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Results: 1 to 20 of 124

Similar articles for PubMed (Select 23834315)

1.

Application of Box-Behnken design in the preparation and optimization of fenofibrate-loaded self-microemulsifying drug delivery system (SMEDDS).

Lee DW, Marasini N, Poudel BK, Kim JH, Cho HJ, Moon BK, Choi HG, Yong CS, Kim JO.

J Microencapsul. 2014;31(1):31-40. doi: 10.3109/02652048.2013.805837. Epub 2013 Jul 8.

PMID:
23834315
2.

Enhancement of oral bioavailability of fenofibrate by solid self-microemulsifying drug delivery systems.

Kim GG, Poudel BK, Marasini N, Lee DW, Hiep TT, Yang KY, Kim JO, Yong CS, Choi HG.

Drug Dev Ind Pharm. 2013 Sep;39(9):1431-8. doi: 10.3109/03639045.2012.719903. Epub 2012 Oct 9.

PMID:
23046292
3.

Optimization of self-microemulsifying drug delivery system for telmisartan using Box-Behnken design and desirability function.

Cho HJ, Lee DW, Marasini N, Poudel BK, Kim JH, Ramasamy T, Yoo BK, Choi HG, Yong CS, Kim JO.

J Pharm Pharmacol. 2013 Oct;65(10):1440-50. doi: 10.1111/jphp.12115. Epub 2013 Jul 24.

PMID:
24028611
4.

Development and optimization of self-nanoemulsifying drug delivery system with enhanced bioavailability by Box-Behnken design and desirability function.

Marasini N, Yan YD, Poudel BK, Choi HG, Yong CS, Kim JO.

J Pharm Sci. 2012 Dec;101(12):4584-96. doi: 10.1002/jps.23333. Epub 2012 Sep 28.

PMID:
23023800
5.

In vitro and in vivo evaluation of a self-microemulsifying drug delivery system for the poorly soluble drug fenofibrate.

Cho YD, Park YJ.

Arch Pharm Res. 2014 Feb;37(2):193-203. doi: 10.1007/s12272-013-0169-4. Epub 2013 Jun 11.

PMID:
23754165
6.

Comparison of solid self-microemulsifying drug delivery system (solid SMEDDS) prepared with hydrophilic and hydrophobic solid carrier.

Oh DH, Kang JH, Kim DW, Lee BJ, Kim JO, Yong CS, Choi HG.

Int J Pharm. 2011 Nov 28;420(2):412-8. doi: 10.1016/j.ijpharm.2011.09.007. Epub 2011 Sep 16.

PMID:
21944892
7.

Optimized formulation of solid self-microemulsifying sirolimus delivery systems.

Cho W, Kim MS, Kim JS, Park J, Park HJ, Cha KH, Park JS, Hwang SJ.

Int J Nanomedicine. 2013;8:1673-82. doi: 10.2147/IJN.S43299. Epub 2013 Apr 26.

8.

Formulation, characterization and optimization of valsartan self-microemulsifying drug delivery system using statistical design of experiment.

Poudel BK, Marasini N, Tran TH, Choi HG, Yong CS, Kim JO.

Chem Pharm Bull (Tokyo). 2012;60(11):1409-18.

9.

Characterisation of fenofibrate dissolution delivered by a self-microemulsifying drug-delivery system.

Wei JD, Ho HO, Chen CH, Ke WT, Chen ET, Sheu MT.

J Pharm Pharmacol. 2010 Dec;62(12):1685-96. doi: 10.1111/j.2042-7158.2010.01182.x. Epub 2010 Oct 5.

PMID:
21054394
10.

A novel nanomatrix system consisted of colloidal silica and pH-sensitive polymethylacrylate improves the oral bioavailability of fenofibrate.

Jia Z, Lin P, Xiang Y, Wang X, Wang J, Zhang X, Zhang Q.

Eur J Pharm Biopharm. 2011 Sep;79(1):126-34. doi: 10.1016/j.ejpb.2011.05.009. Epub 2011 May 30.

PMID:
21658449
11.

Liquid and solid self-microemulsifying drug delivery systems for improving the oral bioavailability of andrographolide from a crude extract of Andrographis paniculata.

Sermkaew N, Ketjinda W, Boonme P, Phadoongsombut N, Wiwattanapatapee R.

Eur J Pharm Sci. 2013 Nov 20;50(3-4):459-66. doi: 10.1016/j.ejps.2013.08.006. Epub 2013 Aug 22.

PMID:
23973887
12.
13.

Enhanced oral bioavailability of Coenzyme Q10 by self-emulsifying drug delivery systems.

Balakrishnan P, Lee BJ, Oh DH, Kim JO, Lee YI, Kim DD, Jee JP, Lee YB, Woo JS, Yong CS, Choi HG.

Int J Pharm. 2009 Jun 5;374(1-2):66-72. doi: 10.1016/j.ijpharm.2009.03.008. Epub 2009 Mar 19.

PMID:
19446761
14.

In situ formation of nanocrystals from a self-microemulsifying drug delivery system to enhance oral bioavailability of fenofibrate.

Lin YM, Wu JY, Chen YC, Su YD, Ke WT, Ho HO, Sheu MT.

Int J Nanomedicine. 2011;6:2445-57. doi: 10.2147/IJN.S25339. Epub 2011 Oct 19.

15.

Improved oral bioavailability of poorly water-soluble indirubin by a supersaturatable self-microemulsifying drug delivery system.

Chen ZQ, Liu Y, Zhao JH, Wang L, Feng NP.

Int J Nanomedicine. 2012;7:1115-25. doi: 10.2147/IJN.S28761. Epub 2012 Feb 23. Erratum in: Int J Nanomedicine. 2012;7:1709.

16.

Formulation and in vivo evaluation of a self-microemulsifying drug delivery system of dutasteride.

Choo GH, Park SJ, Hwang SJ, Kim MS.

Drug Res (Stuttg). 2013 Apr;63(4):203-9. doi: 10.1055/s-0033-1334965. Epub 2013 Mar 13.

PMID:
23487399
17.

Design of fenofibrate microemulsion for improved bioavailability.

Hu L, Wu H, Niu F, Yan C, Yang X, Jia Y.

Int J Pharm. 2011 Nov 28;420(2):251-5. doi: 10.1016/j.ijpharm.2011.08.043. Epub 2011 Sep 3.

PMID:
21907776
18.
19.

Solid self-microemulsifying dispersible tablets of celastrol: formulation development, charaterization and bioavailability evaluation.

Qi X, Qin J, Ma N, Chou X, Wu Z.

Int J Pharm. 2014 Sep 10;472(1-2):40-7. doi: 10.1016/j.ijpharm.2014.06.019. Epub 2014 Jun 11.

PMID:
24929011
20.

[Design and in vitro evaluation of self-microemulsifying drug delivery systems for piroxicam].

Zhou XT, Wang J, Wang Y, Sun JY, Nie SF, Pan WS.

Yao Xue Xue Bao. 2008 Apr;43(4):415-20. Chinese.

PMID:
18664206
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