Literature DB >> 15019028

Penciclovir solubility in Eudragit films: a comparison of X-ray, thermal, microscopic and release rate techniques.

A Ahmed1, B W Barry, A C Williams, A F Davis.   

Abstract

The solubility of penciclovir (C(10)N(5)O(3)H(17)) in a novel film formulation designed for the treatment of cold sores was determined using X-ray, thermal, microscopic and release rate techniques. Solubilities of 0.15-0.23, 0.44, 0.53 and 0.42% (w/w) resulted for each procedure. Linear calibration lines were achieved for experimentally and theoretically determined differential scanning calorimetry (DSC) and X-ray powder diffractometry (XRPD) data. Intra- and inter-batch data precision values were determined; intra values were more precise. Microscopy was additionally useful for examining crystal shape, size distribution and homogeneity of drug distribution within the film. Whereas DSC also determined melting point, XRPD identified polymorphs and release data provided relevant kinetics.

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Year:  2004        PMID: 15019028     DOI: 10.1016/j.jpba.2003.11.018

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  2 in total

1.  Solid-state characterization of Felodipine-Soluplus amorphous solid dispersions.

Authors:  Jiannan Lu; Kristina Cuellar; Nathan I Hammer; Seongbong Jo; Andreas Gryczke; Karl Kolter; Nigel Langley; Michael A Repka
Journal:  Drug Dev Ind Pharm       Date:  2015-11-04       Impact factor: 3.225

2.  Solid-State Characterization and Compatibility Studies of Penciclovir, Lysine Hydrochloride, and Pharmaceutical Excipients.

Authors:  Rafaela Z C Meira; Isabela F B Biscaia; Camila Nogueira; Fabio S Murakami; Larissa S Bernardi; Paulo R Oliveira
Journal:  Materials (Basel)       Date:  2019-09-27       Impact factor: 3.623

  2 in total

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