Yung-Ya Lin

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Name: Lin, Yung Ya
Organization: University of California , USA
Department: Department of Chemistry & Biochemistry
Title: (PhD)

TOPICS

Co-reporter:Zhao Li;Chao-Hsiung Hsu;Nikolay Dimitrov;Dennis W. Hwang;Hsin-Wei Chang;Lian-Pin Hwang
Magnetic Resonance in Medicine 2015 Volume 74( Issue 1) pp:
Publication Date(Web):
DOI:10.1002/mrm.25832

Purpose

Sensitive imaging of superparamagnetic nanoparticles or aggregates is of great importance in MR molecular imaging and medical diagnosis. For this purpose, a conceptually new approach, termed active feedback magnetic resonance, was developed.

Methods

In the presence of the Zeeman field, a dipolar field is induced by the superparamagnetic nanoparticles or aggregates. Such dipolar field creates spatial and temporal (due to water diffusion) variations to the precession frequency of the nearby water 1H magnetization. Sensitive imaging of magnetic nanoparticles or aggregates can be achieved by manipulating the intrinsic spin dynamics by selective self-excitation and fixed-point dynamics under active feedback fields.

Results

Phantom experiments of superparamagnetic nanoparticles; in vitro experiments of brain tissue with blood clots; and in vivo mouse images of colon cancers, with and without labeling by magnetic nanoparticles, suggest that this new approach provides enhanced, robust, and positive contrast in imaging magnetic nanoparticles or aggregates for cancer detection.

Conclusion

The spin dynamics originated from selective self-excitation and fixed-point dynamics under active feedback fields have been shown to be sensitive to dipolar fields generated by magnetic nanoparticles. Magn Reson Med 74:33–41, 2015. © 2014 Wiley Periodicals, Inc.

Co-reporter:Zhao Li;Chao-Hsiung Hsu;Nikolay Dimitrov;Dennis W. Hwang;Hsin-Wei Chang;Lian-Pin Hwang
Magnetic Resonance in Medicine 2015 Volume 74( Issue 1) pp:33-41
Publication Date(Web):
DOI:10.1002/mrm.25632

Purpose

Sensitive imaging of superparamagnetic nanoparticles or aggregates is of great importance in MR molecular imaging and medical diagnosis. For this purpose, a conceptually new approach, termed active feedback magnetic resonance, was developed.

Methods

In the presence of the Zeeman field, a dipolar field is induced by the superparamagnetic nanoparticles or aggregates. Such dipolar field creates spatial and temporal (due to water diffusion) variations to the precession frequency of the nearby water 1H magnetization. Sensitive imaging of magnetic nanoparticles or aggregates can be achieved by manipulating the intrinsic spin dynamics by selective self-excitation and fixed-point dynamics under active feedback fields.

Results

Phantom experiments of superparamagnetic nanoparticles; in vitro experiments of brain tissue with blood clots; and in vivo mouse images of colon cancers, with and without labeling by magnetic nanoparticles, suggest that this new approach provides enhanced, robust, and positive contrast in imaging magnetic nanoparticles or aggregates for cancer detection.

Conclusion

The spin dynamics originated from selective self-excitation and fixed-point dynamics under active feedback fields have been shown to be sensitive to dipolar fields generated by magnetic nanoparticles. Magn Reson Med 74:33–41, 2015. © 2014 Wiley Periodicals, Inc.

Co-reporter:Lin-Chen Ho, Chao-Hsiung Hsu, Chung-Mao Ou, Chia-Wei Wang, Tsang-Pai Liu, Lian-Pin Hwang, Yung-Ya Lin, Huan-Tsung Chang
Biomaterials 2015 37() pp: 436-446
Publication Date(Web):
DOI:10.1016/j.biomaterials.2014.10.006
Co-reporter:Stephanie M. Wolahan, Zhao Li, Chao-Hsiung Hsu, Shing-Jong Huang, Robert Clubb, Lian-Pin Hwang, Yung-Ya Lin
Journal of Magnetic Resonance 2014 248() pp: 19-22
Publication Date(Web):November 2014
DOI:10.1016/j.jmr.2014.09.008
•Strong, chaotic self-induced dynamic frequency shifts (DFS) in NMR was discovered.•Its physical origin was identified: nonlinearity in spin dynamics by feedback fields.•DFS induces significant errors in frequencies and other quantities (e.g., temperature).•A spin control scheme to mitigate the disastrous effects of DFS was demonstrated.•It showed a 10× improvement in the accuracy of measuring samples’ temperatures.Accurate temperature measurement is a requisite for obtaining reliable thermodynamic and kinetic information in all NMR experiments. A widely used method to calibrate sample temperature depends on a secondary standard with temperature-dependent chemical shifts to report the true sample temperature, such as the hydroxyl proton in neat methanol or neat ethylene glycol. The temperature-dependent chemical shift of the hydroxyl protons arises from the sensitivity of the hydrogen-bond network to small changes in temperature. The frequency separation between the alkyl and the hydroxyl protons are then converted to sample temperature. Temperature measurements by this method, however, have been reported to be inconsistent and incorrect in modern NMR, particularly for spectrometers equipped with cryogenically-cooled probes. Such errors make it difficult or even impossible to study chemical exchange and molecular dynamics or to compare data acquired on different instruments, as is frequently done in biomolecular NMR. In this work, we identify the physical origins for such errors to be unequal amount of dynamical frequency shifts on the alkyl and the hydroxyl protons induced by strong radiation damping (RD) feedback fields. Common methods used to circumvent RD may not suppress such errors. A simple, easy-to-implement solution was demonstrated that neutralizes the RD effect on the frequency separation by a “selective crushing recovery” pulse sequence to equalize the transverse magnetization of both spin species. Experiments using cryoprobes at 500 MHz and 800 MHz demonstrated that this approach can effectively reduce the errors in temperature measurements from about ±4.0 K to within ±0.4 K in general.
Co-reporter:Kuan-Ju Chen, Stephanie M. Wolahan, Hao Wang, Chao-Hsiung Hsu, Hsing-Wei Chang, Armando Durazo, Lian-Pin Hwang, Mitch A. Garcia, Ziyue K. Jiang, Lily Wu, Yung-Ya Lin, Hsian-Rong Tseng
Biomaterials 2011 32(8) pp: 2160-2165
Publication Date(Web):
DOI:10.1016/j.biomaterials.2010.11.043
Co-reporter:Susie Y. Huang;Sophia S. Yang
Magnetic Resonance in Medicine 2009 Volume 61( Issue 4) pp:925-936
Publication Date(Web):
DOI:10.1002/mrm.21584

Abstract

Nonlinear feedback interactions have been shown to amplify contrast due to small differences in resonance frequency arising from microscopic susceptibility variations. Determining whether the selectivity of feedback-based contrast enhancement for small resonance frequency variations remains valid even in the presence of macroscopic field inhomogeneity is important for transitioning this new methodology into in vivo applications in imaging systems with lower field strengths and poorer homogeneity. This work shows that contrast enhancement under the radiation damping (RD) feedback field is sensitive to microscopic intravoxel frequency variations. Feedback-enhanced contrast provides superior signal differentiation from voxels with distinct microscopic frequency distributions compared with T-weighted imaging, while remaining robust to macroscopic field gradients, which frequently give rise to artifacts by other frequency-sensitive methods. Applying multiple RF pulses during evolution under RD and actively adjusting the phase and amplitude of the feedback field are shown to further improve signal differentiation. Experimental results reveal that feedback-enhanced contrast can generate positive contrast, reflecting microscopic field variations induced by strong local dipole fields, such as those created by blood vessels and superparamagnetic iron oxide nanoparticles. Extensions to in vivo imaging at lower field strengths are discussed in the context of amplifying the RD field via active electronic feedback. Magn Reson Med, 2009. © 2009 Wiley-Liss, Inc.

Co-reporter:Susie Y. Huang;Stephanie M. Wolahan;Gary W. Mathern;Dennis J. Chute;Massoud Akhtari;Snow T. Nguyen;My N. Huynh;Noriko Salamon
Magnetic Resonance in Medicine 2006 Volume 56(Issue 4) pp:776-786
Publication Date(Web):29 AUG 2006
DOI:10.1002/mrm.20987

A new method for enhancing MRI contrast between gray matter (GM) and white matter (WM) in epilepsy surgery patients with symptomatic lesions is presented. This method uses the radiation damping feedback interaction in high-field MRI to amplify contrast due to small differences in resonance frequency in GM and WM corresponding to variations in tissue susceptibility. High-resolution radiation damping-enhanced (RD) images of in vitro brain tissue from five patients were acquired at 14 T and compared with corresponding conventional T1-, T-, and proton density (PD)-weighted images. The RD images yielded a six times better contrast-to-noise ratio (CNR = 44.8) on average than the best optimized T1-weighted (CNR = 7.92), T-weighted (CNR = 4.20), and PD-weighted images (CNR = 2.52). Regional analysis of the signal as a function of evolution time and initial pulse flip angle, and comparison with numerical simulations confirmed that radiation damping was responsible for the observed signal growth. The time evolution of the signal in different tissue regions was also used to identify subtle changes in tissue composition that were not revealed in conventional MR images. RD contrast is compared with conventional MR methods for separating different tissue types, and its value and limitations are discussed. Magn Reson Med, 2006. © 2006 Wiley-Liss, Inc.

Co-reporter:Jamie D. Walls, Yung-Ya Lin
Solid State Nuclear Magnetic Resonance 2006 Volume 29(1–3) pp:22-29
Publication Date(Web):February 2006
DOI:10.1016/j.ssnmr.2005.09.007
We present a general method for constructing a subset of the constants of motion in terms of products of spin operators. These operators are then used to give insight into the multi-spin orders comprising the quasi-equilibrium state formed under a Jeener–Broekaert sequence in small, dipolar-coupled, spin systems. We further show that constants of motion that represent single-quantum coherences are present due to the symmetry of the dipolar Hamiltonian under 180° spin rotations, and that such coherences contribute a DC component to the FID which vanishes in the absence of the flip-flop terms and is only present for spin clusters with an odd number of spins.
Silicide
Platinum silicide(PtSi)
Germanium, compd. with iron (3:5)
Nickel silicide (NiSi)(6CI,7CI,8CI,9CI)
Ethanaminium,2-hydroxy-N,N,N-trimethyl-
NICKEL SILICIDE