Optimization of a convenient route to produce N-succinimidyl 4-radiodobenzoate for radioiodination of proteins

Applied Radiation and Isotopes

Volumn 58, Issue 6, 2003, Pages 667-673

  Araujo, E B ^a   Santos, J S ^a   Colturato, M T ^a   Muramoto, E ^a   Silva, C P G ^a  

^a INSTITUTO DE PESQUISAS ENERGÉTICAS E NUCLEARES   (Brazil)

Author keywords

131I; Conjugation; In vivo stability; Prosthetic group; Proteins

Indexed keywords

CHEMICAL REACTIONS; OPTIMIZATION; ORGANIC ACIDS; RADIOISOTOPES;

PROTEIN CONJUGATION;

PROTEINS;

4 BROMOBENZOIC ACID; 4 IODOBENZOIC ACID I 131; BENZOIC ACID DERIVATIVE; BROMOBENZOIC ACID DERIVATIVE; COPPER CHLORIDE; COPPER ION; IMMUNOGLOBULIN G; N SUCCINIMIDYL 4 RADIODOBENZOATE; O (N SUCCINIMIDYL) N,N,N',N' TETRAMETHYLURONIUM; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CHEMICAL REACTION; CONJUGATION; CONTROLLED STUDY; DEBROMINATION; FEMALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN STABILITY; PURIFICATION; RADIOIODINATION; REACTION TIME;

EID: 0038241504     PISSN: 09698043     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0969-8043(03)00068-X     Document Type: Article

References (13)

1. Garg P.K., Archer J.R.G.E., Bigner D.D., Zalutsky M.R. Synthesis of radioiodinated N-succinimidyl iodobenzoate. optimization for use in antibody labelling Appl. Radiat. Isot. 40(6):1989;485-490.
2. Garg P.K., Slade S.K., Harrison C.L., Zalutsky M.R. Labeling proteins using aryl iodide acylation agents. influence of meta vs. para substitution on in vivo stability Nucl. Med. Biol. 16(7):1989;669-673.
3. 18F]Fluoroacetic acids. Appl. Radiat. Isot. 45(6):1994;715-717.
4. Koziorowski J., Henssen C., Weinreich R. A new convenient route to radioiodinated N-succinimidyl 3- and 4-iodobenzoate, two reagents for radioiodination of proteins. Appl. Radiat. Isot. 49(8):1998;955-959.
5. Lindegren S., Skarnemark G., Jacobsson L., Karlsson B. Chloramine-T in high-specific-activity radioiodination of antibodies using N-succinimidyl-3-(trimethylstannyl)benzoate as an intermediate. Nucl. Med. Biol. 25:1998;659-665.
6. Moerlein S.M. Regioespecific aromatic radioiodination via n.c.a. copper (I) assisted iododebromination. Radiochim. Acta. 50:1990;55-61.
7. Salacinsky P.R.P. Iodination of proteins, glycoproteins and peptides using a solid-phase oxidizing agent, 1.3.4.6.-tetrachloro-3α-6α-diphenylglycoluril (Iodogen). Anal. Biochem. 117:1981;136-146.
8. 18F] fluorobenzoate. Nucl. Med. Biol. 19:1992;275.
9. +-channel syntheses and in-vivo evaluation in NMRI mice J. Labelled Compds. Radiopharm. 37:1995;513-515.
10. Wester H.J., Hamacher K., Stocklin G. A comparative study of n.c.a. Fluorine-18 labeling of proteins via acylation and photochemical conjugation. Nucl. Med. Biol. 23:1996;365-372.
11. Wilbur D.S. Radiohalogenation of proteins. Na overview of radionuclides Bioconjugate Chem. 3:1992;433.
12. Wilbur D.S., Hadley S.W., Hylarides M.D., Abrams P.G., Beaumier P.A., Morgan A.C., Reno J.M., Fritzberg A.R. Development of a stable radioiodinating reagent to label monoclonal antibodies for radiotherapy of cancer. J. Nucl. Med. 30:1989;216-226.
13. Zalutsky M.R., Narula A.S. A method for the radiohalogenation of proteins resulting in decreased thyroid uptake of radioiodine. Appl. Radiat. Isot. 38(12):1987;1051-1055.