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Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective
Preparation of drug nanoparticles via wet media milling (nanomilling) is a very versatile drug delivery platform and is suitable for oral, injectable, inhalable, and buccal applications. Wet media milling followed by various drying processes has become a well-established and proven formulation appro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932480/ https://www.ncbi.nlm.nih.gov/pubmed/27213434 http://dx.doi.org/10.3390/pharmaceutics8020017 |
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author | Li, Meng Azad, Mohammad Davé, Rajesh Bilgili, Ecevit |
author_facet | Li, Meng Azad, Mohammad Davé, Rajesh Bilgili, Ecevit |
author_sort | Li, Meng |
collection | PubMed |
description | Preparation of drug nanoparticles via wet media milling (nanomilling) is a very versatile drug delivery platform and is suitable for oral, injectable, inhalable, and buccal applications. Wet media milling followed by various drying processes has become a well-established and proven formulation approach especially for bioavailability enhancement of poorly water-soluble drugs. It has several advantages such as organic solvent-free processing, tunable and relatively high drug loading, and applicability to a multitude of poorly water-soluble drugs. Although the physical stability of the wet-milled suspensions (nanosuspensions) has attracted a lot of attention, fundamental understanding of the process has been lacking until recently. The objective of this review paper is to present fundamental insights from available published literature while summarizing the recent advances and highlighting the gap areas that have not received adequate attention. First, stabilization by conventionally used polymers/surfactants and novel stabilizers is reviewed. Then, a fundamental understanding of the process parameters, with a focus on wet stirred media milling, is revealed based on microhydrodynamic models. This review is expected to bring a holistic formulation-process perspective to the nanomilling process and pave the way for robust process development scale-up. Finally, challenges are indicated with a view to shedding light on future opportunities. |
format | Online Article Text |
id | pubmed-4932480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-49324802016-07-13 Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective Li, Meng Azad, Mohammad Davé, Rajesh Bilgili, Ecevit Pharmaceutics Review Preparation of drug nanoparticles via wet media milling (nanomilling) is a very versatile drug delivery platform and is suitable for oral, injectable, inhalable, and buccal applications. Wet media milling followed by various drying processes has become a well-established and proven formulation approach especially for bioavailability enhancement of poorly water-soluble drugs. It has several advantages such as organic solvent-free processing, tunable and relatively high drug loading, and applicability to a multitude of poorly water-soluble drugs. Although the physical stability of the wet-milled suspensions (nanosuspensions) has attracted a lot of attention, fundamental understanding of the process has been lacking until recently. The objective of this review paper is to present fundamental insights from available published literature while summarizing the recent advances and highlighting the gap areas that have not received adequate attention. First, stabilization by conventionally used polymers/surfactants and novel stabilizers is reviewed. Then, a fundamental understanding of the process parameters, with a focus on wet stirred media milling, is revealed based on microhydrodynamic models. This review is expected to bring a holistic formulation-process perspective to the nanomilling process and pave the way for robust process development scale-up. Finally, challenges are indicated with a view to shedding light on future opportunities. MDPI 2016-05-20 /pmc/articles/PMC4932480/ /pubmed/27213434 http://dx.doi.org/10.3390/pharmaceutics8020017 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Li, Meng Azad, Mohammad Davé, Rajesh Bilgili, Ecevit Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title | Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title_full | Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title_fullStr | Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title_full_unstemmed | Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title_short | Nanomilling of Drugs for Bioavailability Enhancement: A Holistic Formulation-Process Perspective |
title_sort | nanomilling of drugs for bioavailability enhancement: a holistic formulation-process perspective |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932480/ https://www.ncbi.nlm.nih.gov/pubmed/27213434 http://dx.doi.org/10.3390/pharmaceutics8020017 |
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