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It is conventional to use standard Positron Emission Tomography (PET) radionuclides (11C, 13N, 15O, 18F) for imaging; however,
the decay energy <3 MeV and β+ intensity (>10%) of some other radionuclides (called non-standard) also makes them
correspondingly suitable for PET imaging. The importance of non-standard PET radionuclides (e.g. 45Ti, 60Cu, 61Cu, 64Cu, 86Y,
124I) in clinical nuclear medicine has been realized by imaging the biological systems. Cyclotrons are the best solution to produce
desired beta emitters. Smart choice of target and projectile makes it possible to produce the PET radionuclides in most economical
way. Keeping in view the importance of medical radioisotopes, we investigated the production route and production cross-section
of few non-standard radionuclides (55Co, 61,64Cu, 66,68Ga, 86Y, 89Zr, 90Nb, 94mTc) using medium energy proton and alpha beams.
Stacked-foil activation technique was applied to irradiate the samples (natNi, natFe, natCu, 89Y, 93Nb and natMo) with external
beam of MC-50 cyclotron installed at Korea Institute of Radiological and Medical Sciences (KIRAMS), Korea. Off-line γ-ray
spectrometric technique was used for spectrum analysis and measurement of production cross-sections of radionuclides of
interest. Based on the cross-section, thick target yield information was also obtained. We studied natNi(p,x)55Co, natFe(p,x)55Co,
natCu(α,x)61,64Cu, natCu(α,x)66,68Ga, natCu(p,x)61,64Cu, 89Y(p,x)86Y, 89Y(p,x)89Zr, 93Nb(p,x)90Nb, 89Y(α,x)90Nb, 93Nb(α,x)94mTc and
natMo(p,x)94mTc reactions in the energy range from their threshold to 45 MeV. Proton and alpha beams were bombarded on
different targets to investigate the production routes and production cross-sections of different radionuclides. However, chemical
separation of these non-standard PET radionuclides or their application to image biological systems was not studied. Stacked-foil
activation technique was applied to irradiate the sample with external beam of MC-50 cyclotron installed at Korea Institute of
Radiological and Medical Sciences, Korea. Thin metallic foils (10-50 nm) of 1×1 cm2 area were placed in front of beam of 10 mm
diameter (100-200 nA current) to irradiate for 0.5-1 hours depending on the experimental setup. Off-line γ-ray spectrometric
technique was used for spectrum analysis and measurement of production cross-sections of produced radionuclides. Besides
aforementioned reaction products, some other short lived non-standard PET radionuclides were also produced but their
production could not be identified due to their very short half-lives. As the produced radioisotopes are medically important,
therefore, the integral yields for thick target of the investigated radio-nuclides were also calculated from the measured excitation
functions. The measured results were compared with the literature data as well as with the theoretical values obtained from the
TENDL-2015 library based on the TALYS 1.8 code. The study of the production of non-standard PET radionuclides from different
reactions describes the cross-sections and yield information in the energy range of 2-45 MeV. Most of the reaction products are
directly produced so chances of contamination and unwanted impurities are minimum. One of the advantages of this technique is
carrier free production of desired radioisotopes and easy separation through chemical process. We did not investigate the methods
to separate chemically the desired radionuclides and their applications to image biological systems. However, based on our study
the best production route and suitable energy for maximum production can be identified to produce the desired radionuclide
in the economical way. Though the study has been provided by other investigators, yet discrepancies were observed in their
measurements, so the current study is enough to enrich the literature data except a few where further investigations are required
to make the production economically viable. The information provided about integral yield is pertinent for those involved in
radioisotope production