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Items: 17

1.

Development of a Resveratrol Nanosuspension Using the Antisolvent Precipitation Method without Solvent Removal, Based on a Quality by Design (QbD) Approach.

Kuk DH, Ha ES, Ha DH, Sim WY, Lee SK, Jeong JS, Kim JS, Baek IH, Park H, Choi DH, Yoo JW, Jeong SH, Hwang SJ, Kim MS.

Pharmaceutics. 2019 Dec 17;11(12). pii: E688. doi: 10.3390/pharmaceutics11120688.

2.

Pharmacokinetic Study of a Soft Gelatin Capsule and a Solid-Supersaturatable SMEDDS Tablet of Dutasteride in Beagle Dogs.

Kim JS, Ha ES, Park H, Choi DH, Kim MS, Baek IH.

Eur J Drug Metab Pharmacokinet. 2019 Nov 29. doi: 10.1007/s13318-019-00594-4. [Epub ahead of print]

PMID:
31782125
3.

Preparation and Evaluation of Resveratrol-Loaded Composite Nanoparticles Using a Supercritical Fluid Technology for Enhanced Oral and Skin Delivery.

Ha ES, Sim WY, Lee SK, Jeong JS, Kim JS, Baek IH, Choi DH, Park H, Hwang SJ, Kim MS.

Antioxidants (Basel). 2019 Nov 14;8(11). pii: E554. doi: 10.3390/antiox8110554.

4.

Application of the Discrete Element Method for Manufacturing Process Simulation in the Pharmaceutical Industry.

Yeom SB, Ha ES, Kim MS, Jeong SH, Hwang SJ, Choi DH.

Pharmaceutics. 2019 Aug 15;11(8). pii: E414. doi: 10.3390/pharmaceutics11080414. Review.

5.

Scale-Up Strategy in Quality by Design Approach for Pharmaceutical Blending Process with Discrete Element Method Simulation.

Yeom SB, Choi DH.

Pharmaceutics. 2019 Jun 6;11(6). pii: E264. doi: 10.3390/pharmaceutics11060264.

6.
7.

Quality by Design (QbD) approach to optimize the formulation of a bilayer combination tablet (Telmiduo®) manufactured via high shear wet granulation.

Lee AR, Kwon SY, Choi DH, Park ES.

Int J Pharm. 2017 Dec 20;534(1-2):144-158. doi: 10.1016/j.ijpharm.2017.10.004. Epub 2017 Oct 12.

PMID:
29031980
8.

A new lignan and a new alkaloid, and α-glucosidase inhibitory compounds from the grains of Echinochloa utilis Ohwi & Yabuno.

Nguyen TT, Nguyen DH, Zhao BT, Le DD, Choi DH, Kim YH, Nguyen TH, Woo MH.

Bioorg Chem. 2017 Oct;74:221-227. doi: 10.1016/j.bioorg.2017.08.007. Epub 2017 Aug 20.

PMID:
28865293
9.

Formulation Optimization and in Vitro Characterization of Orally Disintegrating Films Using a Factorial Design and Mathematical Modeling for Drug Release.

Lee Y, Thapa P, Jeong SH, Woo MH, Choi DH.

Chem Pharm Bull (Tokyo). 2017 Feb 1;65(2):166-177. doi: 10.1248/cpb.c16-00757. Epub 2016 Nov 30.

10.

A novel experimental design method to optimize hydrophilic matrix formulations with drug release profiles and mechanical properties.

Choi du H, Lim JY, Shin S, Choi WJ, Jeong SH, Lee S.

J Pharm Sci. 2014 Oct;103(10):3083-94. doi: 10.1002/jps.24080. Epub 2014 Jul 23.

PMID:
25055971
11.

Bioequivalence of tacrolimus formulations with different dynamic solubility and in-vitro dissolution profiles.

Kwon M, Yeom D, Kim NA, Choi du H, Park J, Wang H, Yoo SD, Jeong SH.

Arch Pharm Res. 2015 Jan;38(1):73-80. doi: 10.1007/s12272-014-0343-3. Epub 2014 Feb 11.

PMID:
24627339
12.

Comprehensive evaluation of layer separation tendency of novel three-layered tablets with geometric and mechanical properties.

Choi du H, Lim DG, Son HM, Jeong SH.

Int J Pharm. 2014 Apr 25;465(1-2):347-59. doi: 10.1016/j.ijpharm.2014.02.014. Epub 2014 Feb 12.

PMID:
24530386
13.

Evaluation of drug delivery profiles in geometric three-layered tablets with various mechanical properties, in vitro-in vivo drug release, and Raman imaging.

Choi du H, Kim KH, Park JS, Jeong SH, Park K.

J Control Release. 2013 Dec 28;172(3):763-72. doi: 10.1016/j.jconrel.2013.08.301. Epub 2013 Sep 12.

PMID:
24035977
14.

Evaluation of taste-masking effects of pharmaceutical sweeteners with an electronic tongue system.

Choi du H, Kim NA, Nam TS, Lee S, Jeong SH.

Drug Dev Ind Pharm. 2014 Mar;40(3):308-17. doi: 10.3109/03639045.2012.758636. Epub 2013 Jun 20.

PMID:
23786206
15.

Investigation of polymeric excipients for dutasteride solid dispersion and its physicochemical characterization.

Kim NA, Choi du H, Lim JY, Kim KH, Lim DG, Lee E, Park ES, Jeong SH.

Arch Pharm Res. 2014 Feb;37(2):214-24. doi: 10.1007/s12272-013-0180-9. Epub 2013 Jun 18.

PMID:
23775474
16.

A new experimental design method to optimize formulations focusing on a lubricant for hydrophilic matrix tablets.

Choi du H, Shin S, Khoa Viet Truong N, Jeong SH.

Drug Dev Ind Pharm. 2012 Sep;38(9):1117-27. doi: 10.3109/03639045.2011.641563. Epub 2012 Feb 20.

PMID:
22348254
17.

Time-oriented experimental design method to optimize hydrophilic matrix formulations with gelation kinetics and drug release profiles.

Shin S, Choi du H, Truong NK, Kim NA, Chu KR, Jeong SH.

Int J Pharm. 2011 Apr 4;407(1-2):53-62. doi: 10.1016/j.ijpharm.2011.01.013. Epub 2011 Jan 18.

PMID:
21251963

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