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1 However, a notable amount of accumulation of 67Ga also occurs, both in vitro and in vivo, by a transf
3 DTPA, 131I-albumin (HSA), 99mTc-nanocolloid, 67Ga and 99mTc-gluceptate were evaluated as in vivo cont
4 ficity of 3Auger electron emitters, (111)In, 67Ga, and 125I, and to evaluate beta-particle emitters,
6 eviously that normal soft tissues accumulate 67Ga by a transferrin-dependent route, but uptake by tum
8 en efforts to improve oncologic imaging with 67Ga by increasing the tumor activity, or by decreasing
9 o experiments demonstrate that the uptake of 67Ga by the transferrin-independent route can be enhance
13 -methylene diphosphonate (MDP) (3-5 mCi) and 67Ga-citrate (500 microCi), were performed starting at t
14 111In-DTPA, 131I-albumin, 99mTc-nanocolloid, 67Ga-citrate and 99mTc-gluceptate with an infection Imax
20 cterize the patterns of hilar uptake (HU) on 67Ga-citrate imaging after cyclophosphamide, doxorubicin
22 ditional combination of three-phase bone and 67Ga-citrate scintigraphy can be replaced by a single in
24 Ga-DF-folate, 67Ga-deferoxamine (67Ga-DF) or 67Ga-citrate was administered by intravenous injection.
27 ellular uptake of [18F]holo-transferrin and [67Ga]citrate in various conditions, and washout of label
28 5 days, at which time either 67Ga-DF-folate, 67Ga-deferoxamine (67Ga-DF) or 67Ga-citrate was administ
30 me either 67Ga-DF-folate, 67Ga-deferoxamine (67Ga-DF) or 67Ga-citrate was administered by intravenous
33 67Ga-labeled deferoxamine-folate conjugate (67Ga-DF-folate) to target tumor cells in vivo was examin
34 20 g tumors in 15 days, at which time either 67Ga-DF-folate, 67Ga-deferoxamine (67Ga-DF) or 67Ga-citr
35 3 %ID/g for 45Ti and 8.72 +/- 0.98 %ID/g for 67Ga [%ID/g = percentage injected dose per gram]) and re
36 escent light strongly promotes the uptake of 67Ga in the cultured cells in a time-dependent and conce
37 f nuclear medicine scanning, especially with 67Ga, in the presumptive diagnosis and clinical manageme
40 of photodegraded nifedipine on the uptake of 67Ga is independent of expression of the transferrin rec
41 idity, the transferrin-independent uptake of 67Ga is significant and can be augmented to exceed trans
43 ect of calcium channel blockers on uptake of 67Ga, it was observed that, after exposure to light (eit
50 The negative predictive value of posttherapy 67Ga scan was 83.5% for all patients; however, when calc
54 mong the remaining 97 patients with negative 67Ga scans, 16 patients relapsed, including five with st
63 to reconcile the differences with respect to 67Ga uptake as a function of tumor grade and type in the
65 ors are variable in gallium-avidity, whether 67Ga uptake is a transferrin-independent or dependent pr
66 ial therapy for RPMP, resolution of abnormal 67Ga uptake over time may provide an objective endpoint
70 ficant differences were found when 201Tl and 67Ga were compared in the intermediate, high or Hodgkin'
71 delivered disintegrations per cell, 131I and 67Ga were the most potent of the radionuclides tested, w
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