• Title/Summary/Keyword: Gallium-68 ($^{68}Ga$)

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PET/CT에서 Phantom을 이용한 Fluorine-18, Gallium-68 방사성 핵종의 PET 영상 평가 (Evaluation of PET Image for Fluorine-18 and Gallium-68 using Phantom in PET/CT)

  • 윤석환
    • 대한방사선기술학회지:방사선기술과학
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    • 제41권4호
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    • pp.321-327
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    • 2018
  • The purpose of this study is to compare PET imaging performance with Fluorine-18 ($^{18}F$) and Gallium-68 ($^{68}Ga$) for influence of physical properties of PET tracer. Measurement were performed on a Siemens Biograph mCT64 PET/CT scanner using NEMA IEC body phantom and Flangeless Esser PET phantom containing filled with $^{18}F$ and $^{68}Ga$. Emission scan duration(ESD) was set to 1, 2, 3, 4 and 5min/bed for $^{68}Ga$ and 1min/bed for $^{18}F$. The PET image were evaluated in terms of contrast, spatial resolution. Under same condition, The percentage of contrast recovery measured in the phantom ranged from 16.88% to 72.56% for $^{68}Ga$ and from 27.51% to 74.43% for $^{18}F$ and The FWHM value to evaluate spatial resolution was 10.96 mm for $^{68}Ga$ and 9.19 mm for $^{18}F$. For this study, $^{18}F$ produces better image contrast and spatial resolution than $^{68}Ga$ due to higher positron yield and lower positron energy ($^{18}F$: 96.86%, 633.5 keV, $^{68}Ga$: 88.9%, 1899 keV), The physical properties of PET tracer effect on the PET image. $^{68}Ga$ image applying ESD of 3, 4, 5min/bed were showed similar to $^{18}F$ image with ESD of 1min/bed. This study suggests that increasing ESD for acquiring $^{68}Ga$ PET image seem to be similar to $^{18}F$ image.

임상용 Ga-68 표지 방사성의약품의 합성을 위한 자동합성장치 개발 (Development of an Automated Synthesizer for the Routine Production of Ga-68 Radiopharmaceuticals)

  • 박준영;손정민;강원준
    • 대한임상검사과학회지
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    • 제55권4호
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    • pp.253-260
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    • 2023
  • Germanium-68/gallium-68 (68Ge/68Ga) 제너레이터는 의료용가속기에 비해 크기가 작아 공간적 활용도가 높고 유지비가 저렴하고, Ga-68 표지 방사성의약품의 생산방식이 간편하기 때문에 세계적으로 사용빈도가 급격히 증가하고 있다. 이에 본 연구에서는 제작비용이 낮으며 사용이 쉽고 유지보수가 용이한 Ga-68 표지 방사성의약품 전용 자동합성장치를 개발하고자 하였다. 본 연구에서 개발한 자동합성장치에 사용된 부품들은 대부분 국내에서 생산된 제품들을 사용하여 생산 단가를 낮추었고, 자체 구동프로그램을 개발하여 사용자 편의성을 높였다. 또한, 자동합성장치의 시스템 평가를 통해 작동에 이상이 없음을 확인하였고, 68Ga-DOTA-[Tyr3]-octreotide 합성 프로그램을 사용하여 조제 시 안정된 표지 수율과 임상적용 기준을 만족하는 품질관리 결과를 획득하였다. 최근 다양한 Ga-68 표지 방사성 의약품이 개발되고 있어 본 연구를 통해 개발한 방사성의약품 전용 자동합성장치는 추후 보다 유용하게 사용될 것으로 사료된다.

Preliminary Study on Separation of Germanium and Gallium for Development of a 68Ge/68Ga Generator

  • Lee, Heung Nae;Kim, Sang Wook;Park, Jeong Hoon;Kim, Injong;Yang, Seung Dae;Hur, Min Goo
    • 방사선산업학회지
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    • 제5권2호
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    • pp.101-106
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    • 2011
  • The separation of germanium and gallium ion with metal oxide was introduced into the development of $^{68}Ge/^{68}Ga$ generator. Germanium and gallium within mixed solution were respectively separated by using a liquid-liquid extraction and a column chromatographic method. The separation of Ge within high concentrated hydrochloric and sulfuric acid was conducted by the extraction to $CCl_4$ and the back-extraction to 0.05 M HCl. An optimum condition of the extraction by $CCl_4$ was in 5~7 M HCl and efficiency was around 80%. The gallium was selectively separated by using $Al_2O_3$ among metal oxides as sorbents from the mixed solution in 0.04~0.10 M HCl condition.

카세트 기반 자동합성장치를 사용한 [68Ga]Ga-FAPI-04의 합성방법 연구 (Development of a Synthetic Method for [68Ga]Ga-FAPI-04 Using a Cassette-based Synthesizer)

  • 박준영;강원준
    • 대한임상검사과학회지
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    • 제56권1호
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    • pp.43-51
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    • 2024
  • [68Ga]Ga-FAPI-04는 암세포에 과발현 되어 있는 fibroblast activation protein (FAP)에 특이적으로 결합하는 FAP 저해제(FAP inhibitor, FAPI)에 방사성동위원소 68Ga을 표지한 방사성의약품이다. 본 연구에서는 국내에서 제작된 카세트기반 자동합성장치를 사용하여 [68Ga]Ga-FAPI-04를 제조하는 방법을 개발하였다. [68Ga]Ga-FAPI-04의 합법을 개발하기 위해 완충액 HEPES의 농도, 반응시간, FAPI-04 전구체 양, 반응온도에 따른 표지효율을 확인하였다. [68Ga]Ga-FAPI-04는 2 M HEPES를 사용하여 pH 3.85에서 반응할 경우 가장 높은 표지효율을 획득할 수 있었고, 반응시간이 10분일 경우와 25 ㎍의 FAPI-04 전구체를 사용할 경우 및 100℃에서 반응할 경우 가장 높은 표지효율을 획득할 수 있었다. 또한 최종 합성된 [68Ga]Ga-FAPI-04는 모든 품질기준을 만족하여 본 연구를 통해 개발된 [68Ga]Ga-FAPI-04의 합성법은 FAPI 기반 방사성의 약품생산에 활용도가 높을 것으로 예상된다.

Chelators for 68Ga radiopharmaceuticals

  • Seelam, Sudhakara Reddy;Lee, Yun-Sang;Jeong, Jae Min
    • 대한방사성의약품학회지
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    • 제2권1호
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    • pp.22-36
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    • 2016
  • $^{68}Ga$ is a promising radionuclide for positron emission tomography (PET). It is a generator-produced ($^{68}Ge/^{68}Ga$-generator) radionuclide with a half-life of 68 min. The employment of $^{68}Ga$ for basic research and clinical applications is growing exponentially. Bifunctional chelators (BFCs) that can be efficiently radiolabeled with $^{68}Ga$ to yield complexes with good in vivo stability are needed. Given the practical advantages of $^{68}Ga$ in PET applications, gallium complexes are gaining increasing attention in biomedical imaging. However, new $^{68}Ga$-labeled radiopharmaceuticals that can replace $^{18}F$-labeled agents like [$^{18}F$]fluorodeoxyglucose (FDG) are needed. The majority of $^{68}Ga$-labeled derivatives currently in use consist of peptide agents, but the development of other agents, such as amino acid or nitroimidazole derivatives and glycosylated human serum albumin, is being actively pursued in many laboratories. Thus, the availability of new $^{68}Ga$-labeled radiopharmaceuticals with high impact is expected in the near future. Here, we present an overview of the different new classes of chelators for application in molecular imaging using $^{68}Ga$ PET.

Fully automated radiosynthesis of [68Ga]edotreotide ([68Ga]DOTA-TOC) and its quality controls

  • Park, Hyun Sik;Lee, Hong Jin;An, Hyun Ho;Moon, Byung Seok;Lee, Byung Chul;Lee, Won Woo;Kim, Sang Eun
    • 대한방사성의약품학회지
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    • 제3권2호
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    • pp.85-90
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    • 2017
  • $^{68}Ga-PET$ is of growing importance in the practice of nuclear medicine diagnostic imaging for neuroendocrine tumors as well as prostate cancers. Following this interests, we herein present the radiosynthesis process of [$^{68}Ga$]edotreotide ([$^{68}Ga$]DOTA-TOC) based on the fully automated procedure for clinical doses that can be provided the reduction of radiation exposure and high reproducibility. The quality controls of clinical doses in compliant with European Pharmacopoeia are also discussed.

Development of Freeze-Dried DOTMP Kits for Labeling with 68Ga

  • Lim, Jae Cheong;Choi, Sang Mu;Cho, Eun Ha;Lee, So Young;Dho, So Hee;Kim, Soo Yong
    • 방사선산업학회지
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    • 제9권2호
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    • pp.63-68
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    • 2015
  • Lyophilized DOTMP kits were prepared using DOTMP, ammonium acetate, and ascorbic acid. The $^{68}Ga$-DOTMP was prepared by incubating the kit dissolved in 0.5 ml of concentrated $^{68}Ga$ using NaCl method and 0.5 ml of DDW, at $100^{\circ}C$ for 7 min. The labeling yield was evaluated by two solvent systems of TLC. 1 MBq of concentrated $^{68}Ga$ was labeled with $0.8{\mu}g$ of DOTMP by high radiolabeling yield (>98%), which was determined by two TLC methods. The composition of the prepared freeze-dried vial is $400{\mu}g$ of DOTMP, 19.27 mg of ammonium acetate and 17.62 mg of ascorbic acid. ~555 MBq of $^{68}Ga$-DOTMP was prepared with excellent radiochemical purity (>98%) and it was stable for 4 hr at room temperature. In conclusion, Freeze-dried DOTMP kits for the convenient preparation of $^{68}Ga$-DOTMP have been developed. Availability of this kit is expected to stimulate the widespread use of $^{68}Ga$-DOTMP in the fields of nuclear medicine.

니트로벤젠溶液 및 1,2,4-트리클로로벤젠 溶液內에서의 브롬化갤륨과 브롬化에칠과의 相互作用 (The Interaction of Gallium Bromide with Ethyl Bromide in Nitrobenzene and in 1,2,4-Trichlorobenzene)

  • 최상업
    • 대한화학회지
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    • 제7권1호
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    • pp.65-68
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    • 1963
  • The solubility of ethyl bromide in nitrobenzene and in 1,2,4-trichlorobenzene has been measured at $19^{\circ}$ in the presence and absence of gallium bromide. When gallium bromide does not exist in the system, the solubility of ethyl bromide in nitrobenzene is greater than in 1,2,4-trichlorobenzene, indicating the stronger interaction of ethyl bromide with nitrobenzene than with 1,2,4-trichlorobenzene. When there exists gallium bromide in the system, an unstable 1: 1 complex, C2H5Br·GaBr3, of gallium bromide with ethyl bromide is formed in the solution. The 1: 1 complex in solution dissociates into the components to a large extent according to one of the following equilibria or both: $C_2H_5Br{\cdot}GaBr_3{\rightleftarrows}C_2H_5Br+GaBr_3$C_2H_5Br{\cdot}GaBr_3{\rightleftarrows}C_2H_5Br+1}2GaBr_3$$ The stability of the 1: 1 complex of ethyl bromide with gallium bromide is compared with that of the corresponding complex of methyl bromide.

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양전자 방출핵종 $^{68}$Ga을 이용한 NOTA와 DOTA의 표지 및 시험관내 특성 연구 (Radiolabeling of NOTA and DOTA with Positron Emitting $^{68}$Ga and Investigation of In Vitro Properties)

  • 정재민;김영주;이윤상;이동수;정준기;이명철
    • Nuclear Medicine and Molecular Imaging
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    • 제43권4호
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    • pp.330-336
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    • 2009
  • 목적: $^{68}$Ge/$^{68}$Ga-제너레이터에서 생산되는 PET용 방사성동위원소인 $^{68}$Ga을 NOTA와 DOTA에 표지하는 조건을 확립하고 이의 안정성 및 단백질 결합 특성을 연구하였고, 여러 가지의 금속이온 공존시 표지효율에 미치는 영향도 관찰하였다. 대상 및 방법: 여러 가지 농도의 NOTA 3HCl과 DOTA 4HCl에 $^{68}$Ge/$^{68}$Ga-제너레이터에서 0.1 M HCl로 용출한 $^{68}$GaCl$_3$ 6.66$\sim$272.8 MBq 1.0 mL와 합치고 초산나트륨 또는 탄산나트륨 완충액을 사용하여 다양한 pH 조건에서 반응하였다. 다양한 금속이온(CuCl$_2$, FeCl$_2$, InCl$_3$, FeCl$_3$), GaCl$_3$, MgCl$_2$, CaCl$_2$)과 0.373 mM NOTA를 $^{68}$Ga(6.77$\sim$8.58 MBq)으로 표지할 때 표지효율을 관찰하였다. $^{68}$Ga의 표지효율은 ITLC-SG고정상으로 하고 아세톤과 생리식염수를 이동상으로 하여 측정하였다. 최적의 pH 조건에서 $^{68}$Ga-NOTA와 $^{68}$Ga-DOTA를 표지한 후 4 시간 동안 안정성을 확인하고, 사람 혈청에서의 단백질 결합능을 평가하였으며, 지용성 정도를 측정하기 위하여 octhanol distribulion 실험을 실시하여 log P값을 구하였다. 결과: $^{68}$Ga-NOTA와 $^{68}$Ga-DOTA의 치적 표지 pH 조건은 각각 pH 6.5와 3.5였고, NOTA는 실온에서 표지가 잘 되었으나 DOTA는 가열이 필요하였다. MgCl$_2$와 CaCl$_2$의 존재는 $^{68}$Ga-NOTA의 표지 효율에 영향을 미치지 않았으나 CuCl$_2$, FeCl$_2$, InCl$_3$, FeCl$_3$, GaCl$_3$이 존재할 경우에는 표지효율이 감소하였다. $^{68}$Ga-NOTA와 $^{68}$Ga-DOTA는 실온에 그대로 두거나 사람혈청과 37$^{\circ}C$에 두었을 때 4 시간 이상 안정하였고, 사람 혈청 단백질 결합능은 2.04$\sim$3.32%로 낮았으며, log P 값은 -3.07로 수용성을 보였다. 결론: $^{68}$Ga의 표지에는 NOTA가 DOTA에 비하여 이상적인 양기능성 킬레이트제로 쓰일 수 있음을 알았다. 또한 $^{68}$Ga-NOTA는 금속이온 존재시 표지효율이 떨어질 수 있지만 안정하고 낮은 단백질 결합을 보였다.

68Ga 표지 PET/CT 검사의 최적화된 매개변수에 대한 연구 (Study of 68Ga Labelled PET/CT Scan Parameters Optimization)

  • 곽인석;이혁;김시활;문승철
    • 핵의학기술
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    • 제27권2호
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    • pp.111-127
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    • 2023
  • Purpose: Gallium-68 (68Ga) is increasingly used in nuclear medicine imaging for various conditions such as lymphoma and neuroendocrine tumors by labeling tracers like Prostate Specific Membrane Antigen (PSMA) and DOTA-TOC. However, compared to Fluorine-18 (18F) used in conventional nuclear medicine imaging, 68Ga has lower spatial resolution and relatively higher Signal to Background Ratio (SBR). Therefore, this study aimed to investigate the optimized parameters and reconstruction methods for PET/CT imaging using the 68Ga radiotracer through model-based image evaluation. Materials and Methods: Based on clinical images of 68Ga-PSMA PET/CT, a NEMA/IEC 2008 PET phantom model was prepared with a Hot vs Background (H/B) ratio of 10:1. Images were acquired for 9 minutes in list mode using DMIDR (GE, Milwaukee WI, USA). Subsequently, reconstructions were performed for 1 to 8 minutes using OS-EM (Ordered Subset Expectation Maximization) + TOF (Time of Flight) + Sharp IR (VPFX-S), and BSREM (Block Sequential Regularized Expectation Maximization) + TOF + Sharp IR (QCFX-S-400), followed by comparative evaluation. Based on the previous experimental results, images were reconstructed for BSREM + TOF + Sharp IR / 2 minutes (QCFX-S-2min) with varying β-strength values from 100 to 700. The image quality was evaluated using AMIDE (freeware, Ver.1.0.1) and Advanced Workstation (GE, USA). Results: Images reconstructed with QCFX-S-400 showed relatively higher values for SNR (Signal to Noise Ratio), CNR (Contrast to Noise Ratio), count, RC (Recovery Coefficient), and SUV (Standardized Uptake Value) compared to VPFX-S. SNR, CNR, and SUV exhibited the highest values at 2 minutes/bed acquisition time. RC showed the highest values for a 10 mm sphere at 2 minutes/bed acquisition time. For small spheres of 10 mm and 13 mm, an inverse relationship between β-strength increase and count was observed. SNR and CNR peaked at β-strength 400 and then decreased, while SUV and RC exhibited a normal distribution based on sphere size for β-strength values of 400 and above. Conclusion: Based on the experiments, PET/CT imaging using the 68Ga radiotracer yielded the most favorable quantitative and qualitative results with a 2 minutes/bed acquisition time and BSREM reconstruction, particularly when applying β-strength 400. The application of BSREM can enhance accurate quantification and image quality in 68Ga PET/CT imaging, and an optimization process tailored to each institution's imaging objectives appears necessary.