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Evaluation of the Effect of Chelating Arms and Carrier Agents on t he Radiotoxicity of TAT Agents. 螯合臂和载体对TAT放射毒性影响的评价。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471015666220510161047
Soghra Farzipour, Zahra Shaghaghi, Marziyeh Raeispour, Maryam Alvandi, Fatemeh Jalali, Amirhossein Yazdi

Targeted Alpha Therapy (TAT) is considered an evolving therapeutic option for cancer cells, in which a carrier molecule labeling with an α-emitter radionuclide make the bond with a specific functional or molecular target. α-particles with high Linear Energy Transfer (LET) own an increased Relative Biological Effectiveness (RBE) over common β-emitting radionuclides. Normal tissue toxicity due to non-specific uptake of mother and daughter α-emitter radionuclides seems to be the main conflict in clinical applications. The present survey reviews the available preclinical and clinical studies investigating healthy tissue toxicity of the applicable α -emitters and particular strategies proposed for optimizing targeted alpha therapy success in cancer patients.

靶向α治疗(TAT)被认为是癌症细胞的一种不断发展的治疗选择,其中带有α-发射器放射性核素标记的载体分子与特定的功能或分子靶标结合。具有高线性能量传递(LET)的α-粒子比普通β-释放放射性核素具有更高的相对生物有效性(RBE)。正常组织毒性由于母亲和女儿α-发射器放射性核素的非特异性摄取似乎是在临床应用的主要冲突。本研究综述了现有的临床前和临床研究,研究了适用的α -发射器的健康组织毒性,并提出了优化癌症患者靶向α治疗成功的特定策略。
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引用次数: 2
Evaluating the Mitigation Effect of Spirulina Against Radiation-Induced Heart Injury. 评价螺旋藻对辐射性心脏损伤的缓解作用。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666221027142145
Mohammad Hootan Ahmadvand, Safoora Nikzad, Sayed Payam Hashemi, Alireza Khoshghadam, Fereshte Kalhori, Fatemeh Mirzaei

Background: During a radiological or nuclear disaster, exposure to a high dose of ionizing radiation usually results in cardiovascular diseases such as heart failure, attack, and ischemia.

Objective: The purpose of this study was to examine the mitigation effects of Spirulina in comparison to Metformin's.

Methods: 25 male Wistar rats were randomly assigned to five groups (5 rats in each): for the control group, rats did not receive any intervention. In group 2, spirulina was administered orally to rats. In group 3, rats were irradiated to the chest region with 15 Gray(Gy) x-radiation. In groups 4 and 5, rats were irradiated in the same way as group 3. Forty-eight hours after irradiation, treatment with Spirulina and Metformin began. All rats were sacrificed after ten weeks, and their heart tissues were removed for histopathological and biochemical assays.

Results: Results showed an elevation in Malondialdehyde (MDA) and decreasing superoxide dismutase (SOD) activity. Moreover, pathological changes of radiation were irregularities in the arrangement of myofibrils, proliferation, migration of mononuclear cells, vacuolation of the cytoplasm, and congestion. Administration of spirulina enhanced the SOD activity while did not affect MDA level and pathological change in heart tissue. Despite spirulina, metformin had a considerable effect on pathological lesions and decreased the level of MDA.

Conclusion: Reactive oxygen species (ROS) may be involved in the late effects of radiationinduced heart injury, and scavenging these particles may contribute to reduced radiation side effects. Based on these results, Spirulina had no effect on radiation-induced cardiac damage, while metformin did. Higher Spirulina doses given over a longer period of time will likely have a greater heart-mitigate effect.

背景:在放射性或核灾难中,暴露于高剂量电离辐射通常会导致心血管疾病,如心力衰竭、发作和缺血。目的:本研究的目的是比较螺旋藻与二甲双胍的缓解作用。方法:雄性Wistar大鼠25只,随机分为5组,每组5只,对照组不进行任何干预。第二组大鼠口服螺旋藻;第3组大鼠胸部接受15 Gy x射线照射。第4、5组大鼠照第3组照射。照射48小时后,开始螺旋藻和二甲双胍治疗。10周后处死大鼠,取心脏组织进行组织病理学和生化分析。结果:丙二醛(MDA)升高,超氧化物歧化酶(SOD)活性降低。病理改变为肌原纤维排列不规则、单核细胞增生、迁移、细胞质空泡化、充血。螺旋藻可提高心肌组织SOD活性,但对心肌组织MDA水平及病理改变无明显影响。尽管螺旋藻,二甲双胍对病理病变有相当大的影响,并降低MDA水平。结论:活性氧(ROS)可能参与了辐射致心脏损伤的后期效应,清除这些粒子可能有助于减少辐射的副作用。基于这些结果,螺旋藻对辐射引起的心脏损伤没有影响,而二甲双胍有影响。在较长时间内服用较高剂量的螺旋藻可能会有更大的心脏缓解效果。
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引用次数: 0
Comparative Study of Extremely Low-Frequency Electromagnetic Field, Radiation, and Temozolomide Administration in Spheroid and Monolayer Forms of the Glioblastoma Cell Line (T98). 极低频电磁场、辐射和替莫唑胺在球状和单层胶质母细胞瘤细胞系中的比较研究(T98)。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666221207163043
Rasoul Yahyapour, Samideh Khoei, Zeinab Kordestani, Mohammad Hasan Larizadeh, Ali Jomehzadeh, Maryam Amirinejad, Meysam Ahmadi-Zeidabadi

Background: Glioblastoma is the most common primary malignant tumor of the central nervous system. The patient's median survival rate is 13.5 months, so it is necessary to explore new therapeutic approaches.

Objective: Extremely low-frequency electromagnetic field (EMF) has been explored as a noninvasive cancer treatment. This study applied the EMF with previous conventional chemoradiotherapy for glioblastoma.

Methods: In this study, we evaluated the cytotoxic effects of EMF (50 Hz, 100 G), temozolomide (TMZ), and radiation (Rad) on gene expression of T98 glioma cell lines in monolayer and spheroid cell cultures.

Results: Treatment with Rad and EMF significantly increased apoptosis-related gene expression compared to the control group in monolayers and spheroids (p<0.001). The expression of apoptotic-related genes in monolayers was higher than the similar spheroid groups (p<0.001). We found that treatment with TMZ and EMF could increase the gene expression of the autophagy cascade markers compared to the control group (p<0.001). Autophagy-related gene expression in spheroids was higher than in the similar monolayer group (p<0.001). We demonstrated that coadministration of EMF, TMZ, and Rad significantly reduced cell cycle and drug resistance gene expression in monolayers and spheroids (p<0.001) compared to the control group.

Conclusion: The combinational use of TMZ, Rad and, EMF showed the highest antitumor activity by inducing apoptosis and autophagy signaling pathways and inhibiting cell cycle and drug resistance gene expression. Furthermore, EMF increased TMZ or radiation efficiency.

背景:胶质母细胞瘤是中枢神经系统最常见的原发性恶性肿瘤。患者的中位生存期为13.5个月,因此有必要探索新的治疗方法。目的:探讨极低频电磁场(EMF)作为一种无创治疗癌症的方法。本研究将电磁场与以往的常规放化疗联合应用于胶质母细胞瘤。方法:在本研究中,我们评估了电磁场(50 Hz, 100 G)、替莫唑胺(TMZ)和辐射(Rad)对单层和球状细胞培养的T98胶质瘤细胞系基因表达的细胞毒性作用。结果:与对照组相比,Rad和EMF可显著提高细胞单层和球状组织中凋亡相关基因的表达(p)。结论:TMZ、Rad和EMF联合使用可诱导细胞凋亡和自噬信号通路,抑制细胞周期和耐药基因表达,显示出最高的抗肿瘤活性。此外,EMF增加了TMZ或辐射效率。
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引用次数: 0
Status of α-emitter Radioimmunoconjugates for Targeted Therapy. 靶向治疗α-发射器放射免疫偶联物的现状
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666230106111119
Mobina Rabiei, Ahmad Reza Vaez Alaei, Hassan Yousefnia

This minireview describes the global situation of ongoing research and development and the clinical application of alpha emitter labeled immunoconjugates with various alpha emitters with an overview of the future trends. The potentially helpful alpha emitter radioisotopes for medical applications, chelators, and immunomolecules of interest for future alpha radioimmunotherapy are discussed. Challenges and some suggested future works on chelators are also presented.

本文简要介绍了α发射器标记免疫偶联物在全球范围内的研究开发情况和临床应用,并对未来的发展趋势进行了展望。讨论了在医疗应用中潜在有用的α发射器放射性同位素、螯合剂和未来α放射免疫治疗感兴趣的免疫分子。本文还提出了螯合剂研究中存在的挑战和一些建议。
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引用次数: 0
A New Buffer for Gallium-68 Labeling Suitable for use in Nuclear Medicine; Triethanolamine (TEA). 一种适用于核医学的镓-68标记缓冲液三乙醇胺(茶)。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666230522100024
Ayşe Uğur, Olga Yaylali, Doğangün Yüksel

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.

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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引用次数: 0
Synthesis and Ready to Use Kit Formulation of EDTMP for the Preparation of 177Lu-EDTMP as a Bone Palliation Radiopharmaceutical. 骨缓解放射性药物177Lu-EDTMP的合成及即用型试剂盒配制
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471015666220721095938
Guldem Mercanoglu, Kani Zilbeyaz, Nuri Arslan

Introduction: With its suitable nuclear decay characteristics and large-scale production feasibility with adequate specific activity, 177Lu is regarded as an excellent radionuclide for developing bone pain palliation agent. Ethylenediamine-tetramethylene phosphonic acid (EDTMP) is a preferred carrier molecule for radiolanthanides, such as 177Lu. The present paper describes the synthesis of EDTMP and the development of a ready-to-use kit for the preparation of 177Lu-EDTMP and its quality control in accordance with the quality and safety criteria required for medicinal use.

Material and methods: EDTMP was synthesized by a modified Mannich-type reaction, and the structure was characterized using NMR and IR spectroscopy. Optimization of radiolabeling conditions was done with two different salt forms of EDTMP. The labeling yield was checked by paper chromatography with radiation detection. Kit was developed as a lyophilized mixture of EDTMP and sodium bicarbonate in a maximum volume of 5 mL. Labeling efficiency, radionuclidic purity, radiochemical purity, sterility, and pyrogenicity analysis were performed as the quality control of the labeled kit.

Results: The analytical data for the structure determination and purity of the synthesized ligand were in agreement with authentic commercial samples used in radiopharmacy.177Lu-EDTMP complex was prepared using synthesized EDTMP ligand under optimized labeling conditions with high labelling yield (>99%). The radiolabeling yields of the EDTMP kit at room temperature after 30 min and 48 hours were 99.46% and 99.00%.

Conclusion: The developed EDTMP kit enables an instant one-step preparation of the radiopharmaceutical of high radiochemical purity (>99%) and has a sufficiently long shelf life. This enables the routine production of the 177Lu-EDTMP in nuclear medicine clinics without requiring experienced staff.

177Lu具有适宜的核衰变特性和规模化生产的可行性,具有足够的比活性,被认为是开发骨痛缓解剂的优良放射性核素。乙二胺-四亚甲基膦酸(EDTMP)是放射性镧系元素如177Lu的首选载体分子。本文介绍了EDTMP的合成、制备177Lu-EDTMP即用型试剂盒的研制及其按照药用质量安全标准进行的质量控制。材料与方法:采用改性mannich型反应合成了EDTMP,并用核磁共振和红外光谱对其结构进行了表征。对两种不同盐态EDTMP的放射性标记条件进行了优化。用辐射检测的纸层析法检测标签收率。试剂盒为EDTMP和碳酸氢钠的冻干混合物,最大体积为5 mL。标记效率、放射性核素纯度、放射化学纯度、无菌性和热原性分析作为标记试剂盒的质量控制。结果:合成的配体的结构测定和纯度分析数据与放射药学中真实的商业样品一致。在优化的标记条件下,用合成的EDTMP配体制备了177Lu-EDTMP配合物,标记率高(>99%)。EDTMP试剂盒在室温下30 min和48 h的放射性标记率分别为99.46%和99.00%。结论:所开发的EDTMP试剂盒可快速一步制备高放射化学纯度(>99%)的放射性药物,且具有足够长的保质期。这使得在核医学诊所常规生产177Lu-EDTMP无需经验丰富的工作人员。
{"title":"Synthesis and Ready to Use Kit Formulation of EDTMP for the Preparation of 177Lu-EDTMP as a Bone Palliation Radiopharmaceutical.","authors":"Guldem Mercanoglu,&nbsp;Kani Zilbeyaz,&nbsp;Nuri Arslan","doi":"10.2174/1874471015666220721095938","DOIUrl":"https://doi.org/10.2174/1874471015666220721095938","url":null,"abstract":"<p><strong>Introduction: </strong>With its suitable nuclear decay characteristics and large-scale production feasibility with adequate specific activity, <sup>177</sup>Lu is regarded as an excellent radionuclide for developing bone pain palliation agent. Ethylenediamine-tetramethylene phosphonic acid (EDTMP) is a preferred carrier molecule for radiolanthanides, such as <sup>177</sup>Lu. The present paper describes the synthesis of EDTMP and the development of a ready-to-use kit for the preparation of <sup>177</sup>Lu-EDTMP and its quality control in accordance with the quality and safety criteria required for medicinal use.</p><p><strong>Material and methods: </strong>EDTMP was synthesized by a modified Mannich-type reaction, and the structure was characterized using NMR and IR spectroscopy. Optimization of radiolabeling conditions was done with two different salt forms of EDTMP. The labeling yield was checked by paper chromatography with radiation detection. Kit was developed as a lyophilized mixture of EDTMP and sodium bicarbonate in a maximum volume of 5 mL. Labeling efficiency, radionuclidic purity, radiochemical purity, sterility, and pyrogenicity analysis were performed as the quality control of the labeled kit.</p><p><strong>Results: </strong>The analytical data for the structure determination and purity of the synthesized ligand were in agreement with authentic commercial samples used in radiopharmacy.<sup>177</sup>Lu-EDTMP complex was prepared using synthesized EDTMP ligand under optimized labeling conditions with high labelling yield (>99%). The radiolabeling yields of the EDTMP kit at room temperature after 30 min and 48 hours were 99.46% and 99.00%.</p><p><strong>Conclusion: </strong>The developed EDTMP kit enables an instant one-step preparation of the radiopharmaceutical of high radiochemical purity (>99%) and has a sufficiently long shelf life. This enables the routine production of the <sup>177</sup>Lu-EDTMP in nuclear medicine clinics without requiring experienced staff.</p>","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":"16 1","pages":"38-43"},"PeriodicalIF":2.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186375/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9474341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Novel Tumor Hypoxia Imaging Agent: [99mTc]Tc(CO)3-CPA-2-NIM. 新型肿瘤缺氧显像剂:[99mTc]Tc(CO)3-CPA-2-NIM。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666230320144641
Xiao Lin, Xiaojie Tan, Fengyu Wu, Qian Yu

Introduction: Hypoxia imaging agents can selectively remain in hypoxic tissue, which can directly reflect the location and degree of hypoxia.

Methods: Synthesized a novel tumor hypoxia imaging probe [99mTc]Tc(CO)3-CPA-2-NIM and evaluated its biological behavior with the purpose to assess its possibility of becoming a qualified tumor hypoxia imaging agent.

Results: Radiochemcial purity of [99mTc]Tc(CO)3-CPA-2-NIM was greater than 95% after HPLC purification. Lipophilicity coefficient of this complex was -1.74 ± 0.10 (n = 5, number of experiments), indicating it was a hydrophilic complex. In vitro cell experiments demonstrated that this complex has selectivity for hypoxia at oxygen concentrations < 10 ppm (parts per million). Biodistribution experiment in S180 tumor bearing mice showed that tumor uptake reached its highest at 2 h post-injection with mice tumor-to-muscle ratio.

Conclusions: Complex [99mTc]Tc(CO)3-CPA-2-NIM has the possibility of becoming a tumor hypoxia imaging agent.

简介:低氧显像剂可以选择性地停留在缺氧组织中,可以直接反映缺氧的部位和程度。方法:合成一种新型肿瘤缺氧显像探针[99mTc]Tc(CO)3-CPA-2-NIM,并对其生物学行为进行评价,评价其成为合格肿瘤缺氧显像剂的可能性。结果:HPLC纯化后[99mTc]Tc(CO)3-CPA-2-NIM的放射化学纯度大于95%。该配合物的亲脂性系数为-1.74±0.10 (n = 5,实验次数),表明该配合物为亲水性配合物。体外细胞实验表明,该复合物对氧浓度< 10 ppm(百万分之一)的缺氧具有选择性。在S180荷瘤小鼠体内的生物分布实验表明,注射后2 h,肿瘤摄取以小鼠瘤肌比达到最高。结论:配合物[99mTc]Tc(CO)3-CPA-2-NIM有可能成为肿瘤缺氧显像剂。
{"title":"A Novel Tumor Hypoxia Imaging Agent: [<sup>99m</sup>Tc]Tc(CO)<sub>3</sub>-CPA-2-NIM.","authors":"Xiao Lin,&nbsp;Xiaojie Tan,&nbsp;Fengyu Wu,&nbsp;Qian Yu","doi":"10.2174/1874471016666230320144641","DOIUrl":"https://doi.org/10.2174/1874471016666230320144641","url":null,"abstract":"<p><strong>Introduction: </strong>Hypoxia imaging agents can selectively remain in hypoxic tissue, which can directly reflect the location and degree of hypoxia.</p><p><strong>Methods: </strong>Synthesized a novel tumor hypoxia imaging probe [<sup>99m</sup>Tc]Tc(CO)<sub>3</sub>-CPA-2-NIM and evaluated its biological behavior with the purpose to assess its possibility of becoming a qualified tumor hypoxia imaging agent.</p><p><strong>Results: </strong>Radiochemcial purity of [<sup>99m</sup>Tc]Tc(CO)<sub>3</sub>-CPA-2-NIM was greater than 95% after HPLC purification. Lipophilicity coefficient of this complex was -1.74 ± 0.10 (n = 5, number of experiments), indicating it was a hydrophilic complex. <i>In vitro</i> cell experiments demonstrated that this complex has selectivity for hypoxia at oxygen concentrations < 10 ppm (parts per million). Biodistribution experiment in S180 tumor bearing mice showed that tumor uptake reached its highest at 2 h post-injection with mice tumor-to-muscle ratio.</p><p><strong>Conclusions: </strong>Complex [<sup>99m</sup>Tc]Tc(CO)<sub>3</sub>-CPA-2-NIM has the possibility of becoming a tumor hypoxia imaging agent.</p>","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":"16 4","pages":"300-307"},"PeriodicalIF":2.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10144638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of Bone Scan Index as a Prognostic Tool in Breast Cancer Patients with Bone Metastasis. 骨扫描指数作为乳腺癌骨转移患者预后工具的评价。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666230509113108
Maria Silvia De Feo, Viviana Frantellizzi, Arianna Di Rocco, Alessio Farcomeni, Antonio Matto, Andrea Marongiu, Susanna Nuvoli, Angela Spanu, Giuseppe De Vincentis

Background: Bone metastatic involvement represents a leading cause of death in patients with advanced breast cancer (BC). At present, it is not clear whether the bone metastatic load might impact Overall Survival (OS) in patients with bone metastatic BC at diagnosis. For this purpose, we used the Bone Scan Index (BSI), which is a reproducible and quantitative expression of tumor load observed at bone scintigraphy.

Objective: The aim of this study was to associate BSI with OS in bone metastatic BC patients.

Methods: In this retrospective study, we enrolled BC patients with bone metastases at the scintigraphic bone scan performed for staging purposes. The BSI was calculated through the DASciS software, and statistical analysis was carried out. Other clinical variables relevant to OS analysis were taken into account.

Results: Of a total of 94 patients, 32% died. In most cases, the histotype was ductal infiltrating carcinoma. The median OS from diagnosis was 72 months (CI 95%: 62-NA). The univariate analysis with COX regression showed that only hormone therapy significantly correlates with OS (HR 0.417, CI 95%: 0.174-0.997, p < 0.049). As concerning BSI, the statistical analysis showed that it does not predict OS in BC patients (HR 0.960, 95% CI: 0.416-2.216, p < 0.924).

Conclusion: Although the BSI significantly predicts OS in prostate cancer and in other tumors, we observed that the metastatic load of bone disease has not a key role in prognostic stratification in our population.

背景:骨转移累及是晚期乳腺癌(BC)患者死亡的主要原因。目前尚不清楚骨转移负荷是否会影响骨转移性BC患者诊断时的总生存期(OS)。为此,我们使用骨扫描指数(Bone Scan Index, BSI),这是在骨扫描中观察到的肿瘤负荷的可重复和定量表达。目的:本研究的目的是将骨转移性BC患者的BSI与OS联系起来。方法:在这项回顾性研究中,我们招募了在骨扫描中进行分期的骨转移的BC患者。通过DASciS软件计算BSI,并进行统计分析。其他与OS分析相关的临床变量也被考虑在内。结果:94例患者中,32%死亡。大多数病例的组织类型为导管浸润性癌。诊断后的中位OS为72个月(CI 95%: 62-NA)。单因素COX回归分析显示,只有激素治疗与OS显著相关(HR 0.417, CI 95%: 0.174 ~ 0.997, p < 0.049)。BSI不能预测BC患者的OS (HR 0.960, 95% CI: 0.416-2.216, p < 0.924)。结论:尽管BSI可以显著预测前列腺癌和其他肿瘤的OS,但我们观察到骨病的转移负荷在我们的人群中并不是预后分层的关键作用。
{"title":"Evaluation of Bone Scan Index as a Prognostic Tool in Breast Cancer Patients with Bone Metastasis.","authors":"Maria Silvia De Feo,&nbsp;Viviana Frantellizzi,&nbsp;Arianna Di Rocco,&nbsp;Alessio Farcomeni,&nbsp;Antonio Matto,&nbsp;Andrea Marongiu,&nbsp;Susanna Nuvoli,&nbsp;Angela Spanu,&nbsp;Giuseppe De Vincentis","doi":"10.2174/1874471016666230509113108","DOIUrl":"https://doi.org/10.2174/1874471016666230509113108","url":null,"abstract":"<p><strong>Background: </strong>Bone metastatic involvement represents a leading cause of death in patients with advanced breast cancer (BC). At present, it is not clear whether the bone metastatic load might impact Overall Survival (OS) in patients with bone metastatic BC at diagnosis. For this purpose, we used the Bone Scan Index (BSI), which is a reproducible and quantitative expression of tumor load observed at bone scintigraphy.</p><p><strong>Objective: </strong>The aim of this study was to associate BSI with OS in bone metastatic BC patients.</p><p><strong>Methods: </strong>In this retrospective study, we enrolled BC patients with bone metastases at the scintigraphic bone scan performed for staging purposes. The BSI was calculated through the DASciS software, and statistical analysis was carried out. Other clinical variables relevant to OS analysis were taken into account.</p><p><strong>Results: </strong>Of a total of 94 patients, 32% died. In most cases, the histotype was ductal infiltrating carcinoma. The median OS from diagnosis was 72 months (CI 95%: 62-NA). The univariate analysis with COX regression showed that only hormone therapy significantly correlates with OS (HR 0.417, CI 95%: 0.174-0.997, p < 0.049). As concerning BSI, the statistical analysis showed that it does not predict OS in BC patients (HR 0.960, 95% CI: 0.416-2.216, p < 0.924).</p><p><strong>Conclusion: </strong>Although the BSI significantly predicts OS in prostate cancer and in other tumors, we observed that the metastatic load of bone disease has not a key role in prognostic stratification in our population.</p>","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":"16 4","pages":"284-291"},"PeriodicalIF":2.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10132987","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of the Mitigation Effect of Spirulina Against Lung Injury Induced by Radiation in Rats. 螺旋藻对大鼠放射性肺损伤的缓解作用评价。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471015666220418133919
Mohammad Hootan Ahmadvand, Safoora Nikzad, Vahid Changizi, Abdolazim Sedighi Pashaki, Masoud Najafi, Fatemeh Mirzaei

Background: Some compounds have been investigated to mitigate the effect of radiation on the lung, such as pneumonitis and fibrosis.

Objective: This study aimed to examine the mitigation efficiency of Spirulina compared to the effect of Metformin.

Methods: 25 male Wistar rats were allotted in five groups: control, Spirulina, Radiation, Radiation plus Spirulina, and Radiation plus Metformin. Rat chest regions were irradiated by 15 Gray (Gy) xradiation using aLINAC. Forty-eight hours after irradiation, treatment with Spirulina and Metformin began. Eighty days after irradiation, all rats were sacrificed, and their lung tissues were removed for histopathological, and biochemical assays.

Results: The results demonstrated that irradiation increased MDA (Malondialdehyde) levels while suppressing the SOD (superoxide dismutase) and GPx(glutathione peroxidase) activity in the irradiated group. MDA levels in lung tissues were reduced with Metformin but not with Spirulina. Both Metformin and Spirulina increased the SOD and GPx activity in lung tissue. Moreover, histopathological evaluations showed extensive changes in the lung tissue including infiltration of lymph cells around the bronchioles and blood vessels, thickening of the alveolar wall, and the disruption of the alveolar structure, as well as accumulation of collagen fibers. Administration of Spirulina and Metformin significantly reduced pathological changes in lung tissue, although the effect of Metformin was greater than that of Spirulina.

Conclusion: Spirulina could mitigate radiation-induced lung injury moderately, although Metformin is more effective than Spirulina as a mitigator agent.

背景:一些化合物已被研究用于减轻辐射对肺的影响,如肺炎和纤维化。目的:本研究旨在比较螺旋藻与二甲双胍的缓解效果。方法:雄性Wistar大鼠25只,随机分为5组:对照组、螺旋藻组、放射线组、放射线加螺旋藻组、放射线加二甲双胍组。用aLINAC对大鼠胸部进行15 Gy x射线照射。照射48小时后,开始螺旋藻和二甲双胍治疗。照射后80 d处死大鼠,取肺组织进行组织病理学和生化分析。结果:结果表明,辐照组MDA(丙二醛)水平升高,超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)活性降低。二甲双胍可降低肺组织中丙二醛的含量,而螺旋藻则无此作用。二甲双胍和螺旋藻均能提高肺组织SOD和GPx活性。此外,组织病理学检查显示肺组织广泛改变,包括细支气管和血管周围淋巴细胞浸润,肺泡壁增厚,肺泡结构破坏以及胶原纤维积聚。螺旋藻和二甲双胍联合用药可显著降低肺组织的病理改变,但二甲双胍的作用大于螺旋藻。结论:螺旋藻对放射性肺损伤有中度缓解作用,但二甲双胍的缓解效果优于螺旋藻。
{"title":"Evaluation of the Mitigation Effect of Spirulina Against Lung Injury Induced by Radiation in Rats.","authors":"Mohammad Hootan Ahmadvand,&nbsp;Safoora Nikzad,&nbsp;Vahid Changizi,&nbsp;Abdolazim Sedighi Pashaki,&nbsp;Masoud Najafi,&nbsp;Fatemeh Mirzaei","doi":"10.2174/1874471015666220418133919","DOIUrl":"https://doi.org/10.2174/1874471015666220418133919","url":null,"abstract":"<p><strong>Background: </strong>Some compounds have been investigated to mitigate the effect of radiation on the lung, such as pneumonitis and fibrosis.</p><p><strong>Objective: </strong>This study aimed to examine the mitigation efficiency of Spirulina compared to the effect of Metformin.</p><p><strong>Methods: </strong>25 male Wistar rats were allotted in five groups: control, Spirulina, Radiation, Radiation plus Spirulina, and Radiation plus Metformin. Rat chest regions were irradiated by 15 Gray (Gy) xradiation using aLINAC. Forty-eight hours after irradiation, treatment with Spirulina and Metformin began. Eighty days after irradiation, all rats were sacrificed, and their lung tissues were removed for histopathological, and biochemical assays.</p><p><strong>Results: </strong>The results demonstrated that irradiation increased MDA (Malondialdehyde) levels while suppressing the SOD (superoxide dismutase) and GPx(glutathione peroxidase) activity in the irradiated group. MDA levels in lung tissues were reduced with Metformin but not with Spirulina. Both Metformin and Spirulina increased the SOD and GPx activity in lung tissue. Moreover, histopathological evaluations showed extensive changes in the lung tissue including infiltration of lymph cells around the bronchioles and blood vessels, thickening of the alveolar wall, and the disruption of the alveolar structure, as well as accumulation of collagen fibers. Administration of Spirulina and Metformin significantly reduced pathological changes in lung tissue, although the effect of Metformin was greater than that of Spirulina.</p><p><strong>Conclusion: </strong>Spirulina could mitigate radiation-induced lung injury moderately, although Metformin is more effective than Spirulina as a mitigator agent.</p>","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":"16 1","pages":"71-77"},"PeriodicalIF":2.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9431074","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Impact of Radiolabeled Nanomaterials. 放射性标记纳米材料的影响。
IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.2174/1874471016666230523155711
Martha Sahylí Ortega Pijeira, Natália Cristina Gomes da Silva, Luciana Magalhaes Rebelo Alencar, Eduardo Ricci-Junior, Ralph Santos-Oliveira

Nanotechnology has changed the world, with a great impact on industry and medicine. In this commentary, we discuss the importance of radiolabeled nanomaterials for the construction of theranostic, imaging and therapeutic agents in order to pave the future of medicine.

纳米技术改变了世界,对工业和医学产生了巨大影响。在这篇评论中,我们讨论了放射性标记纳米材料在构建治疗剂、成像剂和治疗剂方面的重要性,为医学的未来铺平道路。
{"title":"The Impact of Radiolabeled Nanomaterials.","authors":"Martha Sahylí Ortega Pijeira,&nbsp;Natália Cristina Gomes da Silva,&nbsp;Luciana Magalhaes Rebelo Alencar,&nbsp;Eduardo Ricci-Junior,&nbsp;Ralph Santos-Oliveira","doi":"10.2174/1874471016666230523155711","DOIUrl":"10.2174/1874471016666230523155711","url":null,"abstract":"<p><p>Nanotechnology has changed the world, with a great impact on industry and medicine. In this commentary, we discuss the importance of radiolabeled nanomaterials for the construction of theranostic, imaging and therapeutic agents in order to pave the future of medicine.</p>","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":"16 4","pages":"337-339"},"PeriodicalIF":2.3,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10479849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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Current radiopharmaceuticals
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