Literature DB >> 7816760

Solid-state emulsions: evaluation by 1H and 13C solid-state nuclear magnetic resonance.

M L Shively1, S F Dec.   

Abstract

The molecular environment of sucrose and mineral oil within sucrose and mineral oil solid state emulsions was investigated by NMR techniques. The 13C and 1H chemical shifts of sucrose and mineral oil to those observed in solid state emulsions (comprised of sucrose and mineral oil) were equivalent, indicating that the local structure of sucrose is unaffected by the presence of mineral oil in the solid-state emulsion. Cross-polarization, magic angle spinning 13C (CP-MAS) in conjunction with single-pulse studies indicated that the 1H-13C dipole-dipole interactions are very weak, i.e., mineral oil is highly mobile. Spinning side bands were observed, however, in 1H single-pulse, magic angle spinning (SPMAS) spectra of the solid-state emulsion, indicating that the mineral oil has solid properties. Although the mineral oil was shown to be highly mobile, it also appears to be constrained or included by the sucrose.

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Year:  1994        PMID: 7816760     DOI: 10.1023/a:1018946512445

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


  6 in total

1.  Characterization of oil-in-water emulsions prepared from solid-state emulsions: effect of matrix and oil phase.

Authors:  M L Shively
Journal:  Pharm Res       Date:  1993-08       Impact factor: 4.200

Review 2.  Solid-state nuclear magnetic resonance spectroscopy: theory and pharmaceutical applications.

Authors:  D E Bugay
Journal:  Pharm Res       Date:  1993-03       Impact factor: 4.200

3.  Solid-state emulsions: the effects of process and storage conditions.

Authors:  M L Shively; S Myers
Journal:  Pharm Res       Date:  1993-07       Impact factor: 4.200

4.  Solid-state emulsions: the effects of maltodextrin on microcrystalline aging.

Authors:  S L Myers; M L Shively
Journal:  Pharm Res       Date:  1993-09       Impact factor: 4.200

5.  Quantitation of the relative amounts of anhydrous carbamazepine (C15H12N2O) and carbamazepine dihydrate (C15H12N2O.2H2O) in a mixture by solid-state nuclear magnetic resonance (NMR).

Authors:  R Suryanarayanan; T S Wiedmann
Journal:  Pharm Res       Date:  1990-02       Impact factor: 4.200

6.  Analysis of solid-state Carbon-13 NMR spectra of polymorphs (benoxaprofen and nabilone) and pseudopolymorphs (cefazolin).

Authors:  S R Byrn; G Gray; R R Pfeiffer; J Frye
Journal:  J Pharm Sci       Date:  1985-05       Impact factor: 3.534

  6 in total

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