1H-19F cross-polarization magic angle spinning dynamic nuclear polarization NMR investigation of advanced pharmaceutical formulations

被引:0
作者
Soltesova, Maria [1 ]
Pinon, Arthur C. [1 ]
Aussenac, Fabien [2 ]
Schlagnitweit, Judith [3 ]
Reiter, Christian [4 ]
Purea, Armin [4 ]
Melzi, Roberto [5 ]
Engelke, Frank [4 ]
Martin, Dave [6 ]
Krambeck, Stefanie [7 ]
Biscans, Annabelle [7 ]
Kay, Emma [8 ]
Emsley, Lyndon [9 ]
Schantz, Staffan [10 ]
机构
[1] Univ Gothenburg, Swedish NMR Ctr, S-41390 Gothenburg, Sweden
[2] Bruker Biospin France, Wissembourg, France
[3] Univ Claude Bernard Lyon 1, Ctr RMN Tres Hauts Champs Lyon, UMR5082 CNRS, ENS Lyon, Villeurbanne, France
[4] Bruker BioSpin Germany, Ettlingen, Germany
[5] Bruker Biospin Italy, Milan, Italy
[6] AstraZeneca, Oral Prod Dev, Pharmaceut Technol & Dev, Macclesfield, England
[7] AstraZeneca, Cell Gene & RNA Therapy, Discovery Sci, BioPharmaceut R&D, Gothenburg, Sweden
[8] AstraZeneca, Assays Profiling & Cell Sci, Discovery Sci, Gothenburg, Sweden
[9] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[10] AstraZeneca, Oral Prod Dev, Operat, Pharmaceut Technol & Dev, Gothenburg, Sweden
关键词
Nuclear magnetic resonance; Dynamic nuclear polarization; Fluorine; NMR probe; Pharmaceutical formulation; SOLID-STATE NMR; SPECTROSCOPY; RESOLUTION; PROTEINS; FIELD;
D O I
10.1016/j.jmr.2024.107827
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new 3.2 mm H-1-F-19-X magic angle spinning dynamic nuclear polarization NMR (MAS DNP-NMR) probe was developed with a unique coil design with separate radiofrequency channels for H-1 excitation and C-13 or F-19 detection to enable acquisition of H-1-F-19 cross-polarization (CP) MAS experiments, direct-detected F-19 spectra with proton decoupling, and acquisition on C-13 with simultaneous double decoupling on the H-1 and 19F channels as well as H-1-F-19-C-13 double-CP experiments under low temperature MAS DNP conditions. We use these sequences to study AZD2811, which is an active pharmaceutical ingredient (API), in its pure dry state as well as in its corresponding drug delivery formulation consisting of drug-loaded polymeric nanoparticles (PNPs). Included in this study are also small interfering RNAs (siRNAs) for therapeutic targeting of peptidyl-prolyl cis-trans isomerase B (Ppib) mRNA. We demonstrate that H-1-F-19 CP MAS experiments performed on the new HFX probe represent a notable advantage over usually acquired direct-detected F-19 experiments. The indirect F-19 DNP enhancement epsilon(on/off)(F-19) = 26 was obtained via H-1-F-19 CP for the pure API impregnated with DNP solution, with an overall 30-fold sensitivity gain compared to the direct-detected F-19 experiment under similar conditions. DNP enhancement value of epsilon(on/off)(F-19) = 42 was obtained via H-1-F-19 CP for the polymeric nanoparticle suspension and epsilon(on/off)(F-19) approximate to 150 were obtained for two different siRNAs in frozen DNP solution.
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页数:7
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