FFr RetentionIn order to test retention of the 225Ac decay products

FFr RetentionIn order to test retention of the 225Ac decay products in vitro, the 225 Ac-NPs were loaded into a dialysis membrane and dialyzed against 400 mL of 18 MV water. The dialysis tube was stirred for a sufficient time for daughter equilibrium to be established (.3 hours), then a 5 mL aliquot was taken for c-ray spectrometry analysis. Each sample was re-analyzed at a later time to determine the level of 225Ac in the removed dialysate fraction. The measured activities were corrected for decay and dialysate loss from prior aliquot removals. The 213Bi activity in the dialysate was used as a measure of the 221Fr that was released from the NP, as 213Bi which 12926553 escaped from the particles did not move across the dialysis membrane [28].Surface ModificationSurfaces were modified using a lipoamide-dPEG12-acid linker (Quanta Biodesign). Two mg of dPEG were added, followed by 6 mg of Tris(2-carboxyethyl)phosphine reducing agent to cleave the disulfide bond. The pH of the solution was adjusted to 7 using 0.1 M NaOH and the reaction mixture was stirred for 4 hours. Connection of the linker was determined by a shift in the plasmon resonance near 530 nm as monitored by UV-Vis spectroscopy before and after the addition of the linker.MicroSPECT/CT ImagingSmall animal imaging was performed using a microCAT II SPECT dual modality platform (Siemens Preclinical Imaging, Knoxville, TN). Mice were injected with approximately 40 times more NP than were the mice for tert-Butylhydroquinone web biodistribution studies. Thus the mice for competition with cold mAb 201b did not have the same ratio of cold competitor to radiolabeled NP and competition was not as complete.Animals were sacrificed by overdose of isoflurane at 1 h postinjection and imaged via microSPECT/CT 3 h later when the 225Ac and its daughters had reached equilibrium. SPECT data for the final images were acquired as previously described by Woodward et al. [28].Antibody ConjugationTo attach antibodies to the linker, the carboxylate group on the PEG linker was first activated using 8 mL of 10 mg/mL aqueous 3sulfo-N-hydroxysuccinimide (sulfo-NHS) and 80 mL of 10 mg/mL 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC). 4 mg of EDC and 0.4 mg of sulfo-NHS were used per mg of NPs. After 15 minutes, the solutions were centrifuged to remove excess EDC/ NHS, the supernatant removed, and the particles redispersed in phosphate buffered saline (0.01 M NaPO4 pH 7.6 in 0.15 M NaCl, PBS). MAb 201b was added (, 1 mg of 1516647 mAb/mg of NP), and the mixture was mixed by rotation overnight. The reaction was then quenched with 1 mg of glycine, which was allowed to react for 15 minutes. The particles were then centrifuged to remove excess antibody. The supernatant was removed and the particles were redispersed in PBS containing 5 mg/mL bovine serum albumin (BSA/PBS). The particles were sonicated with aAuthor ContributionsConceived and designed the experiments: MFM JW SJK SM JDR. Performed the experiments: MFM JW RAB SJK. Analyzed the data: MFM SJK SM. Contributed reagents/materials/analysis tools: AJR. Wrote the paper: MFM SJK SM JDR.
Many experiments involving the manipulation of nucleic acids and proteins require multiple strong linkages that can be established in-situ, and can be used together and thus must be specific. For certain applications the molecules involved are immobilized on surfaces, either because the experimental setup requires fixing and controlling the position of the get 548-04-9 molecular ends or because the molecular phenomenon is measur.FFr RetentionIn order to test retention of the 225Ac decay products in vitro, the 225 Ac-NPs were loaded into a dialysis membrane and dialyzed against 400 mL of 18 MV water. The dialysis tube was stirred for a sufficient time for daughter equilibrium to be established (.3 hours), then a 5 mL aliquot was taken for c-ray spectrometry analysis. Each sample was re-analyzed at a later time to determine the level of 225Ac in the removed dialysate fraction. The measured activities were corrected for decay and dialysate loss from prior aliquot removals. The 213Bi activity in the dialysate was used as a measure of the 221Fr that was released from the NP, as 213Bi which 12926553 escaped from the particles did not move across the dialysis membrane [28].Surface ModificationSurfaces were modified using a lipoamide-dPEG12-acid linker (Quanta Biodesign). Two mg of dPEG were added, followed by 6 mg of Tris(2-carboxyethyl)phosphine reducing agent to cleave the disulfide bond. The pH of the solution was adjusted to 7 using 0.1 M NaOH and the reaction mixture was stirred for 4 hours. Connection of the linker was determined by a shift in the plasmon resonance near 530 nm as monitored by UV-Vis spectroscopy before and after the addition of the linker.MicroSPECT/CT ImagingSmall animal imaging was performed using a microCAT II SPECT dual modality platform (Siemens Preclinical Imaging, Knoxville, TN). Mice were injected with approximately 40 times more NP than were the mice for biodistribution studies. Thus the mice for competition with cold mAb 201b did not have the same ratio of cold competitor to radiolabeled NP and competition was not as complete.Animals were sacrificed by overdose of isoflurane at 1 h postinjection and imaged via microSPECT/CT 3 h later when the 225Ac and its daughters had reached equilibrium. SPECT data for the final images were acquired as previously described by Woodward et al. [28].Antibody ConjugationTo attach antibodies to the linker, the carboxylate group on the PEG linker was first activated using 8 mL of 10 mg/mL aqueous 3sulfo-N-hydroxysuccinimide (sulfo-NHS) and 80 mL of 10 mg/mL 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC). 4 mg of EDC and 0.4 mg of sulfo-NHS were used per mg of NPs. After 15 minutes, the solutions were centrifuged to remove excess EDC/ NHS, the supernatant removed, and the particles redispersed in phosphate buffered saline (0.01 M NaPO4 pH 7.6 in 0.15 M NaCl, PBS). MAb 201b was added (, 1 mg of 1516647 mAb/mg of NP), and the mixture was mixed by rotation overnight. The reaction was then quenched with 1 mg of glycine, which was allowed to react for 15 minutes. The particles were then centrifuged to remove excess antibody. The supernatant was removed and the particles were redispersed in PBS containing 5 mg/mL bovine serum albumin (BSA/PBS). The particles were sonicated with aAuthor ContributionsConceived and designed the experiments: MFM JW SJK SM JDR. Performed the experiments: MFM JW RAB SJK. Analyzed the data: MFM SJK SM. Contributed reagents/materials/analysis tools: AJR. Wrote the paper: MFM SJK SM JDR.
Many experiments involving the manipulation of nucleic acids and proteins require multiple strong linkages that can be established in-situ, and can be used together and thus must be specific. For certain applications the molecules involved are immobilized on surfaces, either because the experimental setup requires fixing and controlling the position of the molecular ends or because the molecular phenomenon is measur.