The Polymorphism of Drugs: New Approaches to the Synthesis of Nanostructured Polymorphs.

cryosynthesis cryotemperature nanoparticles polymorphism poorly soluble drug

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
01 Jan 2020
Historique:
received: 07 11 2019
revised: 12 12 2019
accepted: 25 12 2019
entrez: 8 1 2020
pubmed: 8 1 2020
medline: 8 1 2020
Statut: epublish

Résumé

Among the significant problems of modern pharmacology are the low solubility and bioavailability of drugs. One way to resolve this problem is to obtain new polymorphic forms of drugs with improved physicochemical properties. Various approaches have been developed with this aim, including the preparation of co-crystals, the use of nanoparticles, or the use of compounds in the form of a salt. A promising direction in pharmacology concerns the production of new stable polymorphic structures. In this mini-review, we consider certain aspects of drug polymorphism, methods for the synthesis of polymorphs, and the stability, size, and transformation of crystalline polymorphs. Moreover, we summarize our results from several studies demonstrating the problems associated with the synthesis of new polymorphous modifications based on inert gases and cryotemperatures. The results indicate that the problems specific to drug polymorphisms have only been partly resolved, are of current interest, and require further development.

Identifiants

pubmed: 31906357
pii: pharmaceutics12010034
doi: 10.3390/pharmaceutics12010034
pmc: PMC7022426
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Dmitry Chistyakov (D)

Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.

Gleb Sergeev (G)

Department of Chemistry, M. V. Lomonosov Moscow State University, 119991 Moscow, Russia.

Classifications MeSH