scholarly journals In vitro antibacterial screening of methanolic extract of whole body tissue and ethylene diamine tetra acetate (EDTA) extract of cuttlebone of Sepia pharaonis (Ehrenberg, 1831) against selected clinical isolates

2014 ◽  
Vol 8 (40) ◽  
pp. 3551-3557 ◽  
Author(s):  
Krishnamoorthi Jayalakshmi ◽  
Sudharsan Sadhasivam ◽  
Shanmugam Vairamani ◽  
Shanmugam Annaian
Keyword(s):  
Methanolic Extract ◽  
Clinical Isolates ◽  
Body Tissue ◽  
Ethylene Diamine ◽  
Whole Body ◽  
Antibacterial Screening ◽  
Sepia Pharaonis ◽  
Ethylene Diamine Tetra Acetate

scholarly journals Pseudothrombocytopenia: an immunologic study on platelet antibodies dependent on ethylene diamine tetra-acetate

Blood ◽  
1982 ◽  
Vol 59 (1) ◽  
pp. 157-161 ◽  
Author(s):  
JG Pegels ◽  
EC Bruynes ◽  
CP Engelfriet ◽  
AE von dem Borne
Keyword(s):  
Ethylene Diamine ◽  
Igg Antibodies ◽  
Immunofluorescence Test ◽  
Igm Antibodies ◽  
Platelet Antibodies ◽  
Group Specificity ◽  
Iga Antibodies ◽  
Ethylene Diamine Tetra Acetate

Abstract Antibodies specifically reacting with platelets only in the presence of EDTA, by the platelet immunofluorescence test, were found in the serum of 20 patients with pseudothrombocytopenia due to in vitro EDTA- dependent platelet agglutination. These antibodies reacted optimally at 0–4 degree C. In 19 patients, IgG antibodies were detected; in 8 patients, IgM or IgA antibodies were also found. In one patient, only IgM antibodies were found. In 14 patients, the IgG antibodies were IgG1, but IgG2, IgG3, and IgG4 antibodies were also seen in 7 patients. The reaction of platelets with the antibodies was detectable in the presence of Na2EDTA, the K, Ca, and Mg salts of EDTA, and K2EGTA. F(ab')2 or F(ab') fragments of the IgG antibodies reached as strongly as the intact antibodies, indicating that the reaction is dependent on the antibody-combining site. The EDTA-dependent antibodies did not show platelet-group specificity. However, platelets from patients with Glanzmann disease did not react with the antibodies.

scholarly journals Antimicrobial activity of leaves extracts against bacteria isolated from wound infections

2020 ◽  
Vol 8 (3) ◽  
pp. 114-120
Author(s):  
Goris BMT ◽  
Sabahalkheir KG ◽  
Ibrahim AA ◽  
Ibrahim AA ◽  
Ishaq MM ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Aqueous Extract ◽  
Methanolic Extract ◽  
Clinical Isolates ◽  
University Hospital ◽  
Diffusion Method ◽  
Klebsiella Pneumonia ◽  
Lawsonia Inermis ◽  
Perennial Plant

Background: Lawsonia inermis (L. inermis) is perennial plant commonly called henna. It is frequently cultivated in Sudan. Beside its uses cosmetics for staining hands and as hairs dyes‚ it was reported to be useful in jaundice, enlargement of spleen, calculus affliction and skin disease. Method: This descriptive study was done during the period from December 2014 to April 2015 in order to determine the invitro antimicrobial activity of L. inermis (henna) leaves extract against standard and clinical isolates from wound swabs, including Staphylococcus aureus, Escherichia coli, Proteus species, Klebsiella pneumonia, and Pseudomonas aeruginosa. These organisms were collected from different hospitals in Khartoum State including: Soba University Hospital, Military Teaching Hospital, and Laboratory Management Center. The in vitro antimicrobial susceptibly testing was performed using cup plate diffusion method. The activity of L. inermis Linn leaves extract was controlled with four reference antibiotics including gentamicin, oxacillin, ciprofloxacin, and impinim. Results: When aqueous extract of L. inermis Linn examined against standard bacteria and clinical isolates result showed that all standard bacteria were inhibited at 100%, 50%, and 25% concentration. All clinical isolates were successfully inhibited at 100%, 50%, 25%, and 12.5%. In contrary, the activity of methanolic extract of L. inermis Linn against standard bacteria showed that all standard bacteria were inhibited at 100%, 50% concentration, However, the clinical isolates showed an inhibition rate various depending on the concentration of methanolic extract of L. inermis Linn with S. aureus being most sensitive isolate. Conclusion: We conclude that aqueous and methanolic extract of henna exhibited antimicrobial activity against all types of tested organisms both clinical and standard isolates. But the aqueous extract shows superior inhibition ability than the methanolic.

scholarly journals In vitro evaluation of antimicrobial activity of methanolic extract from selected species of Cephalopods on clinical isolates

2011 ◽  
Vol 5 (23) ◽  
pp. 3884-3889 ◽  
Author(s):  
Ramasamy Pasiyappazham ◽  
Subhapradha Namasivayam ◽  
Srinivasan Alagiri ◽  
Shanmugam Vairamani ◽  
Krishnamoorthy Jayalakshmi ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Methanolic Extract ◽  
Clinical Isolates ◽  
In Vitro Evaluation

scholarly journals ACTIVITY OF THE MEDICINAL PLANT PARKIA JAVANICA AGAINST NEISSERIA GONORRHOEAE MULTI DRUG RESISTANT AND OTHER CLINICAL ISOLATES

2019 ◽  
pp. 83-86 ◽  
Author(s):  
JHINUK BASU MULLICK ◽  
TAPAN MAJUMDAR ◽  
KUDUMULA VENKATA RAMI REDDY ◽  
SUMITA MUKHERJEE ◽  
SAMIR KUMAR SIL
Keyword(s):  
Neisseria Gonorrhoeae ◽  
Ethyl Acetate ◽  
Methanolic Extract ◽  
Ethyl Acetate Fraction ◽  
Multidrug Resistant ◽  
Clinical Isolates ◽  
Chloroform Fraction ◽  
Standard Strain ◽  
Water Fraction

Objective: The objective of this study was to look into the in vitro activity of Parkia javanica against isolates of Neisseria gonorrhoeae. Methods: Methanolic extract of P. javanica bark (MEPJ) and organic fractionation were tested against one standard strain and 10 clinical isolates including one multidrug-resistant (MDR) isolate of N. gonorrhoeae through minimum inhibitory concentrations (MIC) and minimum bactericidal concentrations (MBC) tests. Results: The MDR isolate, standard strain, as well as all the clinical isolates were inhibited by MEPJ as well as all the fractions except water fraction. Chloroform fraction showed the best activity with MIC and MBC values, both being 0.2 mg/ml. Ethyl acetate fraction also showed MIC value at 0.2 mg/ml; however, MBC value was at 0.3 mg/ml. MIC and MBC values of MEPJ were both 0.3 mg/ml. Conclusion: Chloroform fraction, ethyl acetate fraction, and MEPJ bark showed the lowest MIC values and can be considered as prospective candidates for the development of antigonococcal topical drugs.

scholarly journals Pseudothrombocytopenia: an immunologic study on platelet antibodies dependent on ethylene diamine tetra-acetate

Blood ◽  
1982 ◽  
Vol 59 (1) ◽  
pp. 157-161 ◽  
Author(s):  
JG Pegels ◽  
EC Bruynes ◽  
CP Engelfriet ◽  
AE von dem Borne
Keyword(s):  
Ethylene Diamine ◽  
Igg Antibodies ◽  
Immunofluorescence Test ◽  
Igm Antibodies ◽  
Platelet Antibodies ◽  
Group Specificity ◽  
Iga Antibodies ◽  
Ethylene Diamine Tetra Acetate

Antibodies specifically reacting with platelets only in the presence of EDTA, by the platelet immunofluorescence test, were found in the serum of 20 patients with pseudothrombocytopenia due to in vitro EDTA- dependent platelet agglutination. These antibodies reacted optimally at 0–4 degree C. In 19 patients, IgG antibodies were detected; in 8 patients, IgM or IgA antibodies were also found. In one patient, only IgM antibodies were found. In 14 patients, the IgG antibodies were IgG1, but IgG2, IgG3, and IgG4 antibodies were also seen in 7 patients. The reaction of platelets with the antibodies was detectable in the presence of Na2EDTA, the K, Ca, and Mg salts of EDTA, and K2EGTA. F(ab')2 or F(ab') fragments of the IgG antibodies reached as strongly as the intact antibodies, indicating that the reaction is dependent on the antibody-combining site. The EDTA-dependent antibodies did not show platelet-group specificity. However, platelets from patients with Glanzmann disease did not react with the antibodies.

Minimal contribution of cell-bound antibodies to the immunoscintigraphy of inflamed joints with 99mTc-anti-CD4 monoclonal antibodies

2002 ◽  
Vol 41 (03) ◽  
pp. 129-134 ◽  
Author(s):  
A. Wolski ◽  
E. Palombo-Kinne ◽  
F. Wolf ◽  
F. Emmrich ◽  
W. Becker ◽  
...  
Keyword(s):  
T Cells ◽  
Monoclonal Antibodies ◽  
Synovial Membrane ◽  
In Vitro Release ◽  
Peritoneal Macrophages ◽  
Lymphoid Organs ◽  
Whole Body ◽  
Free Form ◽  
Ankle Joints

Summary Aim: The cellular joint infiltrate in rheumatoid arthritis patients is rich in CD4-positive T-helper lymphocytes and macrophages, rendering anti-CD4 monoclonal antibodies (mAbs) suitable for specific immunoscintigraphy of human/ experimental arthritis. Following intravenous injection, however, mAbs are present both in the free form and bound to CD4-positive, circulating monocytes and T-cells. Thus, the present study aimed at analyzing the relative contribution of the free and the cell-bound component to the imaging of inflamed joints in experimental adjuvant arthritis (AA). Methods: AA rat peritoneal macrophages or lymph node T-cells were incubated in vitro with saturating amounts of 99mTc-anti-CD4 mAb (W3/25) and injected i.v. into rats with AA. Results: In vitro release of 99mTc-anti-CD4 mAb from the cells was limited (on average 1.57%/h for macrophages and 0.84%/h for T-cells). Following i.v. injection, whole body/joint scans and tissue measurements showed only negligible accumulation of radioactivity in inflamed ankle joints (tissue: 0.22 and 0.34% of the injected activity, respectively), whereas the radioactivity was concentrated in liver (tissue: 79% and 71%, respectively), kidney, and urinary bladder. Unlike macrophages, however, anti-CD4 mAb-coated T-cells significantly accumulated in lymphoid organs, the inflamed synovial membrane of the ankle joints, as well as in elbow and knee joints. Conclusion: While the overall contribution of cell-bound mAbs to the imaging of arthritic joints with anti-CD4 mAbs is minimal, differential accumulation of macrophages and T-cells in lymphoid organs and the inflamed synovial membrane indicates preferential migration patterns of these 2 cell populations in arthritic rats. Although only validated for 99mTc-anti-CD4 mAbs, extrapolation of the results to other anticellular mAbs with similar affinity for their antigen may be possible.

A Simple and Inexpensive Clinical Whole Body Counter

1976 ◽  
Vol 15 (05) ◽  
pp. 248-253
Author(s):  
A. K. Basu ◽  
S. K. Guha ◽  
B. N. Tandon ◽  
M. M. Gupta ◽  
M. ML. Rehani
Keyword(s):  
The Body ◽  
Whole Body ◽  
Vitro Assay ◽  
Body Counter ◽  
Optimum Parameters ◽  
Whole Body Counter ◽  
Single Detector ◽  
Background Index ◽  
Iodide Crystal

SummaryThe conventional radioisotope scanner has been used as a whole body counter. The background index of the system is 10.9 counts per minute per ml of sodium iodide crystal. The sensitivity and derived sensitivity parameters have been evaluated and found to be suitable for clinical studies. The optimum parameters for a single detector at two positions above the lying subject have been obtained. It has been found that for the case of 131I measurement it is possible to assay a source located at any point in the body with coefficient of variation less than 5%. To add to the versatility, a fixed geometry for in-vitro counting of large samples has been obtained. The retention values obtained by the whole body counter have been found to correlate with those obtained by in-vitro assay of urine and stool after intravenous administration of 51Cr-albumin.

Evaluation of a New Preparation of Urokinase

1973 ◽  
Vol 30 (01) ◽  
pp. 114-122
Author(s):  
C.R.M Prentice ◽  
K.M Rogers ◽  
G.P McNicol
Keyword(s):  
Body Weight ◽  
Maintenance Therapy ◽  
Initial Dose ◽  
Fibrinolytic Activity ◽  
Pharmacological Effect ◽  
Whole Body ◽  
Fibrinolytic Agent ◽  
Thromboplastic Activity

SummaryThe pharmacological effect of a new preparation of urokinase (Leo) has been studied, both in vitro and in six patients suffering from thrombo-embolic disorders. It was a non-toxic, effective fibrinolytic agent if given in sufficient dosage. A regimen consisting of an initial dose of 7,200 ploug units per kg body weight, followed by hourly maintenance therapy with 3,600 ploug units per kg intravenously, gave satisfactory evidence of whole body fibrinolytic activity. The preparation had minor but insignificant thromboplastic activity both when assayed in the laboratory and when given to patients.

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