1997
DOI: 10.1016/s0969-8043(96)00041-3
|View full text |Cite
|
Sign up to set email alerts
|

Production of positron-emitting 110mIn via the process

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

2
21
0
2

Year Published

2003
2003
2015
2015

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 23 publications
(25 citation statements)
references
References 9 publications
2
21
0
2
Order By: Relevance
“…11 In particular, careful selection of the irradiation parameters can minimize the production of unwanted radionuclidic impurities. For example, 89 Zr is a promising PET radionuclide for labeling monoclonal antibodies (mAbs) for use in immuno-PET imaging, and its production via the 89 Y( p , n ) 89 Zr transmutation reaction using 100% naturally abundant 89 Y thin metal foils has been studied in detail by several groups. 39 -44 However, many previous attempts to prepare 89 Zr in high radionuclide, radiochemical, and chemical purity have suffered from diffi culties arising from the complex separation chemistry and contamination from the longer-lived nuclides 88 Zr ( t 1/2 = 83.4 days) and 88 Y ( t 1/2 = 106.626 days).…”
Section: Cyclotron-produced Pet Radionuclidesmentioning
confidence: 99%
See 1 more Smart Citation
“…11 In particular, careful selection of the irradiation parameters can minimize the production of unwanted radionuclidic impurities. For example, 89 Zr is a promising PET radionuclide for labeling monoclonal antibodies (mAbs) for use in immuno-PET imaging, and its production via the 89 Y( p , n ) 89 Zr transmutation reaction using 100% naturally abundant 89 Y thin metal foils has been studied in detail by several groups. 39 -44 However, many previous attempts to prepare 89 Zr in high radionuclide, radiochemical, and chemical purity have suffered from diffi culties arising from the complex separation chemistry and contamination from the longer-lived nuclides 88 Zr ( t 1/2 = 83.4 days) and 88 Y ( t 1/2 = 106.626 days).…”
Section: Cyclotron-produced Pet Radionuclidesmentioning
confidence: 99%
“…1 The following discussion provides an up-to-date extension of the aforementioned article and covers a more extensive range of radionuclides. In addition, the potential impact of unconventional PET radionuclides on radiation safety is considered by way of a case study on the increasingly prevalent nuclides 64 Cu, 68 Ga, 86 Y, 89 Zr, and 124 I.…”
mentioning
confidence: 99%
“…110m In can be mainly produced by two methods, direct reaction or indirectly by generator. The generator of 110 In was produced via 110 Cd( 3 He,xn) 110 Sn→ 110 In by Szelecsényi et al (1991) and 110m In generator via the 110 Cd( 3 He,3n) 110 Sn→ 110m In process was produced by Rösch et al (1997). Because of high incident proton energy in generator based production and low production yield, usage of them does not seem to be more interesting than a direct reaction to produce 110m In.…”
Section: Introductionmentioning
confidence: 99%
“…44 Scmarkierten Radiopharmaka ± auch als längerlebige Alternative im Vergleich zu 68 Ga ± neue Aufmerksamkeit zukommt. 44 Ti kann durch die 45 [81,82]. Direkte Produktionen von 110m In nach 110 Cd(p,n)-, 107 Ag(a,n)oder 109 Ag( 3 He,2n)-Prozessen populieren hauptsächlich das Isomer 110g In (T Ý = 4,9 h).…”
unclassified
“…Direkte Produktionen von 110m In nach 110 Cd(p,n)-, 107 Ag(a,n)oder 109 Ag( 3 He,2n)-Prozessen populieren hauptsächlich das Isomer 110g In (T Ý = 4,9 h). Isotop-reines 110m In ist nur über den sekundären Weg des Radionuklid-Generatorsystems 110 Sn/ 110m In zugänglich [81]. 110 Eine Reihe von 72 Se/ 72 As-Generatorkonzeptionen ist publiziert, wobei generell ein makroskopischer Selen-Trägerzusatz verwendet wurde ( [83 ± 86] u.…”
unclassified