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"Jin-Ho Chun"

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"Jin-Ho Chun"

Original Articles
Therapeutic evaluation of sustained-releasing praziquantel (SRP) for clonorchiasis: Phase 1 and 2 clinical studies
Min-Ho Choi, Byung-Chan Chang, Seung-Jin Lee, In-Jin Jang, Sang-Goo Shin, Weon-Gyu Kho, Jin-Ho Chun, Sung-Tae Hong
Korean J Parasitol 2006;44(4):361-366.
Published online December 20, 2006
DOI: https://doi.org/10.3347/kjp.2006.44.4.361

Sustained-releasing praziquantel (SRP) tablet was designed for single dose treatment regimen of clonorchiasis. A previous pre-clinical study confirmed its sustained-releasing characteristics and a better cure rate than conventional praziquantel (PZQ). In this clinical study, the pharmacokinetics of this SRP tablet were investigated in human volunteers (phase 1; 12 volunteers), and its curative efficacy was examined in clonorchiasis patients (phase 2; 20 volunteers). In the phase 1 clinical study, blood concentrations of both tablets showed wide individual variation. The AUClast of SRP was 497.9 ± 519.0 ng · hr/ml (mean ± SD) and PZQ of 628.6 ± 695.5 ng · hr/ml, and the AUCinf of SRP was 776.0 ± 538.5 ng · hr/ml and of PZQ 658.6 ± 709.9 ng · hr/ml. Cmax values of SRP and PZQ were 90.7 ± 82.2 ng/ml and 214.9 ± 251.9 ng/ml, and Tmax values were 3.42 ± 1.43 hr and 1.96 ± 1.23 hr, respectively. SRP tablets showed similar AUC values, but lower Cmax and longer Tmax values than PZQ. In the phase 2 study, SRP at 30 mg/kg (single dose) achieved a 60% cure rate and a 95.5% egg reduction rate. The cure rate of a single dose SRP was unsatisfactory compared with that of the conventional PZQ dose, but much better than that achieved by a single dose PZQ.

Citations

Citations to this article as recorded by  Crossref logo
  • Lack of Clinical Pharmacokinetic Studies to Optimize the Treatment of Neglected Tropical Diseases: A Systematic Review
    Luka Verrest, Thomas P. C. Dorlo
    Clinical Pharmacokinetics.2017; 56(6): 583.     CrossRef
  • Current status and perspectives of Clonorchis sinensis and clonorchiasis: epidemiology, pathogenesis, omics, prevention and control
    Ze-Li Tang, Yan Huang, Xin-Bing Yu
    Infectious Diseases of Poverty.2016;[Epub]     CrossRef
  • Correlation between Discharged Worms and Fecal Egg Counts in Human Clonorchiasis
    Jae-Hwan Kim, Min-Ho Choi, Young Mee Bae, Jin-Kyoung Oh, Min Kyung Lim, Sung-Tae Hong, Akira Ito
    PLoS Neglected Tropical Diseases.2011; 5(10): e1339.     CrossRef
  • Pharmacotherapy of helminth infection
    Erwin van den Enden
    Expert Opinion on Pharmacotherapy.2009; 10(3): 435.     CrossRef
  • Biliary parasites: Diagnostic and therapeutic strategies
    Niraj Khandelwal, Joanna Shaw, Mamta K. Jain
    Current Treatment Options in Gastroenterology.2008; 11(2): 85.     CrossRef
  • 8,217 View
  • 95 Download
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Analysis of polymorphic region of GAM-1 gene in Plasmodium vivax Korean isolates
Weon-Gyu Kho, Joon-Yong Chung, Ui-Wook Hwang, Jin-Ho Chun, Yeong-Hong Park, Woo-Chul Chung
Korean J Parasitol 2001;39(4):313-318.
Published online December 31, 2001
DOI: https://doi.org/10.3347/kjp.2001.39.4.313

The identification, characterization and quantification of Plasmodium sp. genetic polymorphism are becoming increasingly important in the vaccine development. We investigated polymorphism of Plasmodium vivax GAM-1 (PvGAM-1) gene in 30 Korean isolates. The polymorphic region of the PvGAM-1 gene, corresponding to nt 3792-4029, was amplified using polymerase chain reaction (PCR) followed by sequencing. All of the P. vivax Korean isolates were one type of GAM-1 gene, which were identical to that of the Belem strain. It is suggested that PvGAM-1 could not be used as a genetic marker for identifying or classifying P. vivax Korean isolates. It revealed that the polymorphic pattern was acquired basically by duplication and modification or deletion event of a 33 bp-motif fragment ended by poly guanine (G) and that there were at least three complete and one partial 33 bp-motif sequences within the polymorphic region in the longest cases such as those of South Korean and Belem isolates. In addition, we clustered P. vivax isolates with parsimonious criteria on the basis of PvGAM-1 polymorphic patterns (insertion/deletion patterns).

Citations

Citations to this article as recorded by  Crossref logo
  • Complete mitochondrial genome of a malaria vector mosquito Anopheles sinensis from South Korea
    Ashraf Akintayo Akintola, Bia Park, Eun Hwa Choi, Ui Wook Hwang
    Mitochondrial DNA Part B.2022; 7(5): 881.     CrossRef
  • Genetic Diversity of Plasmodium vivax Causing Epidemic Malaria in the Republic of Korea
    Young Yil Bahk, Jeonga Kim, Seong Kyu Ahn, Byoung-Kuk Na, Jong-Yil Chai, Tong-Soo Kim
    The Korean Journal of Parasitology.2018; 56(6): 545.     CrossRef
  • Genetic Characteristics of Polymorphic Antigenic Markers among Korean Isolates of Plasmodium vivax
    Seung-Young Hwang, So-Hee Kim, Weon-Gyu Kho
    The Korean Journal of Parasitology.2009; 47(Suppl): S51.     CrossRef
  • Plasmodium vivax in India
    Hema Joshi, Surendra K. Prajapati, Anju Verma, Simon Kang’a, Jane M. Carlton
    Trends in Parasitology.2008; 24(5): 228.     CrossRef
  • Allelic dimorphism of Plasmodium vivax gam-1 in the Indian subcontinent
    Surendra K Prajapati, Anju Verma, Tridibes Adak, Rajpal S Yadav, Ashwini Kumar, Alex Eapen, Manoj K Das, Neeru Singh, Surya K Sharma, Moshahid A Rizvi, Aditya P Dash, Hema Joshi
    Malaria Journal.2006;[Epub]     CrossRef
  • 8,099 View
  • 58 Download
  • Crossref