Mu H - Search Results

1

Design of lipid matrix particles for fenofibrate: effect of polymorphism of glycerol monostearate on drug incorporation and release.

Xia D, Cui F, Gan Y, Mu H, Yang M. Xia D, et al. Among authors: mu h. J Pharm Sci. 2014 Feb;103(2):697-705. doi: 10.1002/jps.23830. Epub 2013 Dec 20. J Pharm Sci. 2014. PMID: 24375427

2

Solid lipid particles for oral delivery of peptide and protein drugs I--elucidating the release mechanism of lysozyme during lipolysis.

Christophersen PC, Zhang L, Yang M, Nielsen HM, Müllertz A, Mu H. Christophersen PC, et al. Among authors: mu h. Eur J Pharm Biopharm. 2013 Nov;85(3 Pt A):473-80. doi: 10.1016/j.ejpb.2013.07.017. Epub 2013 Aug 2. Eur J Pharm Biopharm. 2013. PMID: 23911434

3

Investigating the correlation between in vivo absorption and in vitro release of fenofibrate from lipid matrix particles in biorelevant medium.

Borkar N, Xia D, Holm R, Gan Y, Müllertz A, Yang M, Mu H. Borkar N, et al. Among authors: mu h. Eur J Pharm Sci. 2014 Jan 23;51:204-10. doi: 10.1016/j.ejps.2013.09.022. Epub 2013 Oct 14. Eur J Pharm Sci. 2014. PMID: 24134899

4

Solid lipid particles for oral delivery of peptide and protein drugs II--the digestion of trilaurin protects desmopressin from proteolytic degradation.

Christophersen PC, Zhang L, Müllertz A, Nielsen HM, Yang M, Mu H. Christophersen PC, et al. Among authors: mu h. Pharm Res. 2014 Sep;31(9):2420-8. doi: 10.1007/s11095-014-1337-z. Epub 2014 Mar 13. Pharm Res. 2014. PMID: 24623481

5

Solid lipid particles for oral delivery of peptide and protein drugs III - the effect of fed state conditions on the in vitro release and degradation of desmopressin.

Christophersen PC, Vaghela D, Müllertz A, Yang M, Nielsen HM, Mu H. Christophersen PC, et al. Among authors: mu h. AAPS J. 2014 Jul;16(4):875-83. doi: 10.1208/s12248-014-9619-2. Epub 2014 May 30. AAPS J. 2014. PMID: 24875052 Free PMC article.

6

Investigation of protein distribution in solid lipid particles and its impact on protein release using coherent anti-Stokes Raman scattering microscopy.

Christophersen PC, Birch D, Saarinen J, Isomäki A, Nielsen HM, Yang M, Strachan CJ, Mu H. Christophersen PC, et al. Among authors: mu h. J Control Release. 2015 Jan 10;197:111-20. doi: 10.1016/j.jconrel.2014.10.023. Epub 2014 Nov 3. J Control Release. 2015. PMID: 25449810

7

Lipophilic prodrugs of apomorphine I: preparation, characterisation, and in vitro enzymatic hydrolysis in biorelevant media.

Borkar N, Li B, Holm R, Håkansson AE, Müllertz A, Yang M, Mu H. Borkar N, et al. Among authors: mu h. Eur J Pharm Biopharm. 2015 Jan;89:216-23. doi: 10.1016/j.ejpb.2014.12.014. Epub 2014 Dec 13. Eur J Pharm Biopharm. 2015. PMID: 25513957

8

Characterization of particulate drug delivery systems for oral delivery of Peptide and protein drugs.

Christophersen PC, Fano M, Saaby L, Yang M, Nielsen HM, Mu H. Christophersen PC, et al. Among authors: mu h. Curr Pharm Des. 2015;21(19):2611-28. doi: 10.2174/1381612821666150416100943. Curr Pharm Des. 2015. PMID: 25876916 Review.

9

Apomorphine and its esters: Differences in Caco-2 cell permeability and chylomicron affinity.

Borkar N, Chen Z, Saaby L, Müllertz A, Håkansson AE, Schönbeck C, Yang M, Holm R, Mu H. Borkar N, et al. Among authors: mu h. Int J Pharm. 2016 Jul 25;509(1-2):499-506. doi: 10.1016/j.ijpharm.2016.06.010. Epub 2016 Jun 6. Int J Pharm. 2016. PMID: 27282537

10

In Vivo Precipitation of Poorly Soluble Drugs from Lipid-Based Drug Delivery Systems.

Sassene PJ, Michaelsen MH, Mosgaard MD, Jensen MK, Van Den Broek E, Wasan KM, Mu H, Rades T, Müllertz A. Sassene PJ, et al. Among authors: mu h. Mol Pharm. 2016 Oct 3;13(10):3417-3426. doi: 10.1021/acs.molpharmaceut.6b00413. Epub 2016 Aug 30. Mol Pharm. 2016. PMID: 27533712

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