Imaging: PET and SPECT Positron Emission Tomography Single Photon Emission Computed Tomography PET and SPECT Properties of ideal imaging nuclides, biological, chemical , physical Production of radionuclides Nuclear fission Charged particle bombardment The Tc-99m Generator Chemistry Chelators vs organic chemistry Delivery strategies Blood brain barrier Metabolic pathways Chemical affinity Clinical applications Tumor imaging and staging Cardiac imaging Gene therapy Brain function Dopamine pathways, addiction Imaging Image removed. Radionuclides SI unit is the Becquerel (Bq) 1 Bq = 1 dps (disintegration per second ) old unit is the Curie (Ci ) 1 Ci = 3.7 X 10 10 dps Activity (A) = rate of decay N o = number of active nuclei at time t = 0 N(t) is the number of active nuclei at time ‘t’ λ is the decay constant λ = 0.693/T (T = half-life) dN/dt = -λ N(t) N(t) = N o e -λt A(t) = A o e -λt Effective Half-Life Physical half-life, T P [radioactive decay] Biological half-life, T B [clearance from the body] t t biol phys eeAA λ λ ? ? = 0 t DP eAA )( 0 λλ +? = λ P +λ B = λ E BP BP E PBE TT TT Tor TTT + =+= 111 Effective Half-Life E.g., for an isotope with a 6-hr half life attached to various carrier molecules with different biological half-lives. T P T B T E 6 hr 1 hr 0.86 hr 6 hr 6 hr 3 hr 6 hr 60 hr 5.5 hr 6 hr 600 hr 5.9 hr Effective Half-Life Assume 10 6 Bq localized in a tumor site, vary T Nuclide Half-life (T) λ (sec -1 ) N 1 6 sec 0.115 8.7 x 10 7 2 6 min 1.75 x 10 -3 5.7 x 10 9 3 6 hrs 3.2 x 10 -5 3.1 x 10 11 4 6 days 1.3 x 10 -6 7.7 x 10 12 5 6 years 4 x 10 -9 2.5 x 10 15 Effective Half-Life Assume 10 10 atoms of radionuclide localized in a tumor site, vary T Nuclide Half-life (T) λ (sec -1 ) Activity (Bq) 1 6 sec 0.115 1.15 x 10 9 2 6 min 1.75 x 10 -3 1.7 x 10 7 3 6 hrs 3.2 x 10 -5 3.2 x 10 6 4 6 days 1.3 x 10 -6 1.3 x 10 4 5 6 years 4 x 10 -9 40 Production of Radionuclides Reactor production, Nuclear fission ? Heavy nuclides (A > 230) capture a neutron; tend to fission ? Daughter nuclides of ~ half the parent mass are produced ? Possible to purify nuclides carrier free (chemically different) ? Nuclides generally neutron rich and decay by β - emission Production of Radionuclides Image removed. Production of Radionuclides Image removed. Production of Radionuclides Cyclotron production: Charged particle bombardment ? Accelerates charged particles to high energies ? Nuclear reactions have threshold energies ? The product is different than the target ? Nuclides can be produced carrier-free Production of Radionuclides Image removed. Properties of the ideal diagnostic radiopharmaceutical 1. Pure gamma emitter 2. 100 < gamma energy < 250 keV. 3. Effective half-life = 1.5 X test duration. 4. High target:nontarget ratio. 5. Minimal radiation dose to patient and Nuclear Medicine personnel 6. Patient Safety 7. Chemical Reactivity 8. Inexpensive, readily available radiopharmaceutical. 9. Simple preparation and quality control if manufactured in house. Properties of the ideal diagnostic radiopharmaceutical One nuclide comes close to being the ideal gamma-emitting nuclide Technetium-99m ( 99m Tc) ? Half-life = 6 hr ? Almost a pure γ ray emitter ? E = 140 keV ? can be obtained at high specific activity and carrier free Nuclides 99m Tc 99m Tc is a decay product of the fission product 99 Mo Image removed. Table of the nuclides 99m Tc Original source: Brookhaven National Laboratories. (site no longer maintained - see http://www2.bnl.gov/CoN/) Decay scheme for 99m Tc 99 Mo decays to 99m Tc by β - emission ( 99 Mo: T= 67 hrs) 99m Tc excited nuclear state decays by γ emission (140 keV) to ground state 99 Tc ( 99m Tc: T=6 hrs) 99 Tc (ground state) decays by β - emission to 99 Ru (stable isotope) ( 99 Tc: T=2x10 5 years) Image removed. Radioactive equilibrium Parent N 1 decays to daughter N 2 , both are radioactive. Special Case: Transient equilibrium N 1 → N 2 T 1 > T 2 , but not greatly so. [A = λN, A = A 0 e -λt ] ttt eAeeAANN dt dN 221 20 12 1 1022211 2 )( λλλ λλ λ λλ ??? +? ? =???= Simplifying assumptions: A 20 = 0; After ~10 half-lives, tt ee 12 λλ ?? << 12 1 1 2 12 1 12 101 12 1 102 11 λλ λ λλ λ λλ λ λλ ? = ? = = ? = ?? A A orAA eAAeAA tt Radioactive Decay Example 99 Mo (T = 67 hrs) 99m Tc (T = 6 hrs) Image removed. Fig. 4.5 in Turner J. E. Atoms, Radiation, and Radiation Protection, 2 nd ed. New York: Wiley-Interscience, 1995. The 99m Tc Generator 99 Mo is adsorbed on an alumina column as ammonium molybdate (NH 4 MoO 4 ) 99 Mo (T = 67 hrs) decays (by β -decay) to 99m Tc (T = 6 hrs) 99 MoO 4 ion becomes the 99m TcO 4 (pertechnetate) ion (chemically different) 99m TcO 4 has a much lower binding affinity for the alumina and can be selectively eluted by passing physiological saline through the column. Image removed. Chelators N N O - OO - O O - O O - O EDTA ethylenediaminetetraacetate Image removed. 99m Tc Mertiatide bond structure Image removed. Technetium Pentetate bond structure DTPA Chelators Image removed. Production of Radionuclides Cyclotron production ? Products are proton rich, neutron deficient ? Decay by β+ decay ? Positron emitters Image removed. Chart of the Nuclides The “organic” elements 13 N[ 13 N]NH 3 15 O[ 15 O]H 2 O 11 C[ 11 C]..various 18 F[ 18 F]FDG (primarily) Original source: Brookhaven National Laboratories. (site no longer maintained - see http://www2.bnl.gov/CoN/) Cyclotron Production Targets O-15: 14 N(d,n) 15 O; deuterons on natural N 2 gas; 15 O 2 directly or C 15 O 2 , by mixing 5% carrier CO 2 gas. C-11: 14 N(p,α) 11 C; protons on natural N 2 gas: including 2% O 2 produces 11 CO 2 N-13: 16 O(p,α) 13 N; protons on distilled water F-18: 18 O(p,n) 18 F; protons on 18 O-enriched water (H 2 18 O),. Fluoride is recovered as an aqueous solution. For nucleophilic substitution. F-18: 20 Ne(d,α) 18 F; deuterons on neon gas. For electrophilic substitutions. PET Radiopharmaceuticals Image removed. PET Radiopharmaceuticals ? 11 CO 2 from the target is converted into a highly reactive methylating agent: 11 CH 3 I or 11 CH 3 Tf ? Elapsed time is 12 minutes.. ? The radiochemical yield, based on 11 CO 2 is about 90%. ? Specific activities of more than 6 Ci/μmol (220 GBq/μmol) can be obtained. ? 11 C-Methylation of various precursors is performed in the second reaction vessel within a few minutes. ? After methylation, the reaction product is separated via a semi preparative Radio-HPLC, purified via a solid phase extraction unit, followed by formulation of the radiotracer as an injectable saline solution. Delivery strategies Blood brain barrier Metabolic pathways Biological affinity Image removed. Late 19 th century German chemist Paul Ehrlich demonstrates that certain dyes injected i.v. do not stain the brain. The same dyes, when injected into the cerebral spinal fluid, stain the brain and spinal cord, but no other tissues. The Blood-Brain Barrier Function Provide neurons with their exact nutritional requirements. Glucose ? Sole source of energy (adult brain consumes ~100 g of glucose/day) ? Neurons need a steady supply at an exact concentration The BBB is selective ? Glucose and other nutrients are transported through ? Proteins, complex carbohydrates, all other foreign compounds are excluded. ? Ion concentrations are tightly regulated Image removed. Drug Delivery Tumors do not have a blood tumor barrier Image removed. Delivery Strategies: Metabolic pathways O OH H OH H H H F H OH OH O OH H OH H H H OH H OH OH FDG 2-fluoro-2-deoxy-glucose Β-D-glucose Delivery Strategies: Metabolic pathways Glu → G6P→ F6P→ FBP ? FDG is transported into the cells ? FDG is phosphorylated to FDG-6P (charged molecules cannot diffuse out) ? FDG is NOT a substrate for the enzyme that catalyzes the next step in glycolysis. Image removed. Mapping Human Brain Function 18 F-FDG PET scans show different patterns of glucose metabolism related to various tasks. Image removed. FDG in Oncology ? FDG transport into tumors occurs at a higher rate than in the surrounding normal tissues. ? FDG is de-phosphorylated and can then leave the cell. ? The dephosphorylation occurs at a slower rate in tumors. Applications of FDG ?Locating unknown primaries ?Differentiation of tumor from normal tissue ?Pre-operative staging of disease (lung, breast, colorectal, melanoma, H&N, pancreas) ?Recurrence vs necrosis ?Recurrence vs post-operative changes (limitations with FDG) ?Monitoring response to therapy Delivery Strategies: Metabolic pathways H 2 NCHC CH 2 OH O CH 2 S CH 3 O HOH FH HH HO HN N O O I FIAU 2'-fluoro-2'-deoxy-1-B-D-arabinofuranosyl-5-[ 124 I]-uracil O HF HH HH HO HN N O O CH 3 FLT 3'deoxy-3-'fluoro-[ 18 F]-L-thymidine methionine PET can provide highly specific metabolic information. ? FDG, MET, FLT are incorporated via transporters ? Uptake is indicative of tumor grade. 11 C-methionine ?specific for tumor ?avoids high brain background problem seen with FDG ?no significant uptake in chronic inflammatory or radiogenic lesions ?MET better than FDG in low-grade gliomas Functional imaging of gliomas Imaging objectives ? Location and relation to surrounding brain activity ? Biological activity = malignancy ? Response to therapy Image removed. Tumor recurrence vs post-radiotherapy changes FDG uptake indicates recurrence Left: MRI Center: PET Right: fused image Image removed. Functional Imaging Tumor vs functional brain 11 C-MET + MRI delineates tumor (GREEN) [ 15 O]H 2 O PET delineates function (blood flow) Stimulation of brain regions causes increased blood flow (RED) finger tapping (A) verb generation (B) Pre-surgical analysis to guide surgery. Tumors cause swelling and deformation of brain anatomy: mapping function is critical. Intra-operative electrical stimulation causes aphasia: correlated well with area mapped by [ 15 O]H 2 O PET. Information can be displayed in neuro-navigation software during surgery. Image removed. Recurrent tumor vs necrosis Image removed. MRI (right) indicates necrosis 11 C-MET (left) shows tumor recurrence Image correlation with different modalities High-grade glioma: three- dimensional determination of ? Localization ? Extent ? Metabolism Top: MRI Middle: 11 C-MET Bottom: 18 FDG [Note lower ipsilateral glucose metabolism.] Image removed. Bone scanning Bone scans are the second most frequent nuclear medicine procedure. Clinical uses: ?Detection of primary and metastatic bone tumors ?Evaluation of unexplained bone pain ?Diagnosis of stress fractures or other musculoskeletal injuries or disorders. E.g., Prostate cancer: ?Incidence is rising ?Most common cause of death in males in many western countries ?Of prostate deaths, 85% have mets in bone ?60% of new cases have mets ?Bone metastases are painful and debilitating ?Diagnosis of bone mets is part of the staging process that determines treatment Breast cancer: ?Bone is the most common site of metastasis ?8% of all cases develop bone mets ?70% of advanced cases experience bone mets Bone Bone is a living tissue comprised of a crystalline matrix of hydroxyapatite Ca 5 (PO 4 ) 3 OH in a collagen matrix. Osteoblasts: responsible for new bone formation, repair of damaged sites, lay down new crystalline hydroxyapatite. Osteoclasts: responsible for bone resorption, dissolve bone. Osteoclasts are more active in metastatic tumor sites. Delivery Strategy POPHO O - OH O O - O PC PHO O - OH O O - OR 1 R 2 pyrophosphate bisphosphonate Pyrophosphate Normal metabolite from ATP hydrolysis Source of phosphate in bone. Bisphosphonates ?have an affinity for the hydroxyapatite component of bone ?are incorporated into the crystalline matrix during bone remodeling or repair. ?are used to slow or prevent bone density loss leading to osteoporosis Bone Scans Normal pediatric bone image Image removed. Bone scans SCHAPHOID fracture ?48 y. o. woman presenting with with painful wrist 2 weeks after fall onto outstretched hand. ?X rays normal ?Blood flow ( 13 NH 3 ) increased to the left wrist (top) ?Left scaphoid fracture revealed on 99m Tc-MDP image (bottom) Image removed. Active metastatic disease 41 y.o. male with lung carcinoma presents with pain in upper right humerus, 2-3 months of bilateral rib pain, 3 weeks of left knee pain. Scan shows multiple focal sites of abnormal tracer uptake ?Right humerus ?Multiple ribs ?Left femur ?Sacral and lumbar vertebrae Image removed. Coronary artery disease Use PET and/or SPECT imaging to assess information on: ? perfusion ? metabolism ? distinguish viable from non-viable myocardium. Cardiac Imaging Image removed. The Cardiac Stress Test Exercise causes ?Increased HR, contractility, BP ?Increased O 2 demand ?Coronary vasodilation Increased myocardial blood flow Image removed. Gene Therapy Image removed. Gene Therapy Use of PET to confirm vector gene expression Specific retention of FIAU PET signal at 68 hrs (left) indicates phosphorylation by HSV TK. Same area shows necrosis after treatment with ganciclovir (right). Image removed. PET in studies of substance abuse Drugs of abuse ? Why are they pleasurable? ? What brain changes reinforce usage and lead to addiction? Brain Function Changes in specific components of this system present in various disease states. Parkinsons Disease aging substance abuse depression. Image removed. Brain Function Quantitative PET ?Signal intensity in regions of interest is monitored as a function of time. ?Concurrent sampling of arterial blood allows correlation of signal to blood concentration. ?Pharmacologic doses of antagonist block PET tracer uptake. Image removed. Drug Addiction Image removed. ?Cocaine: one of the most reinforcing drugs of abuse ?Cocaine binds to the DA re- uptake transporter (DAT) ?DAT blockade results in increased DA concentrations. Effect is greatest in brain regions rich in DA neurons (e.g., basal ganglia). Drug Addiction Control 1 week de-tox 3 months de-tox Image removed. FDG PET: Low frontal metabolism may underlie the loss of control in cocaine addiction. Drug Addiction Image removed. Cocaine and methylphenidate (Ritalin) Image removed. 11 C-cocaine 11 C-methylphenidate ? show identical distribution ? highest in basal ganglia (highest DAT concentrations) ? binding to the same receptors ? cold cocaine blocks 11 C-methylphenidate uptake ? cold methylphenidate blocks 11 C-cocaine uptake Cocaine and methylphenidate (Ritalin) Slow on-rate of oral methylphenidate does not produce a high Peak DAT blockade i.v. cocaine: 4-6 min i.v. methylphenidate: 8-10 min oral methylphenidate 60 min Image removed. Slow off-rate for methylphenydate does not lead to “binging” behavior. Second dose would not produce a high.