Literature DB >> 27324960

Probing the Distribution of Water in a Multi-Component System by Solid-State NMR Spectroscopy.

Pinal Mistry1, Paroma Chakravarty2, Joseph W Lubach3.   

Abstract

PURPOSE: To characterize the distribution of water among various components in a powder blend using solid-state NMR spectroscopy.
METHODS: Water sorption behavior of theophylline anhydrate and excipients was determined by dynamic vapor sorption (DVS) and Karl Fischer Titration (KFT) after storing them in humidity chambers for 1 week at room temperature (RT) and calibration curves were generated for water content vs. (1)H T 1 relaxation times. Powder blends (either with microcrystalline cellulose or lactose as diluent) were stored at different relative humidity (RH) conditions and analyzed periodically using solid-state NMR, powder X-ray diffraction, and KFT.
RESULTS: Anhydrous theophylline converted to the hydrate at ≥ 84% RH. Based on the calibration curves of water content vs. relaxation times, the distribution of water in the powder blends was estimated. The total water content calculated using ssNMR was in good agreement with values measured using KFT. In blends stored at 90% RH, theophylline anhydrate-to-hydrate conversion did not occur in 1 week.
CONCLUSIONS: The distribution of water in multi-component powder blends was successfully determined using correlation between (1)H T 1 relaxation times and total water content. Excipient water sorption inhibited hydrate formation in theophylline at 90% RH. Water distribution was affected by excipient type. The extent of water sorbed by excipients in blends was found to be different than their standalone equilibrium water content.

Entities:  

Keywords:  formulation; hydrate; solid-state NMR; theophylline; water distribution

Mesh:

Substances:

Year:  2016        PMID: 27324960     DOI: 10.1007/s11095-016-1972-7

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  18 in total

1.  Preformulation studies involving moisture uptake in solid dosage forms.

Authors:  D R Heidemann; P J Jarosz
Journal:  Pharm Res       Date:  1991-03       Impact factor: 4.200

2.  Molecular mobility of nifedipine-PVP and phenobarbital-PVP solid dispersions as measured by 13C-NMR spin-lattice relaxation time.

Authors:  Yukio Aso; Sumie Yoshioka
Journal:  J Pharm Sci       Date:  2006-02       Impact factor: 3.534

Review 3.  Correlations between molecular mobility and chemical stability during storage of amorphous pharmaceuticals.

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4.  Wide-ranging molecular mobilities of water in active pharmaceutical ingredient (API) hydrates as determined by NMR relaxation times.

Authors:  Sumie Yoshioka; Yukio Aso; Tsutomu Osako; Toru Kawanishi
Journal:  J Pharm Sci       Date:  2008-10       Impact factor: 3.534

5.  An improved broadband decoupling sequence for liquid crystals and solids.

Authors:  B M Fung; A K Khitrin; K Ermolaev
Journal:  J Magn Reson       Date:  2000-01       Impact factor: 2.229

6.  3-Methylglutaric acid as a 13C solid-state NMR standard.

Authors:  Dewey H Barich; Eric M Gorman; Mark T Zell; Eric J Munson
Journal:  Solid State Nucl Magn Reson       Date:  2006-06-15       Impact factor: 2.293

7.  Polymorphism in anhydrous theophylline--implications on the dissolution rate of theophylline tablets.

Authors:  N V Phadnis; R Suryanarayanan
Journal:  J Pharm Sci       Date:  1997-11       Impact factor: 3.534

8.  Effects of excipients on hydrate formation in wet masses containing theophylline.

Authors:  Sari Airaksinen; Pirjo Luukkonen; Anna Jørgensen; Milja Karjalainen; Jukka Rantanen; Jouko Yliruusi
Journal:  J Pharm Sci       Date:  2003-03       Impact factor: 3.534

9.  Excipient selection can significantly affect solid-state phase transformation in formulation during wet granulation.

Authors:  Sari Airaksinen; Milja Karjalainen; Niina Kivikero; Sari Westermarck; Anna Shevchenko; Jukka Rantanen; Jouko Yliruusi
Journal:  AAPS PharmSciTech       Date:  2005-10-06       Impact factor: 3.246

10.  Effect of moisture on polyvinylpyrrolidone in accelerated stability testing.

Authors:  Shaun Fitzpatrick; James F McCabe; Catherine R Petts; Steven W Booth
Journal:  Int J Pharm       Date:  2002-10-10       Impact factor: 5.875

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