Literature DB >> 12078989

Disordered drug delivery: destiny, dynamics and the Deborah number.

Bruno C Hancock1.   

Abstract

"Disordered drug delivery" is an innovative approach to improving the performance of new chemical entities delivered to the human body. In this technique, the molecules of the drug and/or its delivery system are kinetically trapped in a high energy non-crystalline state. The resulting disordered or "amorphous" material offers potential increases in solubility and biological activity of many thousand fold compared with more conventional crystalline forms of the drug. Despite having a molecular level structure akin to that of liquids, amorphous materials have macroscopic properties that are typical of solids and thus they may be presented to the patient in the form of a convenient solid dosage form. Significant advances in the fundamental understanding of amorphous pharmaceutical materials in the past ten years have permitted major steps forward in the rational design of disordered drug delivery systems. Recognition of significant levels of molecular mobility in the glassy regime and an in-depth appreciation of molecular relaxation times and their distributions have enabled rapid progress to be made in this field. Needs for the future include analytical techniques that can elucidate the complex, dynamic and heterogeneous structure of amorphous materials and reliable models to predict the physical stability and in-vivo performance of disordered drug delivery systems. There are also significant opportunities for the production of disordered drug delivery systems with tailor-made properties through the careful engineering of custom amorphous alloys.

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Year:  2002        PMID: 12078989     DOI: 10.1211/0022357021778989

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  10 in total

1.  Solution behavior of PVP-VA and HPMC-AS-based amorphous solid dispersions and their bioavailability implications.

Authors:  Feng Qian; Jennifer Wang; Ruiling Hartley; Jing Tao; Raja Haddadin; Neil Mathias; Munir Hussain
Journal:  Pharm Res       Date:  2012-10       Impact factor: 4.200

2.  Ordered nanoporous silica as carriers for improved delivery of water insoluble drugs: a comparative study between three dimensional and two dimensional macroporous silica.

Authors:  Ying Wang; Qinfu Zhao; Yanchen Hu; Lizhang Sun; Ling Bai; Tongying Jiang; Siling Wang
Journal:  Int J Nanomedicine       Date:  2013-10-22

3.  Probing the Interplay between Amorphous Solid Dispersion Stability and Polymer Functionality.

Authors:  Derek S Frank; Adam J Matzger
Journal:  Mol Pharm       Date:  2018-06-20       Impact factor: 4.939

4.  Nonlinear optical imaging for sensitive detection of crystals in bulk amorphous powders.

Authors:  Umesh S Kestur; Duangporn Wanapun; Scott J Toth; Lindsay A Wegiel; Garth J Simpson; Lynne S Taylor
Journal:  J Pharm Sci       Date:  2012-07-30       Impact factor: 3.534

5.  Soluble itraconazole in tablet form using disordered drug delivery approach: critical scale-up considerations and bio-equivalence studies.

Authors:  Shankar Swaminathan; Mayur Sangwai; Sharad Wawdhane; Pradeep Vavia
Journal:  AAPS PharmSciTech       Date:  2013-01-19       Impact factor: 3.246

6.  Characterization of dynamics in complex lyophilized formulations: I. Comparison of relaxation times measured by isothermal calorimetry with data estimated from the width of the glass transition temperature region.

Authors:  Norman Chieng; Masayasu Mizuno; Michael Pikal
Journal:  Eur J Pharm Biopharm       Date:  2013-04-20       Impact factor: 5.571

7.  Evaluation of the recrystallization kinetics of hot-melt extruded polymeric solid dispersions using an improved Avrami equation.

Authors:  Xin Feng; Xingyou Ye; Jun-Bom Park; Wenli Lu; Joe Morott; Brad Beissner; Zhuoyang John Lian; Elanor Pinto; Vivian Bi; Stu Porter; Tom Durig; Soumyajit Majumdar; Michael A Repka
Journal:  Drug Dev Ind Pharm       Date:  2015-07-21       Impact factor: 3.225

8.  Liqui-Pellet: the Emerging Next-Generation Oral Dosage Form Which Stems from Liquisolid Concept in Combination with Pelletization Technology.

Authors:  Matthew Lam; Taravat Ghafourian; Ali Nokhodchi
Journal:  AAPS PharmSciTech       Date:  2019-06-24       Impact factor: 3.246

9.  Optimising the release rate of naproxen liqui-pellet: a new technology for emerging novel oral dosage form.

Authors:  Matthew Lam; Taravat Ghafourian; Ali Nokhodchi
Journal:  Drug Deliv Transl Res       Date:  2020-02       Impact factor: 4.617

10.  Formulating a heat- and shear-labile drug in an amorphous solid dispersion: Balancing drug degradation and crystallinity.

Authors:  Daniel A Davis; Dave A Miller; Supawan Santitewagun; J Axel Zeitler; Yongchao Su; Robert O Williams
Journal:  Int J Pharm X       Date:  2021-07-17
  10 in total

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