Quality Assurance

Checklist for sample preparation by U.V. analysis

Checklist for sample preparation by U.V. analysis

Checklist for Do’s for U.V. analysis

  • Cells used for the analysis should be identical and transparent.
  • The solution whose U.V. reading is to be taken should be clear and transparent, it should not contain any foreign particles or fibres.
  • For analysis solvents used should be spectroscopic grade.
  • Where the solution is to be filtered it should be filtered twice and that solution should be discarded, after which the filtered solution should be used for U.V. reading.
  • In the case of volatile solvents, cuvettes should be covered with a lid while taking the reading.
  • Shake the solutions before taking UV reading & should free them from air bubbles.
  • While taking reading the lid of the sample holder chamber should be closed properly.
  • For colour development sample UV reading should take immediately.
  • Reagents used for colour development should be prepared freshly and should be free from foreign particles.

Checklist for Don’ts for U.V. analysis

  • Don’t use unidentical cells for analysis
  • Don’t use a solution for UV reading that has any foreign material/particles
  • Don’t use AR grade or HPLC grade reagents for analysis.
  • Don’t use the solution as such in cases Where the solution is to be filtered.
  • Don’t use cuvettes without lids in case of volatile solvents are used for analysis.
  • Don’t shake the solution at the time of taking the reading because air bubbles would form and would give a wrong reading.
  • Don’t open the lid of the sample holder chamber during reading
  • Don’t take readings if keep colour development samples are kept for a longer time.
  • Don’t use previously prepared reagent solution for Colour development analysis.

ABHA

Abha is the Author  of pharmaceutical guidance, she is a pharmaceutical professional having more than 22 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd. During his experience, she faces many regulatorily audits i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda, Kenya, Tanzania, Zimbabwe. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube