Literature DB >> 7617525

The application of malononitriles as microviscosity probes in pharmaceutical systems.

S L LaPorte1, A Harianawala, R H Bogner.   

Abstract

Three molecules were investigated for their ability to distinguish variations in the microviscosity of the surrounding medium. Julolidinemalononitrile (JMN), p-(N-dimethylaminobenzylidene) malononitrile (BMN), and p-(N-dimethylaminocinnamylidene) malononitrile (CMN) were dissolved in media of various micro- and bulk viscosities. The fluorescence intensity of each dissolved probe and the bulk viscosity of each medium were measured. In solutions of low molecular weight substances, where the micro- and bulk viscosities are expected to correspond, the fluorescence behavior of each probe was a function of bulk viscosity and was independent of solution composition. In contrast, in aqueous solutions of methylcellulose, the fluorescence behavior of the probes corresponds to microviscosities significantly lower than the measured bulk viscosities. Thus, the probes are useful in resolving the microviscosity from bulk viscosity of neat liquid and solution systems. The sensitivity of the probes to viscosity is in the order JMN > BMN > CMN. Due to its limited water solubility, JMN is not particularly useful for pharmaceutical systems. CMN is the preferred probe for these applications due to its high fluorescence intensity over a large viscosity range.

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Year:  1995        PMID: 7617525     DOI: 10.1023/a:1016252518401

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


  13 in total

1.  The use of electron spin resonance to measure microviscosity.

Authors:  T Gebre-Mariam; N A Armstrong; K C James; J C Evans; C C Rowlands
Journal:  J Pharm Pharmacol       Date:  1991-07       Impact factor: 3.765

2.  Microviscosity and drug release from topical gel formulations.

Authors:  K I Al-Khamis; S S Davis; J Hadgraft
Journal:  Pharm Res       Date:  1986-08       Impact factor: 4.200

3.  Microenvironmental kinetic effects within a lyotropic smectic biophase model: conformational restrictions in Fischer indole cyclization.

Authors:  H G Ibrahim; E G Rippie
Journal:  J Pharm Sci       Date:  1976-11       Impact factor: 3.534

4.  The effect of gelatin grade and concentration on the migration of solutes into and through glycerogelatin gels.

Authors:  T Gebre-Mariam; N A Armstrong; K R Brain; K C James
Journal:  J Pharm Pharmacol       Date:  1989-08       Impact factor: 3.765

5.  Mass transport in dissolution kinetics. II: Convective diffusion to assess role of viscosity under conditions of gravitational flow.

Authors:  A C Shah; K G Nelson
Journal:  J Pharm Sci       Date:  1987-12       Impact factor: 3.534

6.  Effects of polyelectrolytes on drug transport. I. Diffusion.

Authors:  K F Farng; K G Nelson
Journal:  J Pharm Sci       Date:  1973-09       Impact factor: 3.534

7.  Influence of viscosity and solubilization on dissolution rate.

Authors:  R J Braun; E L Parrott
Journal:  J Pharm Sci       Date:  1972-02       Impact factor: 3.534

8.  The influence of solution viscosity on the dissolution rate of soluble salts, and the measurement of an "effective" viscosity.

Authors:  A T Florence; P H Elworthy; A Rahman
Journal:  J Pharm Pharmacol       Date:  1973-10       Impact factor: 3.765

9.  Molecular motion of drugs in hydrocolloids measured by electron paramagnetic resonance.

Authors:  J Kristl; S Pecar; J Smid-Korbar; M Schara
Journal:  Pharm Res       Date:  1991-04       Impact factor: 4.200

10.  The influence of viscosity on the migration of chloramphenicol and 4-hydroxybenzoic acid through glycerogelatin gels.

Authors:  N A Armstrong; T Gebre-Mariam; K C James; P Kearney
Journal:  J Pharm Pharmacol       Date:  1987-08       Impact factor: 3.765

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