scispace - formally typeset
Journal ArticleDOI

Pharmaceutical Applications of Polymorphism

John K. Haleblian, +1 more
- 01 Aug 1969 - 
- Vol. 58, Iss: 8, pp 911-929
TLDR
Polymorphism is the ability of any element or compound to crystallize as more than one distinct crystal species (e.g., carbon as cubic diamond or hexagonal graphite).
About
This article is published in Journal of Pharmaceutical Sciences.The article was published on 1969-08-01. It has received 894 citations till now. The article focuses on the topics: Polymorphism (materials science) & Crystal.

read more

Citations
More filters
Journal Article

Influence of solid-state chemistry in drug substances in pharmaceutical products. A review

TL;DR: In this paper, the authors present a number of routes such as co-crystallization, polymorphism and salt formation to improve physico-chemical properties of drugs, which can be implemented through an in detail knowledge of crystallization processes and the molecular properties.
Patent

Malonate salt of 4-((1R,3S)-6-chloro-3-phenylindan-1-yl)-1,2,2-trimethylpiperazine and uses of same

TL;DR: In this article, the use of hydrogen malonate salt for the treatment of schizophrenia and other psychotic disorders is described. But the authors did not specify the uses of the same for other disorders.
Patent

Polymorphs and amorphous forms of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile

Sharona Zamir
TL;DR: In this article, the authors present methods for preparing the novel polymorphs, pseudomorphs and amorphous form, as well as insecticidal or pesticidal compositions comprising same, and methods of use thereof as pesticidal agents.
References
More filters
Journal ArticleDOI

Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices

TL;DR: The analyses suggest that for the latter system the time required to release 50% of the drug would normally be expected to be approximately 10 per cent of that required to dissolve the last trace of the solid drug phase in the center of the pellet.
Journal ArticleDOI

The united states pharmacopeia.

Robert A. Hatcher
- 04 Jan 1908 - 
TL;DR: The Pharmacopeia was called into being by physicians in 1820, and in 1850 pharmacists were admitted to the convention; since then physicians have gradually relinquished control to pharmacists, and to-day the authors are confronted with an anomalous condition.
Book

Thermal methods of analysis

TL;DR: In this article, a revised edition necessitated by the phenomenal growth of the field during the past decade contains 90% new material, focusing on tech niques and applications of thermal analysis.