Ac-EAZY!: Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application

The application of 225Ac (half-life T1/2 = 9.92 d) dramatically reduces the activity used for peptide receptor radionuclide therapy by a factor of 1000 in comparison to 90Y, 177Lu or 188Re while maintaining the therapeutic outcome. Additionally, the range of alpha particles of 225Ac and its daughter...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Pretze, Marc (VerfasserIn) , Kunkel, Falk (VerfasserIn) , Runge, Roswitha (VerfasserIn) , Freudenberg, Robert (VerfasserIn) , Braune, Anja (VerfasserIn) , Hartmann, Holger (VerfasserIn) , Schwarz, Uwe (VerfasserIn) , Brogsitter, Claudia (VerfasserIn) , Kotzerke, Jörg (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 6 July 2021
In: Pharmaceuticals
Year: 2021, Jahrgang: 14, Heft: 7, Pages: 1-10
ISSN:1424-8247
DOI:10.3390/ph14070652
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/ph14070652
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/1424-8247/14/7/652
Volltext
Verfasserangaben:Marc Pretze, Falk Kunkel, Roswitha Runge, Robert Freudenberg, Anja Braune, Holger Hartmann, Uwe Schwarz, Claudia Brogsitter and Jörg Kotzerke

MARC

LEADER 00000caa a2200000 c 4500
001 1806296292
003 DE-627
005 20220820195647.0
007 cr uuu---uuuuu
008 220608s2021 xx |||||o 00| ||eng c
024 7 |a 10.3390/ph14070652  |2 doi 
035 |a (DE-627)1806296292 
035 |a (DE-599)KXP1806296292 
035 |a (OCoLC)1341460724 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 33  |2 sdnb 
100 1 |a Pretze, Marc  |d 1983-  |e VerfasserIn  |0 (DE-588)1054783837  |0 (DE-627)792109120  |0 (DE-576)410510602  |4 aut 
245 1 0 |a Ac-EAZY!  |b Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application  |c Marc Pretze, Falk Kunkel, Roswitha Runge, Robert Freudenberg, Anja Braune, Holger Hartmann, Uwe Schwarz, Claudia Brogsitter and Jörg Kotzerke 
264 1 |c 6 July 2021 
300 |a 10 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
500 |a Published: 6 July 2021 
500 |a Gesehen am 08.06.2022 
520 |a The application of 225Ac (half-life T1/2 = 9.92 d) dramatically reduces the activity used for peptide receptor radionuclide therapy by a factor of 1000 in comparison to 90Y, 177Lu or 188Re while maintaining the therapeutic outcome. Additionally, the range of alpha particles of 225Ac and its daughter nuclides in tissue is much lower (47-85 μm for alpha energies Eα = 5.8-8.4 MeV), which results in a very precise dose deposition within the tumor. DOTA-conjugated commercially available peptides used for endoradiotherapy, which can readily be labeled with 177Lu or 90Y, can also accommodate 225Ac. The benefits are lower doses in normal tissue for the patient, dose reduction of the employees and environment and less shielding material. The low availability of 225Ac activity is preventing its application in clinical practice. Overcoming this barrier would open a broad field of 225Ac therapy. Independent which production pathway of 225Ac proves the most feasible, the use of automated synthesis and feasible and reproducible patient doses are needed. The Modular-Lab EAZY is one example of a GMP-compliant system, and the cassettes used for synthesis are small. Therefore, also the waste after the synthesis can be minimized. In this work, two different automated setups with different purification systems are presented. In its final configuration, three masterbatches were performed on the ML EAZY for DOTA-TATE and PSMA-I&T, respectively, fulfilling all quality criteria with final radiochemical yields of 80-90% for the 225Ac-labeled peptides. 
650 4 |a actinium-225 
650 4 |a endoradiotherapy 
650 4 |a GMP 
650 4 |a module synthesis 
650 4 |a PSMA 
650 4 |a TATE 
700 1 |a Kunkel, Falk  |e VerfasserIn  |4 aut 
700 1 |a Runge, Roswitha  |d 1958-  |e VerfasserIn  |0 (DE-588)139817778  |0 (DE-627)613786610  |0 (DE-576)312614756  |4 aut 
700 1 |a Freudenberg, Robert  |d 1980-  |e VerfasserIn  |0 (DE-588)1028806728  |0 (DE-627)731622804  |0 (DE-576)376265213  |4 aut 
700 1 |a Braune, Anja  |d 1985-  |e VerfasserIn  |0 (DE-588)1150879491  |0 (DE-627)1011139561  |0 (DE-576)497309106  |4 aut 
700 1 |a Hartmann, Holger  |d 1960-  |e VerfasserIn  |0 (DE-588)103011272X  |0 (DE-627)734805705  |0 (DE-576)377919802  |4 aut 
700 1 |a Schwarz, Uwe  |e VerfasserIn  |4 aut 
700 1 |a Brogsitter, Claudia  |e VerfasserIn  |0 (DE-588)1171012802  |0 (DE-627)1040367135  |0 (DE-576)51309380X  |4 aut 
700 1 |a Kotzerke, Jörg  |d 1958-  |e VerfasserIn  |0 (DE-588)1127750178  |0 (DE-627)882204254  |0 (DE-576)485364123  |4 aut 
773 0 8 |i Enthalten in  |t Pharmaceuticals  |d Basel : MDPI, 2004  |g 14(2021), 7, Artikel-ID 652, Seite 1-10  |h Online-Ressource  |w (DE-627)491437528  |w (DE-600)2193542-7  |w (DE-576)281279470  |x 1424-8247  |7 nnas  |a Ac-EAZY! Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application 
773 1 8 |g volume:14  |g year:2021  |g number:7  |g elocationid:652  |g pages:1-10  |g extent:10  |a Ac-EAZY! Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application 
856 4 0 |u https://doi.org/10.3390/ph14070652  |x Verlag  |x Resolving-System  |z lizenzpflichtig  |3 Volltext 
856 4 0 |u https://www.mdpi.com/1424-8247/14/7/652  |x Verlag  |z lizenzpflichtig  |3 Volltext 
951 |a AR 
992 |a 20220608 
993 |a Article 
994 |a 2021 
998 |g 1054783837  |a Pretze, Marc  |m 1054783837:Pretze, Marc  |d 60000  |e 60000PP1054783837  |k 0/60000/  |p 1  |x j 
999 |a KXP-PPN1806296292  |e 4145277260 
BIB |a Y 
SER |a journal 
JSO |a {"recId":"1806296292","origin":[{"dateIssuedKey":"2021","dateIssuedDisp":"6 July 2021"}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"relHost":[{"name":{"displayForm":["Molecular Diversity Preservation International"]},"note":["Gesehen am 05.09.2011"],"disp":"Ac-EAZY! Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical applicationPharmaceuticals","physDesc":[{"extent":"Online-Ressource"}],"id":{"zdb":["2193542-7"],"issn":["1424-8247"],"eki":["491437528"]},"type":{"media":"Online-Ressource","bibl":"periodical"},"recId":"491437528","origin":[{"dateIssuedKey":"2004","dateIssuedDisp":"2004-","publisher":"MDPI","publisherPlace":"Basel"}],"part":{"year":"2021","text":"14(2021), 7, Artikel-ID 652, Seite 1-10","volume":"14","issue":"7","extent":"10","pages":"1-10"},"language":["eng"],"title":[{"title_sort":"Pharmaceuticals","title":"Pharmaceuticals"}],"pubHistory":["1.2004 -"]}],"note":["Published: 6 July 2021","Gesehen am 08.06.2022"],"id":{"eki":["1806296292"],"doi":["10.3390/ph14070652"]},"physDesc":[{"extent":"10 S."}],"name":{"displayForm":["Marc Pretze, Falk Kunkel, Roswitha Runge, Robert Freudenberg, Anja Braune, Holger Hartmann, Uwe Schwarz, Claudia Brogsitter and Jörg Kotzerke"]},"person":[{"family":"Pretze","display":"Pretze, Marc","role":"aut","given":"Marc"},{"family":"Kunkel","display":"Kunkel, Falk","given":"Falk","role":"aut"},{"family":"Runge","display":"Runge, Roswitha","role":"aut","given":"Roswitha"},{"role":"aut","given":"Robert","display":"Freudenberg, Robert","family":"Freudenberg"},{"display":"Braune, Anja","role":"aut","given":"Anja","family":"Braune"},{"family":"Hartmann","role":"aut","given":"Holger","display":"Hartmann, Holger"},{"family":"Schwarz","given":"Uwe","role":"aut","display":"Schwarz, Uwe"},{"family":"Brogsitter","role":"aut","given":"Claudia","display":"Brogsitter, Claudia"},{"family":"Kotzerke","given":"Jörg","role":"aut","display":"Kotzerke, Jörg"}],"language":["eng"],"title":[{"title_sort":"Ac-EAZY!","title":"Ac-EAZY!","subtitle":"Towards GMP-compliant module syntheses of 225Ac-labeled peptides for clinical application"}]} 
SRT |a PRETZEMARCACEAZY6202