Literature DB >> 21223990

Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology.

Elaine Merisko-Liversidge1, Gary G Liversidge.   

Abstract

A significant percentage of active pharmaceutical ingredients identified through discovery screening programs is poorly soluble in water. These molecules are often difficult to formulate using conventional approaches and are associated with innumerable formulation-related performance issues, e.g. poor bioavailability, lack of dose proportionality, slow onset of action and other attributes leading to poor patient compliance. In addition, for parenteral products, these molecules are generally administered with co-solvents and thus have many undesirable side effects. Wet media milling is one of the leading particle size reduction approaches that have been successfully used to formulate these problematic compounds. The approach is a water-based media milling process where micron-sized drug particles are shear-fractured into nanometer-sized particles. Nanoparticle dispersions are stable and typically have a mean diameter of less than 200 nm with 90% of the particles being less than 400 nm. The formulation consists only of water, drug and one or more GRAS excipients. Drug concentrations approaching 300-400mg/g can be targeted with the use of minimal amounts stabilizer. Typically, on average, the drug to stabilizer ratio on a weight basis ranges from 2:1 to 20:1. These liquid nanodispersions exhibit acceptable shelf-life and can be post-processed into various types of solid dosage forms. Nanoparticulate-based drug products have been shown to improve bioavailability and enhance drug exposure for oral and parenteral dosage forms. Suitable formulations for the most commonly used routes of administration can be identified with milligram quantities of drug substance providing the discovery scientist an alternate avenue for screening and identifying superior leads. In the last few years, formulating poorly water soluble compounds as nanosuspensions has evolved from a conception to a realization. The versatility and applicability of this drug delivery platform are just beginning to be realized.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21223990     DOI: 10.1016/j.addr.2010.12.007

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  65 in total

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Authors:  Filippos Kesisoglou; Amitava Mitra
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2.  Nanomanufacturing: A Perspective.

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Journal:  ACS Nano       Date:  2016-02-22       Impact factor: 15.881

3.  The preparation and evaluation of water-soluble SKLB610 nanosuspensions with improved bioavailability.

Authors:  Yunchuang Huang; Xun Luo; Xinyu You; Yong Xia; Xuejiao Song; Luoting Yu
Journal:  AAPS PharmSciTech       Date:  2013-08-10       Impact factor: 3.246

4.  A novel three-dimensional large-pore mesoporous carbon matrix as a potential nanovehicle for the fast release of the poorly water-soluble drug, celecoxib.

Authors:  Yanzhuo Zhang; Hong Wang; Chuanjun Li; Baoxiang Sun; Yu Wang; Siling Wang; Cunqiang Gao
Journal:  Pharm Res       Date:  2013-11-28       Impact factor: 4.200

5.  Development and characterization of solid dispersion for dissolution improvement of furosemide by cogrinding method.

Authors:  Mohammad Reza Siahi-Shadbad; Saeed Ghanbarzadeh; Mohammad Barzegar-Jalali; Hadi Valizadeh; Alireza Taherpoor; Ghobad Mohammadi; Azim Barzegar-Jalali; Khosro Adibkia
Journal:  Adv Pharm Bull       Date:  2014-08-10

6.  An Intensified Vibratory Milling Process for Enhancing the Breakage Kinetics during the Preparation of Drug Nanosuspensions.

Authors:  Meng Li; Lu Zhang; Rajesh N Davé; Ecevit Bilgili
Journal:  AAPS PharmSciTech       Date:  2015-07-17       Impact factor: 3.246

Review 7.  Nanomaterial Drug Products: Manufacturing and Analytical Perspectives.

Authors:  Christie M Sayes; Grace V Aquino; Anthony J Hickey
Journal:  AAPS J       Date:  2016-11-07       Impact factor: 4.009

8.  Formulation, optimization, and in vitro-in vivo evaluation of olmesartan medoxomil nanocrystals.

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Journal:  Drug Deliv Transl Res       Date:  2017-04       Impact factor: 4.617

9.  Using USP I and USP IV for discriminating dissolution rates of nano- and microparticle-loaded pharmaceutical strip-films.

Authors:  Lucas Sievens-Figueroa; Natasha Pandya; Anagha Bhakay; Golshid Keyvan; Bozena Michniak-Kohn; Ecevit Bilgili; Rajesh N Davé
Journal:  AAPS PharmSciTech       Date:  2012-10-23       Impact factor: 3.246

Review 10.  Application of drug nanocrystal technologies on oral drug delivery of poorly soluble drugs.

Authors:  Lei Gao; Guiyang Liu; Jianli Ma; Xiaoqing Wang; Liang Zhou; Xiang Li; Fang Wang
Journal:  Pharm Res       Date:  2012-10-17       Impact factor: 4.200

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