Evaluation of hemostatic effect of polyelectrolyte complex-based dressings

2017 ◽  
Vol 32 (5) ◽  
pp. 638-647 ◽  
Author(s):  
Manisha Buriuli ◽  
Wasupalli Geeta Kumari ◽  
Devendra Verma

The aim of this work was to develop a polyelectrolyte complex-based hemostatic dressing made from chitosan and polygalacturonic acid. Porous dressings were fabricated by ultrasonication of chitosan and alginate solutions followed by freeze-drying. Since chitosan has inherent hemostatic properties, and polygalacturonic acid is anti-inflammatory in nature, it was desired to combine these two polymers to develop an effective hemostatic dressing, which may also promote wound healing. Porous structure of the bandages was observed using field-emission scanning electron microscope. Blood clotting behavior was studied using whole blood clotting assay. Plasma recalcification time, prothrombin time, and activated partial thromboplastin time were also determined to study the mechanism of clotting. The dressings were found to accelerate clotting rates and showed increased thrombin activity with an increase in chitosan concentration.

2021 ◽  
Vol 8 (9) ◽  
pp. 210462
Author(s):  
Bingxian Lin ◽  
Kaiming Liu ◽  
Yunren Qiu

Polysulfone (PSF) works potentially in haemodialysis due to its great mechanical and chemical stability, but performs poorly in haemocompatibility. For promoting the unpleasant haemocompatibility, sulfonated citric chitosan (SCACS) with the structure and groups similar to heparin was primarily synthesized by acylation and sulfonation. Furthermore, the chloroacylated PSF was pretreated by electrophilic chloroacetyl chloride to achieve more active sites for further reaction; the following membranes underwent the amination and were named amination polysulfone (AMPSF) membranes. Moreover, SCACS with abundant carboxyl and sulfonic groups was covalently grafted at the surface of pretreated PSF membranes, called PSF-SCACS membranes. The PSF-SCACS membranes were successfully synthesized and characterized by 1 H NMR, ATR-FTIR and XPS. In addition, the water contact angle of PSF-SCACS membranes decreased by 47° and the morphologies of the membranes changed little compared with the unmodified PSF membranes. The haemocompatible testing results, including protein adsorption, platelet adhesion, haemolysis rate, plasma recalcification time, activated partial thromboplastin time (APTT), prothrombin time (PT) and thrombin time (TT), demonstrated that the PSF-SCACS membranes possessed excellent haemocompatible performances, and SCACS played an important role in the modification.


1972 ◽  
Vol 27 (03) ◽  
pp. 619-633 ◽  
Author(s):  
J Soria ◽  
C Soria ◽  
M Samama ◽  
E Poirot ◽  
C Kling

SummaryTwo new cases of congenital dysfibrinogenemia have been discovered. In the first case, “Fibrinogen TROYES”, the abnormality is characterized by a prolonged thrombin clotting time, the defect being due to abnormal aggregation of fibrin monomers. There is no tendency towards excessive bleeding. The abnormality is found to be present with the same intensity in one of the patient’s brothers and one of his sisters.In the second case, “Fibrinogen METZ”, the abnormality is more pronounced, since, even in the presence of very high thrombin concentrations no clotting occurs. The abnormality is due to a defect in the release of fibrinopeptides, on addition of thrombin. The patient’s blood contains only abnormal fibrinogen. The plasma recalcification time is more prolonged than in the whole blood clotting time. The abnormality is present in both parents in heterozygote form, a milder form than in the patient who is homozygous. The patient has a moderate bleeding tendency, the parents being normal in this respect.


1979 ◽  
Vol 42 (03) ◽  
pp. 959-964 ◽  
Author(s):  
Nasreen Ahmad ◽  
B Dube ◽  
G P Agarwal ◽  
Rama Kanta Dube

Summary1. During hibernation in frogs (Rana tigrina) there occurs prolongation of several clotting tests, viz, whole blood clotting time, plasma recalcification time, cephalin time and prothrombin time.2. The ambient body temperature of the frog during winter hibernation is low and the retarded blood clotting at lower temperature may play an important protective role against intravascular thrombosis.3. Shorter plasma recalcification time in low-spun plasma as compared to high-spun plasma indicated the presence of procoagulant activity in platelets/leucocytes of frogs.


RSC Advances ◽  
2014 ◽  
Vol 4 (78) ◽  
pp. 41551-41560 ◽  
Author(s):  
Chengling Jiang ◽  
Zhiliang Wang ◽  
Xueqin Zhang ◽  
Xiaoqun Zhu ◽  
Jun Nie ◽  
...  

The formation mechanism polyelectrolyte complex nanofibers during the process of freeze drying.


2018 ◽  
Vol 552 (1-2) ◽  
pp. 27-38 ◽  
Author(s):  
Anita Umerska ◽  
Krzysztof J. Paluch ◽  
Maria Jose Santos-Martinez ◽  
Owen I. Corrigan ◽  
Carlos Medina ◽  
...  

1979 ◽  
Author(s):  
M. Colucci ◽  
L. Curatolo ◽  
M.B. Donati ◽  
N. Semeraro

The procoagulant activity of cells from some experimental tumors isolated in culture or as cell suspensions fron ascitic fluid was investigated. Cells from Lewis Lung carcinoma (primary and metastasis), Ehrlich carcinoma ascites and JK sarcoma ascites markedly shortened the recalcification time of normal, F.VIII and F.VII-deficient, not of F.X-deficient human plasma. This suggests a direct activation of coagulation F.X. To verify this assumption, cells were incubated with a BaS04-eluate of normal (N.E.) or F.VII-deficient (VII-D.E.) human serum (as a source of F.X) and CaCl2. The chromogenic substrate S-2222 was used for monitoring F. Xa generation. Substrate cleavage occurred to different degrees with all cell types; it was similar both with VII-D.F. and N.F., proportional to cell number and incubation period and was not influenced by hirudin. When tested separately, neither the eluate nor the cells had any amidolytic activity. Our assay readily discriminated between direct and F.VII-mediated activation of F.X. Indeed when cells with thrombopla-stin-like activity (mouse embryo fibroblasts) were tested, the rate of S-2222 cleavage was markedly lower with VII-D.E. than with N.E. Cells from sarcoma 180 ascites were completely inactive in both plasma recalcification time and amidolytic assay. It is concluded that cells from some experimental tumors directly activate F.X.(Supported by CNR (Italy), and NIK, NCI (USA).


1987 ◽  
Author(s):  
A Blanco ◽  
R Bonfil ◽  
O Bustoabad ◽  
M Lazzari

Increased deposition and lysis of fibrin, associated with malignant tissue, has led to look for activators of both the coagulation and fibrinolytic systems produced by tumor cells. We report the evidences of a procoagblant activity (PA) in the extracts of intratumoral necrosis from two experimental breast adenocarcinomas in murine model (BALB/c). The tumors have different metastatic capacity (MC). M3 without MC and MM3 with high MC.The addition of the extracts to: 1- Normal Plasma, 2- Deficient substrates in coagulation factors, 3- Purified, fibrinogen (I), showed: 1- Shortening of the plasma recalcification time (PRT) and APTT, without ;modification on prothrombin time (PT), 2- Reduction of the PRT on deficient substrates in factors: VIII; VII; VII and X; V; V, VII and X; without modification on II deficient substrate, 3- No PA on I. Table:C: Control, s: seconds, m: minutes. The PA was not affected by heparin. The results suggest that the PA is independent of the presence of either factor VIII or factor VII (intrinsic or extrinsic pathway respectively), as well as presence of either factor V or factor X. Any effect was observed either on factor II deficient substrate or on I, so, there was no evidence of thrombin activity The PA could be act directly on factor II, suggesting that fibrin formation could be induced by a “non-classical” activation pathway. No significant differences (p>0.5) in PA were observed between both tumoral necrosis extracts. The necrotic area in M3 (37%) is bigger than in MM3 (18%). So, much more PA could be present in MM3 and this could play a role in the MC of this tumor.


2019 ◽  
Vol 47 ◽  
Author(s):  
Raissa Lopes Lima ◽  
Paulo Victor Braga ◽  
Nathálye Fernandes Pelegrini ◽  
Arlena Do Bom Parto Ferreira de Almeida ◽  
Adriane Jorge Mendonça ◽  
...  

Background: Snakebites occur frequently among humans and animals. In Brazil, about 23,000 cases of snakebite involving humans were recorded in 2016, 11% of them caused by venomous snakes. In the region of Cuiabá, capital of Mato Grosso, the highest occurrence is of snakes of the genus Bothrops (81%), followed by Crotalus (4%). Bothrops venom has proteolytic, coagulant and hemorrhagic effects, whereas Crotalus venom is neurotoxic, myotoxic and nephrotoxic. This paper reports on three cases of Bothrops snakebites in dogs treated at the Veterinary Hospital of the Federal University of Mato Grosso in 2017.Cases: Three dogs were treated showing clinical signs of snakebite, possibly by Bothrops, since their owners reported that these are the snakes most frequently found where they live. This information is consistent with the known geographic distribution of snakes of the genus Bothrops in the state of Mato Grosso, Brazil. In the first report (Case 11), the patient was bitten on two different occasions in a five-month interval, and died presumably due to anaphylactic shock caused by the venom injected by a second snakebite (Case 12). In both episodes, the animal presented a swollen face and neck, dyspnea and eye bleeding, and these signs were more severe in the second episode. Case 2 was a dog with severe neck and chest swelling and pain. The owner of this dog reported that he had taken his dog for a walk in the countryside, along with the dog of Case 1, and had returned home with both dogs about three hours before the consultation. Case 3 was a Rottweiler living at a small family farm located 67 km from Cuiabá. The animal presented with slight swelling and pain in the left forelimb, and puncture wounds on the lower limb. Neutrophilic leukocytosis was observed in cases 1 and 3.  In addition, Case 12 (the second episode of Case 1) presented with thrombocytopenia and increased prothrombin time and activated partial thromboplastin time. The dog of Case 2 presented no hematological or biochemical alteration. All the dogs received antivenom serum and supportive care.Discussion: Based on the clinical signs of local swelling with bleeding and absence of neurological signs, the snakebites were attributed to the genus Bothrops. In Case 12, blood clotting tests showed non-coagulation. The greater severity of Case 1, which culminated in death, was attributed to anaphylaxis due to prior exposure or the larger amount of venom than that injected in Case 2, since the two injuries were inflicted in the same environment on the same day, probably by the same snake. Neutrophilic leukocytosis may be indicative of an inflammatory reaction, while thrombocytopenia and clotting changes are associated with the hemorrhagic activity of Bothrops venom. Death by snakebite is directly linked to the amount of venom injected, the envenomation site, and the time between the bite and the beginning of treatment. This explains the moderate signs presented by Cases 2 and 3, whose injuries were inflicted on the neck and forelimb, unlike the dog of Case 1, which was bitten on the head on two occasions. It was concluded that Bothrops venom causes systemic and local alterations characterized by pain, swelling, necrosis and bleeding. Early access to antivenom treatment is essential to neutralize clinical signs and prevent worsening of systemic poisoning. The determining factor in snakebite deaths is the amount of injected venom and the time elapsed between the injury and the beginning of treatment.


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