technetium-tc-99m-exametazime has been researched along with Escherichia-coli-Infections* in 5 studies
1 review(s) available for technetium-tc-99m-exametazime and Escherichia-coli-Infections
1 trial(s) available for technetium-tc-99m-exametazime and Escherichia-coli-Infections
4 other study(ies) available for technetium-tc-99m-exametazime and Escherichia-coli-Infections
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99mTc-HMPAO-labeled autologous versus heterologous leukocytes for imaging infection.
Radiolabeled autologous leukocytes are the gold standard for imaging infectious foci in patients. Good results have also been reported for radiolabeled heterologous leukocytes from noninfected donors. Until now, the 2 methods have not been directly compared. In this study, we compared the infection-imaging potential of 99mTc-hexamethylpropyleneamine oxime (HMPAO)-labeled autologous granulocytes with that of 99mTc-HMPAO-labeled granulocytes from either infected or noninfected donors in rabbits with Escherichia coli infection.. The radiolabeled granulocyte preparations were studied in rabbits with an E. coli infection in the left calf muscle. The soft-tissue infections were scintigraphically visualized after injection of 18 MBq of either 99mTc-HMPAO purified autologous granulocytes or radiolabeled purified heterologous granulocytes from infected or noninfected donor rabbits. Gamma camera images were acquired at 2 min and at 1, 2, and 4 h after injection. After the last image, the rabbits were killed and uptake of the radiolabel in the dissected tissues was determined.. The 99mTc-HMPAO autologous granulocytes and heterologous granulocytes from infected donors accurately revealed the infectious focus in the calf muscle at 2 h after injection. At 4 h after injection, a significantly better (P < 0.05) delineation of the infection was established with the 99mTc-HMPAO autologous granulocytes and 99mTc-HMPAO heterologous granulocytes from the infected rabbits than with the heterologous granulocytes from noninfected donors. With both cell preparations, the intensity of uptake in the infected calf muscle continuously increased until 4 h after injection. The 99mTc-HMPAO heterologous granulocytes from noninfected donors showed no significant increase in contrast after 2 h after injection. Absolute uptake in the infected calf muscle was much higher for 99mTc-HMPAO autologous granulocytes (7.81 +/- 1.21 percentage injected dose [%ID]) and 99mTc-HMPAO heterologous infected granulocytes (8.91 +/- 1.92 %ID) than for the radiolabeled heterologous noninfected granulocytes (2.32 +/- 0.75 %ID) (P < 0.04) at 4 h after injection. The ratio of infected muscle to noninfected contralateral muscle was significantly higher for 99mTc-HMPAO autologous granulocytes and 99mTc-HMPAO heterologous granulocytes from infected donors than for 99mTc-HMPAO heterologous granulocytes from noninfected donors (5.53 +/- 1.09, 3.86 +/- 0.75, and 1.86 +/- 0.31, respectively; P < 0.05).. For nuclear medicine imaging of infection, purified granulocytes derived from infected rabbits are superior to purified granulocytes derived from noninfected donor rabbits. In addition, autologous granulocytes gave similar results to heterologous granulocytes from infected donor rabbits, suggesting the need for intrinsic cell activation for specific granulocyte migration. Topics: Abscess; Animals; Escherichia coli Infections; Female; Granulocytes; Hindlimb; Leukocytes; Rabbits; Radionuclide Imaging; Technetium Tc 99m Exametazime; Time Factors; Tissue Distribution; Transplantation, Autologous; Transplantation, Heterologous | 2002 |
Tc-99m HMPAO leukocyte and Tc-99m nanocolloid scintigraphy in posttraumatic bone infection.
Posttraumatic osteomyelitis was investigated in 23 patients using nuclear medicine techniques. Tc-99m hexamethylpropilene amine oxime (HMPAO)-labeled leukocyte scintigraphy was performed in 11 patients, and Tc-99m nanocolloid scanning was performed in the other 12 patients. The scintigraphic findings were compared with clinical, laboratory, radiologic, and bacteriologic results. The findings on leukocyte imaging were consistent with the clinical symptoms in 7 of 11 patients, with the laboratory pattern in 7 of 10 patients, with the radiologic findings in 7 of 11 patients, and with the results of bacteriology in 6 of 7 patients. The findings on nanocolloid scintigraphy corresponded with the clinical symptoms in 9 of 12 patients, with the laboratory pattern in 8 of 10 patients, with the radiologic findings in 8 of 12 patients, and with the bacteriology in 4 of 5 patients. The results suggest that both methods were of similar value for the detection of chronic posttraumatic osteomyelitis regardless of whether the process was active. Conversely, on the basis of semiquantitative analysis of the images, leukocyte scintigraphy seemed to characterize the grade of inflammation better than did nanocolloid scintigraphy. Topics: Adult; Aged; Bone and Bones; Chronic Disease; Escherichia coli Infections; Female; Femur; Follow-Up Studies; Humans; Leukocytes; Male; Middle Aged; Osteomyelitis; Proteus Infections; Radiography; Radionuclide Imaging; Radiopharmaceuticals; Staphylococcal Infections; Technetium Tc 99m Aggregated Albumin; Technetium Tc 99m Exametazime; Thumb; Tibia | 1998 |
Detecting infection and inflammation with technetium-99m-labeled Stealth liposomes.
The performance of 99mTc Stealth liposomes was investigated in various rat models.. Preformed polyethyleneglycol-containing liposomes with encapsulated reduced glutathione, were radiolabeled using the lipophilic 99mTc-HMPAO. The labeled liposomes were intravenously administered to rats with focal S. aureus or E. coli infection, or turpentine-induced inflammation. For comparison, Tc-99m-nanocolloid- and 99mTc-labeled nonspecific IgG were tested. In rats with Pneumocystis carinii pneumonia (PCP), Tc-99m-liposomes were directly compared to In-111 labeled nonspecific IgG.. Technetium-99m-liposomes accumulated in the infectious and inflammatory muscle foci over 24 hr (0.59% injected dose per gram tissue (%ID/g) for S. aureus; 1.18 %ID/g for turpentine). Abscess-to-muscle ratios increased to values as high as 24.0, 41.7 and 44.5 for the respective models at 24 hr postinjection. Technetium-99m-liposomes visualized the foci as early as 1 hr postinjection. Technetium-99m-IgG visualized S. aureus infection, but abscess-to-muscle ratios and abscess uptake at the later time points were significantly lower. Technetium-99m-nanocolloid failed to visualize any of the muscle foci. In PCP however, 99mTc-liposomes did not show preferential localization in the infection. The control agent 111In-IgG showed a significant, two-fold increase in lung uptake.. Technetium-99m-Stealth liposomes preferentially accumulated in abscesses, leading to very high target-to-nontarget ratios. This property appears to be related to a process based on uptake of long-circulating particles. In a specific type of infection, i.c. PCP, 99mTc-liposomes did not accumulate in diseased lung tissue, thus mimicking the in vivo behavior of labeled leukocytes. Topics: Abscess; Animals; Escherichia coli Infections; Female; Immunoglobulin G; Indium Radioisotopes; Inflammation; Liposomes; Male; Organotechnetium Compounds; Oximes; Pneumonia, Pneumocystis; Radioimmunodetection; Rats; Rats, Sprague-Dawley; Rats, Wistar; Staphylococcal Infections; Technetium Tc 99m Aggregated Albumin; Technetium Tc 99m Exametazime; Tissue Distribution | 1996 |
New efficient cell-labeling method with Tc-99m pertechnetate via neutral and lipid soluble Sn(II)--mercaptopyridine N-oxide complex and comparative evaluation with Tc-99m HMPAO labeled platelets.
Topics: Animals; Blood Platelets; Cattle; Cell Survival; Escherichia coli Infections; Humans; Indium Radioisotopes; Isotope Labeling; Lipids; Mice; Organometallic Compounds; Organotechnetium Compounds; Osteomyelitis; Oximes; Pyridines; Rabbits; Radionuclide Imaging; Sodium Pertechnetate Tc 99m; Solubility; Technetium Tc 99m Exametazime; Thiones; Tissue Distribution; Tropolone | 1990 |