1.Changes in erythrocyte, leucocyte and platelet in people having frequent contact with chemicals
Journal of Vietnamese Medicine 2004;295(2):23-26
In this study, 48 long-term exposed people with polychemicals (the male/female ratio is 1/3, the age from 23 to 44): such as organic and iso-organic acids: benzene, toluene and their coequals were investigated. 17 normal people not exposed with polychemicals as the control group. Results were shown following: quantity of erythrocyte was lower than control group but not significantly. Leucocytes especially neutrophils reduced significantly (p<0.001). 15/48 cases (30%) appereared lymphoblast. There is no difference in platelet between studied group and control group
Chemistry
;
Diagnosis
;
Erythrocytes
;
Blood Platelets
3.The results of studying procedure to reduce erythrocytes from cord blood using to long-term storage of CD34 cells
Dung Thi My Pham ; Phan Trung Do ; Tung Quang Nguyen ; Vinh Quang Pham ; Tri Anh Nguyen
Journal of Medical Research 2007;51(4):1-4
Background: The reduction of erythrocytes from cord blood is very need for long - term storage of C034 cells for transplantation. Reduced erythrocyte will reduces preservative blood volume, preservatives and freely HST when defrosting, so stem cells are better protected. Objectives: To study selection of the best centrifugal procedure to reduce maximal erythrocytes and lose minimal C034 cells from cord blood. Subjects and methods: 20 blood samples selected from 60 cord blood units was used for this study. The study was carried out through two steps. In the first step, the centrifugal speed was fixed and the centrifugal time was changed.In the second step, the centrifugal time was fixed, the centrifugal speed was changed. From collected results the best appropriate procedure to reduce erythrocytes from cord blood have been selected. Results: The procedure of gradient centrifuge with speed of 500g in 6 minutes isolated> 50% of erythrocytes, kept > 84% of CD34 cells and then centrifuge of 1000 g in 10 minutes reduced about 40% of volume of nuclear cell - suspension. Conclusion: The procedure can use for preparation of stem cell suspension from cord blood to storage in nitrogen liquid. \r\n', u'\r\n', u'
Erythrocytes/ pathology
;
Fetal Blood/ chemistry
;
drug effects
;
immunology
4.Arginase Level in Suspended Red Blood Cells Storaged for Different Time.
Li-Ping FAN ; Hao-Bo HUANG ; Shi-Jin WEI ; Dan-Hui FU ; Feng ZENG ; Qing-Hua HUANG ; Jin-Quan HONG
Journal of Experimental Hematology 2015;23(5):1459-1463
OBJECTIVETo explore the effect of storage time on arginase level, and the possible source of arginase in suspended red blood cells (RBC).
METHODSThe arginase and myeloperoxidase (MPO) levels in suspended RBC and control plasma were detected by ELISA. The free hemoglobin level in suspended RBC and control plasma were detected by colorimetric method. The relationship between arginase level, MPO level and free hemoglobin level in suspended RBC was analyzed by the related methods.
RESULTSThe arginase and free hemoglobin levels in suspended RBC were higher than those in control plasma. Otherwise, MPO level was not significantly different between suspended RBC and control plasma. All of them did not increase along with prolonging of storage time. There was not a significant correlation between arginase level and free hemoglobin level in suspended RBC of different storage time (r = 0.03), but arginase level positively correlated with MPO level in the suspended RBC of different storage time (r = 0.76).
CONCLUSIONThe arginase level in suspended RBC storaged for different time increases significantly, but not along with prolonging of storage time. The main possible source of arginase in the suspended RBC is the residual white blood cell, especially neutrophils.
Arginase ; chemistry ; Blood Preservation ; Erythrocytes ; enzymology ; Humans ; Peroxidase ; chemistry ; Plasma ; enzymology ; Time Factors
5.Kinetic spectrophotometric study on hemolytic process of polysorbate 80.
Shao-Feng ZHANG ; Dan YAN ; Hui-Ying TANG ; Yun LUO ; Ping ZHANG ; Ming YANG ; Yue-sheng WANG ; Xiao-He XIAO
Acta Pharmaceutica Sinica 2010;45(4):535-538
To establish kinetic assay method for the analysis of hemolysis and to investigate dynamic hemolytic process of polysorbate 80. The UV-VIS spectrum of heme changes when hemoglobin is released continuously during the hemolytic process. Therefore, dynamic hemolytic curve was determined as a new way to characterize the kinetic process of interaction between polysorbate 80 and red blood cells. The effect of polysorbate 80 on blood cells could be perfectly investigated by the hemolytic dynamics. Dynamic hemolytic parameters of polysorbate 80 were calculated according to the hemolytic curves. The constants of hemolytic rate and maximum hemolytic rate of polysorbate 80 had fine linear relationships at the range of 1-20 mg x mL(-1) and 5-20 mg x mL(-1), respectively. In comparison with the present official method such as macroscopic observation and static spectrophotometric methods, kinetic spectrophotometry has the advantages of real time, on-line determination, sensitive, objective, good reproducibility and 2-dimensional information acquired. Therefore, as a biological technique, kinetic spectrophotometry could be applied to evaluate the quality of polysorbate 80 and to screen other solubilizing excipients.
Animals
;
Drug Stability
;
Erythrocytes
;
chemistry
;
Excipients
;
chemistry
;
Hemoglobins
;
analysis
;
Hemolysis
;
Kinetics
;
Polysorbates
;
chemistry
;
Rabbits
;
Reproducibility of Results
;
Spectrophotometry, Ultraviolet
;
methods
6.Measuring the shelf life of CPDA and ACD whole blood stored at above 4 degrees C in vitro.
Wei HAN ; Jing-Han LIU ; Tie-Jun WANG ; Rui LI ; Xi-Lin OUYANG ; Xi-Jin LI
Journal of Experimental Hematology 2004;12(1):95-97
In order to measure the shelf life of whole blood stored at above 4 degrees C and provide experimental data for blood preservation and transportation in battle fields, 200 ml whole blood was collected from each of the 10 donors and anticoagulated by CPDA or ACD, then 50 ml whole blood was separated from each one and marked as control group, the rest was marked as test group. The control group was stored at 4 degrees C and RBC ATP concentrations was measured at the end of its shelf life which signed as critical ATP. The test group was stored at above 4 degrees C condition, some items as ATP, FHb (free hemoglobin), serum K(+) and germiculture were tested daily and ensured all of them eligible. When RBC ATP decreased to the level of critical ATP, the time of preservation was considered as shelf life. The results showed that at temperatures from 10 to 33 degrees C, the shelf life of CPDA whole blood ranges from 2.5 days to 18 days, while shelf life of ACD whole blood ranges from 1 day to 13 days. It is concluded that CPDA whole blood stored at above 4 degrees C condition can be sent to the front hospital in effective shelf life so that the wounded can be cured in time.
Adenosine Triphosphate
;
blood
;
Blood Preservation
;
Erythrocytes
;
chemistry
;
Humans
;
Temperature
;
Time Factors
7.Effect of highway transportation on the quality of red blood cells.
Gen-Hong YAO ; Jian-Feng LUAN ; Dong YE ; Pei-Yuan ZHU ; Jing-Mei YAN ; Ping HONG ; Xin-Yong HU ; Xue-Ming YI
Journal of Experimental Hematology 2008;16(4):922-925
This study was purposed to investigate the effect of highway transportation on the quality of blood components so as to provide experimental basis to meet the needs of military operations. The transport condition was simulated by random vibration test. The red blood cells, leukocyte-reduced red blood cells, washed red blood cells were randomly vibrated (C Road) for 4 hours. Then, these blood components were stored in refrigerator for 15 days (4 degrees C). Six milliliters of blood were collected before vibration, after vibration, and at day 15 days of storage after vibration, respectively. The suspension was isolated. The free hemoglobin (FHb), routine hematological parameters, and biochemical indexes were determined. The results showed that FHb, lactate dehydrogenase (LDH), K(+) of red blood cells and leukocyte-reduced red blood cells did not significantly change after vibration and storage. However, FHb, LDH and K(+) of washed red blood cells increased significantly after simulated transportation (p < 0.05). The levels of these parameters at day 15 of storage after vibration were also significantly higher than those after vibration (p < 0.01). The changes of other hematological parameters were not significant in three blood components after vibration (C Road) and storage for 15 day. In conclusion, red blood cells and leukocyte-reduced red blood cells were qualified for clinic transfusion even after transportation within 4 hours for 15 day storage later, if they were kept in proper blood container and protected from damping. However, the washed red blood cells could not be used for clinic after similar transport in the military operations.
Blood Preservation
;
Cryopreservation
;
Erythrocytes
;
chemistry
;
Humans
;
L-Lactate Dehydrogenase
;
blood
;
Transportation
;
Vibration
8.Establishment of the cell line K562 with stable expression of hermap and hermap-siRNA.
Yan-Mei LI ; Sai-Jun GAO ; Tie-Zhen YE ; Ying-Yi HE
Journal of Experimental Hematology 2010;18(5):1306-1309
In order to establish K562 line with stable expressions of hermap and hermap-siRNA, amplified hermap and hermap-siRNA were cloned into pEGFP-c1 and pRNAT to acquire hermap-pEGFP-c1 and hermap-siRNA-pRNAT, respectively. These two plasmids were electrotransferred into K562 cells, then were followed by culturing with G418. The result showed that the transfer rate of hermap-pEGFP-c1-K562 and hermap-siRNA-pRNAT-K562 plasmids were 10.0% and 9.3%, respectively. After selective culture by G418, these two cell lines were still able to express GFP. It is concluded that the eukaryotic expression plasmids containing hermap and hermap-siRNA have been successfully constructed, and the cell lines of hermap-K562 and hermap-siRNA-K562 are established, definitely contributing to further functional investigation on HERMAP and its interaction with other proteins.
Erythrocytes
;
chemistry
;
Gene Silencing
;
Humans
;
K562 Cells
;
Membrane Proteins
;
genetics
;
Plasmids
;
RNA, Small Interfering
;
Transfection
9.Mechanical properties and biological evaluation of buffalo horn material.
Quanbin ZHANG ; Qunfei ZHOU ; Guanghua SHAN ; Ping CAO ; Yaoxiong HUANG ; Ningjian AO
Journal of Biomedical Engineering 2014;31(6):1298-1304
Mechanical properties and biological evaluation of buffalo horn material were examined in this study. The effects of sampling position of buffalo horn on mechanical properties were investigated with uniaxial tension and micron indentation tests. Meanwhile, the variation of element contents in different parts of buffalo horn was determined with elemental analysis, and the microstructure of the horn was measured with scanning electron microscopy. In addition, biological evaluation of buffalo horn was studied with hemolytic test, erythrocyte morphology, platelet and erythrocyte count, and implantation into mouse. Results showed that the buffalo horn had good mechanical properties and mechanical characteristic values of it gradually increased along with the growth direction of the horn, which may be closely related to its microstructure and element content of C, N, and S in different parts of the buffalo horn. On the other hand, because the buffalo horn does not have toxicity, it therefore does not cause hemolysis of erythrocyte and has a good affinity with it. Buffalo horn has good histocompatibility but meanwhile it may induce the platelet adhesion and aggregation. Even so, it does not continue to rise to induce a large number of platelet to aggregate with resulting blood clotting. Therefore, the buffalo horn material has been proved to possess good blood compatibility according to the preliminary evaluation.
Animals
;
Biocompatible Materials
;
Biomechanical Phenomena
;
Buffaloes
;
Erythrocytes
;
Horns
;
chemistry
;
ultrastructure
;
Mice
;
Microscopy, Electron, Scanning
10.Aquaporin 1 expression in tissues of canines possessing inherited high K+ erythrocytes.
Hideharu OCHIAI ; Nobuya HISHIYAMA ; Shin HISAMATSU ; Nobuyuki KANEMAKI
Journal of Veterinary Science 2008;9(2):203-205
We investigated the expression of aquaporin 1 (AQP1) in tissues from canines with an inherited anomaly that causes their erythrocytes to have high K+. Northern blot analysis revealed abundant AQP1 expression in lung and kidney, though little expression was found in spleen. Using anti-C-terminus for dog AQP1, abundant expression was shown in kidney, trachea, and eye, but little expression was shown in pancreas and cerebrum, indicating that AQP1 expression in canine tissues is similar to that noted in other mammals.
Animals
;
Aquaporin 1/*metabolism
;
Blotting, Northern
;
Dogs
;
Erythrocytes/*chemistry
;
Immunoblotting
;
Potassium/*analysis
;
Viscera/metabolism