Literature DB >> 18539443

In situ dissolution testing using potentiometric sensors.

Karl Peeters1, Roy De Maesschalck, Hugo Bohets, Koen Vanhoutte, Luc Nagels.   

Abstract

Potentiometric sensors can be used to determine the amount of API dissolved in the dissolution medium in function of time by measuring directly in the dissolution vessel of a Paddle (USP type 2) and Basket (USP type 1) apparatus. The prototype potentiometric sensor instrumentation showed very promising results for a selection of APIs with different physico-chemical properties. The applicability, benefits and limitations of the prototype were explored. The applicability of the measurement technique strongly depends on the log(P) of the API. Here, it is shown that measurements can easily be performed for APIs with a log(P)>4. Electrode performance however decreases with decreasing logP of the APIs due to decreased drug selectivity in comparison to the excipients and ionic strength of the applied dissolution medium. The potentiometric sensors are shown to be insensitive towards undissolved particles and air bubbles as opposed to UV spectrometric measurement where these can lead to severe light scattering. For the tested APIs, the obtained dissolution profiles are very reproducible and show a low variation compared to the measurements using manual sampling and UV or HPLC analysis. The measurements demonstrate that potentiometric sensors are a very promising technology that can become a standard for in situ dissolution measurements.

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Year:  2008        PMID: 18539443     DOI: 10.1016/j.ejps.2008.04.009

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  7 in total

1.  Dissolution studies of poorly soluble drug nanosuspensions in non-sink conditions.

Authors:  Peng Liu; Odile De Wulf; Johanna Laru; Teemu Heikkilä; Bert van Veen; Juha Kiesvaara; Jouni Hirvonen; Leena Peltonen; Timo Laaksonen
Journal:  AAPS PharmSciTech       Date:  2013-04-25       Impact factor: 3.246

2.  The Biopharmaceutics Classification System: subclasses for in vivo predictive dissolution (IPD) methodology and IVIVC.

Authors:  Yasuhiro Tsume; Deanna M Mudie; Peter Langguth; Greg E Amidon; Gordon L Amidon
Journal:  Eur J Pharm Sci       Date:  2014-01-28       Impact factor: 4.384

3.  In Vitro Dissolution Testing Strategies for Nanoparticulate Drug Delivery Systems: Recent Developments and Challenges.

Authors:  Jie Shen; Diane J Burgess
Journal:  Drug Deliv Transl Res       Date:  2013-10-01       Impact factor: 4.617

4.  Investigations of the Influences of Processing Conditions on the Properties of Spray Dried Chitosan-Tripolyphosphate Particles loaded with Theophylline.

Authors:  Yang Wei; Yu-Hung Huang; Kuo-Chung Cheng; Yu-Lin Song
Journal:  Sci Rep       Date:  2020-01-24       Impact factor: 4.379

5.  Widening the applications of the Just-Dip-It approach: a solid contact screen-printed ion-selective electrode for the real-time assessment of pharmaceutical dissolution testing in comparison to off-line HPLC analysis.

Authors:  Khadiga M Kelani; Osama M Badran; Mamdouh R Rezk; Mohamed R Elghobashy; Sherif M Eid
Journal:  RSC Adv       Date:  2021-04-09       Impact factor: 3.361

6.  Two Green Micellar HPLC and Mathematically Assisted UV Spectroscopic Methods for the Simultaneous Determination of Molnupiravir and Favipiravir as a Novel Combined COVID-19 Antiviral Regimen.

Authors:  Yasmine Ahmed Sharaf; Sami El Deeb; Adel Ehab Ibrahim; Ahmed Al-Harrasi; Rania Adel Sayed
Journal:  Molecules       Date:  2022-04-04       Impact factor: 4.411

7.  Using ion-selective electrodes to study the drug release from porous cellulose matrices.

Authors:  Hossein Vakili; Natalja Genina; Henrik Ehlers; Johan Bobacka; Niklas Sandler
Journal:  Pharmaceutics       Date:  2012-08-07       Impact factor: 6.321

  7 in total

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