Ethylene C2H3D isotopologue: high resolution study of v6, v4, v8, v7 and v10 fundamentals

High Resolution Fourier transform infrared spectra of the C2H3D molecule were recorded with Doppler limited resolution in the region of 600 - 1250 cm-1 at room temperature. The measurements were carried out under several different absorption conditions using the Bruker 120 HR spectrometer in Braunschweig Technical University. Five fundamentals v6, v4, v8, v7, and v10 were observed and found to be perturbed by different resonance interactions. About 6000 lines were assigned in the recorded spectrum. They were used then in the weighted fit procedure with the effective Hamiltonian taking into account five strongly interacting states

Functional imaging of neuroendocrine tumors

Neuroendocrine tumors (NET) have several distinct pathophysiological features that can be addressed by specific radiolabeled probes. An overview on the different radiopharmaceuticals that have been developed for positron emission tomography (PET) of NET are presented. The focus is on fluordeoxyglucose (F-18 FDG), biogenic amine precursors, somatostatin analogs, and hormone syntheses markers. Due to the highly specific tracers lacking any clear anatomical landmarking, the advantages of integrated functional and morphological imaging systems such as PET-CT are obvious. Based on the up to now published literature and one's own experience, it is concluded that amine precursors (e.g. fluor-dihydroxyphenylalanin and hydroxytryptophane) should be employed in most gastroenteropancreatic NET, whereas F-18 FDG should be preserved for more aggressive less-differentiated NETs. Hormone syntheses markers have up to now only been used in few centers and their broad clinical value remains uncertain. The different available somatostatin analogs are the most promising tracers, since they can improve dosimetry in cases where peptide receptor radiotherapies are planned. Of specific interest are the somatostatin analogs addressing several subtypes of the somatostatin receptor (e.g. DOTANOC) that allow detecting also subtypes not expressing the "classically" addressed subtype 2 and 5. Since NET have a high variety of different features, the individual diagnostic approach using PET or integrated PET-CT should be tailored, depending on the histological classification and the differentiation of the tumor

Comparison of diagnostic accuracy of In-111-pentetreotide SPECT and Ga-68-DOTATOC PET/CT: A lesion-by-lesion analysis in patients with metastatic neuroendocrine tumours

To compare the diagnostic accuracy of In-111-pentetreotide-scintigraphy with Ga-68-DOTATOC-positron emission tomography (PET)/computed tomography (CT) in patients with metastatic-neuroendocrine tumour (NET) scheduled for peptide receptor radionuclide therapy (PRRT). Incremental lesions (ILs) were defined as lesions observed on only one modality. Fifty-three metastatic-NET-patients underwent In-111-pentetreotide-scintigraphy (24 h post-injection; planar+single-photon emission CT (SPECT) abdomen) and whole-body Ga-68-DOTATOC-PET/CT. SPECT and PET were compared in a lesion-by-lesion and organ-by-organ analysis, determining the total lesions and ILs for both modalities. Significantly more lesions were detected on Ga-68-DOTATOC-PET/CT versus In-111-pentetreotide-scintigraphy. More specifically, we observed 1,098 lesions on PET/CT (range: 1-105; median: 15) versus 660 on SPECT (range: 0-73, median: 9) (p <0.0001), with 439 PET-ILs (42/53 patients) and one SPECT-IL (1/53 patients). The sensitivity for PET/CT was 99.9 % (95 % CI, 99.3-100.0), for SPECT 60.0 % (95 % CI, 48.5-70.2). The organ-by-organ analysis showed that the PET-ILs were most frequently visualized in liver and skeleton. Ga-DOTATOC-PET/CT is superior for the detection of NET-metastases compared to In-111-pentetreotide SPECT. aEuro cent Somatostatin receptor PET is superior to SPECT in detecting NET metastases aEuro cent PET is the scintigraphic method for accurate depiction of NET tumour burden aEuro cent The sensitivity of PET is twofold higher than the sensitivity of SPECT