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Items: 1 to 20 of 111

1.

Chemometric methods for the quantification of crystalline tacrolimus in solid dispersion by powder X-ray diffractrometry.

Siddiqui A, Rahman Z, Bykadi S, Khan MA.

J Pharm Sci. 2014 Sep;103(9):2819-2828. doi: 10.1002/jps.23912. Epub 2014 Mar 1.

PMID:
24585357
2.

Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics.

Rahman Z, Siddiqui A, Bykadi S, Khan MA.

Int J Pharm. 2014 Nov 20;475(1-2):462-70. doi: 10.1016/j.ijpharm.2014.08.050. Epub 2014 Aug 27.

PMID:
25173870
4.

Near-infrared and fourier transform infrared chemometric methods for the quantification of crystalline tacrolimus from sustained-release amorphous solid dispersion.

Rahman Z, Siddiqui A, Bykadi S, Khan MA.

J Pharm Sci. 2014 Aug;103(8):2376-85. doi: 10.1002/jps.24055. Epub 2014 Jun 13.

PMID:
24931728
5.

Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis.

Zidan AS, Rahman Z, Sayeed V, Raw A, Yu L, Khan MA.

Int J Pharm. 2012 Feb 28;423(2):341-50. doi: 10.1016/j.ijpharm.2011.11.003. Epub 2011 Nov 12.

PMID:
22100517
6.

Comparison of Univariate and Multivariate Models of ¹³C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs.

Rahman Z, Mohammad A, Siddiqui A, Khan MA.

AAPS PharmSciTech. 2015 Dec;16(6):1368-76. doi: 10.1208/s12249-015-0327-8. Epub 2015 May 9.

7.

Characterization of a nonribosomal peptide antibiotic solid dispersion formulation by process analytical technologies sensors.

Rahman Z, Siddiqui A, Khan MA.

J Pharm Sci. 2013 Dec;102(12):4337-46. doi: 10.1002/jps.23740. Epub 2013 Oct 1.

PMID:
24114944
8.

Quantitative solid-state analysis of three solid forms of ranitidine hydrochloride in ternary mixtures using Raman spectroscopy and X-ray powder diffraction.

Chieng N, Rehder S, Saville D, Rades T, Aaltonen J.

J Pharm Biomed Anal. 2009 Jan 15;49(1):18-25. doi: 10.1016/j.jpba.2008.09.054. Epub 2008 Oct 17.

PMID:
19081220
9.

Application of NIR chemometric methods for quantification of the crystalline fraction of warfarin sodium in drug product.

Korang-Yeboah M, Akhtar S, Siddiqui A, Rahman Z, Khan MA.

Drug Dev Ind Pharm. 2016;42(4):584-94. doi: 10.3109/03639045.2015.1058817. Epub 2015 Jul 10.

PMID:
26161939
10.

Determination of the crystallinity of cephalexin in pharmaceutical formulations by chemometrical near-infrared spectroscopy.

Fukui Y, Otsuka M.

Drug Dev Ind Pharm. 2010 Jan;36(1):72-80. doi: 10.3109/03639040903092327.

PMID:
19656006
11.

Evaluation of chemometric algorithms in quantitative X-ray powder diffraction (XRPD) of intact multi-component consolidated samples.

Moore MD, Cogdill RP, Wildfong PL.

J Pharm Biomed Anal. 2009 Apr 5;49(3):619-26. doi: 10.1016/j.jpba.2008.12.007. Epub 2008 Dec 13.

PMID:
19167855
12.

Chemometric Model Development and Comparison of Raman and (13)C Solid-State Nuclear Magnetic Resonance-Chemometric Methods for Quantification of Crystalline/Amorphous Warfarin Sodium Fraction in the Formulations.

Rahman Z, Mohammad A, Akhtar S, Siddiqui A, Korang-Yeboah M, Khan MA.

J Pharm Sci. 2015 Aug;104(8):2550-8. doi: 10.1002/jps.24524. Epub 2015 Jun 10.

PMID:
26096869
13.

Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products.

Siddiqui A, Rahman Z, Korang-Yeboah M, Khan MA.

Int J Pharm. 2015 Sep 30;493(1-2):1-6. doi: 10.1016/j.ijpharm.2015.07.051. Epub 2015 Jul 21.

PMID:
26209072
14.

Effect of the solid-dispersion method on the solubility and crystalline property of tacrolimus.

Joe JH, Lee WM, Park YJ, Joe KH, Oh DH, Seo YG, Woo JS, Yong CS, Choi HG.

Int J Pharm. 2010 Aug 16;395(1-2):161-6. doi: 10.1016/j.ijpharm.2010.05.023. Epub 2010 May 24.

PMID:
20580799
16.

Evaluation of analytical tools and multivariate methods for quantification of co-former crystals in ibuprofen-nicotinamide co-crystals.

Soares FL, Carneiro RL.

J Pharm Biomed Anal. 2014 Feb;89:166-75. doi: 10.1016/j.jpba.2013.11.005. Epub 2013 Nov 15.

PMID:
24291798
17.

Multivariate Quantification of the Solid State Phase Composition of Co-Amorphous Naproxen-Indomethacin.

Beyer A, Grohganz H, Löbmann K, Rades T, Leopold CS.

Molecules. 2015 Oct 27;20(10):19571-87. doi: 10.3390/molecules201019571.

18.

Non-Sink Dissolution Behavior and Solubility Limit of Commercial Tacrolimus Amorphous Formulations.

Trasi NS, Purohit HS, Wen H, Sun DD, Taylor LS.

J Pharm Sci. 2017 Jan;106(1):264-272. doi: 10.1016/j.xphs.2016.09.016. Epub 2016 Nov 2.

PMID:
27816263
19.

Formation, physical stability, and quantification of process-induced disorder in cryomilled samples of a model polymorphic drug.

Hu Y, Macfhionnghaile P, Caron V, Tajber L, Healy AM, Erxleben A, McArdle P.

J Pharm Sci. 2013 Jan;102(1):93-103. doi: 10.1002/jps.23338. Epub 2012 Oct 9.

PMID:
23047833
20.

Cohesive, multicomponent, dense powder flow characterization by NIR.

Benedetti C, Abatzoglou N, Simard JS, McDermott L, Léonard G, Cartilier L.

Int J Pharm. 2007 May 24;336(2):292-301. Epub 2006 Dec 15.

PMID:
17240094

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