Literature DB >> 31407270

Classification of the crystallization tendency of active pharmaceutical ingredients (APIs) and nutraceuticals based on their nucleation and crystal growth behaviour in solution state.

Sneha Rathi1, Rahul B Chavan1, Nalini R Shastri2.   

Abstract

Supersaturated drug delivery systems are commonly used to address the problems of poor aqueous solubility posed by most of the active pharmaceutical ingredients (APIs). However, the supersaturated systems are highly unstable due to their high free energy levels and demonstrate a tendency to precipitate. Understanding the crystallization tendency based on the mechanisms of crystallization, that is nucleation and crystal growth, is imperative to design formulation strategies and select appropriate precipitation inhibitors. This study aims to provide a classification system, based on both the nucleation and crystal growth tendency in the solution state of 60 APIs and nutraceuticals (in absence of polymer) from their desupersaturation profiles monitored by UV-Visible spectroscopy. The APIs and nutraceuticals are divided into four classes based on their induction time (tind) and crystal growth rate as fast nucleators-fast crystal growth (class I), fast nucleators-slow crystal growth (class II), slow nucleators-fast crystal growth (class III) and slow nucleators-slow crystal growth (class IV). Most of the molecules fall in the class I and class IV. An easy-to-use protocol for nucleation and crystal growth studies has been optimized. This protocol will find application to assess the crystallization tendency of the molecules in the preliminary screening stages, enabling appropriate formulation strategies to inhibit crystallization.

Keywords:  Amorphous solid dispersion; Crystallization; Nucleation induction time; Precipitation inhibitors; Solubility; Supersaturated drug delivery system

Mesh:

Substances:

Year:  2020        PMID: 31407270     DOI: 10.1007/s13346-019-00663-w

Source DB:  PubMed          Journal:  Drug Deliv Transl Res        ISSN: 2190-393X            Impact factor:   4.617


  31 in total

1.  Drug supersaturation in simulated and human intestinal fluids representing different nutritional states.

Authors:  Jan Bevernage; Joachim Brouwers; Sarah Clarysse; Maria Vertzoni; Jan Tack; Pieter Annaert; Patrick Augustijns
Journal:  J Pharm Sci       Date:  2010-11       Impact factor: 3.534

Review 2.  Supersaturating drug delivery systems: the answer to solubility-limited oral bioavailability?

Authors:  Joachim Brouwers; Marcus E Brewster; Patrick Augustijns
Journal:  J Pharm Sci       Date:  2009-08       Impact factor: 3.534

3.  Classification of the crystallization behavior of amorphous active pharmaceutical ingredients in aqueous environments.

Authors:  Bernard Van Eerdenbrugh; Shweta Raina; Yi-Ling Hsieh; Patrick Augustijns; Lynne S Taylor
Journal:  Pharm Res       Date:  2013-11-23       Impact factor: 4.200

Review 4.  Physical and chemical stability of drug nanoparticles.

Authors:  Libo Wu; Jian Zhang; Wiwik Watanabe
Journal:  Adv Drug Deliv Rev       Date:  2011-02-21       Impact factor: 15.470

5.  Supersaturation-nucleation behavior of poorly soluble drugs and its impact on the oral absorption of drugs in thermodynamically high-energy forms.

Authors:  Shunsuke Ozaki; Takuma Minamisono; Taro Yamashita; Takashi Kato; Ikuo Kushida
Journal:  J Pharm Sci       Date:  2011-09-14       Impact factor: 3.534

6.  Phase Behavior of Resveratrol Solid Dispersions Upon Addition to Aqueous media.

Authors:  Lindsay A Wegiel; Laura I Mosquera-Giraldo; Lisa J Mauer; Kevin J Edgar; Lynne S Taylor
Journal:  Pharm Res       Date:  2015-05-15       Impact factor: 4.200

7.  Factors influencing crystal growth rates from undercooled liquids of pharmaceutical compounds.

Authors:  Niraj S Trasi; Jared A Baird; Umesh S Kestur; Lynne S Taylor
Journal:  J Phys Chem B       Date:  2014-08-07       Impact factor: 2.991

8.  Impact of Eudragit EPO and hydroxypropyl methylcellulose on drug release rate, supersaturation, precipitation outcome and redissolution rate of indomethacin amorphous solid dispersions.

Authors:  Tian Xie; Wei Gao; Lynne S Taylor
Journal:  Int J Pharm       Date:  2017-08-24       Impact factor: 5.875

9.  Nucleation.

Authors:  Peter G Vekilov
Journal:  Cryst Growth Des       Date:  2010-11-15       Impact factor: 4.076

10.  Improved Release of Celecoxib from High Drug Loading Amorphous Solid Dispersions Formulated with Polyacrylic Acid and Cellulose Derivatives.

Authors:  Tian Xie; Lynne S Taylor
Journal:  Mol Pharm       Date:  2016-02-02       Impact factor: 4.939

View more
  1 in total

1.  Tailoring Chlorthalidone Aqueous Solubility by Cocrystallization: Stability and Dissolution Behavior of a Novel Chlorthalidone-Caffeine Cocrystal.

Authors:  Christian Rodríguez-Ruiz; Pedro Montes-Tolentino; Jorge Guillermo Domínguez-Chávez; Hugo Morales-Rojas; Herbert Höpfl; Dea Herrera-Ruiz
Journal:  Pharmaceutics       Date:  2022-01-30       Impact factor: 6.321

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.