Seung-Hoi Kim

Prof. Seung-Hoi Kim


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2022 in Nano Convergence
Verified
Journal Article
Open access
PDF file
SKSeung-Hoi Kim
Seung-Hoi Kim
JKJi-Hye Kang
Ji-Hye Kang
JHJi-Young Hwang
Ji-Young Hwang
USUeon Sang Shin
Ueon Sang Shin
Sensors, such as optical, chemical, and electrical sensors, play an important role in our lives. While these sensors already have widespread applications, such as humidity sensors, most are generally incompatible with flexible/inactive substrates and rely on conventional hard materials and complex manufacturing processes. To overcome this, we develop a CNT-based, low-resistance, and flexible humidity sensor. The core–shell structured CNT@CPM is prepared with Chit and PAMAM to achieve reliability, accuracy, consistency, and durability, resulting in a highly sensitive humidity sensor. The average response/recovery time of optimized sensor is only less than 20 s, with high sensitivity, consistent responsiveness, good linearity according to humidity rates, and low hysteresis (− 0.29 to 0.30 %RH). Moreover, it is highly reliable for long-term (at least 1 month), repeated bending (over 15,000 times), and provides accurate humidity measurement results. We apply the sensor to smart-wear, such as masks, that could conduct multi-respiratory monitoring in real-time through automatic ventilation systems. Several multi-respiratory monitoring results demonstrate its high responsiveness (less than 1.2 s) and consistent performance, indicating highly desirable for healthcare monitoring. Finally, these automatic ventilation systems paired with flexible sensors and applied to smart-wear can not only provide comfort but also enable stable and accurate healthcare in all environments.

9 April 2024 in Advanced Healthcare Materials
Verified
Journal Article
Open access
SKSeung-Hoi Kim
Seung-Hoi Kim
CLCheng Ji Li
Cheng Ji Li
SPSung‐Min Park
Sung‐Min Park
KKKyung Wook Kim
Kyung Wook Kim
JMJi‐Hun Mo
Ji‐Hun Mo
JLJung‐Hwan Lee
Jung‐Hwan Lee
Biomimetic stress‐relaxing hydrogels with reversible crosslinks attract significant attention for stem cell tissue regeneration compared with elastic hydrogels. However, stress‐relaxing hyaluronic acid (HA)‐based hydrogels fabricated using conventional technologies lack stability, biocompatibility, and mechanical tunability. Here, it is aimed to address these challenges by incorporating calcium or phosphate components into the HA backbone, which allows reversible crosslinking of HA with alginate to form interpenetrating networks, offering stability and mechanical tunability for mimicking cartilage. Diverse stress‐relaxing hydrogels (τ1/2; SR50, 60–2000 s) are successfully prepared at ≈3 kPa stiffness with self‐healing and shear‐thinning abilities, favoring hydrogel injection. In vitro cell experiments with RNA sequencing analysis demonstrate that hydrogels tune chondrogenesis in a biphasic manner (hyaline or calcified) depending on the stress‐relaxation properties and phosphate components. In vivo studies confirm the potential for biphasic chondrogenesis. These results indicate that the proposed stress‐relaxing HA‐based hydrogel with biphasic chondrogenesis (hyaline or calcified) is a promising material for cartilage regeneration.

11 July 2023 in European Journal of Pharmaceutical Sciences
Verified
Journal Article
Open access
SKSeung-Hoi Kim
Seung-Hoi Kim
JKJi-Hye Kang
Ji-Hye Kang
JJJunHwee Jang
JunHwee Jang
ELEun-Jung Lee
Eun-Jung Lee
JKJin Hee Kim
Jin Hee Kim
USUeon Sang Shin
Ueon Sang Shin
The recent progress in nanoparticle applications, such as tumor-targeting, has enabled specific delivery of chemotherapeutics to malignant tissues with enhanced local efficacy while limiting side effects. However, existing delivery systems leave much room for improvement in terms of achieving enhanced colloidal stability in fluid medium, efficient targeting of intended sites, and effective release of therapeutic drugs into diseased cells. Here, an efficient stimuli-responsive nanocarrier for mammalian cells, termed RGD-NAMs, was developed, which enabled temperature- and pH-sensitive release of drug loads. The RGD-NAMs comprise two parts: a stimuli-responsive copolymer shell (NIBIm-AA-RGD) and drug-container core (MSNs). The RGD-NAMs have a stable drug-loading capacity with a marked difference in the release rate depending on the temperature and pH conditions. The RGD-NAMs also exhibit high colloidal stability in SBF (Stimulated body fluid) solutions and minimal toxicity in skeletal myoblasts (C2C12) and bovine arterial endothelial cells (BAEC). The doxorubicin-loaded RGD-NAMs induced a cytotoxic effect in a dose-dependent manner, which was furthered by an increase in temperature from 37 to 40 °C. Moreover, significant control of the release rate and the amount were achieved through pH change. This novel, smart drug-delivery system with high responsiveness to temperature and pH changes has wide application prospects in biomedical fields, including the theragnosis of tumors and vascular diseases.

11 March 2019 in Catalysis Letters
Verified
Journal Article
Closed access
PDF file
ESEun-Jae Shin
Eun-Jae Shin
SKSeung-Hoi Kim
Seung-Hoi Kim
SJSeong-Ryu Joo
Seong-Ryu Joo
USUeon Sang Shin
Ueon Sang Shin
SKSeung-Hoi Kim
Seung-Hoi Kim

1 June 2019 in Tetrahedron Letters
Verified
Journal Article
Closed access
ESEun-Jae Shin
Eun-Jae Shin
SJSeong-Ryu Joo
Seong-Ryu Joo
SKSeung-Hoi Kim
Seung-Hoi Kim

28 February 2020 in Asian Journal of Organic Chemistry
Verified
Journal Article
Closed access
PDF file
SJSeong‐Ryu Joo
Seong‐Ryu Joo
GKGyu‐Tae Kwon
Gyu‐Tae Kwon
SKSeung-Hoi Kim
Seung-Hoi Kim