Journal of Pharmaceutical Chemistry & Chemical Science

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.
Reach Us +1 (202) 780-3397

Opinion Article - Journal of Pharmaceutical Chemistry & Chemical Science (2023) Volume 7, Issue 4

Pharmaceutical analysis and quality control

Vanden Leufkens*

Department of Pharmacology,Utrecht University Netherlands

*Corresponding Author:
Vanden Leufkens
Department of Pharmacology
Utrecht University
Netherlands
E-mail:vanden@leufkens.nl

Received:27-Jul-2023,Manuscript No.AAPCCS -23- 109675; Editor assigned:31-Jul-2023,PreQC No.AAPCCS -23- 109675 (PQ); Reviewed:14-Aug-2023,QC No.AAPCCS -23- 109675; Revised:21-Aug-2023,Manuscript No.AAPCCS -23- 109675(R); Published:28-Aug-2023,DOI: 10.35841/aapccs-7.4.157

Citation: Leufkens V. Pharmaceutical Analysis and Quality Control. J pharm Chem sci.2023;7(4):157

Introduction

A hook or opening line that grabs the reader's attention and emphasises the importance of pharmaceutical analysis and quality control in medication development and patient safety typically comes first in the introduction.The background material on the pharmaceutical sector in this part emphasises the crucial role that quality control plays in assuring the efficacy, consistency, and safety of pharmaceuticals.The significance of pharmaceutical analysis, which entails the identification and measurement of drug components and contaminants, is discussed in the introduction. It emphasises the significance of analytical methods in defining medicinal products.[1].

The USP, EP, and other international pharmacopoeias, as well as other regulatory organisations and standards that regulate pharmaceutical analysis and quality control, may be mentioned in the introduction. A brief summary of the research methodology can be given, highlighting the analytical methods used or the kinds of pharmaceutical samples examined. The research paper's subsequent sections are outlined in the introduction's final paragraph, offering readers a road map of what to anticipate.[2].

The research paper's subsequent sections are outlined in the introduction's final paragraph, offering readers a road map of what to anticipate. A strong beginning statement that emphasises the significance of pharmaceutical analysis in drug development, manufacturing, and patient safety usually comes first in the introduction.This section defines pharmaceutical analysis in detail and outlines its application.[3].

It describes the objective of pharmaceutical analysis, which entails characterising, identifying, and quantifying pharmacological molecules and the chemicals that are connected to them.The critical function of pharmaceutical analysis in drug development is discussed by the authors. It aids in the selection of suitable drug candidates, formulation optimisation, and assurance of the safety and efficacy of drugs.[4].

The need of quality control using analytical techniques to make sure that pharmaceutical products fulfil the necessary standards and regulatory norms may be emphasised in the introduction.Listing just a few of the standard analytical methods utilised in pharmaceutical analysis, such as chromatography (HPLC, GC), spectroscopy (UV-Vis, IR, NMR), Mass Spectrometry (MS), and dissolution testing.[5].

Conclusion

The main conclusions, their ramifications, and the overall influence on the subject of pharmaceutical analysis are summarised in the conclusion of a research paper on pharmaceutical analysis. It brings the study to a close and frequently offers suggestions for future lines of inquiry. An example of what a conclusion in this field might include is given below:The study's goals are restated in the introduction, reminding readers of the precise research questions or objectives that have been addressed throughout the report.The study's practical consequences for the pharmaceutical business and patient safety are covered in the conclusion. It emphasises how the findings can be used in the processes of medication development, production, and quality control.Strengths and Drawbacks Authors frequently consider the advantages and disadvantages of their research,outlining any challenges faced during the research. They may address factors that could have influenced the results and suggest areas for improvement.

References

  1. Aboagye EA, Chea JD, Yenkie KMSystems level roadmap for solvent recovery and reuse in industries.iscience. 2021;24(10).

    2. Indexed at, Google Scholar, Cross Ref

  2. Beard JC, Swager TMAn organic chemist’s guide to N-nitrosamines: their structure, reactivity, and role as contaminants. J Org Chem. 2021;86(3):2037-57.

    3. Indexed at, Google Scholar, Cross Ref

  3. Fritzsche M, Blom G, Keitel J, et al Discovery solubility measurement and assessment of small molecules with drug development in mind Eur J Pharm Sci. 2022;168:106026.

    4. Indexed at, Google Scholar, Cross Ref

  4. López-Rodríguez R, McManus JA, Murphy NS, et al Pathways for N-nitroso compound formation: secondary amines and beyond Org Process Res Dev. 2020;24(9):1558-85.

    5. Indexed at, Google Scholar, Cross Ref

  5. Nanda KK, Tignor S, Clancy J, et alInhibition of N-nitrosamine formation in drug products: A model study. J Pharm Sci.2021;110(12):3773-5.

    6. Indexed at, Google Scholar, Cross Ref

Get the App