Comparison of D-[F-18]FMAU and L-[F-18]FMAU as PET Imaging Agents for HSV1-TK Gene Expression

Authors
Moon, Byung SeokJo, Nam HyunLee, Kyo ChulEi-Gamal, Mohammed I.An, Gwang IlHong, Su HeeChoi, Tae HyunChoi, Won-KyoungPark, Jin-HunCho, Jung-HyuckCheon, Gi JeongOh, 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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