Yttrium-90 and Rhenium-188 Radiopharmaceuticals for Radionuclide Therapy

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This immunoconjugate solution (1 mL, 5 mg/mL) was prepared in a kit form by lyophilizing with 250 μL of mannitol (80 mg/mL in distilled water). Both the immunoconjugate and mannitol solutions were filtered through sterile 0.45 μm filters (Millipore) prior to lyophilization. On lyophilization, the final product has the appearance of a white pellet. For labelling, 90 Y was obtained from the 90 Sr/ 90 Y generator assembled at AECS. The generator was loaded with ~50 mCi of 90 Sr and the yield of 90 Y was ~45 mCi, equivalent to >90% elution efficiency. Each labelling procedure was carried out at 42°C for 1 h with: (a) (b) Two 700 μL volumes of 90 Y activity of 2.8 mCi, pH5; Two 100 μL volumes of rituximab DOTA in acetate, pH7.5. 11.4.1.2. Quality control (a) HPLC Quality control of the radiopharmaceutical was performed by HPLC using a 2.1 mm × 200 mm Hypersil AA-ODS 5 µm column with a flow rate of 0.4 m/min and wavelength λ = 254 nm. The mobile phase was 95% saline and 5% ACN, and the run was for 20 min. The analysis (HPLC) showed an overall RCP ≥95–98%. (b) TLC ITLC SG (Gelman Sciences) paper chromatography was carried out using various mobile phases (saline, MeOH:ammonia 3:2, MeOH:ammonium acetate 1:1). ITLC radioactivity was analysed by cutting the strips into two segments and measuring the radioactivity using an LSC (Beckman), as shown in Figs 11.6–11.8. The RCP was observed to be 98.1%. In both reactions, carried out at a DOTA:antibody molar ratio of 100:1, specific activities of 10 and 20 mCi/mg with labelling yields of 99.8% and 99.5% were achieved, respectively. These data are reported in Table 11.4. (c) In vivo studies Biodistribution studies of 90 Y DOTA NCS rituximab were carried out on healthy Albino rats. Rats weighing ~175 g were injected with 1 mCi (50 μL) of the radioconjugate in acetate buffer, pH7.5. Biodistribution studies were carried out to confirm the in vivo stability of the radioimmunoconjugate, as shown in Fig. 11.9. 216
FIG. 11.6. RCP measured using ITLC SG eluted with saline. FIG. 11.7. RCP measured using ITLC SG eluted with MeOH:ammonia (3:2). 11.4.2. DOTA hR3 coupling and labelling with 90 Y 11.4.2.1. Materials and method The hR3 antibody was obtained from CIM, p-SCN-Bn-DOTA and DOTA NHS ester were purchased from Macrocyclics Design Technologies and 90 Y was obtained from a 90 Sr/ 90 Y generator assembled at AECS. All other reagents were purchased from Aldrich or Sigma. The centrifuge filter devices used were Amicon Ultra-15 filters (MWCO = 30 000 Da, Millipore). 217
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IAEA RADIOISOTOPES AND RADIOPHARMAC
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YTTRIUM-90 AND RHENIUM-188 RADIOPHA
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IAEA RADIOISOTOPES AND RADIOPHARMAC
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FOREWORD The IAEA helps to promote
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CONTENTS CHAPTER 1. INTRODUCTION ..
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7.4. Discussion ...................
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CHAPTER 12. DEVELOPMENT OF 90 Sr/ 9
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Chapter 1 INTRODUCTION 1.1. BACKGRO
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devices were designed to improve th
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etention of the antibody’s target
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Binding affinity of these derivativ
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Chapter 2 FUNDAMENTAL CONCEPTS IN R
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A special characteristic of radioph
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β particles emitted by 90 Y. Numer
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2.3.1. Exploitation of certain meta
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2.3.3. Antibodies The high specific
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cell cultures, presents one example
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Another very promising form of radi
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destructive processes within the jo
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esearch efforts, since then. Howeve
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[2.18] HAMILTON, J.G., The metaboli
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[2.52] GOLDENBERG, D.M., et al., Mu
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Chapter 3 DEVELOPMENT OF RADIOPHARM
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FIG. 3.3. Elution efficiencies for
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FIG. 3.5. Electrodeposition of yttr
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The results of the experiments of r
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TABLE 3.3. RESULTS FOR 90 Sr/ 90 Y
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FIG. 3.11. Elution yield of a 90 Sr
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According to Fig. 3.12, there is a
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eagent (Sigma). The mean recovery o
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FIG. 3.18. Variation of RCP (%) of
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(20 and 30 min) and volume of 188 R
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FIG. 3.24. Variation of labelling y
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(c) Clodronate: 20 mg of clodronate
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Chapter 4 EVALUATION OF THE 90 Sr/
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Kamadhenu consists of five main com
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Quality control of radiolabelling w
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The electrochemical deposition of 9
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FIG. 4.5. Typical pattern of the wh
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FIG. 4.6. Elution profile from the
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FIG. 4.8. CD20 recognition in Ramos
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4.5. RECOMMENDATIONS AND FUTURE WOR
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adioiodine labelled anti-NCAM antib
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FIG. 5.1. Comparison of biodistribu
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FIG. 5.3. Three step strategy. Biot
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TABLE 5.1. THREE STEP PRETARGETING:
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5.1.4. Therapeutic experiments with
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5.1.4.4. Conclusion The radioiodine
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control procedure for detection of
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6.1.3. Recovery of doped 85/89 Sr 2
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6.2. PREPARATION AND BIOEVALUATION
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(a) (b) (c) FIG. 6.5. PD-10 column
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FIG. 6.7. SDS PAGE pattern of ritux
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FIG. 6.10. HPLC pattern of pure 90
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FIG. 6.13. Cell binding studies wit
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6.2.1.6. Conclusion The procedure f
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FIG. 6.17. Elution profile of 90 Y
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form NADH, which, in turn, causes t
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FIG. 6.19. In vivo distribution pat
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ACKNOWLEDGEMENTS The authors of thi
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Chapter 7 DEVELOPMENT OF THERAPEUTI
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the residual breast tissue becoming
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7.2.5.2. Automatic procedure The la
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FIG. 7.2. RCP values of 90 Y r-BHD
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FIG. 7.3. Pyrogen test shows result
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to avidin at the 1:4 avidin:r-BHD m
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[7.9] SU, F.M., GUSTAVSON, L.M., AX
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8.1. INTRODUCTION In past years, th
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(a) FIG. 8.1. (a) Schematic illustr
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Preliminary synthesis of the biotin
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(a) (b) FIG. 8.4. (a) PEGylated and
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TABLE 8.2. BIODISTRIBUTION IN RATS
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A specific binding to avidin was ev
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[8.13] BOSCHI, A., DUATTI, A., UCCE
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90 Y solution obtained from a 90 Sr
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From each fraction, a ~1 g aliquot
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FIG. 9.2. Relationship between 90 S
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with 188 Re obtained from the 188 W
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9.3.2. Labelling of DPA ale DPA ale
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FIG. 9.8. TLC radiochromatogram of
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(-) 188 Re(CO) 3 (+) (-) 99m Tc(CO)
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the HSA solution containing sodium
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TABLE 9.3. RESULTS OF 99m Tc LABELL
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9.4.4. Yttrium-90 and 177 Lu labell
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FIG. 9.14. In vitro stability of 90
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(a) (b) (c) (d) (e) (f) (g) (h) (i)
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TABLE 9.8. YTTRIUM-90 CITRATE COLLO
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(a) (b) FIG. 9.17. Grain size distr
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TABLE 9.10. BIODISTRIBUTION AFTER A
Page 179 and 180: FIG. 9.19. Structure of DOTA biotin
Page 181 and 182: [9.8] WESTERA, G., GADZE, A., HORST
Page 183 and 184: Chapter 10 DEVELOPMENT, PREPARATION
Page 185 and 186: acidic pH) and the vial heated for
Page 187 and 188: 10.2.2.1. Materials and methods (a)
Page 189 and 190: Using a semiquantitative method, th
Page 191 and 192: FIG. 10.3. Whole body, SPECT and ta
Page 193 and 194: TABLE 10.4. ORGAN DISTRIBUTION STUD
Page 195 and 196: was assessed by measuring the relea
Page 197 and 198: —— Biological studies: The whol
Page 199 and 200: or liver) (see Fig. 10.7). The resu
Page 201 and 202: (b) Results and discussion Healthy
Page 203 and 204: and the pellet (particles of HA lab
Page 205 and 206: FIG. 10.11. Organ distribution stud
Page 207 and 208: The procedure was as follows: —
Page 209 and 210: TABLE 10.5. INFLUENCE OF CHEMICAL I
Page 211 and 212: analysed using ICP OES was within t
Page 213 and 214: suggested for separation of pure 86
Page 215 and 216: adionuclidic purity of the 90 Y sol
Page 217 and 218: FIG. 10.16. (a) Strontium-90/yttriu
Page 219 and 220: [10.5] DJOKIĆ, D.J., JANKOVIĆ, D.
Page 221 and 222: Yttrium-90 is one of the radionucli
Page 223 and 224: (a) (b) (c) The generator was prepa
Page 225 and 226: —— Development of EPC: The EPC
Page 227 and 228: FIG. 11.4. Elution curve of 90 Sr e
Page 229: 11.4. YTTRIUM-90 MAbs The use of th
Page 233 and 234: FIG. 11.9. Biodistribution of 90 Y
Page 235 and 236: 11.5. YTTRIUM-90 EDTMP Bone metasta
Page 237 and 238: FIG. 11.14. Electrophoresis of 90 Y
Page 239 and 240: FIG. 11.15. Particle size distribut
Page 241 and 242: 11.7. CONCLUSION During this CRP, a
Page 243 and 244: Chapter 12 DEVELOPMENT OF 90 Sr/ 90
Page 245 and 246: 12.1.1.4. Acid vapour trap and radi
Page 247 and 248: 12.1.8. Yttrium-90 peptide labellin
Page 249 and 250: (a) FIG. 12.3. Yttrium-90 elution p
Page 251 and 252: FIG. 12.6. HPLC of 90 Y DOTATATE. 1
Page 253 and 254: Chapter 13 BIFUNCTIONAL BISPHOSPHON
Page 255 and 256: latter requirement [13.10]. When th
Page 257 and 258: whether the organometallic core sel
Page 259 and 260: The fate of a targeted imaging prob
Page 261 and 262: FIG. 13.7. SPECT/CT images showing
Page 263 and 264: FIG. 13.9. TLC SG analyses of [ 188
Page 265 and 266: FIG. 13.11. Stability study (toward
Page 267 and 268: Ex vivo biodistribution studies at
Page 269 and 270: was in the form of either pertechne
Page 271 and 272: FIG. 13.19. Absolute uptake of 99m
Page 273 and 274: [13.2] ZHANG, S., GANGAL, G., ULUDA
Page 275 and 276: [13.31] DE ROSALES, R.T.M., et al.,
Page 277 and 278: The activity due to 90 Sr should be
Page 279 and 280: 14.3.1.2. Operation of the 90 Sr/ 9
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antibody were taken, to which 90 Y
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operation, radiopharmaceutical grad
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14.4.1.3. Operation of the stage II
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A typical EPC pattern for a 90 Y pr
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FIG. 14.10. Decay curve of carrier
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FIG. 14.12. ITLC of 90 Y rituximab.
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FIG. 14.13. Reaction scheme for lab
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TABLE 14.6. STABILITY (%) OF 90 Y D
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FIG. 14.18. Microsphere albumin siz
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[14.3] PANDEY, U., DHAMI, P.S., JAG
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naphthalene and 1.2 g of 2,5-diphen
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A-2.2. Materials The method for sep
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out using a Wallac 1411 spectromete
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A-5.3. Procedure The technique was
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Although acyclic chelators offer ma
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(b) (c) and 90 Y colloids, both ser
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CONTRIBUTORS TO DRAFTING AND REVIEW
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INDIA Allied Publishers 1 st Floor,
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A key requirement for the effective
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Yttrium-90 and Rhenium-188 Radiopharmaceuticals for Radionuclide Therapy

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