8 results on '"Edetic Acid standards"'
Search Results
2. Comprehensive Quality Control of the ITG 68Ge/68Ga Generator and Synthesis of 68Ga-DOTATOC and 68Ga-PSMA-HBED-CC for Clinical Imaging.
- Author
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Amor-Coarasa A, Schoendorf M, Meckel M, Vallabhajosula S, and Babich JW
- Subjects
- Drug Contamination prevention & control, Edetic Acid analysis, Edetic Acid chemical synthesis, Edetic Acid standards, Equipment Design, Equipment Failure Analysis, Gallium Isotopes, Gallium Radioisotopes, Isotope Labeling instrumentation, Isotope Labeling standards, New York, Octreotide analysis, Octreotide chemical synthesis, Octreotide standards, Oligopeptides analysis, Organometallic Compounds analysis, Quality Control, Edetic Acid analogs & derivatives, Octreotide analogs & derivatives, Oligopeptides chemical synthesis, Oligopeptides standards, Organometallic Compounds chemical synthesis, Organometallic Compounds standards, Radionuclide Generators instrumentation, Radionuclide Generators standards
- Abstract
Unlabelled: A good-manufacturing-practices (GMP) (68)Ge/(68)Ga generator that uses modified dodecyl-3,4,5-trihydroxybenzoate hydrophobically bound to a octadecyl silica resin (C-18) as an adsorbent has been developed that allows for dilute HCl (0.05N) to efficiently elute metal-impurity-free (68)Ga(3+) ready for peptide labeling. We characterized the performance of this generator system over a year in conjunction with the production of (68)Ga-labeled DOTATOC and Glu-NH-CO-NH-Lys(Ahx)-HBED-CC (PSMA-HBED-CC) intended for clinical studies and established protocols for batch release., Methods: A 2,040-MBq self-shielded (68)Ge/(68)Ga generator provided metal-free (68)GaCl3 ready for peptide labeling in the fluidic labeling module after elution with 4 mL of 0.05N HCl. The compact system was readily housed in a laminar flow cabinet allowing an ISO class-5 environment. (68)Ga labeling of peptides using GMP kits was performed in 15-20 min, and the total production time was 45-50 min. Batch release quality control specifications were established to meet investigational new drug submission and institutional review board approval standards., Results: Over a period of 12 mo, (68)Ga elution yields from the generator averaged 80% (range, 72.0%-95.1%), and (68)Ge breakthrough was less than 0.006%, initially decreasing with time to 0.001% (expressed as percentage of (68)Ge activity present in the generator at the time of elution), a unique characteristic of this generator. The radiochemical purity of both (68)Ga-DOTATOC and (68)Ga-PSMA-HBED-CC determined by high-performance liquid chromatography analysis was greater than 98%, with a minimum specific activity of 12.6 and 42 GBq/μmol, respectively. The radionuclidic ((68)Ge) impurity was 0.00001% or less (under the detection limit). Final sterile, pyrogen-free formulation was provided in physiologic saline with 5%-7% ethanol., Conclusion: The GMP-certified (68)Ge/(68)Ga generator system was studied for a year. The generator system is contained within the fluidic labeling module, and it is compact, self-shielded, and easy to operate using simple manual techniques. The system provides radiolabeled peptides with high (>98%) radiochemical purity and greater than 80% radiochemical yield. The (68)Ge levels in the final drug products were under the detection limits at all times. (68)Ga-DOTATOC and (68)Ga-PSMA-HBED-CC investigational radiopharmaceuticals are currently being studied clinically under investigational new drug (IND) applications submitted to the U.S. Food and Drug Administration., (© 2016 by the Society of Nuclear Medicine and Molecular Imaging, Inc.)
- Published
- 2016
- Full Text
- View/download PDF
3. Reference ranges for 51Cr-EDTA measurements of glomerular filtration rate in children.
- Author
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Blake GM, Gardiner N, Gnanasegaran G, and Dizdarevic S
- Subjects
- Adolescent, Child, Child, Preschool, Female, Humans, Infant, Infant, Newborn, Male, Radioisotope Renography methods, Radiopharmaceuticals standards, Reference Values, Retrospective Studies, United Kingdom epidemiology, Edetic Acid standards, Glomerular Filtration Rate, Kidney diagnostic imaging, Radioisotope Renography standards, Radioisotope Renography statistics & numerical data, Urinary Tract Infections diagnostic imaging, Urinary Tract Infections epidemiology
- Abstract
Background: 51Cr-Ethylenediaminetetraacetic acid (51Cr-EDTA) is widely used to measure the glomerular filtration rate (GFR) in children and adults., Aim: To produce paediatric reference data for use with the British Nuclear Medicine Society (BNMS) GFR guidelines., Methods: This was a retrospective study of children and adolescents, aged 0-17 years, undergoing combined 99mTc-dimercaptosuccinic acid (99mTc-DMSA) scintigraphy and GFR examination. GFR was evaluated from Cr-EDTA plasma clearance using blood samples taken at 2, 3 and 4 h according to the methods set out in the BNMS GFR guidelines. 99mTc-DMSA images were reviewed to identify children with normal scans., Results: Of the 45 children having a combined 99mTc-DMSA and GFR investigation, 27 (12 females, 15 males) had a normal scan result. The mean GFR (standard deviation) in the 24 subjects aged 2-17 years was 109.5 (16.8) ml . min(-1) . (1.73 m2)(-1). This compared with a predicted figure of 107.0 (17.0) ml . min(-1) . (1.73 m2)(-1) when the paediatric reference range published by Piepsz et al. was adjusted to be consistent with the BNMS GFR guidelines. When the GFR results in the present study were calculated according to the single-sample and two-sample methods used by Piepsz et al., there was close agreement with the results obtained in the latter study [116.7 (24.2) vs. 114.7 (25.8) ml . min(-1) . (1.73 m2)(-1)]. Children with abnormal 99mTc-DMSA scans had significantly lower GFR than those with normal scans (P=0.003)., Conclusion: There is a consistent difference between the GFR results in children with normal 99mTc-DMSA scans obtained in the present study and the unadjusted results of Piepsz et al. that can be explained by the different methods of calculating GFR in the two studies. Given the larger number of children in the latter study, it is proposed that centres evaluating GFR according to the BNMS method should adopt the Piepsz et al. reference range adjusted for consistency with the BNMS guidelines. This gives a mean GFR (SD) in children of 2 years and over of 107 (17) ml . min(-1) . (1.73 m2)(-1).
- Published
- 2005
- Full Text
- View/download PDF
4. New Jersey Board of Medical Examiners (NJBME) attempts to ban EDTA.
- Author
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Farfalla S
- Subjects
- Chelating Agents therapeutic use, Edetic Acid therapeutic use, Humans, New Jersey, Patient Participation, Quality Assurance, Health Care legislation & jurisprudence, State Government, Chelating Agents standards, Edetic Acid standards, Legislation, Drug, Legislation, Medical, Specialty Boards
- Published
- 2003
5. Comparison of two heavy metal chelators for treatment of lead toxicosis in cockatiels.
- Author
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Denver MC, Tell LA, Galey FD, Trupkiewicz JG, and Kass PH
- Subjects
- Animals, Body Weight, Chelating Agents standards, Edetic Acid standards, Edetic Acid therapeutic use, Female, Kidney pathology, Lead blood, Lead Poisoning drug therapy, Liver pathology, Male, Random Allocation, Spectrophotometry, Atomic veterinary, Spleen pathology, Succimer standards, Succimer therapeutic use, Survival Analysis, Thyroid Gland pathology, Bird Diseases drug therapy, Chelating Agents therapeutic use, Lead Poisoning veterinary, Psittaciformes
- Abstract
Objective: To compare efficacy and safety of meso-2,3-dimercaptosuccinic acid (DMSA) and Ca EDTA for treatment of experimentally induced lead toxicosis in cockatiels (Nymphicus hollandicus)., Animals: 137 (69 females, 68 males) healthy cockatiels between 6 months and 8 years old., Procedure: Lead toxicosis was induced by placing lead shot in the gastrointestinal tract. Treatment with Ca EDTA (40 mg/kg of body weight, IM, q 12 h), DMSA (40 or 80 mg/kg, PO, q 12 h), and sodium sulfate salts (SSS; 0.5 mg/kg, PO, q 48 h) was initiated 4 days after induction of lead toxicosis. Blood lead concentrations were determined, using atomic absorption spectrophotometry. Number of birds surviving and blood lead concentrations were compared among groups., Results: In Phase II of the study, administration of DMSA and Ca EDTA significantly decreased blood lead concentrations when used alone or in combination in birds with lead toxicosis. Addition of SSS did not result in further decreases in lead concentrations. Eight of 12 (66.7%) birds without lead toxicosis given 80 mg of DMSA/kg did not survive to the end of the study. Lesions related to treatment with chelating agents were not detected during necropsy., Conclusions and Clinical Relevance: DMSA and Ca EDTA are effective chelating agents in cockatiels. Because DMSA is administered orally, it may be easier than other chelating agents for bird owners to administer at home. However, the narrow margin of safety of DMSA indicates that this agent should be used with caution.
- Published
- 2000
- Full Text
- View/download PDF
6. Factors affecting motion characteristics of frozen-thawed stallion spermatozoa.
- Author
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Heitland AV, Jasko DJ, Squires EL, Graham JK, Pickett BW, and Hamilton C
- Subjects
- Animals, Cryopreservation methods, Cryopreservation standards, Edetic Acid standards, Egg Yolk, Glycerol standards, Lactose standards, Male, Milk standards, Semen Preservation methods, Semen Preservation standards, Time Factors, Cryopreservation veterinary, Horses physiology, Semen physiology, Semen Preservation veterinary, Sperm Motility physiology, Spermatozoa physiology
- Abstract
Five experiments were conducted to evaluate damage incurred in each processing step for cryopreservation of stallion spermatozoa. In Experiment 1, semen was centrifuged for 9 centrifugation times and the percentage of spermatozoa recovered after each treatment was calculated and spermatozoal motion characteristics analysed. Recovery of spermatozoa was > or = 80% when spermatozoa were centrifuged for > or = 10 min. Experiment 2 evaluated spermatozoa cryopreserved at 5 different concentrations in each of 2 extenders (skim milk-egg yolk-glycerol, SM-EYG; and lactose-EDTA, LAC). In SM-EYG, TMOT and PMOT were higher at spermatozoal concentrations of 20, 200 and 400 x 10(6)/ml (51%/41%, 52%/44%, 50%/43%, respectively) than for samples frozen at > or = 800 x 10(6) spermatozoa/ml (41%/35%, 32%/27%; P < 0.05). Spermatozoa frozen in LAC at a concentration of 20 x 10(6)/ml resulted in the highest TMOT and PMOT (43% and 30%, respectively, P < 0.05). The effect of freezing rate on motion characteristics of spermatozoa was evaluated in Experiment 3. The VCL of spermatozoa frozen in SM-EYG was the only parameter affected by freezing rate (P < 0.05). Experiment 4 evaluated motion characteristics after cryopreservation of spermatozoa in different sized straws (0.5 or 2.5 ml) in each of 2 extenders (SM-EYG and LAC). In SM-EYG, PMOT (38%) and VCL (109 microns/s) were highest when spermatozoa were frozen in 0.5 ml straws (P < 0.05). In Experiment 5, spermatozoa thawed immediately after cryopreservation or thawed after storage in liquid nitrogen for 24-48 h were evaluated. There was no effect of length of storage in liquid nitrogen on spermatozoal motion characteristics (P < 0.05). Experiment 6 evaluated the effects of cooling time to 5 degrees C (0, 2.5 and 5 h) on motion characteristics of spermatozoa cryopreserved in 2 extenders (SM-EYG and LAC). TMOT and PMOT were effected by cooling time, and there was a cooling-time-by-extender interaction (P < 0.05). In SM-EYG, TMOT and PMOT were higher if spermatozoa were cooled to 5 degrees C prior to initiation of freezing than if freezing was initiated at 20 degrees C (P < 0.05). A suggested protocol for cryopreservation of stallion spermatozoa would include: 1) centrifugation at 400 g for 14 to 16 min; 2) extension at 23 degrees C with SM-EYG to 400 x 10(6) spermatozoa/ml; 3) cool to 5 degrees C for 2.5 h; 4) package in 0.5 ml straws at 5 degrees C; 5) freeze in liquid nitrogen vapour at -160 degrees C; and 6) thaw for 30 s in 37 degrees C water.
- Published
- 1996
- Full Text
- View/download PDF
7. A pilot double-blind study of sodium-magnesium EDTA in peripheral vascular disease.
- Author
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Olszewer E, Sabbag FC, and Carter JP
- Subjects
- Adult, Clinical Trials as Topic, Double-Blind Method, Edetic Acid administration & dosage, Edetic Acid pharmacology, Humans, Infusions, Intravenous, Male, Middle Aged, Pilot Projects, Vascular Diseases classification, Vascular Diseases physiopathology, Edetic Acid standards, Vascular Diseases drug therapy
- Abstract
Ten male patients with peripheral vascular disease, Type 2 (LaFontaine), were randomly assigned in a double-blind study to receive either Na2 ethylene diamine tetra acetic acid (EDTA) plus MgSO4, B complex, and vitamin C, or a placebo of MgSO4, B complex, and vitamin C in Ringer's lactate solution. A total of 20 intravenous infusions were planned for administration to each patient. Clinical and laboratory (noninvasive) tests showed dramatic improvements after 10 infusions in some patients, and thus was broken the code indicating who was receiving EDTA and who was receiving placebo. The group that improved had been receiving EDTA; there was no change in the placebo group. The trial was then completed in a single-blind fashion. Patients originally assigned to receive placebo then received 10 EDTA infusions, while the group originally assigned to EDTA received 20 EDTA infusions. The group that had formerly received placebo showed improvements comparable to those seen in the first EDTA group after 10 treatments.
- Published
- 1990
8. Fluress, fluorescein and benoxinate: recovery from bacterial contamination.
- Author
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Yolton DP and German CJ
- Subjects
- Anesthetics, Local pharmacology, Anesthetics, Local standards, Chlorobutanol pharmacology, Drug Combinations pharmacology, Drug Combinations standards, Edetic Acid pharmacology, Fluoresceins pharmacology, Povidone pharmacology, Procaine pharmacology, Procaine standards, Pseudomonas aeruginosa drug effects, Staphylococcus aureus drug effects, Chlorobutanol standards, Drug Contamination prevention & control, Edetic Acid standards, Fluoresceins standards, Ophthalmic Solutions standards, Povidone standards, Procaine analogs & derivatives
- Abstract
The ability to recover from bacterial contaminations with Staphylococcus auresus and Pseudomonas aeruginosa was determined for three optometric DPAs: Fluress, fluorescein and benoxinate. Results show that Fluress recovers from contamination more rapidly than benoxinate or fluorescein. This ability to recover from contamination and the relative ease of use of Fluress may make it the DPA choice for a number of optometric procedures including applanation tonometry.
- Published
- 1980
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