• Nuclear Medicine and Molecular Imaging
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• 제41권2호
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• pp.78-84
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• 2007

Quantitative analysis of dynamic brain PET data using a tracer kinetic modeling has played important roles in the investigation of functional and molecular basis of various brain diseases. Parametric imaging of the kinetic parameters (voxel-wise representation of the estimated parameters) has several advantages over the conventional approaches using region of interest (ROI). Therefore, several strategies have been suggested to generate the parametric images with a minimal bias and variability in the parameter estimation. In this paper, we will review the several approaches for parametric imaging with linearized methods which include graphical analysis and mulilinear regression analysis.

• 대한핵의학회:학술대회논문집
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• 대한핵의학회 2001년도 제40차 춘계학술대회 및 연수교육
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• pp.51-55
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• 2001

Regional MBF and MRGlc can be accurately estimated with N-13 ammonia and FDG PET using tracer kinetic methods including compartmental and non-compartmental approaches. Compartment modeling approaches are physiologically well characterized, but are methodologically more complicated. Noncompartmental analysis are easier to implement while the limitations and assumptions of the methods should be understood prior to the application of the method.

• Nuclear Medicine and Molecular Imaging
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• 제43권4호
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• pp.253-258
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• 2009

Bone scintigraphy using $^{99m}$Tc-labeled phosphate agents has long been the standard evaluation method for whole skeletal system. However, recent shortage of $^{99m}$Tc supply and advanced positron emission tomography (PET) technology evoked the attention to surrogate radiopharmaceuticals and imaging modalities for bone. Actually, fluorine-18 ($^{18}$F) was the first bone seeking radiotracer before the introduction of $^{99m}$Tc-labeled agents even though its clinical application failed to become pervasive anymore after the rapid spread of Anger type gamma camera systems in early 1970s. However, rapidly developed PET technology made us refocus on the usefulness of $^{18}$F as a PET tracer. Early study comparing $^{18}$F-Na PET scan and planar bone scintigraphy reported that PET has higher sensitivity and specificity in the diagnosis of metastatic bone lesions than planar bone scan. Subsequent reports comparing between PET and both planar and SPECT bone image also revealed better results of PET scan in similar study groups. Rapid clinical application of PET/CT also accumulated considerable amount of experiences in skeletal evaluation and this modality is known to have better diagnostic power than stand alone PET system as well as bone scan. Furthermore $^{18}$F-Na PET/CT revealed better or at least equal results in detection of primary and metastatic bone lesions compared with CT and MRI. Therefore, it is obvious that $^{18}$F-Na PET/CT has potential to become new imaging modality for practical skeletal evaluation so continuous and careful evaluation of this modality and radiopharmaceutical must be required.

• 한국컴퓨터정보학회논문지
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• 제12권2호
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• pp.123-130
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• 2007

본 논문에서는 소동물 생체내 실험시 서로 다른 장비에서 획득된 영상의 융합 및 정합을 위한 방법을 제안한다. 마우스의 꼬리 정맥에 $[[^{18}F]FDG$를 주사하여 60분 섭취후 서로 다른 장비에서 동일한 위치의 영상을 획득하기 위하여 아크릴 재질의 소동물 가이드에 기준마크를 설정하고 microPET과 CT 영상을 획득하였다. MicroPET으로 획득된 리스트모드(list-mode) 데이터는 Fourier Rebinning(FRB) 방법을 사용하여 사이노그램(Sinogram)으로 변환 후 4 번의 반복횟수를 가지는 Ordered Subset Expectation Maximization(OSEM) 알고리즘으로 재구성하였다. MicroPET 영상획득후 PET/CT의 CT를 이용하여 CT영상을 획득하였다. MicroPET 영상에서 폐영역을 정확히 찾아내는 어려움이 있어. 해부학적 정보를 제공하는 CT 영상을 이용하여 폐 영역을 구분하였다. 영상 융합을 위한 불일치 부분을 해결하기 위하여 기준마크의 정보와 폐 영역의 정보를 이용하여 회전과 이동정보를 가지는 어파인 (affine) 변환 행렬 구하여 영상 정합에 사용하였다. 이 방법은 정량적 정확성과 영상 해석의 정확성을 개선할 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제25권4호
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• pp.506-510
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• 2004

There have been intensive studies concerning $[^{11}F]$choline ($[^{11}F]$methyldimethyl( ${\beta}$ -hydroxyethyl) ammonium) (1) which is known as a very effective tracer in imaging various human tumors localized in brain, lung, esophagus, rectum, prostate and urinary bladder using Positron Emission Tomography (PET) and there is increasing interest in $^{18}F$ labelled choline (2) and proved to be useful to visualize prostate cancer. We have prepared six $^{18}F$ labelled alkyl choline derivatives (3a-3c, 4a-4c) from ditosylated and dibrominated alkanes in moderate yields. The six alkyl tosylate or bromate ammonium salts have been synthesized as precursors. Radiofluorination was achieved by the treatment of precursors with $^{18}F$ - in the presence of Kryptofix-2.2.2.. The labeling yields varied ranging from 7 to 25%.

• 대한핵의학회지
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• 제29권4호
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• pp.533-540
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• 1995

정량적인 PET 영상에서는 감쇠보정이 매우 중요하며 가장 정확한 방법은 투과스캔을 관심부위에 실시하여 측정된 감쇠보정영상을 만들고, 이를 같은 부위에서 실시한 방출 영상의 재구성에 적용하는 것이다. 기존의 방법은 투과스캔 후에 추적자가 섭취되기까지 장시간이 경과된 후 방출스캔을 하므로 PET스캐너의 효율적 사용에 제한이 있었다. 따라서, 스캔시간을 단축하고 촬영중 환자가 움직일 가능성을 최소화시켜 영상의 질을 개선하고 PET스캐너의 효율을 높이기 위하여, 추적자를 주사한 후 투과 및 방출스캔을 동시에 실시하여, 투과스캔에서의 측정치를 왜곡시키는 방출계수를 빼주는 T+E 감쇠보정 방법을 실행하였다. 배후에는 F-l8 fluoride ion $0.4{\mu}Ci/cc$의 방사능을 가진 물을 실린더 모형(5750 cc)에 채우고, 목적물을 나다내는 1개의 삽입물 실린더(276 cc)에는 F-18 fluoride ion $4.3{\mu}Ci/cc$의 방사능을 주입하고 공기를 주입한 삽입물 실린더와 테플론으로 이루어진 삽입물 실린더를 사용하여 T+E 방법의 특성을 고찰하였다. 투과용선원으로 Ge-68(10 mCi) 회전 핀선원을 사용하여 5시간 동안에 T+E 스캔을 5분, 10분, 20분, 방출스캔을 20분씩 교대로 5차례 실행하여 투과 및 방출영상이 최종 방출영상에 미치는 오차를 측정하였다. T+E 스캔으로 감쇠보정한 방출영상과 기준 투과영상으로 감쇠보정한 방출영상을 비교하면, 목적물의 방사능이 $1.0{\mu}Ci/cc$일 경우 T+E 감쇠보정 방법의 오차는 2.6%이었으며 이 오차는 목적물의 방사능이 줄어들수록 더욱 감소하였다. 또한, T+E 방법으로 구성된 방출영상의 노이즈는 기준 투과스캔 방법으로 보정된 영상에 비하여 유의한 차이를 보이지 않았다. 그러므로, 회전 핀선원과 투과 및 방출 동시 영상 방법을 사용하여 정확한 감쇠보정을 할 수 있었으며 이 방법은 임상 PET 영상에서 환자당 스캔시간을 줄임으로써, 환자의 움직임으로 인하여 발생할 수 있는 오차를 최소화하여 PET 스캐너의 효율을 높일 수 있었다.

• Brain Tumor Research and Treatment
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• 제6권2호
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• pp.47-53
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• 2018

Brain tumors represent a diverse spectrum of histology, biology, prognosis, and treatment options. Although MRI remains the gold standard for morphological tumor characterization, positron emission tomography (PET) can play a critical role in evaluating disease status. This article focuses on the use of PET with radiolabeled glucose and amino acid analogs to aid in the diagnosis of tumors and differentiate between recurrent tumors and radiation necrosis. The most widely used tracer is $^{18}F$-fluorodeoxyglucose (FDG). Although the intensity of FDG uptake is clearly associated with tumor grade, the exact role of FDG PET imaging remains debatable. Additionally, high uptake of FDG in normal grey matter limits its use in some low-grade tumors that may not be visualized. Because of their potential to overcome the limitation of FDG PET of brain tumors, $^{11}C$-methionine and $^{18}F$-3,4-dihydroxyphenylalanine (FDOPA) have been proposed. Low accumulation of amino acid tracers in normal brains allows the detection of low-grade gliomas and facilitates more precise tumor delineation. These amino acid tracers have higher sensitivity and specificity for detecting brain tumors and differentiating recurrent tumors from post-therapeutic changes. FDG and amino acid tracers may be complementary, and both may be required for assessment of an individual patient. Additional tracers for brain tumor imaging are currently under development. Combinations of different tracers might provide more in-depth information about tumor characteristics, and current limitations may thus be overcome in the near future. PET with various tracers including FDG, $^{11}C$-methionine, and FDOPA has improved the management of patients with brain tumors. To evaluate the exact value of PET, however, additional prospective large sample studies are needed.

• 대한방사성의약품학회지
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• 제2권2호
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• pp.113-117
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• 2016

As a neurotransmitter, serotonin plays important roles in brain. It relates various neuropsychiatric disorders such as anxiety, depression, schizophrenia. [$^{11}C$]DASB is a well-known PET tracer for serotonin transporter imaging. In this study, we synthesized [$^{11}C$]DASB in HPLC loop for simple and rapid production. Total synthesis time was about 40 minutes and the radiochemical purities were over 99%. The specific activity was $51.4GBq/{\mu}mole$ (n=16). [$^{11}C$]DASB showed highest uptake in mid-brain that serotonergic nerves are abundant and lowest uptake in cerebellum. In conclusion, we used HPLC loop method for [$^{11}C$]DASB labeling and this method is useful for production of $^{11}C$ labeled PET tracers.

• 대한방사성의약품학회지
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• 제6권2호
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• pp.69-74
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• 2020

PIB is the first amyloid plaque PET image tracer reported for the first time in 2003, and is considered to be the best and is still being utilized due to its very high uptake and kinetic properties. Initially, it was synthesized by radioisotope labeling using a precursor containing a methoxy methyl protection group, but now it is synthesized using a 6-OH precursor that can be easily synthesized in one step using [¹¹C]methyl triflate. Carbon-11 has several limitations in clinical studies using PET because its half-life is as short as 20 minutes. In this study, in order to overcome the difficulty of this half-life, a rapid method using Sep-Pak was adopted instead of HPLC purification to significantly reduce the burden of the purification process and attempted synthesis. As a result, the synthesis time was shortened by more than 50%, and the yield of the final compound was higher than the previous result and showed relatively high specific radioactivity, confirming that it is a strategic method with high applicability for various precursors having primary amines.

• Bulletin of the Korean Chemical Society
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• 제26권1호
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• pp.91-96
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• 2005

O-(3-[$^{18}$F]Fluoropropyl)-L-tyrosine (L-[$^{18}$F]FPT) was synthesized by nucleophilic radiofluorination followed by acidic hydrolysis of protective groups and evaluated with 9 L tumor bearing rat. L-[$^{18}$F]FPT is an homologue of O-(2-[$^{18}$F]fluoroethyl)-L-tyrosine (L-[$^{18}$F]FET) which recently is studied as a tracer for tumor imaging using positron emission tomography (PET). [$^{18}$F]FPT was directly prepared from the precursor of O-(3-ptoluenesulfonyloxypropyl)- N-(tert-butoxycarbonyl)-L-tyrosine methyl ester. FPT-PET image was obtained at 60 min in 9 L tumor bearing rats. The radiochemical yield of [$^{18}$F]FPT was 0-45% (decay corrected) and the radiochemical purity was more than 95% after HPLC purification. The total time elapsed for the synthesis of [$^{18}$F]FPT was 100 min from EOB (End-of-bombardment). A comparison of uptake studies between [$^{18}$F]FPT and [$^{18}$F]FET was performed. In biodistribution, [$^{18}$F]FPT showed similar pattern with [$^{18}$F]FET in various tissues, but [$^{18}$F]FPT showed low uptake in brain. Furthermore, [$^{18}$F]FPT showed higher tumor-to-brain ratio than [$^{18}$F]FET. In conclusion, [$^{18}$F]FPT seems to be more useful amino acid tracer than [$^{18}$F]FET for brain tumors imaging with PET.