Author(s): Manohar D. Kengar, Rohit S. Howal, Dattatray B. Aundhakar, Amit V. Nikam, Priyajit S. Hasabe

Email(s): manojkengar200@gmail.com

DOI: 10.5958/2231-5713.2019.00010.2   

Address: Manohar D. Kengar*, Rohit S. Howal, Dattatray B. Aundhakar, Amit V. Nikam, Priyajit S. Hasabe
Rajarambapu College of Pharmacy, Kasegaon, Dist – Sangli, Maharashtra, India – 415404.
*Corresponding Author

Published In:   Volume - 9,      Issue - 1,     Year - 2019


ABSTRACT:
The every drug has intrinsic chemical and physical properties in which has been consider before development of pharmaceutical formulation. This property provides great framework for drugs combination with pharmaceutical ingredients in the fabrication of dosage form. The objective of preformulation study is to develop the elegant, stable, effective and safe dosage form by establishing kinetic rate profile, compatibility with the other ingredients and establish Physico-chemical parameter of new drug substances. Among these properties, drug solubility, dissolution rate, Particle size partition coefficient polymorphic forms and stability are plays important role in preformulation study. Polymorphism having crystal and amorphous forms shows different chemical physical and therapeutic description of the drug molecule. This article explains some Physical properties and physic-chemical techniques for preformulation evaluation parameters of drug.


Cite this article:
Manohar D. Kengar, Rohit S. Howal, Dattatray B. Aundhakar, Amit V. Nikam, Priyajit S. Hasabe. Physico-chemical Properties of Solid Drugs: A Review. Asian J. Pharm. Tech. 2019; 9 (1):53-59. doi: 10.5958/2231-5713.2019.00010.2


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