Affiliation:
1. Department of Pharmaceutical Analysis, JSS College of Pharmacy, JSS Academy of Higher Education & Research,
Ooty, Nilgiris, Tamil Nadu, India
Abstract
Background:
Several analytical approaches for assessing anti-cancer drugs in pharmaceutical
formulations have been developed over the last few years. QbD plays an important role in
establishing accurate analytical methods to analyze anti-cancer compounds. Quality by Design has
become a risk analysis and a science-based strategy, implemented by experimental methods to optimize
system output with known variables for data. The influence of highly complex and correlations
of input variables on the output reactions of pharmaceutical drugs and empirical approaches
have been widely used to explain the design of experiments.
Objective:
The efficiency of the anti-cancer drugs and their formulation in the various dosage
forms has been made convenient with the help of QbD designs such as Plackett Burman, full factorial
design, etc. QbD contains various steps, which help enhance and sustain the quality of the
drug in its dosage form.
Conclusion:
This review covers a basic, efficient, and accurate analytical approach technique using
Quality by Design for anti-cancer drugs. Thus, an outline of the experimental methods used in
anti-cancer drugs was identified and discussed.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmaceutical Science,Molecular Medicine,Biochemistry,Biophysics
Cited by
1 articles.
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