Comparison of D-[F-18]FMAU and L-[F-18]FMAU as PET Imaging Agents for HSV1-TK Gene Expression
- Authors
- Moon, Byung Seok; Jo, Nam Hyun; Lee, Kyo Chul; Ei-Gamal, Mohammed I.; An, Gwang Il; Hong, Su Hee; Choi, Tae Hyun; Choi, Won-Kyoung; Park, Jin-Hun; Cho, Jung-Hyuck; Cheon, Gi Jeong; Oh, Chang-Hyun
- Issue Date
- 2010-11-20
- Publisher
- KOREAN CHEMICAL SOC
- Citation
- BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.31, no.11, pp.3309 - 3312
- Abstract
- D-[(18) F]FMAU and L-[F-18]FMAU are F-18 labeled nucleoside analogue which have been efficiently synthesized in order to be a PET imaging probe D-[F-18]FMAU and L-[F-18]FMAU were compared as PET imaging agents using HSV1-TK gene expressing tumor-bearing mice Their cellular uptake profiles were also compared using MCA and MCA-TK cell lines D-[F-18]FMAU demonstrated higher cellular uptake and higher accumulation in MCA-TK tumor regions than L-[F-18]FMAU On the other hand, L-[F-18]FMAU showed higher MCA-TK/MCA ratio of %ID/g than that of D-[F-18]FMAU L-[F-18]FMAU can be utilized as a good candidate for HSV1-TK PET imaging It can be used for antiviral drug evaluation
- Keywords
- VIRUS THYMIDINE KINASE; IN-VIVO; DNA-SYNTHESIS; FIALURIDINE; CARCINOMA; THERAPY; FIAU; VIRUS THYMIDINE KINASE; IN-VIVO; DNA-SYNTHESIS; FIALURIDINE; CARCINOMA; THERAPY; FIAU; HSV1-TK; D-[F-18]FMAU; L-[F-18]FMAU; PET imaging; MicroPET
- ISSN
- 0253-2964
- URI
- https://pubs.kist.re.kr/handle/201004/130911
- DOI
- 10.5012/bkcs.2010.31.11.3309
- Appears in Collections:
- KIST Article > 2010
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