A New Buffer for Gallium-68 Labeling Suitable for use in Nuclear Medicine; Triethanolamine (TEA).

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Current radiopharmaceuticals Pub Date : 2023-01-01 DOI:10.2174/1874471016666230522100024
Ayşe Uğur, Olga Yaylali, Doğangün Yüksel
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Abstract

Background: Radiopharmaceuticals labeled with [68Ga] from positron emission tomography (PET) radionuclides are utilized in nuclear medicine for non-invasive in vivo molecular imaging. Buffer solutions for radiolabeling play an important role as choosing the right buffer for the reaction helps to obtain high yield radiopharmaceuticals. Zwitterionic organic buffer 4-(2- hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), sodium acetate (CH3COONa), sodium bicarbonate (NaHCO3) buffers are widely used for labeling of peptides with [68Ga]Cl3. They can be used for peptide labelings with the acidic [68Ga]Cl3 precursor of triethanolammonium (TEA) buffer. The cost and toxicity of TAE buffer are relatively low.

Method: For [68Ga]GaPSMA-HBED-CC and [68Ga]GaDOTA-TATE labeling, the effectiveness of TEA buffer without chemical impurities in radiolabeling reactions and QC parameters in successful labeling was investigated.

Results: The method used to label [68Ga]Cl3 with PSMA-HBED-CC peptide in the presence of TEA buffer was successful when applied at room temperature. High purity radiosynthesis suitable for clinical use was performed to obtain DOTA-TATE peptide with the addition of 363K temperature and radical scavenger. Quality control tests with R-HPLC have shown that this method is suitable for clinical use.

Conclusion: We present an alternative procedure for labeling PSMA-HBED-CC and DOTATATE peptides with [68GaCl3] to obtain high radioactive doses of final radiopharmaceutical products used in nuclear medicine clinical applications. We have provided a quality-controlled final product that can be used in clinical diagnostic procedures. With the use of an alternative buffer, these methods could be adapted to semi-automatic or automated modules routinely used in nuclear medicine laboratories to label [68Ga]-based radiopharmaceuticals.

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一种适用于核医学的镓-68标记缓冲液三乙醇胺(茶)。
背景:用正电子发射断层扫描(PET)放射性核素标记[68Ga]的放射性药物在核医学中用于无创体内分子成像。用于放射性标记的缓冲液起着重要的作用,因为为反应选择合适的缓冲液有助于获得高产量的放射性药物。两性离子有机缓冲液4-(2-羟乙基)-1-哌嗪乙磺酸(HEPES)、乙酸钠(CH3COONa)、碳酸氢钠(NaHCO3)缓冲液被广泛用于用[68Ga]Cl3标记肽。它们可用于与三乙醇铵(TEA)缓冲液的酸性[68Ga]Cl3前体进行肽标记。TAE缓冲液的成本和毒性相对较低。方法:针对[68Ga]GaPSMA-HBED-CC和[68Ga]GaDOTA-TATE标记,考察了不含化学杂质的TEA缓冲液在放射性标记反应中的有效性和QC参数对标记成功的影响。结果:在室温条件下,在TEA缓冲液存在下,用PSMA-HBED-CC肽标记[68Ga]Cl3是成功的。采用适合临床使用的高纯度放射合成,添加363K温度和自由基清除剂,得到DOTA-TATE肽。反相高效液相色谱法质量控制试验表明,该方法适合临床使用。结论:我们提出了一种用[68GaCl3]标记psma - hbedcc和DOTATATE肽的替代方法,以获得用于核医学临床应用的高放射性剂量的最终放射性药物产品。我们提供了可用于临床诊断程序的质量控制的最终产品。通过使用替代缓冲液,这些方法可以适用于核医学实验室常规使用的半自动或自动化模块,用于标记基于[68Ga]的放射性药物。
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来源期刊
Current radiopharmaceuticals
Current radiopharmaceuticals PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
4.30%
发文量
43
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