Literature DB >> 17879289

Measurement of surface pH of pharmaceutical solids: a critical evaluation of indicator dye-sorption method and its comparison with slurry pH method.

Madhu Pudipeddi1, Erika A Zannou, Madhav Vasanthavada, Aruna Dontabhaktuni, Alan E Royce, Yatindra M Joshi, Abu T M Serajuddin.   

Abstract

Two methods for the measurement of surface pH of pharmaceutical solids, namely, the dye-sorption method and the slurry pH method, were compared. High purity drug substances, instead of excipients, were used as model solids, because acidic or basic impurities present in excipients could influence slurry pH. Solid test samples were prepared by sorption of methanol-water solutions of several indicator dyes, and their diffuse reflectance UV-visible spectra were measured. The solid surface pH values were estimated by comparing base-to-acid peak ratios of the diffuse reflectance UV-visible spectra of solid samples to the calibration plots of dye solutions in aqueous standard buffers of known pH. In the slurry pH method, pH values of concentrated slurries of the compounds in water were considered to represent solid surface pH. The agreement between the two methods was mixed and depended on the compound or the indicator used. It was concluded that in many cases calibration plots of indicator dye spectra in aqueous buffers were not applicable to the solid state, and, as a result, the reliability of the method was low. The slurry method provided a simple and reliable measurement of surface pH indicating that concentrated slurry may closely represent solid surface pH.

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Year:  2008        PMID: 17879289     DOI: 10.1002/jps.21052

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


  8 in total

Review 1.  Controlled release systems containing solid dispersions: strategies and mechanisms.

Authors:  Phuong Ha-Lien Tran; Thao Truong-Dinh Tran; Jun Bom Park; Beom-Jin Lee
Journal:  Pharm Res       Date:  2011-05-07       Impact factor: 4.200

2.  Implementing quality by design in pharmaceutical salt selection: a modeling approach to understanding disproportionation.

Authors:  Jeremy M Merritt; Shekhar K Viswanath; Gregory A Stephenson
Journal:  Pharm Res       Date:  2012-08-24       Impact factor: 4.200

3.  Surface acidity and solid-state compatibility of excipients with an acid-sensitive API: case study of atorvastatin calcium.

Authors:  Ramprakash Govindarajan; Margaret Landis; Bruno Hancock; Larry A Gatlin; Raj Suryanarayanan; Evgenyi Y Shalaev
Journal:  AAPS PharmSciTech       Date:  2014-10-16       Impact factor: 3.246

4.  Apparent basicities of the surfaces characterizing the dominant crystal habits of distinct polymorphic forms of 4-aminosulfonamide.

Authors:  Piotr Cysewski
Journal:  J Mol Model       Date:  2014-06-17       Impact factor: 1.810

Review 5.  Population-based mechanistic prediction of oral drug absorption.

Authors:  Masoud Jamei; David Turner; Jiansong Yang; Sibylle Neuhoff; Sebastian Polak; Amin Rostami-Hodjegan; Geoffrey Tucker
Journal:  AAPS J       Date:  2009-04-21       Impact factor: 4.009

6.  Role of salt and excipient properties on disproportionation in the solid-state.

Authors:  Peter Guerrieri; Lynne S Taylor
Journal:  Pharm Res       Date:  2009-06-09       Impact factor: 4.200

7.  Formulating weakly basic HCl salts: relative ability of common excipients to induce disproportionation and the unique deleterious effects of magnesium stearate.

Authors:  Christopher T John; Wei Xu; Lisa K Lupton; Paul A Harmon
Journal:  Pharm Res       Date:  2013-03-20       Impact factor: 4.200

8.  Investigation of possible solubility and dissolution advantages of cocrystals, I: Aqueous solubility and dissolution rates of ketoconazole and its cocrystals as functions of pH.

Authors:  Jaydip M Vasoya; Ankita V Shah; Abu T M Serajuddin
Journal:  ADMET DMPK       Date:  2019-04-05
  8 in total

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