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Items: 1 to 20 of 105

1.

Development and characterization of dilutable self-microemulsifying premicroemulsion systems (SMEPMS) as templates for preparation of nanosized particulates.

Lin SF, Chen YC, Ho HO, Huang WY, Sheu MT, Liu DZ.

Int J Nanomedicine. 2013;8:3455-66. doi: 10.2147/IJN.S48465. Epub 2013 Sep 11.

2.

Continuous and scalable process for water-redispersible nanoformulation of poorly aqueous soluble APIs by antisolvent precipitation and spray-drying.

Hu J, Ng WK, Dong Y, Shen S, Tan RB.

Int J Pharm. 2011 Feb 14;404(1-2):198-204. doi: 10.1016/j.ijpharm.2010.10.055. Epub 2010 Nov 5.

PMID:
21056643
3.

Preparation and in vitro/in vivo evaluation of fenofibrate nanocrystals.

Zuo B, Sun Y, Li H, Liu X, Zhai Y, Sun J, He Z.

Int J Pharm. 2013 Oct 15;455(1-2):267-75. doi: 10.1016/j.ijpharm.2013.07.021. Epub 2013 Jul 20.

PMID:
23876497
4.

Fabrication of fenofibrate nanocrystals by probe sonication method for enhancement of dissolution rate and oral bioavailability.

Ige PP, Baria RK, Gattani SG.

Colloids Surf B Biointerfaces. 2013 Aug 1;108:366-73. doi: 10.1016/j.colsurfb.2013.02.043. Epub 2013 Mar 23.

PMID:
23602990
5.

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.

6.

Investigation of preparation parameters to improve the dissolution of poorly water-soluble meloxicam.

Ambrus R, Kocbek P, Kristl J, Sibanc R, Rajkó R, Szabó-Révész P.

Int J Pharm. 2009 Nov 3;381(2):153-9. doi: 10.1016/j.ijpharm.2009.07.009. Epub 2009 Jul 17.

PMID:
19616609
7.

Physical properties of griseofulvin-lipid nanoparticles in suspension and their novel interaction mechanism with saccharide during freeze-drying.

Kamiya S, Kurita T, Miyagishima A, Itai S, Arakawa M.

Eur J Pharm Biopharm. 2010 Mar;74(3):461-6. doi: 10.1016/j.ejpb.2009.12.004. Epub 2009 Dec 14.

PMID:
20018239
8.

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
9.

Controlled crystallization of the lipophilic drug fenofibrate during freeze-drying: elucidation of the mechanism by in-line Raman spectroscopy.

de Waard H, De Beer T, Hinrichs WL, Vervaet C, Remon JP, Frijlink HW.

AAPS J. 2010 Dec;12(4):569-75. doi: 10.1208/s12248-010-9215-z. Epub 2010 Jul 13.

10.

Preparation and evaluation of raloxifene-loaded solid dispersion nanoparticle by spray-drying technique without an organic solvent.

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

Int J Pharm. 2013 Feb 25;443(1-2):50-7. doi: 10.1016/j.ijpharm.2013.01.013. Epub 2013 Jan 11.

PMID:
23318367
11.

Biorelevant in vitro dissolution testing of products containing micronized or nanosized fenofibrate with a view to predicting plasma profiles.

Juenemann D, Jantratid E, Wagner C, Reppas C, Vertzoni M, Dressman JB.

Eur J Pharm Biopharm. 2011 Feb;77(2):257-64. doi: 10.1016/j.ejpb.2010.10.012. Epub 2010 Nov 11.

PMID:
21074611
12.

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
13.

The improvement of ibuprofen dissolution rate through microparticles spray drying processed in an aqueous system.

Wikarsa S, Durand D, Delarbre JL, Baylac G, Bataille B.

Drug Dev Ind Pharm. 2008 May;34(5):485-91. doi: 10.1080/03639040701743949 .

PMID:
18473230
14.

Spray-freeze-drying of nanosuspensions: the manufacture of insulin particles for needle-free ballistic powder delivery.

Schiffter H, Condliffe J, Vonhoff S.

J R Soc Interface. 2010 Aug 6;7 Suppl 4:S483-500. doi: 10.1098/rsif.2010.0114.focus. Epub 2010 Jun 2.

15.

A comparison between use of spray and freeze drying techniques for preparation of solid self-microemulsifying formulation of valsartan and in vitro and in vivo evaluation.

Singh SK, Vuddanda PR, Singh S, Srivastava AK.

Biomed Res Int. 2013;2013:909045. doi: 10.1155/2013/909045. Epub 2013 Jul 18.

16.

Preparation of fenofibrate immediate-release tablets involving wet grinding for improved bioavailability.

Zhang L, Chai G, Zeng X, He H, Xu H, Tang X.

Drug Dev Ind Pharm. 2010 Sep;36(9):1054-63. doi: 10.3109/03639041003642081.

PMID:
20818965
17.

Design and physicochemical characterization of advanced spray-dried tacrolimus multifunctional particles for inhalation.

Wu X, Hayes D Jr, Zwischenberger JB, Kuhn RJ, Mansour HM.

Drug Des Devel Ther. 2013;7:59-72. doi: 10.2147/DDDT.S40166. Epub 2013 Feb 4.

18.

Selection of excipient, solvent and packaging to optimize the performance of spray-dried formulations: case example fenofibrate.

Hugo M, Kunath K, Dressman J.

Drug Dev Ind Pharm. 2013 Feb;39(2):402-12. doi: 10.3109/03639045.2012.685176. Epub 2012 May 17.

PMID:
22591213
19.

Fast drying of biocompatible polymer films loaded with poorly water-soluble drug nano-particles via low temperature forced convection.

Susarla R, Sievens-Figueroa L, Bhakay A, Shen Y, Jerez-Rozo JI, Engen W, Khusid B, Bilgili E, Romañach RJ, Morris KR, Michniak-Kohn B, Davé RN.

Int J Pharm. 2013 Oct 15;455(1-2):93-103. doi: 10.1016/j.ijpharm.2013.07.051. Epub 2013 Jul 31.

PMID:
23911341
20.

Techniques to develop and characterize nanosized formulation for salbutamol sulfate.

Bhavna, Ahmad FJ, Khar RK, Sultana S, Bhatnagar A.

J Mater Sci Mater Med. 2009 Dec;20 Suppl 1:S71-6. doi: 10.1007/s10856-008-3483-5. Epub 2008 Jun 10.

PMID:
18543087
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