Hyeong-Seok Lim

Prof. Dr. Hyeong-Seok Lim


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

View All Publications
1 January 2018 in Translational and Clinical Pharmacology
Verified
Journal Article
Open access
PDF file
YCYong-Soon Cho
Yong-Soon Cho
HLHyeong-Seok Lim
Hyeong-Seok Lim
Cho YS, et al. Transl Clin Pharmacol. 2018 Mar;26(1):39-47. https://doi.org/10.12793/tcp.2018.26.1.39

1 November 2022 in Gut and Liver
Verified
Journal Article
Open access
PDF file
SHSungpil Han
Sungpil Han
HCHee Youn Choi
Hee Youn Choi
YKYo Han Kim
Yo Han Kim
SCSeungChan Choi
SeungChan Choi
SKSeokuee Kim
Seokuee Kim
KBKyun-Seop Bae
Kyun-Seop Bae
Sungpil Han, Hee Youn Choi, Yo Han Kim, SeungChan Choi, Seokuee Kim, Ji Yeon Nam, Bongtae Kim, Geun Seog Song, Hyeong-Seok Lim, and Kyun-Seop Bae. Gut and Liver 2023;17:92-9. https://doi.org/10.5009/gnl220050


1 January 2019 in Translational and Clinical Pharmacology
Verified
Journal Article
Open access
PDF file
HLHyeong-Seok Lim
Hyeong-Seok Lim
Lim HS. Transl Clin Pharmacol. 2019 Mar;27(1):19-23. https://doi.org/10.12793/tcp.2019.27.1.19

1 March 2015 in Clinical Therapeutics
Verified
Journal Article
Closed access
HJHae-Sun Jeon
Hae-Sun Jeon
MKMi-Jo Kim
Mi-Jo Kim
HCHee-Youn Choi
Hee-Youn Choi
YKYo-Han Kim
Yo-Han Kim
EKEun-Hwa Kim
Eun-Hwa Kim
HLHyeong-Seok Lim
Hyeong-Seok Lim

1 January 2018 in Drug Design, Development and Therapy
Verified
Journal Article
Open access
PDF file
HKHyungsub Kim
Hyungsub Kim
HCHee Youn Choi
Hee Youn Choi
YKYo-Han Kim
Yo-Han Kim
KBKyun-Seop Bae
Kyun-Seop Bae
JJJina Jung
Jina Jung
HLHyeong-Seok Lim
Hyeong-Seok Lim
Purpose: Rosuvastatin is a synthetic 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor that effectively reduces low-density lipoprotein cholesterol levels. However, statin monotherapy does not always achieve acceptable low-density lipoprotein cholesterol levels in patients with severe hypercholesterolemia. Ezetimibe, a selective cholesterol-absorption inhibitor, is approved for use as a monotherapy or combination therapy with 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors for patients with hypercholesterolemia. The aim of this study was to examine the pharmacokinetics (PKs) of drug interactions between rosuvastatin and ezetimibe, and the tolerability of combined administration in healthy Korean male volunteers. Subjects and methods: Healthy subjects (n=24) were randomly allocated to 3 treatment groups: rosuvastatin (20 mg) alone, ezetimibe (10 mg) alone, and rosuvastatin (20 mg) plus ezetimibe (10 mg). The drugs were taken once every 24 hours over a period of 10 days. Blood samples were collected to analyze steady-state PKs. Results: All adverse events observed during the study were mild, and the frequency was no higher for combined administration than for mono administration. For rosuvastatin, the steady-state mean ratios (90% CI) of the combined over the single dose were 1.076 (1.019-1.136) for AUC(tau,ss) and 1.099 (1.003-1.204) for concentration at steady-state, respectively. In the case of free and total ezetimibe, the steady-state ratios of AUC(tau,ss) and concentration at steady-state were 1.131 (1.051-1.218) and 1.182 (1.038-1.346), and 1.055 (0.969-1.148) and 0.996 (0.873-1.135), respectively. Conclusion: Combined administration of rosuvastatin and ezetimibe was well tolerated. No clinically significant PK interactions between rosuvastatin and ezetimibe were observed when the 2 drugs were administered concomitantly.