Literature DB >> 8901076

Preparation, characterization, and in vivo evaluation of an oil suspension of a bovine growth hormone releasing factor analog.

L X Yu1, T P Foster, R W Sarver, W M Moseley.   

Abstract

Pharmacia & Upjohn Inc. has discovered a superior bovine growth hormone releasing factor analog, [IIe2,Ser8,28,Ala15,Leu27,Hse30] bGRF (1-30)-NH-ethyl, acetate salt (U-90699F), for enhancement of animal growth. This report delineates the preparation, characterization, and in vivo evaluation of a U-90699F oil suspension. The oil suspension formulation was selected because of its simplicity, inexpensiveness, and ability to produce sustained U-90699F release. 40% U-90699F monomers were incorporated into Miglyol oil with acceptable injectability. Both reversed-phase-high-pressure liquid chromatography (RP-HPLC) and Fourier transform infrared spectroscopy (FTIR) were utilized to evaluate its chemical and structural stability. This suspension formulation demonstrated no significant changes in concentration as determined by RP-HPLC for 10 weeks at both 25 and 39 degrees C. The U-90699F dispersed in oil also showed no signs of structural conversion from alpha-helix to beta-sheet as monitored by FTIR. However, there was an increase in alpha-helix/disordered coil structure after initial drug incorporation. The suspension was subcutaneously administered to Holstein steers. Areas under the serum somatotropin concentration curve were used to determine the duration of action. It was found that the suspension was able to effectively elevate serum somatotropin for at least 14 days.

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Year:  1996        PMID: 8901076     DOI: 10.1021/js9503901

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  3 in total

1.  Stability of nonaqueous suspension formulations of plasma derived factor IX and recombinant human alpha interferon at elevated temperatures.

Authors:  V M Knepp; A Muchnik; S Oldmark; L Kalashnikova
Journal:  Pharm Res       Date:  1998-07       Impact factor: 4.200

2.  Low viscosity highly concentrated injectable nonaqueous suspensions of lysozyme microparticles.

Authors:  Maria A Miller; Joshua D Engstrom; Baltej S Ludher; Keith P Johnston
Journal:  Langmuir       Date:  2010-01-19       Impact factor: 3.882

3.  Preparation of an oil suspension containing ondansetron hydrochloride as a sustained release parenteral formulation.

Authors:  Thi-Thao-Linh Nguyen; Van-An Duong; Han-Joo Maeng; Sang-Cheol Chi
Journal:  Drug Deliv Transl Res       Date:  2020-02       Impact factor: 4.617

  3 in total

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