanza, May 2023. http://dx.doi.org/10.60096/fundacionavanza/2902022.

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In this study we assess and validate the method of extraction of extracellular vesicles found in blood plasma with commercial kits to exclude potential contamination by plasma HDL and LDL particles using immunoblot analysis.
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Valeri, C. R., Linda E. Pivacek, Hiliary Siebens, and Mark D. Altschule. Red Blood Cell Volume, Plasma Volume and Total Blood Volume in Healthy Elderly Men and Women Aged 64 to 100. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada360250.

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Bedina, S. A., E. E. Mozgovaia, E. A. Tikhomirova, M. A. Mamus, S. S. Dotsenko, and A. S. Trofimenko. Xanthine oxidase and xanthine dehydrogenase activity in rheumatoid arthritis: the enzyme profile of blood plasma. ООО "ИМА-Пресс", 2018. http://dx.doi.org/10.18411/1995-4484-2018-56-33-8.

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Mozgovaya, E. E., S. A. Bedina, I. A. Zborovskaya, A. S. Trofimenko, M. A. Mamus, E. A. Tikhomirova, and S. S. Spitsina. XANTHINE OXIDOREDUCTASE AND SUPEROXIDE DISMUTASE ACTIVITIES OF BLOOD PLASMA DEPENDING ON TYPE OF SYSTEMIC SCLEROSIS. "PLANET", 2019. http://dx.doi.org/10.18411/978-5-907192-54-6-2019-xxxvi-120-127.

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Gunn, Patrick J., Allie L. Lundberg, Robert A. Cushman, Harvey C. Freetly, Olivia L. Amundson, Julie A. Walker, and George A. Perry. Effect of Circulating Blood or Plasma Urea Nitrogen Concentrations on Reproductive Efficiency in Beef Heifers and Cows. Ames (Iowa): Iowa State University, January 2016. http://dx.doi.org/10.31274/ans_air-180814-542.

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Bedina, S. A., E. E. Mozgovaya, I. A. Zborovskaya, A. S. Trofimenko, and E. G. Korenskaya. ENZYMATIC PROFILE OF BLOOD PLASMA IN RHEUMATOID ARTHRITIS: ACTIVITY OF XANTHINE OXIDASE, XANTHINE DEHYDROGENASE AND SUPEROXIDE DISMUTASE. Планета, 2018. http://dx.doi.org/10.18411/978-5-907109-24-7-2018-xxxv-54-61.

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Bedina, S. A., E. E. Mozgovaya, A. S. Trofimenko, S. S. Spitsina, M. A. Mamus, and E. A. Tikhomirova. ENZYMATIC PROFILE OF BLOOD PLASMA IN SYSTEMIC SCLEROSIS: ACTIVITY OF XANTHINE OXIDASE, XANTHINE DEHYDROGENASE AND SUPEROXIDE DISMUTASE. "PLANET", 2019. http://dx.doi.org/10.18411/978-5-907192-54-6-2019-xxxvi-38-45.

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Minchev, Velko, Kalina Kamenova, Nadya Hristova-Avakumova, Slavina Surcheva, and Rumen Nikolov. ihydropyrimidine Dehydrogenase (DPD) Screening in Blood Plasma of Cancer Patients Indicated to Fluoropyrimidine Chemotherapy by ELISA Method. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, May 2021. http://dx.doi.org/10.7546/crabs.2021.05.15.

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Bedina, S. A., E. E. Mozgovaya, A. S. Trofimenko, N. M. Devyataeva, M. A. Mamus, S. S. Spitsyna, and E. A. Tikhomirova. XANTHINE OXIDASE, XANTHINE DEHYDROGENASE AND SUPEROXIDE DISMUTASE ACTIVITIES OF BLOOD PLASMA DEPENDING ON CLINICAL FEATURES OF SYSTEMIC SCLEROSIS. Academy of Natural Knowledge, 2019. http://dx.doi.org/10.18411/1996-3955-2019-10-268-272.

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Mozgovaya, E. E., S. A. Bedina, I. A. Zborovskaya, A. S. Trofimenko, and S. S. Khortieva. XANTINOXIDASE, XANTINDEGHYROGENASE, SUPEROXIDEDISMUTASIS ACTIVITY OF BLOOD PLASMA IN THE GROUP OF PATIENTS WITH EXTRA ARTICULAR MANIFESTATIONS OF RHEUMATOID ARTHRITIS. Планета, 2018. http://dx.doi.org/10.18411/978-5-907109-24-7-2018-xxxv-212-218.

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