| Literature DB >> 32661173 |
Qingbin Zeng1, Binglin Bie2, Qianni Guo3,4, Yaping Yuan1,4, Qi Han2, Xiaocang Han5, Mingwei Chen5, Xu Zhang1,4, Yunhuang Yang1,4, Maili Liu1,4, Pan Liu5, Hexiang Deng6,7, Xin Zhou3,4.
Abstract
We report hyperpolarized Xe signal advancement by metal-organic framework (MOF) entrapment (Hyper-SAME) in aqueous solution. The 129Xe NMR signal is drastically promoted by entrapping the Xe into the pores of MOFs. The chemical shift of entrapped 129Xe is clearly distinguishable from that of free 129Xe in water, due to the surface and pore environment of MOFs. The influences from the crystal size of MOFs and their concentration in water are studied. A zinc imidazole MOF, zeolitic imidazole framework-8 (ZIF-8), with particle size of 110 nm at a concentration of 100 mg/mL, was used to give an NMR signal with intensity four times that of free 129Xe in water. Additionally, Hyper-SAME is compatible with hyperpolarized 129Xe chemical exchange saturation transfer. The 129Xe NMR signal can be amplified further by combining the two techniques. More importantly, Hyper-SAME provides a way to make detection of hyperpolarized 129Xe in aqueous solution convenient and broadens the application area of MOFs.Entities:
Keywords: Hyper-CEST; MOFs; MRI; NMR; signal advancement
Year: 2020 PMID: 32661173 PMCID: PMC7395552 DOI: 10.1073/pnas.2004121117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205