192 related articles for article (PubMed ID: 24585357)
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. PubMed ID: 24585357
[TBL] [Abstract][Full Text] [Related]
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; 475(1-2):462-70. PubMed ID: 25173870
[TBL] [Abstract][Full Text] [Related]
3. Comparison of X-ray powder diffraction and solid-state nuclear magnetic resonance in estimating crystalline fraction of tacrolimus in sustained-release amorphous solid dispersion and development of discriminating dissolution method.
Rahman Z; Bykadi S; Siddiqui A; Khan MA
J Pharm Sci; 2015 May; 104(5):1777-86. PubMed ID: 25753829
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 24931728
[TBL] [Abstract][Full Text] [Related]
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; 423(2):341-50. PubMed ID: 22100517
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 25956485
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 24114944
[TBL] [Abstract][Full Text] [Related]
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; 49(1):18-25. PubMed ID: 19081220
[TBL] [Abstract][Full Text] [Related]
9. Quantification of gabapentin polymorphs in gabapentin/excipient mixtures using solid state
Tinmanee R; Larsen SC; Morris KR; Kirsch LE
J Pharm Biomed Anal; 2017 Nov; 146():29-36. PubMed ID: 28843174
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 26161939
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 19656006
[TBL] [Abstract][Full Text] [Related]
12. 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; 49(3):619-26. PubMed ID: 19167855
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 26096869
[TBL] [Abstract][Full Text] [Related]
14. 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; 493(1-2):1-6. PubMed ID: 26209072
[TBL] [Abstract][Full Text] [Related]
15. Univariate and Multivariate Models for Determination of Prasugrel Base in the Formulation of Prasugrel Hydrochloride Using XRPD Method.
Dharani S; Barakh Ali SF; Afrooz H; Khan MA; Rahman Z
J Pharm Sci; 2019 Nov; 108(11):3575-3581. PubMed ID: 31276685
[TBL] [Abstract][Full Text] [Related]
16. 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; 395(1-2):161-6. PubMed ID: 20580799
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 24291798
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 23047833
[TBL] [Abstract][Full Text] [Related]
19. 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; 336(2):292-301. PubMed ID: 17240094
[TBL] [Abstract][Full Text] [Related]
20. L-Leucine as an excipient against moisture on in vitro aerosolization performances of highly hygroscopic spray-dried powders.
Li L; Sun S; Parumasivam T; Denman JA; Gengenbach T; Tang P; Mao S; Chan HK
Eur J Pharm Biopharm; 2016 May; 102():132-41. PubMed ID: 26970252
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]