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Dive into the research topics where Jinwoo Cheon is active.

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Featured researches published by Jinwoo Cheon.


Nature Nanotechnology | 2011

Exchange-coupled magnetic nanoparticles for efficient heat induction.

Jae Hyun Lee; Jung Tak Jang; Jin Sil Choi; Seung Ho Moon; Seung Hyun Noh; Ji Wook Kim; Jin Gyu Kim; Il Sun Kim; Kook In Park; Jinwoo Cheon

The conversion of electromagnetic energy into heat by nanoparticles has the potential to be a powerful, non-invasive technique for biotechnology applications such as drug release, disease treatment and remote control of single cell functions, but poor conversion efficiencies have hindered practical applications so far. In this Letter, we demonstrate a significant increase in the efficiency of magnetic thermal induction by nanoparticles. We take advantage of the exchange coupling between a magnetically hard core and magnetically soft shell to tune the magnetic properties of the nanoparticle and maximize the specific loss power, which is a gauge of the conversion efficiency. The optimized core-shell magnetic nanoparticles have specific loss power values that are an order of magnitude larger than conventional iron-oxide nanoparticles. We also perform an antitumour study in mice, and find that the therapeutic efficacy of these nanoparticles is superior to that of a common anticancer drug.


Nature Materials | 2012

A magnetic switch for the control of cell death signalling in in vitro and in vivo systems

Mi Hyeon Cho; Eun Jung Lee; Mina Son; Jae Hyun Lee; Dongwon Yoo; Ji Wook Kim; Seung Woo Park; Jeon Soo Shin; Jinwoo Cheon

The regulation of cellular activities in a controlled manner is one of the most challenging issues in fields ranging from cell biology to biomedicine. Nanoparticles have the potential of becoming useful tools for controlling cell signalling pathways in a space and time selective fashion. Here, we have developed magnetic nanoparticles that turn on apoptosis cell signalling by using a magnetic field in a remote and non-invasive manner. The magnetic switch consists of zinc-doped iron oxide magnetic nanoparticles (Zn(0.4)Fe(2.6)O(4)), conjugated with a targeting antibody for death receptor 4 (DR4) of DLD-1 colon cancer cells. The magnetic switch, in its On mode when a magnetic field is applied to aggregate magnetic nanoparticle-bound DR4s, promotes apoptosis signalling pathways. We have also demonstrated that the magnetic switch is operable at the micrometre scale and that it can be applied in an in vivo system where apoptotic morphological changes of zebrafish are successfully induced.


Angewandte Chemie | 2013

On‐Demand Drug Release System for In Vivo Cancer Treatment through Self‐Assembled Magnetic Nanoparticles

Jae Hyun Lee; Kuan Ju Chen; Seung Hyun Noh; Mitch A. Garcia; Hao Wang; Wei-Yu Lin; Heeyeong Jeong; Brian Junoh Kong; David Stout; Jinwoo Cheon; Hsian-Rong Tseng

The intrinsic nature of small-molecule chemotherapeutics, including i) limited aqueous solubility, ii) systemic toxicity due to non-specific whole-body distribution, and iii) potential development of drug resistance after initial administration, compromises their treatment efficacy.[1] Recently, nanoparticle (NP)-based drug delivery systems have been considered as promising alternatives to overcome some of these limitations and begin to resolve obstacles in the disease management in clinical oncology.[2] The intraparticular space of a NP vector can be employed to package drug payloads without constrain associated with their solubility. Further, NP vectors exhibit enhanced permeability and retention (EPR) effects[3] that facilitate the differential uptake, leading to preferential spatio-distribution in tumor.[4] However, conventional NP drug delivery systems tend to passively release drug payloads, limiting the ability to release an effective drug concentration at a desired time window. Therefore, there is a need to develop next-generation NP drug delivery system such as a stimuli-responsive drug release system with a goal of achieving spatio-temporal control, by which an acute level of drug concentration can be delivered at the time point the NP vectors reach maximum tumor accumulation.[5] By doing so, it is expected to dramatically improve therapeutic effects in tumor and effectively reduce systematic toxicity at a minute drug dosage.[6]


Chemical Reviews | 2015

Recent Developments in Magnetic Diagnostic Systems.

Hakho Lee; Tae Hyun Shin; Jinwoo Cheon; Ralph Weissleder

Rapid point-of-care (POC) diagnostics that enable specific cellular and molecular detection are currently being developed while some have already become clinical reality. These diagnostics are often based on portable, handheld instruments and reagent-containing test kits. Overall, the development has largely been driven by technological advances, medical needs and cost-saving initiatives. For example, POC systems allow care providers to obtain test results quicker1, which in turn enables immediate clinical management decisions, elimination of costly delays to result in better care. The introduction of POC systems into primary and home care will ultimately preempt unnecessary hospitalization, improve inefficiencies associated with expensive hospital-based medical care and reduce dependence on large, centralized clinics for routine diagnosis.2, 3 POC technologies are also expected to have major impacts in resource-limited settings and low/middle income countries where access to healthcare is often limited.4


Angewandte Chemie | 2013

Magnetically Triggered Dual Functional Nanoparticles for Resistance-Free Apoptotic Hyperthermia†

Dongwon Yoo; Heeyeong Jeong; Seung-hyun Noh; Jae Hyun Lee; Jinwoo Cheon

Overcoming resistance: Heat-treated cancer cells possess a protective mechanism for resistance and survival. Resistance-free apoptosis-inducing magnetic nanoparticles (RAINs) successfully promote hyperthermic apoptosis, obstructing cell survival by triggering two functional units of heat generation and the release of geldanamycin (GM) for heat shock protein (Hsp) inhibition under an alternating magnetic field (AMF).


Angewandte Chemie | 2012

Double-Effector Nanoparticles: A Synergistic Approach to Apoptotic Hyperthermia

Dongwon Yoo; Heeyeong Jeong; Christian Preihs; Jin-sil Choi; Tae-Hyun Shin; Jonathan L. Sessler; Jinwoo Cheon

Highly efficient apoptotic hyperthermia is achieved using a double-effector nanoparticle that can generate reactive oxygen species (ROS) and heat. ROS render cancer cells more susceptible to subsequent heat treatment, which remarkably increases the degree of apoptotic cell death. Xenograft tumors (100 mm(3)) in mice are completely eliminated within 8 days after a single mild magnetic hyperthermia treatment at 43 °C for 30 min.


Cell | 2016

A Mechanogenetic Toolkit for Interrogating Cell Signaling in Space and Time

Daeha Seo; Kaden M. Southard; Ji Wook Kim; Hyunjung Lee; Justin Farlow; Jung Uk Lee; David B. Litt; Thomas J. Haas; A. Paul Alivisatos; Jinwoo Cheon; Zev J. Gartner; Young-wook Jun

Tools capable of imaging and perturbing mechanical signaling pathways with fine spatiotemporal resolution have been elusive, despite their importance in diverse cellular processes. The challenge in developing a mechanogenetic toolkit (i.e., selective and quantitative activation of genetically encoded mechanoreceptors) stems from the fact that many mechanically activated processes are localized in space and time yet additionally require mechanical loading to become activated. To address this challenge, we synthesized magnetoplasmonic nanoparticles that can image, localize, and mechanically load targeted proteins with high spatiotemporal resolution. We demonstrate their utility by investigating the cell-surface activation of two mechanoreceptors: Notch and E-cadherin. By measuring cellular responses to a spectrum of spatial, chemical, temporal, and mechanical inputs at the single-molecule and single-cell levels, we reveal how spatial segregation and mechanical force cooperate to direct receptor activation dynamics. This generalizable technique can be used to control and understand diverse mechanosensitive processes in cell signaling. VIDEO ABSTRACT.


Molecules and Cells | 2013

Magnetic Nanoparticles for Multi-Imaging and Drug Delivery

Jae Hyun Lee; Ji Wook Kim; Jinwoo Cheon

Various bio-medical applications of magnetic nanoparticles have been explored during the past few decades. As tools that hold great potential for advancing biological sciences, magnetic nanoparticles have been used as platform materials for enhanced magnetic resonance imaging (MRI) agents, biological separation and magnetic drug delivery systems, and magnetic hyperthermia treatment. Furthermore, approaches that integrate various imaging and bioactive moieties have been used in the design of multi-modality systems, which possess synergistically enhanced properties such as better imaging resolution and sensitivity, molecular recognition capabilities, stimulus responsive drug delivery with on-demand control, and spatio-temporally controlled cell signal activation. Below, recent studies that focus on the design and synthesis of multi-mode magnetic nanoparticles will be briefly reviewed and their potential applications in the imaging and therapy areas will be also discussed.


Inorganic Chemistry | 2013

Recent developments in texaphyrin chemistry and drug discovery.

Christian Preihs; Jonathan F. Arambula; Darren Magda; Heeyeong Jeong; Dongwon Yoo; Jinwoo Cheon; Zahid H. Siddik; Jonathan L. Sessler

Texaphyrins are pentaaza expanded porphyrins with the ability to form stable complexes with a variety of metal cations, particularly those of the lanthanide series. In biological milieus, texaphyrins act as redox mediators and mediate the production of reactive oxygen species (ROS). In this review, newer studies involving texaphyrin complexes targeting several different applications in anticancer therapy are described. In particular, the preparation of bismuth and lead texaphyrin complexes as potential α-core emitters for radiotherapy is detailed, as are gadolinium texaphyrin functionalized magnetic nanoparticles with features that make them of interest as dual-mode magnetic resonance imaging contrast agents and as constructs with anticancer activity mediated through ROS-induced sensitization and concurrent hyperthermia. Also discussed are gadolinium texaphyrin complexes as possible carrier systems for the targeted delivery of platinum payloads.


ACS Nano | 2014

Magnetic nanoparticles for ultrafast mechanical control of inner ear hair cells.

Jae Hyun Lee; Ji Wook Kim; Michael Levy; Albert Kao; Seung Hyun Noh; Dolores Bozovic; Jinwoo Cheon

We introduce cubic magnetic nanoparticles as an effective tool for precise and ultrafast control of mechanosensitive cells. The temporal resolution of our system is ∼1000 times faster than previously used magnetic switches and is comparable to the current state-of-the-art optogenetic tools. The use of a magnetism-gated switch reported here can address the key challenges of studying mechanotransduction in biological systems. The cube-shaped magnetic nanoparticles are designed to bind to components of cellular membranes and can be controlled with an electromagnet to exert pico-Newtons of mechanical force on the cells. The cubic nanoparticles can thus be used for noncontact mechanical control of the position of the stereocilia of an inner ear hair cell, yielding displacements of tens of nanometers, with sub-millisecond temporal resolution. We also prove that such mechanical stimulus leads to the influx of ions into the hair cell. Our study demonstrates that a magnetic switch can yield ultrafast temporal resolution, and has capabilities for remote manipulation and biological specificity, and that such magnetic system can be used for the study of mechanotransduction processes of a wide range of sensory systems.

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Christian Preihs

University of Texas at Austin

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