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Amorphous Drug-Polymer Salts

Amorphous formulations provide a general approach to improving the solubility and bioavailability of drugs. Amorphous medicines for global health should resist crystallization under the stressful tropical conditions (high temperature and humidity) and often require high drug loading. We discuss the...

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Detalles Bibliográficos
Autores principales: Yao, Xin, Neusaenger, Amy Lan, Yu, Lian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401805/
https://www.ncbi.nlm.nih.gov/pubmed/34452231
http://dx.doi.org/10.3390/pharmaceutics13081271
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author Yao, Xin
Neusaenger, Amy Lan
Yu, Lian
author_facet Yao, Xin
Neusaenger, Amy Lan
Yu, Lian
author_sort Yao, Xin
collection PubMed
description Amorphous formulations provide a general approach to improving the solubility and bioavailability of drugs. Amorphous medicines for global health should resist crystallization under the stressful tropical conditions (high temperature and humidity) and often require high drug loading. We discuss the recent progress in employing drug–polymer salts to meet these goals. Through local salt formation, an ultra-thin polyelectrolyte coating can form on the surface of amorphous drugs, immobilizing interfacial molecules and inhibiting fast crystal growth at the surface. The coated particles show improved wetting and dissolution. By forming an amorphous drug–polymer salt throughout the bulk, stability can be vastly enhanced against crystallization under tropical conditions without sacrificing the dissolution rate. Examples of these approaches are given, along with suggestions for future work.
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spelling pubmed-84018052021-08-29 Amorphous Drug-Polymer Salts Yao, Xin Neusaenger, Amy Lan Yu, Lian Pharmaceutics Perspective Amorphous formulations provide a general approach to improving the solubility and bioavailability of drugs. Amorphous medicines for global health should resist crystallization under the stressful tropical conditions (high temperature and humidity) and often require high drug loading. We discuss the recent progress in employing drug–polymer salts to meet these goals. Through local salt formation, an ultra-thin polyelectrolyte coating can form on the surface of amorphous drugs, immobilizing interfacial molecules and inhibiting fast crystal growth at the surface. The coated particles show improved wetting and dissolution. By forming an amorphous drug–polymer salt throughout the bulk, stability can be vastly enhanced against crystallization under tropical conditions without sacrificing the dissolution rate. Examples of these approaches are given, along with suggestions for future work. MDPI 2021-08-17 /pmc/articles/PMC8401805/ /pubmed/34452231 http://dx.doi.org/10.3390/pharmaceutics13081271 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Perspective
Yao, Xin
Neusaenger, Amy Lan
Yu, Lian
Amorphous Drug-Polymer Salts
title Amorphous Drug-Polymer Salts
title_full Amorphous Drug-Polymer Salts
title_fullStr Amorphous Drug-Polymer Salts
title_full_unstemmed Amorphous Drug-Polymer Salts
title_short Amorphous Drug-Polymer Salts
title_sort amorphous drug-polymer salts
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8401805/
https://www.ncbi.nlm.nih.gov/pubmed/34452231
http://dx.doi.org/10.3390/pharmaceutics13081271
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AT neusaengeramylan amorphousdrugpolymersalts
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